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组蛋白尾部切割作为一种表观遗传调控机制。

Histone Tail Cleavage as a Mechanism for Epigenetic Regulation.

机构信息

Department of Biochemistry and Molecular Medicine, Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA 90033, USA.

出版信息

Int J Mol Sci. 2024 Oct 8;25(19):10789. doi: 10.3390/ijms251910789.

Abstract

Histones are essential for DNA packaging and undergo post-translational modifications that significantly influence gene regulation. Among these modifications, histone tail cleavage has recently garnered attention despite being less explored. Cleavage by various proteases impacts processes such as stem cell differentiation, aging, infection, and inflammation, though the mechanisms remain unclear. This review delves into recent insights on histone proteolytic cleavage and its epigenetic significance, highlighting how chromatin, which serves as a dynamic scaffold, responds to signals through histone modification, replacement, and ATP-dependent remodeling. Specifically, histone tail cleavage is linked to critical cellular processes such as granulocyte differentiation, viral infection, aging, yeast sporulation, and cancer development. Although the exact mechanisms connecting histone cleavage to gene expression are still emerging, it is clear that this process represents a novel epigenetic transcriptional mechanism intertwined with chromatin dynamics. This review explores known histone tail cleavage events, the proteolytic enzymes involved, their impact on gene expression, and future research directions in this evolving field.

摘要

组蛋白对于 DNA 包装至关重要,并经历着翻译后修饰,这些修饰显著影响着基因调控。在这些修饰中,尽管组蛋白尾部切割的研究较少,但它最近引起了人们的关注。各种蛋白酶的切割影响着干细胞分化、衰老、感染和炎症等过程,尽管其机制尚不清楚。本综述深入探讨了组蛋白蛋白水解切割及其表观遗传意义的最新见解,强调了作为动态支架的染色质如何通过组蛋白修饰、替换和 ATP 依赖性重塑来响应信号。具体来说,组蛋白尾部切割与关键的细胞过程有关,如粒细胞分化、病毒感染、衰老、酵母孢子形成和癌症发展。尽管将组蛋白切割与基因表达联系起来的确切机制尚不清楚,但很明显,这一过程代表了一种与染色质动力学交织在一起的新型表观遗传转录机制。本综述探讨了已知的组蛋白尾部切割事件、涉及的蛋白水解酶、它们对基因表达的影响以及该不断发展领域的未来研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ae9/11477362/5c661b883c9e/ijms-25-10789-g001.jpg

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