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组蛋白尾部切割作为一种新型的表观遗传调控机制参与基因表达。

Histone tail cleavage as a novel epigenetic regulatory mechanism for gene expression.

机构信息

School of Biological Sciences, College of Natural Sciences, Chungbuk National University, Cheongju 28644, Korea.

出版信息

BMB Rep. 2018 May;51(5):211-218. doi: 10.5483/bmbrep.2018.51.5.053.

Abstract

Chromatin is an intelligent building block that can express either external or internal needs through structural changes. To date, three methods to change chromatin structure and regulate gene expression have been well-documented: histone modification, histone exchange, and ATP-dependent chromatin remodeling. Recently, a growing body of literature has suggested that histone tail cleavage is related to various cellular processes including stem cell differentiation, osteoclast differentiation, granulocyte differentiation, mammary gland differentiation, viral infection, aging, and yeast sporulation. Although the underlying mechanisms suggesting how histone cleavage affects gene expression in view of chromatin structure are only beginning to be understood, it is clear that this process is a novel transcriptional epigenetic mechanism involving chromatin dynamics. In this review, we describe the functional properties of the known histone tail cleavage with its proteolytic enzymes, discuss how histone cleavage impacts gene expression, and present future directions for this area of study. [BMB Reports 2018; 51(5): 211-218].

摘要

染色质是一种智能建筑砌块,可以通过结构变化来表达外部或内部需求。迄今为止,已有三种方法可以改变染色质结构并调节基因表达,这三种方法分别是组蛋白修饰、组蛋白交换和 ATP 依赖性染色质重塑。最近,越来越多的文献表明,组蛋白尾部切割与包括干细胞分化、破骨细胞分化、粒细胞分化、乳腺分化、病毒感染、衰老和酵母孢子形成在内的各种细胞过程有关。尽管关于组蛋白切割如何影响染色质结构的基因表达的潜在机制才刚刚开始被理解,但很明显,这个过程是一个涉及染色质动力学的新型转录表观遗传机制。在这篇综述中,我们描述了已知的具有蛋白水解酶活性的组蛋白尾部切割的功能特性,讨论了组蛋白切割如何影响基因表达,并为该研究领域提出了未来的方向。[BMB 报告 2018;51(5):211-218]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd8f/5988574/721cebbcd26e/bmb-51-211f1.jpg

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