Underhill C, Qutob M S, Yee S P, Torchia J
Departments of Pharmacology and Toxicology, Oncology, and Biochemistry, Cancer Research Laboratories, London Regional Cancer Centre, The University of Western Ontario, London, Ontario, Canada.
J Biol Chem. 2000 Dec 22;275(51):40463-70. doi: 10.1074/jbc.M007864200.
Transcriptional silencing by many transcription factors is mediated by the nuclear receptor corepressor (N-CoR). The mechanism by which N-CoR represses basal transcription involves the direct or indirect recruitment of histone deacetylases (HDACs). We have isolated two multiprotein N-CoR complexes, designated N-CoR-1 and N-CoR-2, which possess histone deacetylase activity that is mediated by distinct HDACs. Based on Western blotting using antibodies against known subunits, the only HDAC found in the N-CoR-1 complex was HDAC3. In contrast, N-CoR-2 contained predominantly HDAC1 and HDAC2 as well as several other subunits that are found in the Sin3A.HDAC complex. Using mass spectrometry and Western blotting, we have identified several novel components of the N-CoR-1 complex including the SWI/SNF-related proteins BRG1, BAF 170, BAF 155, BAF 47/INI1, and the corepressor KAP-1 that is involved in silencing heterochromatin. Indirect immunofluorescence has revealed that both KAP-1 and N-CoR colocalize throughout the nucleus. These results suggest that N-CoR is found in distinct multiprotein complexes, which are involved in multiple pathways of transcriptional repression.
许多转录因子介导的转录沉默是由核受体辅阻遏物(N-CoR)实现的。N-CoR抑制基础转录的机制涉及组蛋白去乙酰化酶(HDAC)的直接或间接募集。我们分离出了两种多蛋白N-CoR复合物,分别命名为N-CoR-1和N-CoR-2,它们具有由不同HDAC介导的组蛋白去乙酰化酶活性。基于使用针对已知亚基的抗体进行的蛋白质印迹分析,在N-CoR-1复合物中发现的唯一HDAC是HDAC3。相比之下,N-CoR-2主要包含HDAC1和HDAC2以及在Sin3A.HDAC复合物中发现的其他几个亚基。通过质谱分析和蛋白质印迹分析,我们鉴定出了N-CoR-1复合物的几个新组分,包括与SWI/SNF相关的蛋白BRG1、BAF 170、BAF 155、BAF 47/INI1,以及参与异染色质沉默的辅阻遏物KAP-1。间接免疫荧光显示KAP-1和N-CoR在整个细胞核中都共定位。这些结果表明,N-CoR存在于不同的多蛋白复合物中,这些复合物参与多种转录抑制途径。