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异染色质蛋白 1α对肌源性基因表达的表观遗传调控。

Epigenetic regulation of myogenic gene expression by heterochromatin protein 1 alpha.

机构信息

Department of Medicine, Center for Cardiovascular Biology, Institute for Stem Cell Research, University of Washington School of Medicine, Seattle, Washington, United States of America.

出版信息

PLoS One. 2013;8(3):e58319. doi: 10.1371/journal.pone.0058319. Epub 2013 Mar 11.

DOI:10.1371/journal.pone.0058319
PMID:23505487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3594309/
Abstract

Heterochromatin protein 1 (HP1) is an essential heterochromatin-associated protein typically involved in the epigenetic regulation of gene silencing. However, recent reports have demonstrated that HP1 can also activate gene expression in certain contexts including differentiation. To explore the role of each of the three mammalian HP1 family members (α, β and γ) in skeletal muscle, their expression was individually disrupted in differentiating skeletal myocytes. Among the three isoforms of HP1, HP1α was specifically required for myogenic gene expression in myoblasts only. Knockdown of HP1α led to a defect in transcription of skeletal muscle-specific genes including Lbx1, MyoD and myogenin. HP1α binds to the genomic region of myogenic genes and depletion of HP1α results in a paradoxical increase in histone H3 lysine 9 trimethylation (H3K9me3) at these sites. JHDM3A, a H3K9 demethylase also binds to myogenic gene's genomic regions in myoblasts in a HP1α-dependent manner. JHDM3A interacts with HP1α and knockdown of JHDM3A in myoblasts recapitulates the decreased myogenic gene transcription seen with HP1α depletion. These results propose a novel mechanism for HP1α-dependent gene activation by interacting with the demethylase JHDM3A and that HP1α is required for maintenance of myogenic gene expression in myoblasts.

摘要

异染色质蛋白 1(HP1)是一种必需的异染色质相关蛋白,通常参与基因沉默的表观遗传调控。然而,最近的报告表明,HP1 也可以在某些情况下激活基因表达,包括分化。为了探讨三种哺乳动物 HP1 家族成员(α、β和γ)在骨骼肌中的作用,分别在分化的骨骼肌细胞中破坏它们的表达。在三种 HP1 同工型中,只有 HP1α 特异性地需要在成肌细胞中表达肌源性基因。HP1α 的敲低导致包括 Lbx1、MyoD 和 myogenin 在内的骨骼肌特异性基因的转录缺陷。HP1α 结合到肌源性基因的基因组区域,HP1α 的耗竭导致这些位点上组蛋白 H3 赖氨酸 9 三甲基化(H3K9me3)的反常增加。JHDM3A 是一种 H3K9 去甲基酶,也以 HP1α 依赖的方式结合到成肌细胞中肌源性基因的基因组区域。JHDM3A 与 HP1α 相互作用,在成肌细胞中敲低 JHDM3A 可再现 HP1α 耗竭时观察到的肌源性基因转录减少。这些结果提出了一种新的机制,即 HP1α 通过与去甲基酶 JHDM3A 相互作用来激活基因,并且 HP1α 对于维持成肌细胞中肌源性基因的表达是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1822/3594309/d22367a5a9b2/pone.0058319.g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1822/3594309/cae7b833ab9e/pone.0058319.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1822/3594309/074f66bb82f1/pone.0058319.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1822/3594309/faabb7a0581d/pone.0058319.g003.jpg
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