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着丝粒:后基因组时代的狂野西部。

Centromeres: the wild west of the post-genomic age.

机构信息

Ludwig Institute for Cancer Research, University of California, San Diego and Department of Bioengineering, University of California, Irvine, Irvine, CA, USA.

出版信息

Epigenetics. 2010 Jan 1;5(1):34-40. doi: 10.4161/epi.5.1.10629. Epub 2010 Jan 13.

Abstract

Centromeric repetitive DNA is the largest missing piece of the Human Genome Project. Rather than being necessary or sufficient to specify the site of mitotic spindle attachment to the chromosome, centromeric DNA sequence is all but irrelevant. Instead, centromeres are thought to be specified by a protein component, a histone H3 variant called Centromere Protein A (CENP-A). This review includes a brief overview of the history of the centromere field, and the current status of knowledge on CENP-A assembly. New evidence for CENP-A recruitment in response to DNA damage implies a mechanism for neocentromere formation, and raises new questions about the epigenetic model of centromere maintenance.

摘要

着丝粒重复 DNA 是人类基因组计划中最大的缺失部分。着丝粒 DNA 序列对于有丝分裂纺锤体附着到染色体的位置来说并非必需或充分,而几乎是不相关的。相反,着丝粒被认为是由一个蛋白质成分指定的,一种称为着丝粒蛋白 A(CENP-A)的组蛋白 H3 变体。这篇综述包括对着丝粒领域历史的简要概述,以及当前关于 CENP-A 组装的知识状况。新的证据表明,CENP-A 在响应 DNA 损伤时的募集意味着形成新着丝粒的机制,并对着丝粒维持的表观遗传模型提出了新的问题。

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