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进出之间:染色质中的组蛋白变体交换

In and out: histone variant exchange in chromatin.

作者信息

Jin Jingji, Cai Yong, Li Bing, Conaway Ronald C, Workman Jerry L, Conaway Joan Weliky, Kusch Thomas

机构信息

Stowers Institute for Medical Research, 1000 East 50th Street, Kansas City, MO 64110, USA.

出版信息

Trends Biochem Sci. 2005 Dec;30(12):680-7. doi: 10.1016/j.tibs.2005.10.003. Epub 2005 Oct 28.

Abstract

Alterations in nucleosome structure affect the accessibility of the DNA and can generate specialized domains of chromatin in the genome. Such changes can be introduced by posttranslational modifications of histones, by chromatin remodeling, or by the incorporation of variants of H2A and H3 into nucleosomes. In contrast to the canonical histones, which are deposited behind the replication fork during S phase, histone variants are incorporated in a process that is independent of DNA replication. Recent studies have shown that distinct multiprotein complexes are responsible for the targeted deposition of histone variants at active genes, centromeres and silent loci. The incorporation of histone variants most probably has epigenetic consequences and contributes to architectural changes in chromosomes.

摘要

核小体结构的改变会影响DNA的可及性,并能在基因组中产生染色质的特殊结构域。这种变化可通过组蛋白的翻译后修饰、染色质重塑或通过将H2A和H3变体掺入核小体来实现。与在S期复制叉后方沉积的经典组蛋白不同,组蛋白变体是通过一个独立于DNA复制的过程掺入的。最近的研究表明,不同的多蛋白复合物负责组蛋白变体在活跃基因、着丝粒和沉默位点的靶向沉积。组蛋白变体的掺入很可能具有表观遗传学后果,并有助于染色体的结构变化。

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