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核小体重塑:一种机制,多种现象?

Nucleosome remodeling: one mechanism, many phenomena?

作者信息

Längst Gernot, Becker Peter B

机构信息

Adolf-Butenandt-Institut, Molekularbiologie, Ludwig-Maximilians-University Munchen, Schillerstrasse 44, D-80336 Munich, Germany.

出版信息

Biochim Biophys Acta. 2004 Mar 15;1677(1-3):58-63. doi: 10.1016/j.bbaexp.2003.10.011.

Abstract

The term 'nucleosome remodeling' subsumes a large number of energy-dependent alterations of canonical nucleosome structure, catalyzed by dedicated ATPases in large multiprotein complexes. The importance of these factors for gene regulation and other processes with chromatin substrate have emerged from genetic studies. Mechanistic analyses of nucleosome remodeling by different enzymes provided a diverse, almost confusing phenomenology of ATP-dependent derangement of nucleosomes in vitro, suggesting that different remodeling machines follow different strategies to disrupt histone-DNA interactions. This review explores the alternative possibility that the rich phenomenology of nucleosome remodeling may be brought about by variations of one basic remodeling reaction.

摘要

“核小体重塑”一词涵盖了由大型多蛋白复合物中的专用ATP酶催化的大量依赖能量的经典核小体结构改变。这些因子对基因调控和其他涉及染色质底物的过程的重要性已从遗传学研究中显现出来。对不同酶介导的核小体重塑的机制分析在体外提供了一种多样的、几乎令人困惑的核小体ATP依赖性紊乱现象,这表明不同的重塑机器采用不同的策略来破坏组蛋白与DNA的相互作用。本综述探讨了另一种可能性,即核小体重塑丰富的现象可能是由一种基本重塑反应的变化引起的。

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