Sumoylated NHR-25/NR5A regulates cell fate during C. elegans vulval development
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S.
Grantová podpora
R01 CA020535
NCI NIH HHS - United States
P40 OD010440
NIH HHS - United States
CA20535
NCI NIH HHS - United States
#234765
CIHR - Canada
R21 ES021412
NIEHS NIH HHS - United States
ES021412-01
NIEHS NIH HHS - United States
R37 CA020535
NCI NIH HHS - United States
PubMed
24348269
PubMed Central
PMC3861103
DOI
10.1371/journal.pgen.1003992
PII: PGENETICS-D-13-00622
Knihovny.cz E-zdroje
- MeSH
- buněčná diferenciace genetika MeSH
- Caenorhabditis elegans genetika růst a vývoj MeSH
- DNA vazebné proteiny biosyntéza genetika MeSH
- mapy interakcí proteinů MeSH
- protein SUMO-1 genetika metabolismus MeSH
- sekvence aminokyselin MeSH
- signální transdukce genetika MeSH
- sumoylace * MeSH
- transkripční faktory biosyntéza genetika MeSH
- vulva cytologie růst a vývoj MeSH
- vývojová regulace genové exprese MeSH
- zvířata MeSH
- Check Tag
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
- Názvy látek
- DNA vazebné proteiny MeSH
- nuclear hormone receptor NHR-25, C elegans MeSH Prohlížeč
- protein SUMO-1 MeSH
- transkripční faktory MeSH
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° 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° 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° fated VPCs, intermediate levels in 2° fated VPCs, and low levels in 3° fated VPCs. We conclude that sumoylation operates at multiple levels to affect NHR-25 activity in a highly coordinated spatial and temporal manner.
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