Suppr超能文献

修饰组蛋白并启动减数分裂重组;一个老问题的新答案。

Modifying histones and initiating meiotic recombination; new answers to an old question.

作者信息

Maleki Shohreh, Keeney Scott

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, Box 97, New York, NY 10021, USA.

出版信息

Cell. 2004 Aug 20;118(4):404-6. doi: 10.1016/j.cell.2004.08.008.

Abstract

It is well documented that the formation of the DNA double-strand breaks (DSBs) that initiate meiotic recombination is influenced by chromatin and larger scale chromosome organization, but the molecular nature of this influence has remained elusive. Several recent studies, including (this issue of Cell), shed light on this issue by revealing roles for posttranslational histone modifications in promoting DSB formation.

摘要

有充分的文献记载,引发减数分裂重组的DNA双链断裂(DSB)的形成受染色质和更大规模的染色体组织影响,但其影响的分子本质仍不清楚。最近的几项研究,包括(本期《细胞》杂志),通过揭示翻译后组蛋白修饰在促进DSB形成中的作用,为这个问题提供了线索。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验