Keppler Brian R, Archer Trevor K, Kinyamu H Karimi
Chromatin and Gene Expression Section, Laboratory of Molecular Carcinogenesis, NIEHS/NIH, Research Triangle Park, NC 27709, USA.
Biochim Biophys Acta. 2011 Feb;1809(2):109-18. doi: 10.1016/j.bbagrm.2010.08.005. Epub 2010 Aug 20.
The mechanisms by which nuclear hormone receptors (NHRs) regulate transcription are highly dynamic and require interplay between a myriad of regulatory protein complexes including the 26S proteasome. Protein degradation is the most well-established role of the proteasome; however, an increasing body of evidence suggests that the 26S proteasome may regulate transcription in proteolytic and nonproteolytic mechanisms. Here we review how these mechanisms may apply to NHR-mediated transcriptional regulation. This article is part of a Special Issue entitled The 26S Proteasome: When degradation is just not enough!
核激素受体(NHRs)调节转录的机制高度动态,需要包括26S蛋白酶体在内的众多调节蛋白复合物之间相互作用。蛋白质降解是蛋白酶体最确定的作用;然而,越来越多的证据表明,26S蛋白酶体可能通过蛋白水解和非蛋白水解机制调节转录。在这里,我们综述这些机制如何应用于NHR介导的转录调控。本文是名为“26S蛋白酶体:降解并不够!”的特刊的一部分。