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组蛋白去乙酰化酶及其在矿化组织再生中的作用。

Histone deacetylases and their roles in mineralized tissue regeneration.

作者信息

Huynh Nam Cong-Nhat, Everts Vincent, Ampornaramveth Ruchanee Salingcarnboriboon

机构信息

Department of Dental Basic Sciences, Faculty of Odonto-Stomatology, University of Medicine and Pharmacy at Ho Chi Minh City, Viet Nam.

Department of Oral Cell Biology, Academic Centre for Dentistry Amsterdam (ACTA), University of Amsterdam and Vrije Universiteit Amsterdam, Research Institute MOVE, Gustav Mahlerlaan 3004, 1081 LA Amsterdam, The Netherlands.

出版信息

Bone Rep. 2017 Aug 16;7:33-40. doi: 10.1016/j.bonr.2017.08.001. eCollection 2017 Dec.

Abstract

Histone acetylation is an important epigenetic mechanism that controls expression of certain genes. It includes non-sequence-based changes of chromosomal regional structure that can alter the expression of genes. Acetylation of histones is controlled by the activity of two groups of enzymes: the histone acetyltransferases (HATs) and histone deacetylases (HDACs). HDACs remove acetyl groups from the histone tail, which alters its charge and thus promotes compaction of DNA in the nucleosome. HDACs render the chromatin structure into a more compact form of heterochromatin, which makes the genes inaccessible for transcription. By altering the transcriptional activity of bone-associated genes, HDACs control both osteogenesis and osteoclastogenesis. This review presents an overview of the function of HDACs in the modulation of bone formation. Special attention is paid to the use of HDAC inhibitors in mineralized tissue regeneration from cells of dental origin.

摘要

组蛋白乙酰化是一种重要的表观遗传机制,可控制某些基因的表达。它包括基于非序列的染色体区域结构变化,这种变化可改变基因的表达。组蛋白的乙酰化由两组酶的活性控制:组蛋白乙酰转移酶(HATs)和组蛋白去乙酰化酶(HDACs)。HDACs从组蛋白尾部去除乙酰基,这会改变其电荷,从而促进核小体中DNA的压缩。HDACs使染色质结构转变为更紧密的异染色质形式,这使得基因无法进行转录。通过改变与骨相关基因的转录活性,HDACs控制成骨作用和破骨细胞生成。本综述概述了HDACs在调节骨形成中的功能。特别关注HDAC抑制剂在源自牙齿细胞的矿化组织再生中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a773/5565747/b9efa0b9af65/gr1.jpg

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