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RNA 聚合酶 II 的 C 末端结构域通过特异性位点甲基化修饰。

The C-terminal domain of RNA polymerase II is modified by site-specific methylation.

机构信息

Howard Hughes Medical Institute (HHMI), Department of Biochemistry, New York University School of Medicine, 522 First Avenue, Smilow 211, New York, NY 10016, USA.

Department of Molecular Epigenetics, Helmholtz Center Munich, Center of Integrated Protein Science Munich (CIPSM), Marchioninistrasse 25, 81377 Munich, Germany.

出版信息

Science. 2011 Apr 1;332(6025):99-103. doi: 10.1126/science.1202663.

Abstract

The carboxy-terminal domain (CTD) of RNA polymerase II (RNAPII) in mammals undergoes extensive posttranslational modification, which is essential for transcriptional initiation and elongation. Here, we show that the CTD of RNAPII is methylated at a single arginine (R1810) by the coactivator-associated arginine methyltransferase 1 (CARM1). Although methylation at R1810 is present on the hyperphosphorylated form of RNAPII in vivo, Ser2 or Ser5 phosphorylation inhibits CARM1 activity toward this site in vitro, suggesting that methylation occurs before transcription initiation. Mutation of R1810 results in the misexpression of a variety of small nuclear RNAs and small nucleolar RNAs, an effect that is also observed in Carm1(-/-) mouse embryo fibroblasts. These results demonstrate that CTD methylation facilitates the expression of select RNAs, perhaps serving to discriminate the RNAPII-associated machinery recruited to distinct gene types.

摘要

哺乳动物 RNA 聚合酶 II(RNAPII)的羧基末端结构域(CTD)经历广泛的翻译后修饰,这对于转录起始和延伸至关重要。在这里,我们表明 RNAPII 的 CTD 被共激活因子相关精氨酸甲基转移酶 1(CARM1)在单个精氨酸(R1810)处甲基化。尽管在体内 RNAPII 的高度磷酸化形式上存在 R1810 甲基化,但 Ser2 或 Ser5 磷酸化在体外抑制 CARM1 对该位点的活性,表明甲基化发生在转录起始之前。R1810 突变导致多种小核 RNA 和小核仁 RNA 的错误表达,在 Carm1(-/-)小鼠胚胎成纤维细胞中也观察到这种效应。这些结果表明 CTD 甲基化有助于选择性 RNA 的表达,可能有助于区分募集到不同基因类型的 RNAPII 相关机制。

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