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.
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Dagang Chen
Rice Research Institute
Han Ma
Fourth Affiliated Hospital of Guangxi Medical University
Heng Hong
Wake Forest University
Science
University of Southern California
University of California, Irvine
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Chen et al. (Fri,) studied this question.
synapsesocial.com/papers/6a0068f4581c6e761e77bc82 — DOI: https://doi.org/10.1126/science.284.5423.2174