RIP140 directs histone and DNA methylation to silence Ucp1 expression in white adipocytes

被引:82
作者
Kiskinis, Evangelos
Hallberg, Magnus
Christian, Mark
Olofsson, Martina
Dilworth, Stephen M.
White, Roger
Parker, Malcolm G.
机构
[1] Imperial Coll London, Inst Reprod & Dev Biol, Mol Endocrinol Lab, London W12 0NN, England
[2] Imperial Coll London, Fac Med, Dept Metabol Med, London, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
adipocytes; DNA methylation; nuclear receptors; RIP140; Ucp1;
D O I
10.1038/sj.emboj.7601908
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nuclear receptors control the function of cells by regulating transcription from specific gene networks. The establishment and maintenance of epigenetic gene marks is fundamental to the regulation of gene transcription and the control of cell function. RIP140 is a corepressor for nuclear receptors that suppresses transcription from a broad programme of metabolic genes and thereby controls energy homoeostasis in vivo. Here we show by analysis of Ucp1, a gene which is typically expressed in brown but not white adipocytes, that RIP140 is essential for both DNA and histone methylation to maintain gene repression. RIP140 expression promotes the assembly of DNA and histone methyltransferases ( HMTs) on the Ucp1 enhancer and leads to methylation of specific CpG residues and histones as judged by bisulphite genomic sequencing and chromatin immunoprecipitation assays. Our results suggest that RIP140 serves as a scaffold for both DNA and HMT activities to inhibit gene transcription by two key epigenetic repression systems.
引用
收藏
页码:4831 / 4840
页数:10
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