Zhou Yonggang, Santoro Raffaella, Grummt Ingrid
Division of Molecular Biology of the Cell II, Deutsches Krebsforschungszentrum, D-69120 Heidelberg, Germany.
EMBO J. 2002 Sep 2;21(17):4632-40. doi: 10.1093/emboj/cdf460.
Mammalian chromatin remodeling complexes are involved in both activation and repression of transcription. Here, we show that NoRC, a SNF2h- containing nucleolar chromatin remodeling complex, represses ribosomal gene transcription. NoRC-mediated rDNA silencing was alleviated by trichostatin A, indicating that histone deacetylation is causally involved in silencing. Chromatin immunoprecipitation experiments demonstrate that overexpression of TIP5, the large subunit of NoRC, mediates deacetylation of nucleosomes in the vicinity of the rDNA promoter. Protein-protein interaction assays reveal association of TIP5 with the histone deacetylase HDAC1 in vivo and in vitro. Deletion of the C-terminal PHD finger and bromodomain abolishes the interaction of TIP5 and HDAC1, and abrogates transcriptional repression. The results suggest that NoRC silences the rDNA locus by targeting the SIN3 corepressor complex to the rDNA promoter, thereby establishing a repressed chromatin structure.
哺乳动物染色质重塑复合物参与转录的激活与抑制过程。在此,我们发现NoRC,一种含SNF2h的核仁染色质重塑复合物,可抑制核糖体基因转录。曲古抑菌素A可缓解NoRC介导的核糖体DNA沉默,这表明组蛋白去乙酰化与沉默存在因果关系。染色质免疫沉淀实验表明,NoRC的大亚基TIP5的过表达介导了核糖体DNA启动子附近核小体的去乙酰化。蛋白质-蛋白质相互作用分析揭示了TIP5在体内和体外均与组蛋白去乙酰化酶HDAC1相关联。C端PHD指结构域和溴结构域的缺失消除了TIP5与HDAC1的相互作用,并消除了转录抑制。结果表明,NoRC通过将SIN3共抑制复合物靶向核糖体DNA启动子,使核糖体DNA位点沉默,从而建立起一种抑制性染色质结构。