Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0043137
Title: SUMO modification of Stra13 is required for repression of cyclin D1 expression and cellular growth arrest
Authors: Wang, Y.
Rao, V.K. 
Kok, W.K. 
Roy, D.N. 
Sethi, S. 
Ling, B.M.T. 
Lee, M.B.H. 
Taneja, R. 
Issue Date: 14-Aug-2012
Citation: Wang, Y., Rao, V.K., Kok, W.K., Roy, D.N., Sethi, S., Ling, B.M.T., Lee, M.B.H., Taneja, R. (2012-08-14). SUMO modification of Stra13 is required for repression of cyclin D1 expression and cellular growth arrest. PLoS ONE 7 (8) : -. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0043137
Abstract: Stra13, a basic helix-loop-helix (bHLH) transcription factor is involved in myriad biological functions including cellular growth arrest, differentiation and senescence. However, the mechanisms by which its transcriptional activity and function are regulated remain unclear. In this study, we provide evidence that post-translational modification of Stra13 by Small Ubiquitin-like Modifier (SUMO) dramatically potentiates its ability to transcriptionally repress cyclin D1 and mediate G1 cell cycle arrest in fibroblast cells. Mutation of SUMO acceptor lysines 159 and 279 located in the C-terminal repression domain has no impact on nuclear localization; however, it abrogates association with the co-repressor histone deacetylase 1 (HDAC1), attenuates repression of cyclin D1, and prevents Stra13-mediated growth suppression. HDAC1, which promotes cellular proliferation and cell cycle progression, antagonizes Stra13 sumoylation-dependent growth arrest. Our results uncover an unidentified regulatory axis between Stra13 and HDAC1 in progression through the G1/S phase of the cell cycle, and provide new mechanistic insights into regulation of Stra13-mediated transcriptional repression by sumoylation. © 2012 Wang et al.
Source Title: PLoS ONE
URI: http://scholarbank.nus.edu.sg/handle/10635/125311
ISSN: 19326203
DOI: 10.1371/journal.pone.0043137
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