Stem Cells, CABIMER (CSIC), Avenida Americo Vespucio, Seville E-41092, Spain.
EMBO Rep. 2011 Sep 30;12(10):1018-23. doi: 10.1038/embor.2011.152.
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.
蛋白质的小泛素样修饰物(SUMO)的共价附着调节真核细胞中的许多过程。该反应类似于泛素化,通常需要 E3 连接酶进行底物修饰。然而,迄今为止仅描述了少数 SUMO 连接酶,它们通常通过将 SUMO 连接酶 Ubc9 和靶蛋白聚集在一起来促进 sumoylation。Ubc9 是转录因子 Krox20 的相互作用伙伴,Krox20 是后脑发育的关键调节因子。在这里,我们表明 Krox20 作为其共调节剂 Nab 蛋白的 SUMO 连接酶发挥作用,并且 Nab sumoylation 负调节体内 Krox20 的转录活性。