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Mol. Cells 2021; 44(10): 723-735

Published online October 31, 2021

https://doi.org/10.14348/molcells.2021.0055

© The Korean Society for Molecular and Cellular Biology

Goosecoid Controls Neuroectoderm Specification via Dual Circuits of Direct Repression and Indirect Stimulation in Xenopus Embryos

Zobia Umair1,3,4 , Vijay Kumar1,4 , Ravi Shankar Goutam1 , Shiv Kumar1 , Unjoo Lee2,* , and Jaebong Kim1,*

1Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University, Chuncheon 24252, Korea, 2Department of Electrical Engineering, Hallym University, Chuncheon 24252, Korea, 3Department of Molecular Medicine, School of Medicine, Gachon University, Incheon 21999, Korea, 4These authors contributed equally to this work.

Correspondence to : jbkim@hallym.ac.kr (JK); ejlee@hallym.ac.kr (UL)

Received: March 5, 2021; Revised: August 3, 2021; Accepted: August 16, 2021

This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.

Spemann organizer is a center of dorsal mesoderm and itself retains the mesoderm character, but it has a stimulatory role for neighboring ectoderm cells in becoming neuroectoderm in gastrula embryos. Goosecoid (Gsc) overexpression in ventral region promotes secondary axis formation including neural tissues, but the role of gsc in neural specification could be indirect. We examined the neural inhibitory and stimulatory roles of gsc in the same cell and neighboring cells contexts. In the animal cap explant system, Gsc overexpression inhibited expression of neural specific genes including foxd4l1.1, zic3, ncam, and neurod. Genome-wide chromatin immunoprecipitation sequencing (ChIP-seq) and promoter analysis of early neural genes of foxd4l1.1 and zic3 were performed to show that the neural inhibitory mode of gsc was direct. Site-directed mutagenesis and serially deleted construct studies of foxd4l1.1 promoter revealed that Gsc directly binds within the foxd4l1.1 promoter to repress its expression. Conjugation assay of animal cap explants was also performed to demonstrate an indirect neural stimulatory role for gsc. The genes for secretory molecules, Chordin and Noggin, were up-regulated in gsc injected cells with the neural fate only achieved in gsc uninjected neighboring cells. These experiments suggested that gsc regulates neuroectoderm formation negatively when expressed in the same cell and positively in neighboring cells via soluble factors. One is a direct suppressive circuit of neural genes in gsc expressing mesoderm cells and the other is an indirect stimulatory circuit for neurogenesis in neighboring ectoderm cells via secreted BMP antagonizers.

Keywords chordin, dorsal organizer, Gsc, Gsc response element, neuroectoderm, Noggin, transcriptional regulation, Xenopus

Spemann organizer has been established as a center of dorsal mesoderm in the early embryo; this is demonstrated by the organizer transplantation into the ventral side of another embryo, resulting in duplication of the body axis including the head and trunk (Cho et al., 1991; De Robertis et al., 2000; Nieto, 1999). In the same experiment, the duplicated complete axis contained well-organized body patterning of all three germ layers. This structural patterning of Spemann organizer was considered to be due to instructive signaling to induce neuroectoderm formation from the ectoderm. However, search for such instructive signal(s) led to the unexpected finding that instead of providing instructive signals, inhibitory signals emanate from the organizer. The main organizer genes including chordin, noggin, dkk, and cerberus have shown to be inhibitory for instructive signals such as Bmps, Wnts and Nodals (De Robertis et al., 2000; Nieto, 1999; Roskoski, 2020). Also for the organizer in frog, chick, mouse and fish, the organizer is dually active in neural and mesodermal specification. This is demonstrated with the transplanted organizer altering the fate of adjacent tissue/cells and modifying the dorsoventral and anteroposterior pattern of the developing embryos while the organizer maintains its own dorsal mesoderm property as the transplanted tissues always differentiate into chordamesoderm, lastly the notochord (Beddington and Robertson, 1999; De Robertis et al., 2000; Harland and Gerhart, 1997; Lemaire and Kodjabachian, 1996; Nieto, 1999; Yao and Kessler, 2001). Thus far, the mechanism(s) behind the aforementioned dual characteristics of the organizer have remained largely undefined.

Consistent with the conserved natured of the organizer across species, a conserved group of genes have been identified associated with the organizer. One of the first genes identified in the organizer was the homeobox transcription factor (TF) goosecoid (Cho et al., 1991). Gsc is one of the earliest genes expressed in the organizer and it replicates the inductive activities of the Spemann organizer found across the animal phyla, from hydra to human (Cho et al., 1991; Yao and Kessler, 2001), and a gain-of-function experiment by gsc injection to the ventral side remarkably mimics organizer function with complete axis duplication at the later stage (Cho et al., 1991). Gsc transcriptionally represses target genes including wnt8a and BMP signaling components identified in mouse, zebrafish and Xenopus (Artinger et al., 1997; Christian and Moon, 1993; Dixon Fox and Bruce, 2009; Fainsod et al., 1994; Latinkic and Smith, 1999; Latinkic et al., 1997; Seiliez et al., 2006; Steinbeisser et al., 1995; Yasuo and Lemaire, 2001). Binding of Gsc to DNA is via a paired-type homeodomain and it contains a repressor domain composed of a conserved N-terminal heptapeptide, also known as the engrailed homology domain of Gsc. As such, Gsc functions as a transcriptional repressor with several studies demonstrating a repressor activity for Gsc in cell culture and also in developing embryos (Danilov et al., 1998; Ferreiro et al., 1998; Latinkic and Smith, 1999; Mailhos et al., 1998; Smith and Jaynes, 1996).

Gsc is also one of the organizer genes responsible for dorso-ventral patterning (Niehrs et al., 1993). Introduction of gsc leads to dorsalization of embryos, while knock-down of gsc prevents head formation in Xenopus (Steinbeisser et al., 1995) and zebrafish embryos (Rivera-Perez et al., 1995). The expression pattern and repressor function of gsc suggest that gsc represses the genes interfering in the function of organizer or/or dorsal mesoderm differentiation (such as formation of chordamesoderm) (Christian and Moon, 1993; Fainsod et al., 1994; Steinbeisser et al., 1995). However, the direct target gene(s) of Gsc are still largely unexplored, especially for neuro-ectoderm specification. Although Gsc is a repressor TF, it also promotes neural fate of the neighboring dorsal ectodermal cells, leading to neuro-ectoderm in a “noncell-autonomous” manner (a small number of injected cells orchestrating additional uninjected neighboring cells). It is known that Gsc induces ectopic expression of chordin but not that of noggin (Sasai et al., 1994). Chordin and noggin are Bmp antagonizers which promote ectoderm to neuroectoderm formation (Kuroda et al., 2004; Sasai et al., 1994). With the cell-autonomous and noncell-autonomous regulation of the organizer genes in neuroectoderm and mesoderm specification requiring further study, gsc is a good candidate gene for such studies.

Foxd4l1.1 is a forkhead/winged helix TF that functions in a variety of differentiation processes (Jackson et al., 2010; Katoh et al., 2013; Katoh and Katoh, 2004; Pohl and Knochel, 2005). Foxd4l1.1 is one of the earliest genes expressed in the neuro-ectoderm as an upstream gene for various neural regulatory networks and it maintains the neural fate during gastrulation (Yan et al., 2009). Foxd4l1.1 functions to maintain undifferentiated neuro-ectoderm through suppression of neural inhibitory Bmp/Ventx1.1 axis and neural differentiation towards the neural plate (Fetka et al., 2000; Lee et al., 2009; Sullivan et al., 2001; Yan et al., 2009; Yu et al., 2002). Inhibition of Bmp also induces neuro-ectoderm specific earliest genes, foxd4l1.1 and zic3, in animal cap (AC) explants (Shim et al., 2005; Umair et al., 2018; Yoon et al., 2013; Yu et al., 2016). Foxd4l1.1 transcription is necessary to maintain the neuro-ectoderm. In addition, Foxd4l1.1 expression is up-regulated by over-expression of siamois and noggin (Sullivan et al., 2001) and down-regulated by neural inhibitory axis of Bmp-Ventx1.1 axis in ventral mesoderm and ectoderm (Yoon et al., 2014). Study of the transcriptional repression of foxd4l1.1 in the organizer (dorsal mesoderm) is still pending for identifying a role in proper patterning and maintenance of dorsal mesoderm (chordamesoderm) in normal embryogenesis.

In the present study, we hypothesized that organizer gene gsc displays the dual activity of being neural inhibitory as to maintain dorsal mesoderm in a cell-autonomous manner and being neural stimulatory to convert neighboring ectoderm to neuroectoderm in a noncell-autonomous manner. As expected, Gsc co-expression inhibited dominant negative BMP receptor (DNBR) and chordin/noggin mediated early and late neural-specific genes including foxd4l1.1, zic3, ncam, neurod, ngnr, and otx2 in AC explants. A genome-wide Xenopus chromatin immunoprecipitation sequencing (ChIP-seq) analysis of Gsc and promoter analysis of foxd4l1.1 showed that Gsc directly binds to the Gsc response cis-acting element (GRE) within the 5’-flanking upstream region of foxd4l1.1 and represses foxd4l1.1 transcription. Reporter gene assay and site-directed mutagenesis of foxd4l1.1 promoter constructs defined the GREs as directly inhibiting foxd4l1.1 transcription in Xenopus embryos. Noncell-autonomous and stimulatory roles of gsc in neuroectoderm formation were confirmed with conjugation assays of AC explants of gsc-injected and non-injected ACs. Collectively, these results suggest that Gsc is a direct repressor of foxd4l1.1 transcription in order to inhibit neurogenesis in the organizer/dorsal mesoderm while to promote neuroectoderm formation of dorsal ectoderm cells via gsc-stimulated positive regulation of chordin and noggin.

Ethics statement

This animal study was conducted in accordance with the regulations of the Institutional Animal Care and Use Committee (IACUC) of Hallym University (Hallym 2019-79, 2019-80). All the research members attended both the educational and training courses for the appropriate care and use of experimental animals at our institution in order to receive an animal use permit. Adult Xenopus laevis were grown and tended in approved containers, maintained at a 12-h light/dark (LD 12:12 h) cycle and 18°C ambient temperature, by authorized personnel and according to the guidelines of the Institute of Laboratory Animal Resources of Hallym University for laboratory animal maintenance.

DNA and RNA preparation

All mRNA used for this study were synthesized by linearizing the target vectors with the appropriate restriction enzymes, including Sp6/SacII for flag-gsc, Sp6/Acc651 for flag-chordin, Sp6/Not1 for noggin and Sp6/EcoR1 for DNBR constructs. Each vector was linearized with the appropriate restriction enzyme and used for in-vitro transcription using the MEGA script kit according to the manufacturer’s instructions (Ambion, USA). Synthetic mRNAs were quantified by a spectrophotometer at 260/280 nm wavelengths (SpectraMax; Molecular Devices, USA).

Cloning of genomic DNA

Cloning of Foxd4l1.1 and zic3 genomic DNA (gDNA) into the pGL3-Basic plasmid (Promega, USA) was performed as described previously (Lee et al., 2004).

Promoter constructs

The 5’-flanking region of reporter construct of foxd4l1.1 (1.5 kb) and zic3 (1.8 kb) in the pGL3-basic plasmid (Promega) were made by using specific restriction sites, KpnI/XhoI and KpnI/HindIII, respectively. Serially-deleted promoter constructs of foxd4l1.1 were generated and sub-cloned into a pGL3-basic plasmid by polymerase chain reaction (PCR) amplification (Table 1).

Embryo injection and explants culture

X. laevis were obtained from the Korean Xenopus Resource Center for Research (Korea). Xenopus embryos were injected after in vitro fertilization of oocytes, induced by injection of 500 units of human chorionic gonadotropin (Sigma, USA). RNAs were injected into the animal pole at the one or 2-cell stage embryos and cultured in 30% Marc’s Modified Ringer’s (MMR) solution. The ACs were then dissected from injected and un-injected embryos at stage 8.0-8.5 and incubated in 1X L-15 growth medium (Gibco/Thermo Fisher Scientific, USA) until stage 11 and 24 in preparation for reverse transcription PCR (RT-PCR).

RNA isolation and RT-PCR

DNBR mRNA (0.5 ng/embryo), chordin mRNA (0.5 ng/embryo), noggin (0.5 ng/embryo), and gsc (1 ng/embryo) were injected into the animal pole at the one or 2-cell stage of Xenopus embryos and cultured in 30% MMR solution. ACs were then dissected from the injected and un-injected embryos and incubated until stage 11 and 24 in 1X L-15 growth medium as described previously (Kumar et al., 2019). Total RNA was isolated from whole embryos and AC explants using RNA-Bee reagent, following the manufacturer’s instructions (Tel-Test, USA), and was then treated with DNase I to remove genomic DNA contamination. RT-PCR was performed with Superscript II (Invitrogen, USA) as described by the manufacturer and with 2 μg total RNA per reaction. PCR was performed according to the following conditions: 30 s at 94 °C, 30 s at each annealing temperature and 30 s at 72°C, all for with 20-30 cycles of amplification (Table 2).

Morpholino oligomers and activin treatment

Antisense morpholinos (MOs) for Chordin and Gsc were obtained having similar MOs sequences as previously reported (Oelgeschlager et al., 2003; Sander et al., 2007). Nog-MO1 had the sequence (5’-ATTTTGTGCAGCTGTGTGCAGCATG) and Nog-MO2 had the sequence (5’-TGAAAGTGAAGAATATTTAAGAGA). All MOs were obtained from Gene Tools (USA). For use, the MOs were diluted in sterile water and then heated at 65°C for 10 min before microinjections as described previously (Ryu et al., 2021). The harvested ACs were treated with activin (25 ng/ml) as described previously (Umair et al., 2020).

Whole mount in situ hybridization

Embryos were injected with mRNAs as indicated and subsequently processed for whole-mount in situ hybridization using standard methods with anti-sense probes for Foxd4l1.1 (Moore et al., 2004).

Luciferase assays

Relative promoter activities were measured using a luciferase assay system according to the manufacturer’s instructions (Promega) and were performed as previously described (Yoon et al., 2014). Five different groups of embryos (3 embryos per group) were harvested and homogenized in 10 μl lysis buffer per embryo. Embryo homogenates at 10 μl each were assayed with 40 μl luciferase substrate and the reporter gene activity was read by an illuminometer (Berthold Technologies, Germany). All experiments were repeated at least three times for independently derived sample sets.

Site-directed mutagenesis

Mutagenesis was performed by a site-directed mutagenesis kit (Muta-Direct; iNtRON Biotechnology, Korea) using primer oligonucleotides in accordance with the manufacturer’s instructions (Table 3).

Chromatin immunoprecipitation (ChIP)

Chromatin immunoprecipitation assay was performed as described previously (Blythe et al., 2009). Embryos were injected at one-cell stage with mRNA encoding 3Flag-Gsc (1 ng/embryo). Injected embryos were collected at stage 11 (100 embryos/sample) and processed according to protocol. Anti-Flag monoclonal antibodies (F-1804; Sigma) or normal mouse IgG (SC-2025; Santa Cruz Biotechnology, USA) were then added to the cell lysates to immune-precipitate the chromatin. ChIP-PCR was performed with the immune-precipitated chromatin using foxd4l1.1, promoter region primers for GRE. These primers are shown in (Table 4).

ChIP-sequencing analysis

The Gsc mRNA (0.5 ng/embryo) was injected at the one-cell stage. Approximately 1,000 embryos were harvested at stage 11. The ChIP assay was performed accordingly to a previously described method (Blythe et al., 2009). Total immunoprecipitated chromatin was sequenced by Macrogen (Korea), and raw data with short reads were received in FASTA format. Galaxy (https://usegalaxy.org), an online tool, was used for data analysis as described previously (Zhang et al., 2008). MACS call peak data were used for visualization, and Gsc coverage within the foxd4l1.1 and zic3 promoter region was plotted.

Conjugation assay

AC explants were dissected at stages 8 and conjugation of the two required AC explants together was in 30% MMR containing 50 mg/ml gentamycin. The recombinants were cultured for 40 min at 16°C to heal the torn ends of the tissue explants before being transferred to fresh L-15 media.

Statistical analysis

Data were analyzed by unpaired two-tailed Student’s t-test using GraphPad Prism9 (GraphPad Software, USA). Asterisks designations are ** for P ≤ 0.01 and *** for P ≤ 0.001. Non-significance was denoted as “ns”.

Gsc suppresses transcription of early and late neural genes expressed by dnbr, chordin, and noggin

Previous reports demonstrate that gsc is expressed in the dorsal organizer and involving dorsal mesoderm cells. The mesoderm cells expressing gsc sustain their mesodermal identity; however, they greatly influence the interacting neighbor cells (ectoderm) to adopt the neural fate, (Cho et al., 1991; De Robertis et al., 1992). These results indicate that gsc has dual roles of directly inhibiting neural gene expression in mesoderm territory and indirectly stimulating neural fate in neighboring ectoderm cells. To examine the role of Gsc on neural specific gene expression, gsc mRNA was co-injected with or without dnbr, chordin, and noggin. RT-PCR results showed that dnbr, which is known to inhibit BMP signaling and elicit neural genes, prompted expression of early neural marker genes including foxd4l1.1 and zic3, but did not increase those of organizer genes including chordin and noggin (Fig. 1A, lane 1 vs 4). While gsc (with or without introduced DNBR) strongly reduced the expression of early neural genes foxd4l1.1 and zic3 (Fig. 1A, lane 1 vs 2) as well as the neural repressor gene ventx1.1, ectopic gsc expression strongly induced chordin and noggin expression (Fig. 1A, lane 2 and 4). Similar results for neural gene expression were obtained when chordin/noggin combination, instead of DNBR, was injected (Fig. 1B). The ACs showed an elevated expression of foxd4l1.1 and zic3. However, ACs co-injected with gsc abolished neural gene expression (Fig. 1B, lane 1, 2, and 4). As expected, all samples injected with gsc, chordin, and noggin showed no expression of xbra, bmp4, and ventx1.1 (Fig. 1B, lane 1, 2, 3, and 4). These results suggest that gsc plays an inhibitory role in transcription of neural specific genes, which is consistent with previously known role of Gsc as a transcriptional repressor (Yao and Kessler, 2001). To investigate the consequences of gsc overexpression at later stage embryos, the late neural specific markers were also examined. Co-expression of gsc inhibited the expression of later neural genes including ncam, neurod, xngnr1, otx2, and krox2 expressed by dnbr injection (Fig. 1C, lane 1, 2, 3, and 4) and chordin and noggin (Fig. 1D, lane 1, 2, 3, and 4). In co-injected embryos, Gsc diminished ncam and neurod expression, whereas those for xngnr1 and otx2 were not much affected (Fig. 1D, lane 1, 2, 3, and 4). These suggest that xngnr1 and otx2 may not be direct targets of Gsc. In addition, whole mount in situ hybridization (WISH) analysis was performed in whole embryos to examine foxd4l1.1 expression with or without expressed gsc. The WISH results demonstrate that ectopic expression of gsc completely diminishes foxd4l1.1 expression in the injected embryos (Fig. 1E). Taken together, these results indicate gsc inhibits neural gene expression while inducing chordin and noggin expression in AC explants.

Multiple Gsc response elements within foxd4l1.1 promoter are detected using genome-wide ChIP-seq

Several independent studies demonstrate that Gsc has strong repressor activity through direct binding on cis-acting response element within target genes to block their transcription (Cho et al., 1991; Christian and Moon, 1993; Latinkic and Smith, 1999; Yasuo and Lemaire, 2001). To identify the neural specific gene(s) (foxd4l1.1 and zic3) as direct target(s) of gsc, genome wide ChIP-seq analysis was performed using gsc injected gastrula embryos (stage 11). Our ChIP-seq analysis showed that Gsc bound within upstream promoter region of early neural genes (foxd4l1.1 and zic3). Peak calling followed by coverage plot analysis done independently for foxd4l1.1 and zic3 genome sequences led to mapping of the putative binding sites in promoter regions of foxd4l1.1 and zic3 genome (Figs. 2A and 2B). We then selected foxd4l1.1 for a more detailed analysis of the repressive role of Gsc. Foxd4l1.1 is one of the earliest neural TFs that is highly expressed in neuroectoderm to maintain neural identity (Kumar et al., 2020; Neilson et al., 2012; Sherman et al., 2017; Yan et al., 2009). Foxd4l1.1 is one of the most critical genes responsible for neuroectoderm and ectoderm specification (Lee et al., 2014). Foxd4l1.1 is expressed in neuroectoderm cells of BMP inhibited AC explants and overexpression of foxd4l1.1 is sufficient to induce neurogenesis in the ectodermal explants of Xenopus embryos (Yoon et al., 2013). The analysis of ChIP-coverage region of Gsc revealed four putative GRE within upstream region of foxd4l1.1 coding sequences (Figs. 2D and 2E). These results indicate that foxd4l1.1 5’-flanking region may contain more than one GRE to exert repressor activity. Since X. laevis is an allotetraploid that contains two copies of foxd4l1.1 genome on chromosome (chr) 1l and 1s separately, the conserved regions between chr1l and chr1s were analyzed by homology search/alignment (BLAST) of both DNA sequences. Alignment results indicate conserved GRE containing regions (Fig. 2C) in both copies of foxd4l1.1 in chr1l and 1s. The results suggest that foxd4l1.1 and zic3 would be the direct target(s) of Gsc, where Gsc directly binds and negatively regulates the transcription of neural genes in gastrula embryos.

Site-direct mutagenesis of GRE within foxd4l1.1 promoter abolishes the repression activity of Gsc

As shown above, ChIP-seq results indicated putative GREs within foxd4l1.1 and zic3 promoter regions. To identify this functionally active GRE, 1551 bps long 5’-flanking region of foxd4l1.1 respect to putative transcription start site (TSS) was cloned into a reporter vector named foxd4l1.1(–1551). We then examined whether gsc indeed inhibited the relative reporter activity of foxd4l1.1(–1551). Foxd4l1.1(–1551) was injected at one-cell stage with or without dnbr and gsc. The reporter gene assay was performed at the embryonic stage 11. As expected, foxd4l1.1(–1551) relative reporter activity was significantly increased by dnbr (2.5 fold) while co-injection with gsc decreased the reporter activity down to 9 fold (Fig. 3A, bar 1 to 4). To map out the functionally active GRE within the foxd4l1.1(–1551) promoter, serially-deleted promoter constructs were created and sub-cloned into the reporter vector (Fig. 3B). All deleted constructs were then co-injected with or without gsc mRNA for reporter activity assays. Co-injection of gsc mRNA strongly reduced the relative reporter activities of all constructs from –1551 to –301 bps (by approximately 7 to 9 fold), while the reporter constructs containing –186 bps and –78 bps (foxd4l1.1(–186) and foxd4l1.1(–78)) showed no significant changes in the reporter activity assay (Fig. 3C, bar 1 to 14). The results indicate that the functional putative GRE would be between –301 to –186 bps (Fig. 3C, bar 9 to 12). Scrutinizing the sequences of foxd4l1.1(–1551) promoter region between –301 to –186 bps revealed one putative GRE at –218 to –213 bps (ACAAAG) from the putative TSS (Figs. 2D and 2E). To verify the GRE as an active cis-acting element for Gsc, we performed site-directed mutagenesis of GRE (ACAAAG to ACGGGG) in foxd4l1.1(–1551) and foxd4l1.1(–301) reporter constructs separately (Fig. 3D). The mutated foxd4l1.1(–1551)mGRE, foxd4l1.1(–301)mGRE and those wild type promoter constructs were then injected with or without gsc to evaluate the reporter activities. Results show that gsc mediated reduction in foxd4l1.1(–1551) and foxd4l1.1(–301) promoter activities were completely abolished in the mutated foxd4l1.1(–1551)mGRE and foxd4l1.1(–301)mGRE) constructs (Figs. 3E and 3F, lane 1 to 4). These results strongly indicate that functionally active consensus sequences for gsc (its GRE) was located in –218 to –213 bps region within foxd4l1.1(–1551) promoter where Gsc binds to inhibit transcription. We next examined whether Gsc directly bound within the proximal promoter region (–218 to –213 bps) of foxd4l1.1. To determine Gsc binding within foxd4l1.1 promoter, Flag-tagged Gsc construct (3Flag-gsc) was injected at one-cell stage and ChIP-PCR was performed at stage 11 in whole embryos. The results confirm that Gsc directly binds within the proximal region of endogenous foxd4l1.1 promoter (Fig. 3G). In addition, zic3(–1805) promoter was injected with or without gsc mRNA and the reporter assay was performed. As expected, the zic3(–1805) relative reporter activity was markedly reduced in gsc co-injected samples (Fig. 3H, bar 1 and 2). Taken together, these results collectively confirm that foxd4l1.1 promoter contains a cis-acting GRE (–218 to –213 bps) where Gsc directly binds and negatively regulates foxd4l1.1 transcription.

Gsc has dual roles of neural inhibition and stimulation in cell-autonomous and noncell-autonomous fashions, respectively

During early development, Gsc is known as a neural stimulator, probably through induction of chordin in a noncell-autonomous manner (Sander et al., 2007). Ectopic expression of gsc is known to induce a complete secondary axis including head (neural tissue) in ventral region of Xenopus embryos (De Robertis et al., 1992; Latinkic and Smith, 1999; Steinbeisser et al., 1995; Ulmer et al., 2017). However, Gsc also directly binds to within the proximal promoter region (–218 to –213 bps) of the early neural gene foxd4l1.1 to inhibit its transcription. To delineate these contradictory dual regulatory roles for Gsc in neural specification, we designed and performed a conjugation assay for AC explants. Xenopus AC cells are pluripotent in nature and in response to specific signals, AC cells are capable of generating distinct types of tissue, making them excellent for manipulation for developmental studies (Borchers and Pieler, 2010). We designed two different sets of conjugated ACs (described in Fig. 4A). In set-1, embryos were injected with and without foxd4l1.1(–1551) reporter gene separately into the embryos and ACs were then dissected at stage 8. Two ACs were then conjugated as shown in Fig. 4A. In set-2, the embryos were injected with gsc and foxd4l1.1(–1551) separately and those two separately dissected ACs were then conjugated (Fig. 4A). The relative reporter activity was then measured at embryonic stage 11. The results had the reporter activity of set-2 (foxd4l1.1(–1551)/gsc) being significantly higher (2.5 fold) than that of set-1 (foxd4l1.1(–1551)/NI) (Fig. 4B, set-1 vs set-2). These results indicated that Gsc is a stimulatory molecule for neural specification to neighboring ectoderm cells, while Gsc being a direct inhibitor of neural gene expression in cell autonomous manner. We then examined whether gsc would indeed inhibit the endogenous mRNA transcription of neural specific markers in conjugated AC. To ascertain this inhibitory effect of Gsc, we prepared 3 different sets of conjugated ACs (gsc/gsc, gsc/NI, and NI/NI; NI was the not injected control AC) (as depicted in Fig. 4C). The expressed genes were then analyzed by RT-PCR. As expected, AC conjugates of both gsc injected group (gsc/gsc) completely abolished or strongly reduced the expression of early neural marker genes (stage 11) including foxd4l1.1, zic3, fgf8a, chch, and ascl1 (Fig. 4D, lane 2 vs 3). In contrast, in AC conjugates of gsc injected and uninjected AC group (gsc/NI), the neural marker genes were markedly induced when compared to that of the uninjected control conjugates (NI/NI) (Fig. 4D, lane 3 vs 4). The results clearly show that gsc functions as a strong repressor of neural gene transcription in a cell-autonomous manner but a stimulator in noncell-autonomous manner. Noticeably, chordin and noggin expression were strongly increased under both conditions of gsc/gsc and gsc/NI conjugates. There were no significant differences in the expression levels of chordin and noggin in two groups of conjugates for gsc/gsc and gsc/NI (Fig. 4D, lane 2 vs 3), indicating that chordin and noggin expressions were inducible in gsc injected AC samples with gsc being a direct strong repressor of early neural target genes. Similarly, we investigated the expression pattern of late neural markers (stage 24) in the same samples. Neural markers including ncam and xngnr1 (pan-neural markers), xrox20 (mid-brain marker), and otx2 (anterior neural marker) were significantly increased in gsc and not-injected conjugates (gsc/NI) of ACs (Fig. 4E, lane 3 vs 4) when compared to that of conjugates of all NI (NI/NI). These markers were completely abolished in conjugates of both gsc injected group (gsc/gsc) (Fig. 4E, lane 2 vs 3), indicating again that gsc has an inhibitory effect on neural target gene expression. All three sets of AC conjugates were further evaluated using whole-mount in situ hybridization (WISH) with anti-foxd4l1.1 RNA probe. In support of RT-PCR results, the gsc/gsc conjugates showed no expression of foxd4l1.1 in either portions of conjugates. On the other hand, gsc/NI conjugates showed that only the NI portion of conjugated ACs showed strong expression of foxd4l1.1 (Fig. 4F). As expected, NI/NI conjugates showed no expression of foxd4l1.1 in either portions of the conjugates (Fig. 4F). Taken together, the results confirm that Gsc has dual roles of neural inhibition in cell-autonomous and stimulation in noncell-autonomous manner, respectively.

In the present study, we sought to define the role of the homeobox repressor gsc in neural specification as part of its functions in the organizer. The organizer (being dorsal mesoderm) maintains its mesodermal identity while having a stimulatory effect on the naive ectoderm above its layer to become neuroectoderm during gastrula stage of embryos, and we tried to tie a role for gsc in the mechanism for neural gene exclusion seen in the organizer region. With the organizer as dorsal mesoderm needing a mechanism for stimulating naïve ectoderm to neuroectoderm as well as maintaining mesoderm and/or preventing it from being alternate germ layers including ectoderm and/or neuroectoderm, we adopted gsc as a candidate gene possibly performing such dual activity for the organizer. Gsc is a repressive TF and a known factor for enhancing chordin (Sasai et al., 1994), a secretory factor inhibiting BMP and leading to neighboring ectoderm cells to neuroectoderm. We found that gsc, as an organizer specific TF, repressed foxd4l1.1, a neural specific TF. We have previously found that repressive neural and non-neural TFs (foxd4l1.1 vs ventx1.1) are mutually antagonistic in specifying the non-neural versus neural ectoderm activation areas of the nucleus (Kumar et al., 2020). We selected and focused on foxd4l1.1 for the hypothesis that a TF in a distinct germ layer protects it from becoming another type of germ layer. In this view, gsc, a critical TF of dorsal mesoderm (organizer), protects the expression of foxd4l1.1, a critical TF of neuroectoderm. Thus, Gsc protects dorsal mesoderm (organizer) from becoming a neuroectoderm through foxd4l1.1. In addition, AC conjugation experiments demonstrated that gsc induction was neural stimulatory in a noncell-autonomous manner. Together, our results suggest that Gsc is an organizer specific factor performing dual roles of organizer in neural specification. Specifically, Gsc is a repressive TF to protect dorsal mesoderm from expressing neural genes as well as a stimulatory factor of neighboring neuro-ectoderm via expression of chordin and noggin. The implication and interpretation of this study is discussed below in the point of view of representative repressor TFs preserving each germ layer of dorsal and ventral mesoderm as well as dorsal (neural ectoderm) and ventral ectoderm (non-neural ectoderm).

We have previously reported on various mechanisms existing in reciprocally exclusive germ-layer specifications in early vertebrate embryogenesis (ectoderm, mesoderm and neuroectoderm) (Kumar et al., 2020). In the ventral mesoderm and ectoderm region, neural repressor ventx1.1 is expressed and it inhibits neuroectoderm specific genes including foxd4l1.1 and zic3 (Umair et al., 2018). On the other hand, the neuroectoderm region requires the neuroectoderm specific repressor foxd4l1.1 to inhibit the neural repressor ventx1.1 expression (Kumar et al., 2020). These studies suggested reciprocal repression of ventx1.1 and foxd4l1.1 being at least part of specifying mechanisms for non-neural versus neural ectoderm fate specification in Xenopus embryos (Kumar et al., 2020; Umair et al., 2018). In the present study, we asked whether the two adjacent layers of organizer and neuro-ectoderm cells also follow such a mechanism of reciprocal repression in gastrula embryos, especially in the dorsal mesoderm territory (the Spemann organizer) (De Robertis and Kuroda, 2004; Harland, 2000; Nieuwkoop and Nigtevecht, 1954; Spemann, 1967). Here, we found that gain-of-function study of gsc pointed to gsc acting as a strong repressor in dnbr, chordin, and noggin mediated neuroectoderm formation in AC explants. A direct binding of Gsc in an early neural specific gene foxd4l1.1 was also demonstrated in ChIP-seq and reporter gene analysis of gastrula embryos. Gsc-mediated repression of the neural specific repressor TF Foxd4l1.1 is important in protecting the organizer from expressing nonspecific neural genes as well as maintaining organizer as gsc expressing dorsal mesoderm.

From our preliminary findings, Gsc promoter also contained the direct binding response element for Foxd4l1.1 (from Chip-seq and reporter assay of Gsc promoter) (unpublished data). Whether a reciprocal repression of gsc and foxd4l1.1 is the underlying mechanism for the non-neural organizer versus neural ectoderm fate specification in Xenopus embryos, it requires more elaboration; more immediately, any repressive functions of Foxd4l1.1 on gsc expression in neuro-ectoderm needs to be demonstrated. We designed and performed loss-of function studies for proof of Gsc’s neural repressive role in activin treated AC system. In activin treated AC explants, one may expect increased expression for the neuroectoderm gene foxd4l1.1, and actually gsc MO injected ACs had decreased foxd4l1.1 expression under the activin treated condition. Gsc MO also led to increase a neural repressor ventx1.1 expression compared to the activin treated condition without the Gsc MO. The effects of gsc depletion on expression of foxd4l1.1 in the organizer could have been shown. However, previous work (Sander et al., 2007) has indicated that gsc depletion increases neural repressor gene ventx1.1 and ventx2.1 levels. A gsc MO experiment may lead to neural gene repression in the whole embryos. Our experiments with AC explants allowed certain conditions that were practical to be implemented (such for “activin treated” cases). The results indicated in the activin treated setup was similar to the previous experiment in whole embryos and the results using noggin/chordin MOs were similar to that of Gsc MO (Supplementary Fig. S1A, lane 1 and 2). The Gsc knockdown results supported Gsc suppressing neural genes when Gsc is overexpressed under bmp inhibition in activin treated AC explants (Supplementary Fig. S1A, lane 3 and 4). Taken together, Gsc/noggin/chordin depletion experiments point to a suppressive role for goosecoid and a stimulatory role for noggin/chordin in neuroectoderm formation. It is still need to investigate gsc neural repressive role along with cross-examination of other organizer TFs and signaling molecules in the developing organizer of gastrula embryos. Based on the present results, however, we propose this depicted model for Gsc inhibiting the neural TF foxd4l1.1 in its expressed territory of the organizer, but also inducing secreted Chordin and Noggin, to induce neurogenesis in target tissues (Fig. 5).

In this study, we adopted gsc as an organizer specific gene TF to study the dual inhibitory and stimulatory roles of organizer in neural specification. The reasons on why we selected gsc are the following: First, gsc is the first organizer TF to be recognized as only expressed in the underlying layer of organizer but not in the above layers of the neuroectoderm in gastrula stage of embryos (Cho et al., 1991). Second, gsc is a repressor TF, which would protect the organizer as dorsal mesoderm from expressing neural genes including neural specific repressor TF foxd4l1.1. Third, gsc has been known to induce ectopic expression of chordin. Fourth, overexpression of gsc in ventral side of embryo leads to complete axis duplication including neural tissues of head, indicating somehow the stimulatory role of gsc in neural specification (Dixon Fox and Bruce, 2009; Kuroda et al., 2004; Sander et al., 2007; Seiliez et al., 2006; Yao and Kessler, 2001).

Gsc as an organizer specific repressor TF has been studied in the context of dorso-ventral specification as well as a factor in protecting the organizer by repression of signaling molecules including BMP and Wnt8 (Yao and Kessler, 2001). Gsc has been proposed as a central TF involved in mesoderm patterning (Niehrs et al.,1994). Although showing a direct reciprocal repression between dorsal and ventral specific homeobox genes gsc and ventx1.1/ventx2.1 awaits more studies, involvement of the genes has been demonstrated in dorsoventral patterning of mesoderm by both gain-of function (Cho et al., 1991) and loss-of function (Steinbeisser et al., 1995) studies. Gsc has been suggested as an important TF in dorsoventral patterning, possibly through reciprocal repression of the genes to mediate a self-adjusting mechanism (Sander et al., 2007). Although the studies of gsc have focused on dorso-ventral specification as an organizer repressor gene as well as neuro-ectoderm specification as possibly an indirect inducer of neural stimulatory gene chordin (Sander et al., 2007; Sasai et al., 1994), gsc has not been adequately examined as a direct repressor of neural genes, and the reports have also focused on dorsoventral patterning and not much on organizer/neuroectoderm specification (Thisse et al., 1994).

Additional studies have mainly focused on neural stimulatory effect of Gsc through induction of neural stimulatory factor chordin, possibly through an indirect effect of gsc in chordin expression (Cho et al., 1991; De Robertis and Kuroda, 2004; Sander et al., 2007; Sasai et al., 1994). In the present work, we found that gsc overexpression increased ectopic expression of chordin, as ACs obtained from gsc injected embryos expressed both BMP antagonizer chordin and noggin in AC explants (Fig. 4D); this is different from the report where Gsc induced ectopic expression of chordin but not that of noggin in gsc-injected at 8 cell stage embryos (Sasai et al., 1994). At the present time, we cannot address the exact reason why gsc injection leads to the differences in chordin and noggin expression in AC cells and whole embryos. These may be due to differences for their mode of activation (Sasai et al., 1994). We actually elaborated the expression mode of chordin using the isolated 2.25 kbs in length chordin promoter. The isolated promoter contained a primary response elements for Smad2 and Smad3 of activin signaling, which is slightly different that from Sasai et al. (1994) where chordin was reported as a secondary response gene requiring de novo protein synthesis. In addition, our isolated promoter contained a strong positive cis-acting element of Gsc (GRE) adjacent to the Smad2 and Smad3 response cis-acting elements in the distal region of chordin promoter (Kumar et al., 2021). These results indicate that Gsc functions as a repressor as well as an activator in a context dependent and cell specific manner. Chordin and noggin expression needs more scrutinizing; however, ACs from gsc injected embryos expressed both chordin and noggin, supporting our hypothesis that gsc functions as a neural stimulatory factor via inducing chordin and noggin expression in a noncell-autonomous manner.

In the present paper, we sought to explain the dual roles of the organizer in neuroectoderm specification in the context of the functional activity of the organizer specific TF gsc. The present finding of cell-autonomous and noncell-autonomous regulation of organizer gene in neuroectoderm and mesoderm specification, however, needs further elaboration. The present work suggests that Gsc represses the neural specific gene foxd4l1.1. This, along with our preliminary findings on foxd4l1.1 repression of Gsc promoter (from Chip-seq and reporter assays of Gsc promoter) (unpublished data), a reciprocal repression of gsc and foxd4l1.1 is thought to be the underlying mechanism for the non-neural organizer versus neural ectoderm fate specification in Xenopus embryos. In addition, the results of Gsc repression of ventx1.1 (Fig. 1A) and our previous results of ventx1.1 repression of gsc (Hwang et al., 2003) support the premise of a reciprocal repression existing between ventx1.1 and gsc for ventral and dorsal patterning. A study on the mutual opposing roles of Gsc and Vent homeobox genes in patterning the mesoderm of Xenopus embryo has been reported (Sander et al., 2007). Although it requires further investigation, from our previous and current findings, we propose a reciprocal repressive mechanism for the master repressor TFs including gsc, ventx1.1 and foxd4l1.1 in protecting the organizer, the ventral mesoderm/ectoderm and the neuroectoderm, respectively.

This article was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF), which is funded by the Ministry of Education, Science, and Technology of Korea (2016R1D1A1B02008770, 2018M3C7A1056285, and 2021M3H9A1097557).

Z.U. and V.K. performed the experiments and wrote the primary manuscript. J.K. and U.L. designed and supervised the study. R.S.G. and S.K. contributed to the data analysis and revision of the manuscript.

The authors have no potential conflicts of interest to disclose.

Fig. 1. InhibitIon of neural gene expression either mediated by dnbr or chordin and noggin (Chrd/Nog) in AC explants of Xenopus.
3Flag-gsc (1 ng/embryo), dnbr (0.5 ng/embryo), chordin (0.5 ng/embryo) and noggin (0.5 ng/embryo) (Chrd/Nog) were injected at one-cell stage and the AC explants were dissected at stage 8 to grow until (A and B) stage 11 and (C and D) stage 24. The expression profiles of different germ layer specific marker genes were analyzed by RT-PCR. No RT (no reverse transcriptase added) served as a negative control while WE (whole embryos) served a positive control. (E) 3Flag-gsc (1 ng/embryo) mRNA was injected into one cell embryos, and the injected embryos and non-injected ones (control) were processed for whole mount in situ hybridization (WISH) with anti-sense foxd4l1.1 probe at stage 11.
Fig. 2. Identification of GREs within the neural target genes using ChIP-seq of 3Flag-gsc injected Xenopus embryos. (A and B) Coverage plot of 3Flag-gsc within the foxd4l1.1 and zic3 promoter regions. (C) Similarity within both (chr1s and chr1l) copies of foxd4l1.1 promoter region are shown. The active GRE (–213 to –218 bps) location is highlighted by an arrow. (D) Putative GREs revealed within the foxd4l1.1 promoter region by ChIP-sequencing. (E) Consensus binding motifs of Gsc within both (chr1s and chr1l) copies of foxd4l1.1 promoter region.
Fig. 3. Abolishment of the repressional activity of Gsc by site-directed mutagenesis of GRE within the foxd4l1.1(–1551) reporter construct. (A) foxd4l1.1(–1551) (40 pg/embryo), dnbr (1 ng/embryo), and 3Flag-gsc (1 ng/embryo) were injected at one-cell stage and reporter assay was performed at stage 11. RLU, relative reporter activity. (B) Schematic representation of serially-deleted foxd4l1.1(–1551) promoter constructs. (C) Serially-deleted foxd4l1.1 (40 pg/embryo) promoter constructs were injected with and without 3Flag-gsc (1 ng/embryo) at one-cell stage and relative promoter activity were measured at stage 11. (D) Site-directed mutagenesis scheme for foxd4l1.1(–1551) and foxd4l1.1(–301) promoter constructs, target sequences highlighted (red color and italic). (E and F) Relative reporter assay of foxd4l1.1(–1551), foxd4l1.1(–1551)mGRE, foxd4l1.1(–301), and foxd4l1.1(–301)mGRE with or with gsc were performed at stage 11. (G) 3Flag-gsc was injected at one-cell stage and ChIP-PCR was performed at stage 11. Specific primers of Foxd4l1.1 promoter region (containing GRE) were used for amplification, while ventx2.1 served as negative control. (H) zic3(–1805) reporter construct was injected (40 pg/embryo) with or without 3Flag-gsc (1 ng/embryo) and reporter assay was performed at stage 11. **P ≤ 0.01; ****P ≤ 0.0001; ns, non-significance.
Fig. 4. A dual role of Gsc in transcriptional regulation of foxd4l1.1. In all experiments, 3Flag-gsc (1 ng/embryo) and foxd4l1.1(-1551) (40 pg/embryo) were injected at one-cell stage and the ACs were dissected at stage 8 to grow until stage 11 and 24. (A) Conjugation scheme for AC explants used. (B) The relative promoter activity are measured. RLU, relative reporter activity. ****P ≤ 0.0001. (C) Schematic description of the conjugated AC explants of the embryos injected with 3Flag-gsc and NI. The expression profiles of (D) early (stage 11) and (E) late (stage 24) neural marker genes were analyzed by RT-PCR. No RT (no reverse transcriptase added) served as a negative control while WE (whole embryos) served as positive control. (F) Whole mount in situ hybridization (WISH) was performed with anti-sense foxd4l1.1 probe of at stage 11.
Fig. 5. Schematic diagram depicting the dual role of Gsc in early neurogenesis. In mesoderm (dorsal organizer), Gsc inhibits the neural genes while strongly induces chordin and noggin expression. Newly translated Chordin and Noggin diffuse to neighboring cells (ectoderm) where they induce neurogenesis in a BMP inhibited manner.
Table 1.

Primers used for serially-deleted FoxD5b reporter gene constructs

PrimerPrimer nameSequence
Upstream primerFoxd4l1.1(–1551)5’-CCGGTACCTAGAGGTTGGATAAAGTCAATTGC-3’
Foxd4l1.1(–1316)5’-CCGGTACCTATATGCAGAGCTGCTAATAGTC-3’
Foxd4l1.1(–1016)5’-CCGGTACCTATATGCAGAGCTGCTAATAGTC-3’
Foxd4l1.1(–816)5’-CCGGTACCTAGAATTCCAGTTCCCATAATC-3’
Foxd4l1.1(–301)5’-CCGGTACCTTGGATTGCAAGTTAGTGGCTC-3’
Foxd4l1.1(–186)5’-GGGGTACCTTCATTCAGCAAAAGCACAGCC-3’
Foxd4l1.1(–78)5’-GGGGTACCAATTCAAGTGCAGATGACTGCC-3’
Downstream primerFoxd4l1.1-R5’-ATCTCGAGGCTTGGTTGGCAGTAAGTAG-3’

Table 2.

Primers used for RT-PCR amplification

Gene nameSequenceAnnealing temperature (°C)Cycle
zic3F5’-TCTCAGGATCTGAACACCT-3’4528
R5’-CCCTATAAGACAAGGAATAC-3’
Foxd4l1.1F5’-ACTCTATCAGGCACAACCTGTC-3’5030
R5’-GGTCTGTAGTAAGGCAGAGAGT-3’
xbraF5’-GGATCGTTATCACCTCTG-3’5725
R5’-GTGTAGTCTGTAGCAGCA-3’
Fgf8aF5’-CTGGTGACCGACCAACTAAG-3’5528
R5’-TGCGAACTCTGCTTCCAAAC-3’
chchF5’-ATGTGCGGAGGCTGCGTC-3’6027
R5’-CGTGGGTCATCGGGTAGAAC-3’
ascl1F5’-GAGCTGATGAGGTGCAAGAG-3’6027
R5’-TTTGCTCATCTTCTTGTTGG-3’
ncamF5’-CACAGTTCCACCAAATGC-3’5729
R5’-GGAATCAAGCGGTACAGA-3’
xngnr1F5’-GGATGGTGCTGCTACCGTGCGAGTACC-3’6530
R5’-CAAGCGCAGAGTTCAGGTTGTGCATGC-3’
otx2F5’-GGATGGATTTGTTGCACCAGTC-3’5727
R5’-CACTCTCCCAGCTCACTTCTC-3’
xk81F5’-TGGTGTTGAACAAGTGCAGG-3’5725
R5’-ACCTCCTCGACAATGGTCTT-3’
krox20F5’-AACCGCCCCAGTAAGACC-3’5728
R5’-GTGTCAGCCTGTCCTGTTAG-3’
neurodF5’-GTGAAATCCCAATAGACACC-3’5728
R5’-TTCCCCATATCTAAAGGCAG-3’
HoxB9F5’-TACTTACGGGCTTGGCTGGA-3’6826
R5’-AGCGTGTAACCAGTTGGCTG-3’
gscF5’-GCTGATTCCACCAGTGCCTCACCAG-3’6030
R5’-GGTCCTGTGCCTCCTCCTCCTCCTG-3’
nogginF5’-AGTTGCAGATGTGGCTCT-3’5727
R5’-AGTCCAAGAGTCTGAGCA-3’
chordinF5’-TTAGAGAGGAGAGCAACTCGGGCAAT-3’5725
R5’-GTGCTCCTGTTGCGAAACTCTACAGA-3’
bmp4F5’-CATCATGATTCCTGGTAACCGA-3’5725
R5’-CTCCATGCTGATATCGTGCAG-3’
ventx1.1F5’-CCTTCAGCATGGTTCAACAG-3’5726
R5’-CATCCTTCTTCCTTGGCATC-3’
ef1αF5’-CCTGAATCACCCAGGCCAGATTGTG-3’5719
R5’-GAGGGTACTCTGAGAAAGCTCTCCACG-3’
odcF5’-GTCAATGATGGAGTGTATGGATC-3’5525
R5’-TCCATTCCGCTCTCCTGAGCAC-3’

Table 3.

Primers used for site-directed mutagenesis

Mutated sitePrimer nameSequence
GREFoxd4l1.1mGREF5’-GGACCCTCTCACGTGGGAGCTTATCTGATAR-3’
R5’-TATCAGATAAGCTCCCACGTGAGAGGGTCC-3’

Table 4.

Primers used for ChIP-PCR assay

Prime nameSequenceAnnealing temperature (°C)Cycle
Foxd4l1.1ChIP-GREF5’-ACCTTGTTGGACTACAGATTC-3’5230
R5’-CAGTCATCTGCACTTGAATTGG-3’

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Article

Research Article

Mol. Cells 2021; 44(10): 723-735

Published online October 31, 2021 https://doi.org/10.14348/molcells.2021.0055

Copyright © The Korean Society for Molecular and Cellular Biology.

Goosecoid Controls Neuroectoderm Specification via Dual Circuits of Direct Repression and Indirect Stimulation in Xenopus Embryos

Zobia Umair1,3,4 , Vijay Kumar1,4 , Ravi Shankar Goutam1 , Shiv Kumar1 , Unjoo Lee2,* , and Jaebong Kim1,*

1Department of Biochemistry, Institute of Cell Differentiation and Aging, College of Medicine, Hallym University, Chuncheon 24252, Korea, 2Department of Electrical Engineering, Hallym University, Chuncheon 24252, Korea, 3Department of Molecular Medicine, School of Medicine, Gachon University, Incheon 21999, Korea, 4These authors contributed equally to this work.

Correspondence to:jbkim@hallym.ac.kr (JK); ejlee@hallym.ac.kr (UL)

Received: March 5, 2021; Revised: August 3, 2021; Accepted: August 16, 2021

This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/.

Abstract

Spemann organizer is a center of dorsal mesoderm and itself retains the mesoderm character, but it has a stimulatory role for neighboring ectoderm cells in becoming neuroectoderm in gastrula embryos. Goosecoid (Gsc) overexpression in ventral region promotes secondary axis formation including neural tissues, but the role of gsc in neural specification could be indirect. We examined the neural inhibitory and stimulatory roles of gsc in the same cell and neighboring cells contexts. In the animal cap explant system, Gsc overexpression inhibited expression of neural specific genes including foxd4l1.1, zic3, ncam, and neurod. Genome-wide chromatin immunoprecipitation sequencing (ChIP-seq) and promoter analysis of early neural genes of foxd4l1.1 and zic3 were performed to show that the neural inhibitory mode of gsc was direct. Site-directed mutagenesis and serially deleted construct studies of foxd4l1.1 promoter revealed that Gsc directly binds within the foxd4l1.1 promoter to repress its expression. Conjugation assay of animal cap explants was also performed to demonstrate an indirect neural stimulatory role for gsc. The genes for secretory molecules, Chordin and Noggin, were up-regulated in gsc injected cells with the neural fate only achieved in gsc uninjected neighboring cells. These experiments suggested that gsc regulates neuroectoderm formation negatively when expressed in the same cell and positively in neighboring cells via soluble factors. One is a direct suppressive circuit of neural genes in gsc expressing mesoderm cells and the other is an indirect stimulatory circuit for neurogenesis in neighboring ectoderm cells via secreted BMP antagonizers.

Keywords: chordin, dorsal organizer, Gsc, Gsc response element, neuroectoderm, Noggin, transcriptional regulation, Xenopus

INTRODUCTION

Spemann organizer has been established as a center of dorsal mesoderm in the early embryo; this is demonstrated by the organizer transplantation into the ventral side of another embryo, resulting in duplication of the body axis including the head and trunk (Cho et al., 1991; De Robertis et al., 2000; Nieto, 1999). In the same experiment, the duplicated complete axis contained well-organized body patterning of all three germ layers. This structural patterning of Spemann organizer was considered to be due to instructive signaling to induce neuroectoderm formation from the ectoderm. However, search for such instructive signal(s) led to the unexpected finding that instead of providing instructive signals, inhibitory signals emanate from the organizer. The main organizer genes including chordin, noggin, dkk, and cerberus have shown to be inhibitory for instructive signals such as Bmps, Wnts and Nodals (De Robertis et al., 2000; Nieto, 1999; Roskoski, 2020). Also for the organizer in frog, chick, mouse and fish, the organizer is dually active in neural and mesodermal specification. This is demonstrated with the transplanted organizer altering the fate of adjacent tissue/cells and modifying the dorsoventral and anteroposterior pattern of the developing embryos while the organizer maintains its own dorsal mesoderm property as the transplanted tissues always differentiate into chordamesoderm, lastly the notochord (Beddington and Robertson, 1999; De Robertis et al., 2000; Harland and Gerhart, 1997; Lemaire and Kodjabachian, 1996; Nieto, 1999; Yao and Kessler, 2001). Thus far, the mechanism(s) behind the aforementioned dual characteristics of the organizer have remained largely undefined.

Consistent with the conserved natured of the organizer across species, a conserved group of genes have been identified associated with the organizer. One of the first genes identified in the organizer was the homeobox transcription factor (TF) goosecoid (Cho et al., 1991). Gsc is one of the earliest genes expressed in the organizer and it replicates the inductive activities of the Spemann organizer found across the animal phyla, from hydra to human (Cho et al., 1991; Yao and Kessler, 2001), and a gain-of-function experiment by gsc injection to the ventral side remarkably mimics organizer function with complete axis duplication at the later stage (Cho et al., 1991). Gsc transcriptionally represses target genes including wnt8a and BMP signaling components identified in mouse, zebrafish and Xenopus (Artinger et al., 1997; Christian and Moon, 1993; Dixon Fox and Bruce, 2009; Fainsod et al., 1994; Latinkic and Smith, 1999; Latinkic et al., 1997; Seiliez et al., 2006; Steinbeisser et al., 1995; Yasuo and Lemaire, 2001). Binding of Gsc to DNA is via a paired-type homeodomain and it contains a repressor domain composed of a conserved N-terminal heptapeptide, also known as the engrailed homology domain of Gsc. As such, Gsc functions as a transcriptional repressor with several studies demonstrating a repressor activity for Gsc in cell culture and also in developing embryos (Danilov et al., 1998; Ferreiro et al., 1998; Latinkic and Smith, 1999; Mailhos et al., 1998; Smith and Jaynes, 1996).

Gsc is also one of the organizer genes responsible for dorso-ventral patterning (Niehrs et al., 1993). Introduction of gsc leads to dorsalization of embryos, while knock-down of gsc prevents head formation in Xenopus (Steinbeisser et al., 1995) and zebrafish embryos (Rivera-Perez et al., 1995). The expression pattern and repressor function of gsc suggest that gsc represses the genes interfering in the function of organizer or/or dorsal mesoderm differentiation (such as formation of chordamesoderm) (Christian and Moon, 1993; Fainsod et al., 1994; Steinbeisser et al., 1995). However, the direct target gene(s) of Gsc are still largely unexplored, especially for neuro-ectoderm specification. Although Gsc is a repressor TF, it also promotes neural fate of the neighboring dorsal ectodermal cells, leading to neuro-ectoderm in a “noncell-autonomous” manner (a small number of injected cells orchestrating additional uninjected neighboring cells). It is known that Gsc induces ectopic expression of chordin but not that of noggin (Sasai et al., 1994). Chordin and noggin are Bmp antagonizers which promote ectoderm to neuroectoderm formation (Kuroda et al., 2004; Sasai et al., 1994). With the cell-autonomous and noncell-autonomous regulation of the organizer genes in neuroectoderm and mesoderm specification requiring further study, gsc is a good candidate gene for such studies.

Foxd4l1.1 is a forkhead/winged helix TF that functions in a variety of differentiation processes (Jackson et al., 2010; Katoh et al., 2013; Katoh and Katoh, 2004; Pohl and Knochel, 2005). Foxd4l1.1 is one of the earliest genes expressed in the neuro-ectoderm as an upstream gene for various neural regulatory networks and it maintains the neural fate during gastrulation (Yan et al., 2009). Foxd4l1.1 functions to maintain undifferentiated neuro-ectoderm through suppression of neural inhibitory Bmp/Ventx1.1 axis and neural differentiation towards the neural plate (Fetka et al., 2000; Lee et al., 2009; Sullivan et al., 2001; Yan et al., 2009; Yu et al., 2002). Inhibition of Bmp also induces neuro-ectoderm specific earliest genes, foxd4l1.1 and zic3, in animal cap (AC) explants (Shim et al., 2005; Umair et al., 2018; Yoon et al., 2013; Yu et al., 2016). Foxd4l1.1 transcription is necessary to maintain the neuro-ectoderm. In addition, Foxd4l1.1 expression is up-regulated by over-expression of siamois and noggin (Sullivan et al., 2001) and down-regulated by neural inhibitory axis of Bmp-Ventx1.1 axis in ventral mesoderm and ectoderm (Yoon et al., 2014). Study of the transcriptional repression of foxd4l1.1 in the organizer (dorsal mesoderm) is still pending for identifying a role in proper patterning and maintenance of dorsal mesoderm (chordamesoderm) in normal embryogenesis.

In the present study, we hypothesized that organizer gene gsc displays the dual activity of being neural inhibitory as to maintain dorsal mesoderm in a cell-autonomous manner and being neural stimulatory to convert neighboring ectoderm to neuroectoderm in a noncell-autonomous manner. As expected, Gsc co-expression inhibited dominant negative BMP receptor (DNBR) and chordin/noggin mediated early and late neural-specific genes including foxd4l1.1, zic3, ncam, neurod, ngnr, and otx2 in AC explants. A genome-wide Xenopus chromatin immunoprecipitation sequencing (ChIP-seq) analysis of Gsc and promoter analysis of foxd4l1.1 showed that Gsc directly binds to the Gsc response cis-acting element (GRE) within the 5’-flanking upstream region of foxd4l1.1 and represses foxd4l1.1 transcription. Reporter gene assay and site-directed mutagenesis of foxd4l1.1 promoter constructs defined the GREs as directly inhibiting foxd4l1.1 transcription in Xenopus embryos. Noncell-autonomous and stimulatory roles of gsc in neuroectoderm formation were confirmed with conjugation assays of AC explants of gsc-injected and non-injected ACs. Collectively, these results suggest that Gsc is a direct repressor of foxd4l1.1 transcription in order to inhibit neurogenesis in the organizer/dorsal mesoderm while to promote neuroectoderm formation of dorsal ectoderm cells via gsc-stimulated positive regulation of chordin and noggin.

MATERIALS AND METHODS

Ethics statement

This animal study was conducted in accordance with the regulations of the Institutional Animal Care and Use Committee (IACUC) of Hallym University (Hallym 2019-79, 2019-80). All the research members attended both the educational and training courses for the appropriate care and use of experimental animals at our institution in order to receive an animal use permit. Adult Xenopus laevis were grown and tended in approved containers, maintained at a 12-h light/dark (LD 12:12 h) cycle and 18°C ambient temperature, by authorized personnel and according to the guidelines of the Institute of Laboratory Animal Resources of Hallym University for laboratory animal maintenance.

DNA and RNA preparation

All mRNA used for this study were synthesized by linearizing the target vectors with the appropriate restriction enzymes, including Sp6/SacII for flag-gsc, Sp6/Acc651 for flag-chordin, Sp6/Not1 for noggin and Sp6/EcoR1 for DNBR constructs. Each vector was linearized with the appropriate restriction enzyme and used for in-vitro transcription using the MEGA script kit according to the manufacturer’s instructions (Ambion, USA). Synthetic mRNAs were quantified by a spectrophotometer at 260/280 nm wavelengths (SpectraMax; Molecular Devices, USA).

Cloning of genomic DNA

Cloning of Foxd4l1.1 and zic3 genomic DNA (gDNA) into the pGL3-Basic plasmid (Promega, USA) was performed as described previously (Lee et al., 2004).

Promoter constructs

The 5’-flanking region of reporter construct of foxd4l1.1 (1.5 kb) and zic3 (1.8 kb) in the pGL3-basic plasmid (Promega) were made by using specific restriction sites, KpnI/XhoI and KpnI/HindIII, respectively. Serially-deleted promoter constructs of foxd4l1.1 were generated and sub-cloned into a pGL3-basic plasmid by polymerase chain reaction (PCR) amplification (Table 1).

Embryo injection and explants culture

X. laevis were obtained from the Korean Xenopus Resource Center for Research (Korea). Xenopus embryos were injected after in vitro fertilization of oocytes, induced by injection of 500 units of human chorionic gonadotropin (Sigma, USA). RNAs were injected into the animal pole at the one or 2-cell stage embryos and cultured in 30% Marc’s Modified Ringer’s (MMR) solution. The ACs were then dissected from injected and un-injected embryos at stage 8.0-8.5 and incubated in 1X L-15 growth medium (Gibco/Thermo Fisher Scientific, USA) until stage 11 and 24 in preparation for reverse transcription PCR (RT-PCR).

RNA isolation and RT-PCR

DNBR mRNA (0.5 ng/embryo), chordin mRNA (0.5 ng/embryo), noggin (0.5 ng/embryo), and gsc (1 ng/embryo) were injected into the animal pole at the one or 2-cell stage of Xenopus embryos and cultured in 30% MMR solution. ACs were then dissected from the injected and un-injected embryos and incubated until stage 11 and 24 in 1X L-15 growth medium as described previously (Kumar et al., 2019). Total RNA was isolated from whole embryos and AC explants using RNA-Bee reagent, following the manufacturer’s instructions (Tel-Test, USA), and was then treated with DNase I to remove genomic DNA contamination. RT-PCR was performed with Superscript II (Invitrogen, USA) as described by the manufacturer and with 2 μg total RNA per reaction. PCR was performed according to the following conditions: 30 s at 94 °C, 30 s at each annealing temperature and 30 s at 72°C, all for with 20-30 cycles of amplification (Table 2).

Morpholino oligomers and activin treatment

Antisense morpholinos (MOs) for Chordin and Gsc were obtained having similar MOs sequences as previously reported (Oelgeschlager et al., 2003; Sander et al., 2007). Nog-MO1 had the sequence (5’-ATTTTGTGCAGCTGTGTGCAGCATG) and Nog-MO2 had the sequence (5’-TGAAAGTGAAGAATATTTAAGAGA). All MOs were obtained from Gene Tools (USA). For use, the MOs were diluted in sterile water and then heated at 65°C for 10 min before microinjections as described previously (Ryu et al., 2021). The harvested ACs were treated with activin (25 ng/ml) as described previously (Umair et al., 2020).

Whole mount in situ hybridization

Embryos were injected with mRNAs as indicated and subsequently processed for whole-mount in situ hybridization using standard methods with anti-sense probes for Foxd4l1.1 (Moore et al., 2004).

Luciferase assays

Relative promoter activities were measured using a luciferase assay system according to the manufacturer’s instructions (Promega) and were performed as previously described (Yoon et al., 2014). Five different groups of embryos (3 embryos per group) were harvested and homogenized in 10 μl lysis buffer per embryo. Embryo homogenates at 10 μl each were assayed with 40 μl luciferase substrate and the reporter gene activity was read by an illuminometer (Berthold Technologies, Germany). All experiments were repeated at least three times for independently derived sample sets.

Site-directed mutagenesis

Mutagenesis was performed by a site-directed mutagenesis kit (Muta-Direct; iNtRON Biotechnology, Korea) using primer oligonucleotides in accordance with the manufacturer’s instructions (Table 3).

Chromatin immunoprecipitation (ChIP)

Chromatin immunoprecipitation assay was performed as described previously (Blythe et al., 2009). Embryos were injected at one-cell stage with mRNA encoding 3Flag-Gsc (1 ng/embryo). Injected embryos were collected at stage 11 (100 embryos/sample) and processed according to protocol. Anti-Flag monoclonal antibodies (F-1804; Sigma) or normal mouse IgG (SC-2025; Santa Cruz Biotechnology, USA) were then added to the cell lysates to immune-precipitate the chromatin. ChIP-PCR was performed with the immune-precipitated chromatin using foxd4l1.1, promoter region primers for GRE. These primers are shown in (Table 4).

ChIP-sequencing analysis

The Gsc mRNA (0.5 ng/embryo) was injected at the one-cell stage. Approximately 1,000 embryos were harvested at stage 11. The ChIP assay was performed accordingly to a previously described method (Blythe et al., 2009). Total immunoprecipitated chromatin was sequenced by Macrogen (Korea), and raw data with short reads were received in FASTA format. Galaxy (https://usegalaxy.org), an online tool, was used for data analysis as described previously (Zhang et al., 2008). MACS call peak data were used for visualization, and Gsc coverage within the foxd4l1.1 and zic3 promoter region was plotted.

Conjugation assay

AC explants were dissected at stages 8 and conjugation of the two required AC explants together was in 30% MMR containing 50 mg/ml gentamycin. The recombinants were cultured for 40 min at 16°C to heal the torn ends of the tissue explants before being transferred to fresh L-15 media.

Statistical analysis

Data were analyzed by unpaired two-tailed Student’s t-test using GraphPad Prism9 (GraphPad Software, USA). Asterisks designations are ** for P ≤ 0.01 and *** for P ≤ 0.001. Non-significance was denoted as “ns”.

RESULTS

Gsc suppresses transcription of early and late neural genes expressed by dnbr, chordin, and noggin

Previous reports demonstrate that gsc is expressed in the dorsal organizer and involving dorsal mesoderm cells. The mesoderm cells expressing gsc sustain their mesodermal identity; however, they greatly influence the interacting neighbor cells (ectoderm) to adopt the neural fate, (Cho et al., 1991; De Robertis et al., 1992). These results indicate that gsc has dual roles of directly inhibiting neural gene expression in mesoderm territory and indirectly stimulating neural fate in neighboring ectoderm cells. To examine the role of Gsc on neural specific gene expression, gsc mRNA was co-injected with or without dnbr, chordin, and noggin. RT-PCR results showed that dnbr, which is known to inhibit BMP signaling and elicit neural genes, prompted expression of early neural marker genes including foxd4l1.1 and zic3, but did not increase those of organizer genes including chordin and noggin (Fig. 1A, lane 1 vs 4). While gsc (with or without introduced DNBR) strongly reduced the expression of early neural genes foxd4l1.1 and zic3 (Fig. 1A, lane 1 vs 2) as well as the neural repressor gene ventx1.1, ectopic gsc expression strongly induced chordin and noggin expression (Fig. 1A, lane 2 and 4). Similar results for neural gene expression were obtained when chordin/noggin combination, instead of DNBR, was injected (Fig. 1B). The ACs showed an elevated expression of foxd4l1.1 and zic3. However, ACs co-injected with gsc abolished neural gene expression (Fig. 1B, lane 1, 2, and 4). As expected, all samples injected with gsc, chordin, and noggin showed no expression of xbra, bmp4, and ventx1.1 (Fig. 1B, lane 1, 2, 3, and 4). These results suggest that gsc plays an inhibitory role in transcription of neural specific genes, which is consistent with previously known role of Gsc as a transcriptional repressor (Yao and Kessler, 2001). To investigate the consequences of gsc overexpression at later stage embryos, the late neural specific markers were also examined. Co-expression of gsc inhibited the expression of later neural genes including ncam, neurod, xngnr1, otx2, and krox2 expressed by dnbr injection (Fig. 1C, lane 1, 2, 3, and 4) and chordin and noggin (Fig. 1D, lane 1, 2, 3, and 4). In co-injected embryos, Gsc diminished ncam and neurod expression, whereas those for xngnr1 and otx2 were not much affected (Fig. 1D, lane 1, 2, 3, and 4). These suggest that xngnr1 and otx2 may not be direct targets of Gsc. In addition, whole mount in situ hybridization (WISH) analysis was performed in whole embryos to examine foxd4l1.1 expression with or without expressed gsc. The WISH results demonstrate that ectopic expression of gsc completely diminishes foxd4l1.1 expression in the injected embryos (Fig. 1E). Taken together, these results indicate gsc inhibits neural gene expression while inducing chordin and noggin expression in AC explants.

Multiple Gsc response elements within foxd4l1.1 promoter are detected using genome-wide ChIP-seq

Several independent studies demonstrate that Gsc has strong repressor activity through direct binding on cis-acting response element within target genes to block their transcription (Cho et al., 1991; Christian and Moon, 1993; Latinkic and Smith, 1999; Yasuo and Lemaire, 2001). To identify the neural specific gene(s) (foxd4l1.1 and zic3) as direct target(s) of gsc, genome wide ChIP-seq analysis was performed using gsc injected gastrula embryos (stage 11). Our ChIP-seq analysis showed that Gsc bound within upstream promoter region of early neural genes (foxd4l1.1 and zic3). Peak calling followed by coverage plot analysis done independently for foxd4l1.1 and zic3 genome sequences led to mapping of the putative binding sites in promoter regions of foxd4l1.1 and zic3 genome (Figs. 2A and 2B). We then selected foxd4l1.1 for a more detailed analysis of the repressive role of Gsc. Foxd4l1.1 is one of the earliest neural TFs that is highly expressed in neuroectoderm to maintain neural identity (Kumar et al., 2020; Neilson et al., 2012; Sherman et al., 2017; Yan et al., 2009). Foxd4l1.1 is one of the most critical genes responsible for neuroectoderm and ectoderm specification (Lee et al., 2014). Foxd4l1.1 is expressed in neuroectoderm cells of BMP inhibited AC explants and overexpression of foxd4l1.1 is sufficient to induce neurogenesis in the ectodermal explants of Xenopus embryos (Yoon et al., 2013). The analysis of ChIP-coverage region of Gsc revealed four putative GRE within upstream region of foxd4l1.1 coding sequences (Figs. 2D and 2E). These results indicate that foxd4l1.1 5’-flanking region may contain more than one GRE to exert repressor activity. Since X. laevis is an allotetraploid that contains two copies of foxd4l1.1 genome on chromosome (chr) 1l and 1s separately, the conserved regions between chr1l and chr1s were analyzed by homology search/alignment (BLAST) of both DNA sequences. Alignment results indicate conserved GRE containing regions (Fig. 2C) in both copies of foxd4l1.1 in chr1l and 1s. The results suggest that foxd4l1.1 and zic3 would be the direct target(s) of Gsc, where Gsc directly binds and negatively regulates the transcription of neural genes in gastrula embryos.

Site-direct mutagenesis of GRE within foxd4l1.1 promoter abolishes the repression activity of Gsc

As shown above, ChIP-seq results indicated putative GREs within foxd4l1.1 and zic3 promoter regions. To identify this functionally active GRE, 1551 bps long 5’-flanking region of foxd4l1.1 respect to putative transcription start site (TSS) was cloned into a reporter vector named foxd4l1.1(–1551). We then examined whether gsc indeed inhibited the relative reporter activity of foxd4l1.1(–1551). Foxd4l1.1(–1551) was injected at one-cell stage with or without dnbr and gsc. The reporter gene assay was performed at the embryonic stage 11. As expected, foxd4l1.1(–1551) relative reporter activity was significantly increased by dnbr (2.5 fold) while co-injection with gsc decreased the reporter activity down to 9 fold (Fig. 3A, bar 1 to 4). To map out the functionally active GRE within the foxd4l1.1(–1551) promoter, serially-deleted promoter constructs were created and sub-cloned into the reporter vector (Fig. 3B). All deleted constructs were then co-injected with or without gsc mRNA for reporter activity assays. Co-injection of gsc mRNA strongly reduced the relative reporter activities of all constructs from –1551 to –301 bps (by approximately 7 to 9 fold), while the reporter constructs containing –186 bps and –78 bps (foxd4l1.1(–186) and foxd4l1.1(–78)) showed no significant changes in the reporter activity assay (Fig. 3C, bar 1 to 14). The results indicate that the functional putative GRE would be between –301 to –186 bps (Fig. 3C, bar 9 to 12). Scrutinizing the sequences of foxd4l1.1(–1551) promoter region between –301 to –186 bps revealed one putative GRE at –218 to –213 bps (ACAAAG) from the putative TSS (Figs. 2D and 2E). To verify the GRE as an active cis-acting element for Gsc, we performed site-directed mutagenesis of GRE (ACAAAG to ACGGGG) in foxd4l1.1(–1551) and foxd4l1.1(–301) reporter constructs separately (Fig. 3D). The mutated foxd4l1.1(–1551)mGRE, foxd4l1.1(–301)mGRE and those wild type promoter constructs were then injected with or without gsc to evaluate the reporter activities. Results show that gsc mediated reduction in foxd4l1.1(–1551) and foxd4l1.1(–301) promoter activities were completely abolished in the mutated foxd4l1.1(–1551)mGRE and foxd4l1.1(–301)mGRE) constructs (Figs. 3E and 3F, lane 1 to 4). These results strongly indicate that functionally active consensus sequences for gsc (its GRE) was located in –218 to –213 bps region within foxd4l1.1(–1551) promoter where Gsc binds to inhibit transcription. We next examined whether Gsc directly bound within the proximal promoter region (–218 to –213 bps) of foxd4l1.1. To determine Gsc binding within foxd4l1.1 promoter, Flag-tagged Gsc construct (3Flag-gsc) was injected at one-cell stage and ChIP-PCR was performed at stage 11 in whole embryos. The results confirm that Gsc directly binds within the proximal region of endogenous foxd4l1.1 promoter (Fig. 3G). In addition, zic3(–1805) promoter was injected with or without gsc mRNA and the reporter assay was performed. As expected, the zic3(–1805) relative reporter activity was markedly reduced in gsc co-injected samples (Fig. 3H, bar 1 and 2). Taken together, these results collectively confirm that foxd4l1.1 promoter contains a cis-acting GRE (–218 to –213 bps) where Gsc directly binds and negatively regulates foxd4l1.1 transcription.

Gsc has dual roles of neural inhibition and stimulation in cell-autonomous and noncell-autonomous fashions, respectively

During early development, Gsc is known as a neural stimulator, probably through induction of chordin in a noncell-autonomous manner (Sander et al., 2007). Ectopic expression of gsc is known to induce a complete secondary axis including head (neural tissue) in ventral region of Xenopus embryos (De Robertis et al., 1992; Latinkic and Smith, 1999; Steinbeisser et al., 1995; Ulmer et al., 2017). However, Gsc also directly binds to within the proximal promoter region (–218 to –213 bps) of the early neural gene foxd4l1.1 to inhibit its transcription. To delineate these contradictory dual regulatory roles for Gsc in neural specification, we designed and performed a conjugation assay for AC explants. Xenopus AC cells are pluripotent in nature and in response to specific signals, AC cells are capable of generating distinct types of tissue, making them excellent for manipulation for developmental studies (Borchers and Pieler, 2010). We designed two different sets of conjugated ACs (described in Fig. 4A). In set-1, embryos were injected with and without foxd4l1.1(–1551) reporter gene separately into the embryos and ACs were then dissected at stage 8. Two ACs were then conjugated as shown in Fig. 4A. In set-2, the embryos were injected with gsc and foxd4l1.1(–1551) separately and those two separately dissected ACs were then conjugated (Fig. 4A). The relative reporter activity was then measured at embryonic stage 11. The results had the reporter activity of set-2 (foxd4l1.1(–1551)/gsc) being significantly higher (2.5 fold) than that of set-1 (foxd4l1.1(–1551)/NI) (Fig. 4B, set-1 vs set-2). These results indicated that Gsc is a stimulatory molecule for neural specification to neighboring ectoderm cells, while Gsc being a direct inhibitor of neural gene expression in cell autonomous manner. We then examined whether gsc would indeed inhibit the endogenous mRNA transcription of neural specific markers in conjugated AC. To ascertain this inhibitory effect of Gsc, we prepared 3 different sets of conjugated ACs (gsc/gsc, gsc/NI, and NI/NI; NI was the not injected control AC) (as depicted in Fig. 4C). The expressed genes were then analyzed by RT-PCR. As expected, AC conjugates of both gsc injected group (gsc/gsc) completely abolished or strongly reduced the expression of early neural marker genes (stage 11) including foxd4l1.1, zic3, fgf8a, chch, and ascl1 (Fig. 4D, lane 2 vs 3). In contrast, in AC conjugates of gsc injected and uninjected AC group (gsc/NI), the neural marker genes were markedly induced when compared to that of the uninjected control conjugates (NI/NI) (Fig. 4D, lane 3 vs 4). The results clearly show that gsc functions as a strong repressor of neural gene transcription in a cell-autonomous manner but a stimulator in noncell-autonomous manner. Noticeably, chordin and noggin expression were strongly increased under both conditions of gsc/gsc and gsc/NI conjugates. There were no significant differences in the expression levels of chordin and noggin in two groups of conjugates for gsc/gsc and gsc/NI (Fig. 4D, lane 2 vs 3), indicating that chordin and noggin expressions were inducible in gsc injected AC samples with gsc being a direct strong repressor of early neural target genes. Similarly, we investigated the expression pattern of late neural markers (stage 24) in the same samples. Neural markers including ncam and xngnr1 (pan-neural markers), xrox20 (mid-brain marker), and otx2 (anterior neural marker) were significantly increased in gsc and not-injected conjugates (gsc/NI) of ACs (Fig. 4E, lane 3 vs 4) when compared to that of conjugates of all NI (NI/NI). These markers were completely abolished in conjugates of both gsc injected group (gsc/gsc) (Fig. 4E, lane 2 vs 3), indicating again that gsc has an inhibitory effect on neural target gene expression. All three sets of AC conjugates were further evaluated using whole-mount in situ hybridization (WISH) with anti-foxd4l1.1 RNA probe. In support of RT-PCR results, the gsc/gsc conjugates showed no expression of foxd4l1.1 in either portions of conjugates. On the other hand, gsc/NI conjugates showed that only the NI portion of conjugated ACs showed strong expression of foxd4l1.1 (Fig. 4F). As expected, NI/NI conjugates showed no expression of foxd4l1.1 in either portions of the conjugates (Fig. 4F). Taken together, the results confirm that Gsc has dual roles of neural inhibition in cell-autonomous and stimulation in noncell-autonomous manner, respectively.

DISCUSSION

In the present study, we sought to define the role of the homeobox repressor gsc in neural specification as part of its functions in the organizer. The organizer (being dorsal mesoderm) maintains its mesodermal identity while having a stimulatory effect on the naive ectoderm above its layer to become neuroectoderm during gastrula stage of embryos, and we tried to tie a role for gsc in the mechanism for neural gene exclusion seen in the organizer region. With the organizer as dorsal mesoderm needing a mechanism for stimulating naïve ectoderm to neuroectoderm as well as maintaining mesoderm and/or preventing it from being alternate germ layers including ectoderm and/or neuroectoderm, we adopted gsc as a candidate gene possibly performing such dual activity for the organizer. Gsc is a repressive TF and a known factor for enhancing chordin (Sasai et al., 1994), a secretory factor inhibiting BMP and leading to neighboring ectoderm cells to neuroectoderm. We found that gsc, as an organizer specific TF, repressed foxd4l1.1, a neural specific TF. We have previously found that repressive neural and non-neural TFs (foxd4l1.1 vs ventx1.1) are mutually antagonistic in specifying the non-neural versus neural ectoderm activation areas of the nucleus (Kumar et al., 2020). We selected and focused on foxd4l1.1 for the hypothesis that a TF in a distinct germ layer protects it from becoming another type of germ layer. In this view, gsc, a critical TF of dorsal mesoderm (organizer), protects the expression of foxd4l1.1, a critical TF of neuroectoderm. Thus, Gsc protects dorsal mesoderm (organizer) from becoming a neuroectoderm through foxd4l1.1. In addition, AC conjugation experiments demonstrated that gsc induction was neural stimulatory in a noncell-autonomous manner. Together, our results suggest that Gsc is an organizer specific factor performing dual roles of organizer in neural specification. Specifically, Gsc is a repressive TF to protect dorsal mesoderm from expressing neural genes as well as a stimulatory factor of neighboring neuro-ectoderm via expression of chordin and noggin. The implication and interpretation of this study is discussed below in the point of view of representative repressor TFs preserving each germ layer of dorsal and ventral mesoderm as well as dorsal (neural ectoderm) and ventral ectoderm (non-neural ectoderm).

We have previously reported on various mechanisms existing in reciprocally exclusive germ-layer specifications in early vertebrate embryogenesis (ectoderm, mesoderm and neuroectoderm) (Kumar et al., 2020). In the ventral mesoderm and ectoderm region, neural repressor ventx1.1 is expressed and it inhibits neuroectoderm specific genes including foxd4l1.1 and zic3 (Umair et al., 2018). On the other hand, the neuroectoderm region requires the neuroectoderm specific repressor foxd4l1.1 to inhibit the neural repressor ventx1.1 expression (Kumar et al., 2020). These studies suggested reciprocal repression of ventx1.1 and foxd4l1.1 being at least part of specifying mechanisms for non-neural versus neural ectoderm fate specification in Xenopus embryos (Kumar et al., 2020; Umair et al., 2018). In the present study, we asked whether the two adjacent layers of organizer and neuro-ectoderm cells also follow such a mechanism of reciprocal repression in gastrula embryos, especially in the dorsal mesoderm territory (the Spemann organizer) (De Robertis and Kuroda, 2004; Harland, 2000; Nieuwkoop and Nigtevecht, 1954; Spemann, 1967). Here, we found that gain-of-function study of gsc pointed to gsc acting as a strong repressor in dnbr, chordin, and noggin mediated neuroectoderm formation in AC explants. A direct binding of Gsc in an early neural specific gene foxd4l1.1 was also demonstrated in ChIP-seq and reporter gene analysis of gastrula embryos. Gsc-mediated repression of the neural specific repressor TF Foxd4l1.1 is important in protecting the organizer from expressing nonspecific neural genes as well as maintaining organizer as gsc expressing dorsal mesoderm.

From our preliminary findings, Gsc promoter also contained the direct binding response element for Foxd4l1.1 (from Chip-seq and reporter assay of Gsc promoter) (unpublished data). Whether a reciprocal repression of gsc and foxd4l1.1 is the underlying mechanism for the non-neural organizer versus neural ectoderm fate specification in Xenopus embryos, it requires more elaboration; more immediately, any repressive functions of Foxd4l1.1 on gsc expression in neuro-ectoderm needs to be demonstrated. We designed and performed loss-of function studies for proof of Gsc’s neural repressive role in activin treated AC system. In activin treated AC explants, one may expect increased expression for the neuroectoderm gene foxd4l1.1, and actually gsc MO injected ACs had decreased foxd4l1.1 expression under the activin treated condition. Gsc MO also led to increase a neural repressor ventx1.1 expression compared to the activin treated condition without the Gsc MO. The effects of gsc depletion on expression of foxd4l1.1 in the organizer could have been shown. However, previous work (Sander et al., 2007) has indicated that gsc depletion increases neural repressor gene ventx1.1 and ventx2.1 levels. A gsc MO experiment may lead to neural gene repression in the whole embryos. Our experiments with AC explants allowed certain conditions that were practical to be implemented (such for “activin treated” cases). The results indicated in the activin treated setup was similar to the previous experiment in whole embryos and the results using noggin/chordin MOs were similar to that of Gsc MO (Supplementary Fig. S1A, lane 1 and 2). The Gsc knockdown results supported Gsc suppressing neural genes when Gsc is overexpressed under bmp inhibition in activin treated AC explants (Supplementary Fig. S1A, lane 3 and 4). Taken together, Gsc/noggin/chordin depletion experiments point to a suppressive role for goosecoid and a stimulatory role for noggin/chordin in neuroectoderm formation. It is still need to investigate gsc neural repressive role along with cross-examination of other organizer TFs and signaling molecules in the developing organizer of gastrula embryos. Based on the present results, however, we propose this depicted model for Gsc inhibiting the neural TF foxd4l1.1 in its expressed territory of the organizer, but also inducing secreted Chordin and Noggin, to induce neurogenesis in target tissues (Fig. 5).

In this study, we adopted gsc as an organizer specific gene TF to study the dual inhibitory and stimulatory roles of organizer in neural specification. The reasons on why we selected gsc are the following: First, gsc is the first organizer TF to be recognized as only expressed in the underlying layer of organizer but not in the above layers of the neuroectoderm in gastrula stage of embryos (Cho et al., 1991). Second, gsc is a repressor TF, which would protect the organizer as dorsal mesoderm from expressing neural genes including neural specific repressor TF foxd4l1.1. Third, gsc has been known to induce ectopic expression of chordin. Fourth, overexpression of gsc in ventral side of embryo leads to complete axis duplication including neural tissues of head, indicating somehow the stimulatory role of gsc in neural specification (Dixon Fox and Bruce, 2009; Kuroda et al., 2004; Sander et al., 2007; Seiliez et al., 2006; Yao and Kessler, 2001).

Gsc as an organizer specific repressor TF has been studied in the context of dorso-ventral specification as well as a factor in protecting the organizer by repression of signaling molecules including BMP and Wnt8 (Yao and Kessler, 2001). Gsc has been proposed as a central TF involved in mesoderm patterning (Niehrs et al.,1994). Although showing a direct reciprocal repression between dorsal and ventral specific homeobox genes gsc and ventx1.1/ventx2.1 awaits more studies, involvement of the genes has been demonstrated in dorsoventral patterning of mesoderm by both gain-of function (Cho et al., 1991) and loss-of function (Steinbeisser et al., 1995) studies. Gsc has been suggested as an important TF in dorsoventral patterning, possibly through reciprocal repression of the genes to mediate a self-adjusting mechanism (Sander et al., 2007). Although the studies of gsc have focused on dorso-ventral specification as an organizer repressor gene as well as neuro-ectoderm specification as possibly an indirect inducer of neural stimulatory gene chordin (Sander et al., 2007; Sasai et al., 1994), gsc has not been adequately examined as a direct repressor of neural genes, and the reports have also focused on dorsoventral patterning and not much on organizer/neuroectoderm specification (Thisse et al., 1994).

Additional studies have mainly focused on neural stimulatory effect of Gsc through induction of neural stimulatory factor chordin, possibly through an indirect effect of gsc in chordin expression (Cho et al., 1991; De Robertis and Kuroda, 2004; Sander et al., 2007; Sasai et al., 1994). In the present work, we found that gsc overexpression increased ectopic expression of chordin, as ACs obtained from gsc injected embryos expressed both BMP antagonizer chordin and noggin in AC explants (Fig. 4D); this is different from the report where Gsc induced ectopic expression of chordin but not that of noggin in gsc-injected at 8 cell stage embryos (Sasai et al., 1994). At the present time, we cannot address the exact reason why gsc injection leads to the differences in chordin and noggin expression in AC cells and whole embryos. These may be due to differences for their mode of activation (Sasai et al., 1994). We actually elaborated the expression mode of chordin using the isolated 2.25 kbs in length chordin promoter. The isolated promoter contained a primary response elements for Smad2 and Smad3 of activin signaling, which is slightly different that from Sasai et al. (1994) where chordin was reported as a secondary response gene requiring de novo protein synthesis. In addition, our isolated promoter contained a strong positive cis-acting element of Gsc (GRE) adjacent to the Smad2 and Smad3 response cis-acting elements in the distal region of chordin promoter (Kumar et al., 2021). These results indicate that Gsc functions as a repressor as well as an activator in a context dependent and cell specific manner. Chordin and noggin expression needs more scrutinizing; however, ACs from gsc injected embryos expressed both chordin and noggin, supporting our hypothesis that gsc functions as a neural stimulatory factor via inducing chordin and noggin expression in a noncell-autonomous manner.

In the present paper, we sought to explain the dual roles of the organizer in neuroectoderm specification in the context of the functional activity of the organizer specific TF gsc. The present finding of cell-autonomous and noncell-autonomous regulation of organizer gene in neuroectoderm and mesoderm specification, however, needs further elaboration. The present work suggests that Gsc represses the neural specific gene foxd4l1.1. This, along with our preliminary findings on foxd4l1.1 repression of Gsc promoter (from Chip-seq and reporter assays of Gsc promoter) (unpublished data), a reciprocal repression of gsc and foxd4l1.1 is thought to be the underlying mechanism for the non-neural organizer versus neural ectoderm fate specification in Xenopus embryos. In addition, the results of Gsc repression of ventx1.1 (Fig. 1A) and our previous results of ventx1.1 repression of gsc (Hwang et al., 2003) support the premise of a reciprocal repression existing between ventx1.1 and gsc for ventral and dorsal patterning. A study on the mutual opposing roles of Gsc and Vent homeobox genes in patterning the mesoderm of Xenopus embryo has been reported (Sander et al., 2007). Although it requires further investigation, from our previous and current findings, we propose a reciprocal repressive mechanism for the master repressor TFs including gsc, ventx1.1 and foxd4l1.1 in protecting the organizer, the ventral mesoderm/ectoderm and the neuroectoderm, respectively.

ACKNOWLEDGMENTS

This article was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF), which is funded by the Ministry of Education, Science, and Technology of Korea (2016R1D1A1B02008770, 2018M3C7A1056285, and 2021M3H9A1097557).

AUTHOR CONTRIBUTIONS

Z.U. and V.K. performed the experiments and wrote the primary manuscript. J.K. and U.L. designed and supervised the study. R.S.G. and S.K. contributed to the data analysis and revision of the manuscript.

CONFLICT OF INTEREST

The authors have no potential conflicts of interest to disclose.

Fig. 1.InhibitIon of neural gene expression either mediated by dnbr or chordin and noggin (Chrd/Nog) in AC explants of Xenopus.
3Flag-gsc (1 ng/embryo), dnbr (0.5 ng/embryo), chordin (0.5 ng/embryo) and noggin (0.5 ng/embryo) (Chrd/Nog) were injected at one-cell stage and the AC explants were dissected at stage 8 to grow until (A and B) stage 11 and (C and D) stage 24. The expression profiles of different germ layer specific marker genes were analyzed by RT-PCR. No RT (no reverse transcriptase added) served as a negative control while WE (whole embryos) served a positive control. (E) 3Flag-gsc (1 ng/embryo) mRNA was injected into one cell embryos, and the injected embryos and non-injected ones (control) were processed for whole mount in situ hybridization (WISH) with anti-sense foxd4l1.1 probe at stage 11.
Fig. 2.Identification of GREs within the neural target genes using ChIP-seq of 3Flag-gsc injected Xenopus embryos. (A and B) Coverage plot of 3Flag-gsc within the foxd4l1.1 and zic3 promoter regions. (C) Similarity within both (chr1s and chr1l) copies of foxd4l1.1 promoter region are shown. The active GRE (–213 to –218 bps) location is highlighted by an arrow. (D) Putative GREs revealed within the foxd4l1.1 promoter region by ChIP-sequencing. (E) Consensus binding motifs of Gsc within both (chr1s and chr1l) copies of foxd4l1.1 promoter region.
Fig. 3.Abolishment of the repressional activity of Gsc by site-directed mutagenesis of GRE within the foxd4l1.1(–1551) reporter construct. (A) foxd4l1.1(–1551) (40 pg/embryo), dnbr (1 ng/embryo), and 3Flag-gsc (1 ng/embryo) were injected at one-cell stage and reporter assay was performed at stage 11. RLU, relative reporter activity. (B) Schematic representation of serially-deleted foxd4l1.1(–1551) promoter constructs. (C) Serially-deleted foxd4l1.1 (40 pg/embryo) promoter constructs were injected with and without 3Flag-gsc (1 ng/embryo) at one-cell stage and relative promoter activity were measured at stage 11. (D) Site-directed mutagenesis scheme for foxd4l1.1(–1551) and foxd4l1.1(–301) promoter constructs, target sequences highlighted (red color and italic). (E and F) Relative reporter assay of foxd4l1.1(–1551), foxd4l1.1(–1551)mGRE, foxd4l1.1(–301), and foxd4l1.1(–301)mGRE with or with gsc were performed at stage 11. (G) 3Flag-gsc was injected at one-cell stage and ChIP-PCR was performed at stage 11. Specific primers of Foxd4l1.1 promoter region (containing GRE) were used for amplification, while ventx2.1 served as negative control. (H) zic3(–1805) reporter construct was injected (40 pg/embryo) with or without 3Flag-gsc (1 ng/embryo) and reporter assay was performed at stage 11. **P ≤ 0.01; ****P ≤ 0.0001; ns, non-significance.
Fig. 4.A dual role of Gsc in transcriptional regulation of foxd4l1.1. In all experiments, 3Flag-gsc (1 ng/embryo) and foxd4l1.1(-1551) (40 pg/embryo) were injected at one-cell stage and the ACs were dissected at stage 8 to grow until stage 11 and 24. (A) Conjugation scheme for AC explants used. (B) The relative promoter activity are measured. RLU, relative reporter activity. ****P ≤ 0.0001. (C) Schematic description of the conjugated AC explants of the embryos injected with 3Flag-gsc and NI. The expression profiles of (D) early (stage 11) and (E) late (stage 24) neural marker genes were analyzed by RT-PCR. No RT (no reverse transcriptase added) served as a negative control while WE (whole embryos) served as positive control. (F) Whole mount in situ hybridization (WISH) was performed with anti-sense foxd4l1.1 probe of at stage 11.
Fig. 5.Schematic diagram depicting the dual role of Gsc in early neurogenesis. In mesoderm (dorsal organizer), Gsc inhibits the neural genes while strongly induces chordin and noggin expression. Newly translated Chordin and Noggin diffuse to neighboring cells (ectoderm) where they induce neurogenesis in a BMP inhibited manner.

Tables

Primers used for serially-deleted FoxD5b reporter gene constructs

Primer Primer name Sequence
Upstream primer Foxd4l1.1(–1551) 5’-CCGGTACCTAGAGGTTGGATAAAGTCAATTGC-3’
Foxd4l1.1(–1316) 5’-CCGGTACCTATATGCAGAGCTGCTAATAGTC-3’
Foxd4l1.1(–1016) 5’-CCGGTACCTATATGCAGAGCTGCTAATAGTC-3’
Foxd4l1.1(–816) 5’-CCGGTACCTAGAATTCCAGTTCCCATAATC-3’
Foxd4l1.1(–301) 5’-CCGGTACCTTGGATTGCAAGTTAGTGGCTC-3’
Foxd4l1.1(–186) 5’-GGGGTACCTTCATTCAGCAAAAGCACAGCC-3’
Foxd4l1.1(–78) 5’-GGGGTACCAATTCAAGTGCAGATGACTGCC-3’
Downstream primer Foxd4l1.1-R 5’-ATCTCGAGGCTTGGTTGGCAGTAAGTAG-3’

Primers used for RT-PCR amplification

Gene name Sequence Annealing temperature (°C) Cycle
zic3 F5’-TCTCAGGATCTGAACACCT-3’ 45 28
R5’-CCCTATAAGACAAGGAATAC-3’
Foxd4l1.1 F5’-ACTCTATCAGGCACAACCTGTC-3’ 50 30
R5’-GGTCTGTAGTAAGGCAGAGAGT-3’
xbra F5’-GGATCGTTATCACCTCTG-3’ 57 25
R5’-GTGTAGTCTGTAGCAGCA-3’
Fgf8a F5’-CTGGTGACCGACCAACTAAG-3’ 55 28
R5’-TGCGAACTCTGCTTCCAAAC-3’
chch F5’-ATGTGCGGAGGCTGCGTC-3’ 60 27
R5’-CGTGGGTCATCGGGTAGAAC-3’
ascl1 F5’-GAGCTGATGAGGTGCAAGAG-3’ 60 27
R5’-TTTGCTCATCTTCTTGTTGG-3’
ncam F5’-CACAGTTCCACCAAATGC-3’ 57 29
R5’-GGAATCAAGCGGTACAGA-3’
xngnr1 F5’-GGATGGTGCTGCTACCGTGCGAGTACC-3’ 65 30
R5’-CAAGCGCAGAGTTCAGGTTGTGCATGC-3’
otx2 F5’-GGATGGATTTGTTGCACCAGTC-3’ 57 27
R5’-CACTCTCCCAGCTCACTTCTC-3’
xk81 F5’-TGGTGTTGAACAAGTGCAGG-3’ 57 25
R5’-ACCTCCTCGACAATGGTCTT-3’
krox20 F5’-AACCGCCCCAGTAAGACC-3’ 57 28
R5’-GTGTCAGCCTGTCCTGTTAG-3’
neurod F5’-GTGAAATCCCAATAGACACC-3’ 57 28
R5’-TTCCCCATATCTAAAGGCAG-3’
HoxB9 F5’-TACTTACGGGCTTGGCTGGA-3’ 68 26
R5’-AGCGTGTAACCAGTTGGCTG-3’
gsc F5’-GCTGATTCCACCAGTGCCTCACCAG-3’ 60 30
R5’-GGTCCTGTGCCTCCTCCTCCTCCTG-3’
noggin F5’-AGTTGCAGATGTGGCTCT-3’ 57 27
R5’-AGTCCAAGAGTCTGAGCA-3’
chordin F5’-TTAGAGAGGAGAGCAACTCGGGCAAT-3’ 57 25
R5’-GTGCTCCTGTTGCGAAACTCTACAGA-3’
bmp4 F5’-CATCATGATTCCTGGTAACCGA-3’ 57 25
R5’-CTCCATGCTGATATCGTGCAG-3’
ventx1.1 F5’-CCTTCAGCATGGTTCAACAG-3’ 57 26
R5’-CATCCTTCTTCCTTGGCATC-3’
ef1α F5’-CCTGAATCACCCAGGCCAGATTGTG-3’ 57 19
R5’-GAGGGTACTCTGAGAAAGCTCTCCACG-3’
odc F5’-GTCAATGATGGAGTGTATGGATC-3’ 55 25
R5’-TCCATTCCGCTCTCCTGAGCAC-3’

Primers used for site-directed mutagenesis

Mutated site Primer name Sequence
GRE Foxd4l1.1mGRE F5’-GGACCCTCTCACGTGGGAGCTTATCTGATAR-3’
R5’-TATCAGATAAGCTCCCACGTGAGAGGGTCC-3’

Primers used for ChIP-PCR assay

Prime name Sequence Annealing temperature (°C) Cycle
Foxd4l1.1ChIP-GRE F5’-ACCTTGTTGGACTACAGATTC-3’ 52 30
R5’-CAGTCATCTGCACTTGAATTGG-3’

Fig 1.

Figure 1.InhibitIon of neural gene expression either mediated by dnbr or chordin and noggin (Chrd/Nog) in AC explants of Xenopus.
3Flag-gsc (1 ng/embryo), dnbr (0.5 ng/embryo), chordin (0.5 ng/embryo) and noggin (0.5 ng/embryo) (Chrd/Nog) were injected at one-cell stage and the AC explants were dissected at stage 8 to grow until (A and B) stage 11 and (C and D) stage 24. The expression profiles of different germ layer specific marker genes were analyzed by RT-PCR. No RT (no reverse transcriptase added) served as a negative control while WE (whole embryos) served a positive control. (E) 3Flag-gsc (1 ng/embryo) mRNA was injected into one cell embryos, and the injected embryos and non-injected ones (control) were processed for whole mount in situ hybridization (WISH) with anti-sense foxd4l1.1 probe at stage 11.
Molecules and Cells 2021; 44: 723-735https://doi.org/10.14348/molcells.2021.0055

Fig 2.

Figure 2.Identification of GREs within the neural target genes using ChIP-seq of 3Flag-gsc injected Xenopus embryos. (A and B) Coverage plot of 3Flag-gsc within the foxd4l1.1 and zic3 promoter regions. (C) Similarity within both (chr1s and chr1l) copies of foxd4l1.1 promoter region are shown. The active GRE (–213 to –218 bps) location is highlighted by an arrow. (D) Putative GREs revealed within the foxd4l1.1 promoter region by ChIP-sequencing. (E) Consensus binding motifs of Gsc within both (chr1s and chr1l) copies of foxd4l1.1 promoter region.
Molecules and Cells 2021; 44: 723-735https://doi.org/10.14348/molcells.2021.0055

Fig 3.

Figure 3.Abolishment of the repressional activity of Gsc by site-directed mutagenesis of GRE within the foxd4l1.1(–1551) reporter construct. (A) foxd4l1.1(–1551) (40 pg/embryo), dnbr (1 ng/embryo), and 3Flag-gsc (1 ng/embryo) were injected at one-cell stage and reporter assay was performed at stage 11. RLU, relative reporter activity. (B) Schematic representation of serially-deleted foxd4l1.1(–1551) promoter constructs. (C) Serially-deleted foxd4l1.1 (40 pg/embryo) promoter constructs were injected with and without 3Flag-gsc (1 ng/embryo) at one-cell stage and relative promoter activity were measured at stage 11. (D) Site-directed mutagenesis scheme for foxd4l1.1(–1551) and foxd4l1.1(–301) promoter constructs, target sequences highlighted (red color and italic). (E and F) Relative reporter assay of foxd4l1.1(–1551), foxd4l1.1(–1551)mGRE, foxd4l1.1(–301), and foxd4l1.1(–301)mGRE with or with gsc were performed at stage 11. (G) 3Flag-gsc was injected at one-cell stage and ChIP-PCR was performed at stage 11. Specific primers of Foxd4l1.1 promoter region (containing GRE) were used for amplification, while ventx2.1 served as negative control. (H) zic3(–1805) reporter construct was injected (40 pg/embryo) with or without 3Flag-gsc (1 ng/embryo) and reporter assay was performed at stage 11. **P ≤ 0.01; ****P ≤ 0.0001; ns, non-significance.
Molecules and Cells 2021; 44: 723-735https://doi.org/10.14348/molcells.2021.0055

Fig 4.

Figure 4.A dual role of Gsc in transcriptional regulation of foxd4l1.1. In all experiments, 3Flag-gsc (1 ng/embryo) and foxd4l1.1(-1551) (40 pg/embryo) were injected at one-cell stage and the ACs were dissected at stage 8 to grow until stage 11 and 24. (A) Conjugation scheme for AC explants used. (B) The relative promoter activity are measured. RLU, relative reporter activity. ****P ≤ 0.0001. (C) Schematic description of the conjugated AC explants of the embryos injected with 3Flag-gsc and NI. The expression profiles of (D) early (stage 11) and (E) late (stage 24) neural marker genes were analyzed by RT-PCR. No RT (no reverse transcriptase added) served as a negative control while WE (whole embryos) served as positive control. (F) Whole mount in situ hybridization (WISH) was performed with anti-sense foxd4l1.1 probe of at stage 11.
Molecules and Cells 2021; 44: 723-735https://doi.org/10.14348/molcells.2021.0055

Fig 5.

Figure 5.Schematic diagram depicting the dual role of Gsc in early neurogenesis. In mesoderm (dorsal organizer), Gsc inhibits the neural genes while strongly induces chordin and noggin expression. Newly translated Chordin and Noggin diffuse to neighboring cells (ectoderm) where they induce neurogenesis in a BMP inhibited manner.
Molecules and Cells 2021; 44: 723-735https://doi.org/10.14348/molcells.2021.0055

. Primers used for serially-deleted FoxD5b reporter gene constructs .

PrimerPrimer nameSequence
Upstream primerFoxd4l1.1(–1551)5’-CCGGTACCTAGAGGTTGGATAAAGTCAATTGC-3’
Foxd4l1.1(–1316)5’-CCGGTACCTATATGCAGAGCTGCTAATAGTC-3’
Foxd4l1.1(–1016)5’-CCGGTACCTATATGCAGAGCTGCTAATAGTC-3’
Foxd4l1.1(–816)5’-CCGGTACCTAGAATTCCAGTTCCCATAATC-3’
Foxd4l1.1(–301)5’-CCGGTACCTTGGATTGCAAGTTAGTGGCTC-3’
Foxd4l1.1(–186)5’-GGGGTACCTTCATTCAGCAAAAGCACAGCC-3’
Foxd4l1.1(–78)5’-GGGGTACCAATTCAAGTGCAGATGACTGCC-3’
Downstream primerFoxd4l1.1-R5’-ATCTCGAGGCTTGGTTGGCAGTAAGTAG-3’

. Primers used for RT-PCR amplification .

Gene nameSequenceAnnealing temperature (°C)Cycle
zic3F5’-TCTCAGGATCTGAACACCT-3’4528
R5’-CCCTATAAGACAAGGAATAC-3’
Foxd4l1.1F5’-ACTCTATCAGGCACAACCTGTC-3’5030
R5’-GGTCTGTAGTAAGGCAGAGAGT-3’
xbraF5’-GGATCGTTATCACCTCTG-3’5725
R5’-GTGTAGTCTGTAGCAGCA-3’
Fgf8aF5’-CTGGTGACCGACCAACTAAG-3’5528
R5’-TGCGAACTCTGCTTCCAAAC-3’
chchF5’-ATGTGCGGAGGCTGCGTC-3’6027
R5’-CGTGGGTCATCGGGTAGAAC-3’
ascl1F5’-GAGCTGATGAGGTGCAAGAG-3’6027
R5’-TTTGCTCATCTTCTTGTTGG-3’
ncamF5’-CACAGTTCCACCAAATGC-3’5729
R5’-GGAATCAAGCGGTACAGA-3’
xngnr1F5’-GGATGGTGCTGCTACCGTGCGAGTACC-3’6530
R5’-CAAGCGCAGAGTTCAGGTTGTGCATGC-3’
otx2F5’-GGATGGATTTGTTGCACCAGTC-3’5727
R5’-CACTCTCCCAGCTCACTTCTC-3’
xk81F5’-TGGTGTTGAACAAGTGCAGG-3’5725
R5’-ACCTCCTCGACAATGGTCTT-3’
krox20F5’-AACCGCCCCAGTAAGACC-3’5728
R5’-GTGTCAGCCTGTCCTGTTAG-3’
neurodF5’-GTGAAATCCCAATAGACACC-3’5728
R5’-TTCCCCATATCTAAAGGCAG-3’
HoxB9F5’-TACTTACGGGCTTGGCTGGA-3’6826
R5’-AGCGTGTAACCAGTTGGCTG-3’
gscF5’-GCTGATTCCACCAGTGCCTCACCAG-3’6030
R5’-GGTCCTGTGCCTCCTCCTCCTCCTG-3’
nogginF5’-AGTTGCAGATGTGGCTCT-3’5727
R5’-AGTCCAAGAGTCTGAGCA-3’
chordinF5’-TTAGAGAGGAGAGCAACTCGGGCAAT-3’5725
R5’-GTGCTCCTGTTGCGAAACTCTACAGA-3’
bmp4F5’-CATCATGATTCCTGGTAACCGA-3’5725
R5’-CTCCATGCTGATATCGTGCAG-3’
ventx1.1F5’-CCTTCAGCATGGTTCAACAG-3’5726
R5’-CATCCTTCTTCCTTGGCATC-3’
ef1αF5’-CCTGAATCACCCAGGCCAGATTGTG-3’5719
R5’-GAGGGTACTCTGAGAAAGCTCTCCACG-3’
odcF5’-GTCAATGATGGAGTGTATGGATC-3’5525
R5’-TCCATTCCGCTCTCCTGAGCAC-3’

. Primers used for site-directed mutagenesis .

Mutated sitePrimer nameSequence
GREFoxd4l1.1mGREF5’-GGACCCTCTCACGTGGGAGCTTATCTGATAR-3’
R5’-TATCAGATAAGCTCCCACGTGAGAGGGTCC-3’

. Primers used for ChIP-PCR assay .

Prime nameSequenceAnnealing temperature (°C)Cycle
Foxd4l1.1ChIP-GREF5’-ACCTTGTTGGACTACAGATTC-3’5230
R5’-CAGTCATCTGCACTTGAATTGG-3’

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Mol. Cells
Nov 30, 2021 Vol.44 No.11, pp. 781~860
COVER PICTURE
3D quantitative images of the vesicular structure and the nucleolus using label free optical diffraction tomography (Kim et al., pp. 851-860).

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