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DNA 复制过程中的表达平衡。

Expression homeostasis during DNA replication.

机构信息

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 76100, Israel.

出版信息

Science. 2016 Mar 4;351(6277):1087-90. doi: 10.1126/science.aad1162.

Abstract

Genome replication introduces a stepwise increase in the DNA template available for transcription. Genes replicated early in S phase experience this increase before late-replicating genes, raising the question of how expression levels are affected by DNA replication. We show that in budding yeast, messenger RNA (mRNA) synthesis rate is buffered against changes in gene dosage during S phase. This expression homeostasis depends on acetylation of H3 on its internal K56 site by Rtt109/Asf1. Deleting these factors, mutating H3K56 or up-regulating its deacetylation, increases gene expression in S phase in proportion to gene replication timing. Therefore, H3K56 acetylation on newly deposited histones reduces transcription efficiency from replicated DNA, complementing its role in guarding genome stability. Our study provides molecular insight into the mechanism maintaining expression homeostasis during DNA replication.

摘要

基因组复制为转录提供了逐步增加的 DNA 模板。在 S 期早期复制的基因比晚期复制的基因更早经历这种增加,这就提出了一个问题,即表达水平如何受到 DNA 复制的影响。我们表明,在芽殖酵母中,信使 RNA(mRNA)合成速率在 S 期的基因剂量变化中得到缓冲。这种表达平衡依赖于 Rtt109/Asf1 对 H3 内部 K56 位的乙酰化。删除这些因子、突变 H3K56 或上调其去乙酰化作用,会使 S 期的基因表达按基因复制时间的比例增加。因此,新合成的组蛋白上的 H3K56 乙酰化会降低复制 DNA 的转录效率,这与它在保护基因组稳定性方面的作用是互补的。我们的研究为维持 DNA 复制过程中表达平衡的机制提供了分子见解。

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