Epigenetic codes of PPARγ in metabolic disease

被引:87
作者
Sugii, Shigeki [1 ,2 ,3 ,4 ]
Evans, Ronald M. [1 ,2 ]
机构
[1] Salk Inst Biol Studies, Howard Hughes Med Inst, La Jolla, CA 92037 USA
[2] Salk Inst Biol Studies, Gene Express Lab, La Jolla, CA 92037 USA
[3] Singapore Bioimaging Consortium, Singapore 138667, Singapore
[4] Duke NUS Grad Med Sch, Singapore 138667, Singapore
基金
美国国家卫生研究院;
关键词
Obesity-induced insulin resistance; Adipose tissue; Epigenome; Histone acetyltransferases; Deacetylases; Histone methyltransferases; Demethylases; ACTIVATED-RECEPTOR-GAMMA; NUCLEAR RECEPTORS; ADIPOSE-TISSUE; WHITE ADIPOCYTES; INSULIN SENSITIVITY; ANDROGEN-RECEPTOR; DNA METHYLATION; C/EBP-ALPHA; FAT; EXPRESSION;
D O I
10.1016/j.febslet.2011.05.007
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
Peroxisome proliferator-activated receptor gamma (PPAR gamma), a ligand-regulated nuclear hormone receptor, plays critical roles in metabolism and adipogenesis. PPAR gamma ligands such as thiazolidinediones (TZDs) exert insulin sensitizing and anti-inflammatory effects primarily through action on adipocytes, and are thus widely used to treat metabolic syndrome, especially type II diabetes. A number of PPAR gamma interacting partners have been identified, many of which are known epigenetic regulators, including enzymes for histone acetylation/deacetylation and histone methylation/demethylation. However, their functional roles in the PPAR gamma transcriptional pathway are not well defined. Recent advances in ChIP-based and deep sequencing technology are revealing previously underappreciated epigenomic mechanisms and therapeutic potentials of this nuclear receptor pathway. (C) 2011 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:2121 / 2128
页数:8
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