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作为染色质功能介质的核小体稳定性调控。

Regulation of nucleosome stability as a mediator of chromatin function.

作者信息

Giresi Paul G, Gupta Mayetri, Lieb Jason D

机构信息

Department of Biology and Carolina Center for Genome Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA.

出版信息

Curr Opin Genet Dev. 2006 Apr;16(2):171-6. doi: 10.1016/j.gde.2006.02.003. Epub 2006 Feb 28.

Abstract

Interactions among regulatory proteins, enzymes and DNA are required to use the information encoded in genomes. In eukaryotes, the location and timing of interactions between these proteins and DNA is determined in large part by whether DNA at a given locus is packaged into a nucleosome. Given the central role of nucleosome formation in regulating genome function, many mechanisms have evolved to control nucleosome stability at loci across the genome. New conclusions about the role of the DNA sequence itself in the regulation of nucleosome stability have come from two new types of experiment: high-resolution mapping of in vivo nucleosome occupancy on a genomic scale; and in vivo versus in vitro comparisons of nucleosome stability on natural DNA templates. These new types of data raise intriguing questions about the evolutionary constraints on DNA sequence with regard to nucleosome formation, and at long last might enable the derivation of DNA sequence-based rules that produce reliable predictions of nucleosome behavior.

摘要

利用基因组中编码的信息需要调控蛋白、酶和DNA之间的相互作用。在真核生物中,这些蛋白质与DNA之间相互作用的位置和时间在很大程度上取决于给定基因座处的DNA是否被包装成核小体。鉴于核小体形成在调节基因组功能中的核心作用,已经进化出许多机制来控制全基因组各基因座处的核小体稳定性。关于DNA序列本身在核小体稳定性调控中的作用的新结论来自于两种新型实验:在基因组规模上对体内核小体占据情况进行高分辨率图谱绘制;以及对天然DNA模板上的核小体稳定性进行体内与体外比较。这些新型数据引发了关于核小体形成方面DNA序列进化限制的有趣问题,最终或许能够推导出基于DNA序列的规则,从而对核小体行为做出可靠预测。

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