Mol. Cells 2012; 33(5): 457-463
Published online April 26, 2012
https://doi.org/10.1007/s10059-012-2179-3
© The Korean Society for Molecular and Cellular Biology
Correspondence to : *Correspondence: ojyoo@kaist.ac.kr (OJY); gcha@cnu.ac.kr (GHC); sgpaik@cnu.ac.kr (SGP)
In Drosophila, broad complex, tramtrack, bric ? brac (BTB)/ poxvirus and zinc finger (POZ) transcription factors are essential regulators of development. We searched the Drosophila genome for BTB/POZ-ZF domains and discovered an unknown Drosophila gene, dPLZF, which encodes an orthologue of human PLZF. We then characterized the biological function of the dPLZF via genetic interaction analysis. Ectopic expression of dPLZF in the wing induced extra vein formation during wing development in Drosophila. Genetic interactions between dPLZF and Ras or extracellular signal-regulated kinase (ERK) significantly enhanced the formation of vein cells. On the other hand, loss-of-function mutations in dPLZF resulted in a dramatic suppression of the extra and ectopic vein formation induced by elevated Ras/ERK signaling. Moreover, dPLZF activity upregulated the expression of rhomboid (rho) and spitz, which perform crucial functions in vein cell formation in the developing wing. These results indicate that dPLZF is a transcription factor controlled by the Ras/ERK signaling pathway, which is a prominent regulator of vein cell formation during wing development in Drosophila.
Keywords BTB/POZ, ERK, PLZF, Ras, zinc finger
Mol. Cells 2012; 33(5): 457-463
Published online May 31, 2012 https://doi.org/10.1007/s10059-012-2179-3
Copyright © The Korean Society for Molecular and Cellular Biology.
Oky Maeng1, Wonseok Son2, Jongkyeong Chung3, Kyu-Sun Lee4, Young-Ha Lee1, Ook-Joon Yoo2,6,*, Guang-Ho Cha1,6,*, and Sang-Gi Paik5,6,*
1Department of Infection Biology, College of Medicine and Brain Korea 21 Program for Medical Science, Chungnam National University, Daejeon 301-131, Korea, 2Graduate School of Medical Science and Engineering, Biomedical Research Center, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea, 3School of Biological Science, Seoul National University, Seoul 151-742, Korea, 4Aging Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-806, Korea, 5Department of Biology, Chungnam National University, Daejeon 305-764, Korea, 6These authors contributed equally to this work.
Correspondence to:*Correspondence: ojyoo@kaist.ac.kr (OJY); gcha@cnu.ac.kr (GHC); sgpaik@cnu.ac.kr (SGP)
In Drosophila, broad complex, tramtrack, bric ? brac (BTB)/ poxvirus and zinc finger (POZ) transcription factors are essential regulators of development. We searched the Drosophila genome for BTB/POZ-ZF domains and discovered an unknown Drosophila gene, dPLZF, which encodes an orthologue of human PLZF. We then characterized the biological function of the dPLZF via genetic interaction analysis. Ectopic expression of dPLZF in the wing induced extra vein formation during wing development in Drosophila. Genetic interactions between dPLZF and Ras or extracellular signal-regulated kinase (ERK) significantly enhanced the formation of vein cells. On the other hand, loss-of-function mutations in dPLZF resulted in a dramatic suppression of the extra and ectopic vein formation induced by elevated Ras/ERK signaling. Moreover, dPLZF activity upregulated the expression of rhomboid (rho) and spitz, which perform crucial functions in vein cell formation in the developing wing. These results indicate that dPLZF is a transcription factor controlled by the Ras/ERK signaling pathway, which is a prominent regulator of vein cell formation during wing development in Drosophila.
Keywords: BTB/POZ, ERK, PLZF, Ras, zinc finger
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