Regulation of transcription by a protein methyltransferase

被引:969
作者
Chen, DG
Ma, H
Hong, H
Koh, SS
Huang, SM
Schurter, BT
Aswad, DW
Stallcup, MR
机构
[1] Univ So Calif, Dept Pathol HMR 301, Los Angeles, CA 90033 USA
[2] Univ Calif Irvine, Dept Biochem & Mol Biol, Irvine, CA USA
关键词
D O I
10.1126/science.284.5423.2174
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 CARM 1 substantially reduced both methyltransferase and coactivator activities. Thus, coactivator-mediated methylation of proteins in the transcription machinery may contribute to transcriptional regulation.
引用
收藏
页码:2174 / 2177
页数:4
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