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在脂肪生成分化过程中,PPARγ2基因座处的启动子-增强子环化需要Prmt5甲基转移酶。

Promoter-enhancer looping at the PPARγ2 locus during adipogenic differentiation requires the Prmt5 methyltransferase.

作者信息

LeBlanc Scott E, Wu Qiong, Lamba Pallavi, Sif Saïd, Imbalzano Anthony N

机构信息

Department of Cell and Developmental Biology, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.

Department of Biological and Environmental Sciences, College of Arts and Sciences, Qatar University, P.O. Box 2713, Doha, Qatar Department of Internal Medicine, The Ohio State University College of Medicine, 395 W. 12th Avenue, Third Floor, Columbus, OH 43210, USA.

出版信息

Nucleic Acids Res. 2016 Jun 20;44(11):5133-47. doi: 10.1093/nar/gkw129. Epub 2016 Mar 1.

Abstract

PPARγ2 is a critical lineage-determining transcription factor that is essential for adipogenic differentiation. Here we report characterization of the three-dimensional structure of the PPARγ2 locus after the onset of adipogenic differentiation and the mechanisms by which it forms. We identified a differentiation-dependent loop between the PPARγ2 promoter and an enhancer sequence 10 kb upstream that forms at the onset of PPARγ2 expression. The arginine methyltransferase Prmt5 was required for loop formation, and overexpression of Prmt5 resulted in premature loop formation and earlier onset of PPARγ2 expression. Kinetic studies of regulatory factor interactions at the PPARγ2 promoter and enhancer revealed enhanced interaction of Prmt5 with the promoter that preceded stable association of Prmt5 with enhancer sequences. Prmt5 knockdown prevented binding of both MED1, a subunit of Mediator complex that facilitates enhancer-promoter interactions, and Brg1, the ATPase of the mammalian SWI/SNF chromatin remodeling enzyme required for PPARγ2 activation and adipogenic differentiation. The data indicate a dynamic association of Prmt5 with the regulatory sequences of the PPARγ2 gene that facilitates differentiation-dependent, three-dimensional organization of the locus. In addition, other differentiation-specific, long-range chromatin interactions showed Prmt5-dependence, indicating a more general role for Prmt5 in mediating higher-order chromatin connections in differentiating adipocytes.

摘要

PPARγ2是一种关键的谱系决定转录因子,对脂肪生成分化至关重要。在此,我们报告脂肪生成分化开始后PPARγ2基因座三维结构的特征及其形成机制。我们在PPARγ2表达开始时,在PPARγ2启动子和上游10 kb处的一个增强子序列之间鉴定出一个分化依赖性环。精氨酸甲基转移酶Prmt5是环形成所必需的,Prmt5的过表达导致环过早形成和PPARγ2表达提前开始。对PPARγ2启动子和增强子处调节因子相互作用的动力学研究表明,在Prmt5与增强子序列稳定结合之前,Prmt5与启动子的相互作用增强。Prmt5敲低可阻止MED1(促进增强子-启动子相互作用的中介复合物的一个亚基)和Brg1(PPARγ2激活和脂肪生成分化所需的哺乳动物SWI/SNF染色质重塑酶的ATP酶)的结合。数据表明Prmt5与PPARγ2基因的调控序列存在动态关联,促进了该基因座的分化依赖性三维组织。此外,其他分化特异性的长程染色质相互作用也显示出对Prmt5的依赖性,表明Prmt5在介导分化脂肪细胞中的高阶染色质连接方面具有更广泛的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb12/4914087/05aa11e08514/gkw129fig1.jpg

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