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赖氨酸甲基转移酶G9a在免疫细胞分化和功能中的作用

The Lysine Methyltransferase G9a in Immune Cell Differentiation and Function.

作者信息

Scheer Sebastian, Zaph Colby

机构信息

Infection and Immunity Program, Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia.

出版信息

Front Immunol. 2017 Apr 11;8:429. doi: 10.3389/fimmu.2017.00429. eCollection 2017.

Abstract

G9a (KMT1C, EHMT2) is a lysine methyltransferase (KMT) whose primary function is to di-methylate lysine 9 of histone H3 (H3K9me2). G9a-dependent H3K9me2 is associated with gene silencing and acts primarily through the recruitment of H3K9me2-binding proteins that prevent transcriptional activation. Gene repression via G9a-dependent H3K9me2 is critically required in embryonic stem (ES) cells for the development of cellular lineages by repressing expression of pluripotency factors. In the immune system, lymphoid cells such as T cells and innate lymphoid cells (ILCs) can differentiate from a naïve state into one of several effector lineages that require both activating and repressive mechanisms to maintain the correct gene expression program. Furthermore, the long-term immunity to re-infection is mediated by memory T cells, which also require specific gene expression and repression to maintain a quiescent state. In this review, we examine the molecular machinery of G9a-dependent functions, address the role of G9a in lymphoid cell differentiation and function, and identify potential functions of T cells and ILCs that may be controlled by G9a. Together, this review will highlight the dynamic nature of G9a-dependent H3K9me2 in the immune system and shed light on the nature of repressive epigenetic modifications in cellular lineage choice.

摘要

G9a(KMT1C,EHMT2)是一种赖氨酸甲基转移酶(KMT),其主要功能是使组蛋白H3的赖氨酸9位点发生二甲基化(H3K9me2)。G9a依赖的H3K9me2与基因沉默相关,主要通过招募阻止转录激活的H3K9me2结合蛋白发挥作用。在胚胎干细胞中,通过抑制多能性因子的表达,经由G9a依赖的H3K9me2实现的基因抑制对于细胞谱系的发育至关重要。在免疫系统中,诸如T细胞和固有淋巴细胞(ILC)等淋巴细胞可从幼稚状态分化为几种效应细胞谱系之一,这需要激活和抑制机制来维持正确的基因表达程序。此外,对再次感染的长期免疫由记忆T细胞介导,记忆T细胞也需要特定的基因表达和抑制来维持静止状态。在本综述中,我们研究了G9a依赖性功能的分子机制,探讨了G9a在淋巴细胞分化和功能中的作用,并确定了可能受G9a控制的T细胞和ILC的潜在功能。总之,本综述将突出G9a依赖的H3K9me2在免疫系统中的动态性质,并阐明细胞谱系选择中抑制性表观遗传修饰的本质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa77/5387087/eb421670148e/fimmu-08-00429-g001.jpg

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