Suppr超能文献

蛋白质甲基转移酶对转录的调控。

Regulation of transcription by a protein methyltransferase.

作者信息

Chen D, Ma H, Hong H, Koh S S, Huang S M, Schurter B T, Aswad D W, Stallcup M R

机构信息

Department of Pathology HMR 301, University of Southern California, 2011 Zonal Avenue, Los Angeles, CA 90033, USA.

出版信息

Science. 1999 Jun 25;284(5423):2174-7. doi: 10.1126/science.284.5423.2174.

Abstract

The p160 family of coactivators, SRC-1, GRIP1/TIF2, and p/CIP, mediate transcriptional activation by nuclear hormone receptors. Coactivator-associated arginine methyltransferase 1 (CARM1), a previously unidentified protein that binds to the carboxyl-terminal region of p160 coactivators, enhanced transcriptional activation by nuclear receptors, but only when GRIP1 or SRC-1a was coexpressed. Thus, CARM1 functions as a secondary coactivator through its association with p160 coactivators. CARM1 can methylate histone H3 in vitro, and a mutation in the putative S-adenosylmethionine binding domain of CARM1 substantially reduced both methyltransferase and coactivator activities. Thus, coactivator-mediated methylation of proteins in the transcription machinery may contribute to transcriptional regulation.

摘要

共激活因子的p160家族,即SRC-1、GRIP1/TIF2和p/CIP,介导核激素受体的转录激活。共激活因子相关精氨酸甲基转移酶1(CARM1)是一种先前未被鉴定的与p160共激活因子羧基末端区域结合的蛋白质,它增强了核受体的转录激活作用,但仅在GRIP1或SRC-1a共表达时才会如此。因此,CARM1通过与p160共激活因子结合而作为一种辅助共激活因子发挥作用。CARM1能够在体外使组蛋白H3甲基化,并且CARM1假定的S-腺苷甲硫氨酸结合结构域中的一个突变显著降低了甲基转移酶活性和共激活因子活性。因此,转录机制中共激活因子介导的蛋白质甲基化可能有助于转录调控。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验