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酵母中靶向组蛋白乙酰转移酶的远程抗沉默功能机制

Mechanism of the long range anti-silencing function of targeted histone acetyltransferases in yeast.

作者信息

Yu Qun, Sandmeier Joseph, Xu Hengping, Zou Yanfei, Bi Xin

机构信息

Department of Biology, University of Rochester, New York 14627, USA.

出版信息

J Biol Chem. 2006 Feb 17;281(7):3980-8. doi: 10.1074/jbc.M510140200. Epub 2005 Dec 19.

Abstract

Transcriptionally silent chromatin in Saccharomyces cerevisiae is associated with histone hypoacetylation and is formed through the action of the Sir histone deacetylase complex. A histone acetyltransferase (HAT) targeted near silent chromatin can overcome silencing at a distance by increasing histone acetylation in a sizable region. However, how a tethered HAT acetylates distant nucleosomes has not been resolved. We demonstrate here that targeting the histone H3-specific HAT Gcn5p promotes acetylation of not only histone H3 but also histone H4 in a broad region. We also show that long range anti-silencing and histone acetylation by targeted HATs can be blocked by nucleosome-excluding sequences. These results are consistent with the contention that a tethered HAT promotes stepwise propagation of histone acetylation along the chromatin. Because histone hypoacetylation is key to the formation and maintenance of transcriptionally silent chromatin, it is believed that acetylation promoted by a targeted HAT disrupts silent chromatin thereby overcoming silencing. However, we show that the acetylated and transcriptionally active region created by a tethered HAT retains structural hallmarks of Sir-dependent silent chromatin and remains associated with Sir proteins indicating that tethered HATs overcome silencing without completely dismantling silent chromatin.

摘要

酿酒酵母中转录沉默染色质与组蛋白低乙酰化相关,并通过Sir组蛋白去乙酰化酶复合体的作用形成。靶向沉默染色质附近的组蛋白乙酰转移酶(HAT)可通过增加相当大区域内的组蛋白乙酰化来克服远距离的沉默作用。然而, tethered HAT如何乙酰化远距离核小体尚未得到解决。我们在此证明,靶向组蛋白H3特异性HAT Gcn5p不仅能促进组蛋白H3的乙酰化,还能促进广泛区域内组蛋白H4的乙酰化。我们还表明,靶向HATs的远距离抗沉默和组蛋白乙酰化可被排除核小体的序列阻断。这些结果与tethered HAT促进组蛋白乙酰化沿染色质逐步传播的观点一致。由于组蛋白低乙酰化是转录沉默染色质形成和维持的关键,因此认为靶向HAT促进的乙酰化会破坏沉默染色质从而克服沉默作用。然而,我们表明,tethered HAT产生的乙酰化和转录活性区域保留了Sir依赖性沉默染色质的结构特征,并仍然与Sir蛋白相关,这表明tethered HATs克服沉默作用而无需完全拆解沉默染色质。

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