| Literature DB >> 21836637 |
Pablo García-Gutiérrez1, Francisco Juárez-Vicente, Francisco Gallardo-Chamizo, Patrick Charnay, Mario García-Domínguez.
Abstract
Covalent attachment of small ubiquitin-like modifier (SUMO) to proteins regulates many processes in the eukaryotic cell. This reaction is similar to ubiquitination and usually requires an E3 ligase for substrate modification. However, only a few SUMO ligases have been described so far, which frequently facilitate sumoylation by bringing together the SUMO-conjugating enzyme Ubc9 and the target protein. Ubc9 is an interaction partner of the transcription factor Krox20, a key regulator of hindbrain development. Here, we show that Krox20 functions as a SUMO ligase for its coregulators--the Nab proteins--and that Nab sumoylation negatively modulates Krox20 transcriptional activity in vivo.Entities:
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Year: 2011 PMID: 21836637 PMCID: PMC3185338 DOI: 10.1038/embor.2011.152
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807