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核小体与可及性问题。

Nucleosomes and the accessibility problem.

机构信息

Molecular Biology Program, Sloan Kettering Institute, 1275 York Avenue, New York, NY 10065, USA.

出版信息

Trends Genet. 2011 Dec;27(12):487-92. doi: 10.1016/j.tig.2011.09.001. Epub 2011 Oct 21.

Abstract

Eukaryotic DNA is packaged in nucleosomes. How does this sequestration affect the ability of transcription regulators to access their sites? We cite evidence against the idea that nucleosome positioning is determined primarily by the intrinsic propensities of DNA sequences to form nucleosomes--such that, for example, regulatory sites would be 'nucleosome-free'. Instead, studies in yeast show that nucleosome positioning is primarily determined by specific DNA-binding proteins. Where nucleosomes would otherwise compete with regulatory protein binding (a modest but potentially biologically important effect), this obstacle can be relieved by at least two strategies for exposing regulatory sites. In contrast to their lack of effect on nucleosome positioning, DNA sequence differences do directly affect both the efficiencies with which nucleosomes form in regions flanking regulatory sites before induction, and the extent of their removal upon induction. These nucleosomes, evidently, inhibit basal transcription but are poised to be removed quickly upon command.

摘要

真核生物的 DNA 被包装在核小体中。这种隔离如何影响转录调控因子访问其结合位点的能力?我们列举了一些证据,证明核小体的定位不是主要由 DNA 序列自身形成核小体的倾向决定的——例如,调控位点不会“没有核小体”。相反,酵母的研究表明,核小体的定位主要是由特定的 DNA 结合蛋白决定的。在核小体可能与调控蛋白结合的情况下(这是一种适度但具有潜在生物学意义的影响),这种障碍可以通过至少两种暴露调控位点的策略来缓解。与它们对核小体定位没有影响形成鲜明对比的是,DNA 序列差异确实直接影响诱导前在调控位点侧翼区域形成核小体的效率,以及诱导后核小体去除的程度。这些核小体显然抑制了基础转录,但在接到命令后很快就会被去除。

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