4.6 Article

Sumoylated NHR-25/NR5A Regulates Cell Fate during C. elegans Vulval Development

期刊

PLOS GENETICS
卷 9, 期 12, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1003992

关键词

-

资金

  1. Czech Science Foundation [204/09/H058]
  2. Czech Academy of Sciences [Z60220518, 500960906]
  3. Czech Ministry of Education [MSM6007665801]
  4. MODBIOLIN [7FP-REGPOT-2012-2013-1, GA316304]
  5. Terry Fox Foundation [700046]
  6. Canadian Institutes of Health Research [234765]
  7. NIH [CA20535]
  8. NSF [MCB-1157767]
  9. National Institute of Environmental Health Sciences [ES021412-01]
  10. Program in Breakthrough Biomedical Research
  11. Direct For Biological Sciences [1157767] Funding Source: National Science Foundation
  12. Div Of Molecular and Cellular Bioscience [1157767] Funding Source: National Science Foundation

向作者/读者索取更多资源

Individual metazoan transcription factors (TFs) regulate distinct sets of genes depending on cell type and developmental or physiological context. The precise mechanisms by which regulatory information from ligands, genomic sequence elements, co-factors, and post-translational modifications are integrated by TFs remain challenging questions. Here, we examine how a single regulatory input, sumoylation, differentially modulates the activity of a conserved C. elegans nuclear hormone receptor, NHR-25, in different cell types. Through a combination of yeast two-hybrid analysis and in vitro biochemistry we identified the single C. elegans SUMO (SMO-1) as an NHR-25 interacting protein, and showed that NHR-25 is sumoylated on at least four lysines. Some of the sumoylation acceptor sites are in common with those of the NHR-25 mammalian orthologs SF-1 and LRH-1, demonstrating that sumoylation has been strongly conserved within the NR5A family. We showed that NHR-25 bound canonical SF-1 binding sequences to regulate transcription, and that NHR-25 activity was enhanced in vivo upon loss of sumoylation. Knockdown of smo-1 mimicked NHR-25 overexpression with respect to maintenance of the 3 degrees cell fate in vulval precursor cells (VPCs) during development. Importantly, however, overexpression of unsumoylatable alleles of NHR-25 revealed that NHR-25 sumoylation is critical for maintaining 3 degrees cell fate. Moreover, SUMO also conferred formation of a developmental time-dependent NHR-25 concentration gradient across the VPCs. That is, accumulation of GFP-tagged NHR-25 was uniform across VPCs at the beginning of development, but as cells began dividing, a smo-1-dependent NHR-25 gradient formed with highest levels in 1 degrees fated VPCs, intermediate levels in 2 degrees fated VPCs, and low levels in 3 degrees fated VPCs. We conclude that sumoylation operates at multiple levels to affect NHR-25 activity in a highly coordinated spatial and temporal manner.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据