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AGO1 通过调节 eRNA 介导的 CBP 指导的表观基因组重编程来控制成肌分化。

Ago1 controls myogenic differentiation by regulating eRNA-mediated CBP-guided epigenome reprogramming.

机构信息

King Abdullah University of Science and Technology, KAUST Environmental Epigenetics Research Program, Biological and Environmental Sciences and Engineering Division, Thuwal 23955, Saudi Arabia.

Sequentia Biotech, Carrer Comte D'Urgell 240, 08036 Barcelona, Spain.

出版信息

Cell Rep. 2021 Nov 30;37(9):110066. doi: 10.1016/j.celrep.2021.110066.

Abstract

The role of chromatin-associated RNAi components in the nucleus of mammalian cells and in particular in the context of developmental programs remains to be elucidated. Here, we investigate the function of nuclear Argonaute 1 (Ago1) in gene expression regulation during skeletal muscle differentiation. We show that Ago1 is required for activation of the myogenic program by supporting chromatin modification mediated by developmental enhancer activation. Mechanistically, we demonstrate that Ago1 directly controls global H3K27 acetylation (H3K27ac) by regulating enhancer RNA (eRNA)-CREB-binding protein (CBP) acetyltransferase interaction, a key step in enhancer-driven gene activation. In particular, we show that Ago1 is specifically required for myogenic differentiation 1 (MyoD) and downstream myogenic gene activation, whereas its depletion leads to failure of CBP acetyltransferase activation and blocking of the myogenic program. Our work establishes a role of the mammalian enhancer-associated RNAi component Ago1 in epigenome regulation and activation of developmental programs.

摘要

染色质相关 RNAi 成分在哺乳动物细胞核中的作用,特别是在发育程序的背景下,仍有待阐明。在这里,我们研究了核 Argonaute 1(Ago1)在骨骼肌分化过程中基因表达调控中的功能。我们表明,Ago1 通过支持由发育增强子激活介导的染色质修饰,对于肌生成程序的激活是必需的。从机制上讲,我们证明 Ago1 通过调节增强子 RNA(eRNA)-CREB 结合蛋白(CBP)乙酰转移酶相互作用直接控制全局 H3K27 乙酰化(H3K27ac),这是增强子驱动基因激活的关键步骤。特别是,我们表明 Ago1 特异性地需要肌生成分化 1(MyoD)和下游肌生成基因的激活,而其耗竭会导致 CBP 乙酰转移酶激活失败和肌生成程序受阻。我们的工作确立了哺乳动物增强子相关 RNAi 成分 Ago1 在表观基因组调控和发育程序激活中的作用。

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