TOP

Research Article

Split Viewer

Mol. Cells 2010; 29(3): 291-296

Published online January 14, 2010

https://doi.org/10.1007/s10059-010-0034-y

© The Korean Society for Molecular and Cellular Biology

Predominant Actions of Cytosolic BSU1 and Nuclear BIN2 Regulate Subcellular Localization of BES1 in Brassinosteroid Signaling

Hojin Ryu1,2, Kangmin Kim1,2, Hyunwoo Cho1, and Ildoo Hwang1,*

1Department of Life Sciences, Pohang University of Science and Technology, Pohang 790-894, Korea, 2These authors contributed equally to this work.

Correspondence to : *Correspondence: ihwang@postech.ac.kr

Received: November 3, 2009; Revised: November 26, 2009; Accepted: November 26, 2009

Abstract

During brassinosteroid (BR) signaling in Arabidopsis, BSU1 (bri1 SUPPRESSOR1) phosphatase and BIN2 (BRASSINOSTEROID INSENSITIVE2) kinase regulate the signal intensity by determining the phosphorylation status of the transcription factors BZR1 (BRASSINAZOLE RESISTANT1) and BES1 (bri1 EMS SUPPRESSOR1). Here, we report that BIN2 and BSU1 are nucleocytoplasmic regulators that modulate the subcellular localization of BES1, with differential activities between the nucleus and the cytosol. In our experiments, the nuclear BIN2 induced phosphorylation and nuclear export of BES1 more efficiently than cytosolic BIN2. The cytoplasmic BSU1 mediated the dephosphorylation and nuclear translocation of BES1 more efficiently than the nuclear one. BSU1 com-promised the dwarf phenotype of bri1-5, a weak allele of BRI1 (BR-INSENSITIVE 1) receptor kinase, more effectively when localized in the cytosol than in the nucleus in transgenic plants. In conclusion, the predomi-nance of cytosolic BSU1 and nuclear BIN2 might be re-quired for the efficient subcellular localization of BES1 in BR signaling.

Keywords BES1, BIN2 kinase, Brassinosteroid, BSU1 phosphatase, nucleocytoplasmic shuttling

Article

Research Article

Mol. Cells 2010; 29(3): 291-296

Published online March 31, 2010 https://doi.org/10.1007/s10059-010-0034-y

Copyright © The Korean Society for Molecular and Cellular Biology.

Predominant Actions of Cytosolic BSU1 and Nuclear BIN2 Regulate Subcellular Localization of BES1 in Brassinosteroid Signaling

Hojin Ryu1,2, Kangmin Kim1,2, Hyunwoo Cho1, and Ildoo Hwang1,*

1Department of Life Sciences, Pohang University of Science and Technology, Pohang 790-894, Korea, 2These authors contributed equally to this work.

Correspondence to:*Correspondence: ihwang@postech.ac.kr

Received: November 3, 2009; Revised: November 26, 2009; Accepted: November 26, 2009

Abstract

During brassinosteroid (BR) signaling in Arabidopsis, BSU1 (bri1 SUPPRESSOR1) phosphatase and BIN2 (BRASSINOSTEROID INSENSITIVE2) kinase regulate the signal intensity by determining the phosphorylation status of the transcription factors BZR1 (BRASSINAZOLE RESISTANT1) and BES1 (bri1 EMS SUPPRESSOR1). Here, we report that BIN2 and BSU1 are nucleocytoplasmic regulators that modulate the subcellular localization of BES1, with differential activities between the nucleus and the cytosol. In our experiments, the nuclear BIN2 induced phosphorylation and nuclear export of BES1 more efficiently than cytosolic BIN2. The cytoplasmic BSU1 mediated the dephosphorylation and nuclear translocation of BES1 more efficiently than the nuclear one. BSU1 com-promised the dwarf phenotype of bri1-5, a weak allele of BRI1 (BR-INSENSITIVE 1) receptor kinase, more effectively when localized in the cytosol than in the nucleus in transgenic plants. In conclusion, the predomi-nance of cytosolic BSU1 and nuclear BIN2 might be re-quired for the efficient subcellular localization of BES1 in BR signaling.

Keywords: BES1, BIN2 kinase, Brassinosteroid, BSU1 phosphatase, nucleocytoplasmic shuttling

Mol. Cells
Sep 30, 2023 Vol.46 No.9, pp. 527~572
COVER PICTURE
Chronic obstructive pulmonary disease (COPD) is marked by airspace enlargement (emphysema) and small airway fibrosis, leading to airflow obstruction and eventual respiratory failure. Shown is a microphotograph of hematoxylin and eosin (H&E)-stained histological sections of the enlarged alveoli as an indicator of emphysema. Piao et al. (pp. 558-572) demonstrate that recombinant human hyaluronan and proteoglycan link protein 1 (rhHAPLN1) significantly reduces the extended airspaces of the emphysematous alveoli by increasing the levels of TGF-β receptor I and SIRT1/6, as a previously unrecognized mechanism in human alveolar epithelial cells, and consequently mitigates COPD.

Supplementary File

Share this article on

  • line

Related articles in Mol. Cells

Molecules and Cells

eISSN 0219-1032
qr-code Download