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组蛋白和组蛋白修饰酶通过染色质结构改变参与细胞功能。

Participation of histones and histone-modifying enzymes in cell functions through alterations in chromatin structure.

作者信息

Nakayama T, Takami Y

机构信息

Department of Biochemistry, Miyazaki Medical College, Kihara, Kiyotake, Miyazaki 889-1692, Japan.

出版信息

J Biochem. 2001 Apr;129(4):491-9. doi: 10.1093/oxfordjournals.jbchem.a002882.

DOI:10.1093/oxfordjournals.jbchem.a002882
PMID:11275546
Abstract

Alterations in the chromatin structure are preferentially involved in the regulation of cell functions, including gene expression, in eukaryotes. Three types of mechanisms, by which the alterations are caused have been reported: (i) variants of histone subtypes, (ii) chromatin remodeling, and (iii) post-translational modification. This review focuses mainly on the first and third mechanisms, especially on the acetylation of core histones, one of the third mechanisms. Using the gene targeting technique for the DT40 chicken B cell line, we systematically generated a number of mutants, respectively, devoid of particular genes encoding histones and histone deacetylase(s) (HDACs). Most of the H1 and core histone variants should be involved positively or negatively in the transcription regulation of particular genes. Of the chicken HDACs (chHDACs), chHDAC-2 controls the amount of the IgM H-chain at the steps of both transcription and alternative pre-mRNA processing, and chHDAC-3 is essential for cell viability, whereas chHDAC-1 merely affects gene expression in DT40 cells. These results indicate that HDAC family members should participate, in combination with one another, and/or histone acetyltransferase(s) (HATs), in the acetylation of core histones that regulates gene expression through alterations in the chromatin structure.

摘要

在真核生物中,染色质结构的改变优先参与细胞功能的调控,包括基因表达。已报道引起这些改变的三种机制:(i)组蛋白亚型变体,(ii)染色质重塑,以及(iii)翻译后修饰。本综述主要关注第一种和第三种机制,特别是第三种机制中的核心组蛋白乙酰化。利用针对DT40鸡B细胞系的基因靶向技术,我们分别系统地产生了许多缺失特定组蛋白和组蛋白去乙酰化酶(HDAC)编码基因的突变体。大多数H1和核心组蛋白变体应正向或负向参与特定基因的转录调控。在鸡HDAC(chHDAC)中,chHDAC - 2在转录和前体mRNA可变加工步骤中控制IgM重链的量,chHDAC - 3对细胞活力至关重要,而chHDAC - 1仅影响DT40细胞中的基因表达。这些结果表明,HDAC家族成员应相互结合,和/或与组蛋白乙酰转移酶(HAT)一起参与核心组蛋白的乙酰化,通过染色质结构的改变来调节基因表达。

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