Strohner R, Nemeth A, Jansa P, Hofmann-Rohrer U, Santoro R, Längst G, Grummt I
Division of Molecular Biology of the Cell II, Deutsches Krebsforschungszentrum, D-69120 Heidelberg and Adolf-Butenandt-Institut, Schillerstrasse 44, D-80336 München, Germany.
EMBO J. 2001 Sep 3;20(17):4892-900. doi: 10.1093/emboj/20.17.4892.
Transcription by RNA polymerase I on nucleosomal templates requires binding of the transcription termination factor TTF-I to a cognate site 160 bp upstream of the transcription start site. Binding of TTF-I is accompanied by changes in the chromatin architecture which suggests that TTF-I recruits a remodeling activity to the rDNA promoter. We have cloned a cDNA that encodes TIP5 (TTF-I-interacting protein 5), a 205 kDa protein that shares a number of important protein domains with WSTF (Williams syndrome transcription factor) and hAcf1/WCRF180, the largest subunits of human chromatin remodeling complexes hCHRAC and WCRF. TIP5 co-localizes with the basal RNA polymerase I transcription factor UBF in the nucleolus and is associated with SNF2h. The cellular TIP5-SNF2h complex, termed NoRC (nucleolar remodeling complex), induces nucleosome sliding in an ATP- and histone H4 tail-dependent fashion. The results suggest that NoRC is a novel nucleolar chromatin remodeling machine that may serve a role in the regulation of the rDNA locus.
RNA聚合酶I在核小体模板上进行转录需要转录终止因子TTF-I与转录起始位点上游160 bp处的同源位点结合。TTF-I的结合伴随着染色质结构的变化,这表明TTF-I将一种重塑活性招募到rDNA启动子上。我们克隆了一个编码TIP5(TTF-I相互作用蛋白5)的cDNA,TIP5是一种205 kDa的蛋白质,与WSTF(威廉姆斯综合征转录因子)以及人染色质重塑复合物hCHRAC和WCRF的最大亚基hAcf1/WCRF180共享许多重要的蛋白质结构域。TIP5与基础RNA聚合酶I转录因子UBF在核仁中共定位,并与SNF2h相关联。细胞中的TIP5-SNF2h复合物,称为NoRC(核仁重塑复合物),以ATP和组蛋白H4尾部依赖的方式诱导核小体滑动。结果表明,NoRC是一种新型的核仁染色质重塑机器,可能在rDNA基因座的调控中发挥作用。