Suppr超能文献

Pch2 防止了在芽殖酵母减数分裂中 Red1 独立于 Mec1/Tel1 介导的 Hop1 磷酸化。

Pch2 prevents Mec1/Tel1-mediated Hop1 phosphorylation occurring independently of Red1 in budding yeast meiosis.

机构信息

Institute of Life Science, National Defense Medical Center, Taipei, Taiwan ; Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan.

Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan.

出版信息

PLoS One. 2014 Jan 21;9(1):e85687. doi: 10.1371/journal.pone.0085687. eCollection 2014.

Abstract

A prominent feature of meiosis in most sexually reproducing organisms is interhomolog recombination whereby a significant fraction of the programmed meiotic double-strand breaks are repaired using intact homologous non-sister chromatids rather than sister chromatids. Budding yeast DNA damage checkpoint kinases Mec1 and Tel1 act together with the axial element protein Red1 to promote interhomolog recombination by phosphorylating another axial element protein Hop1. Mec1 and Tel1 also phosphorylate γH2A and the synaptonemal complex protein Zip1 independently of Red1 to facilitate premeiotic DNA replication and to destabilize homology-independent centromere pairing, respectively. It has been unclear why Hop1 phosphorylation is Red1-dependent. Here, we report that the pachytene checkpoint protein 2 (Pch2) specifically prevents Red1-independent Hop1 phosphorylation. Our findings reveal a new function for Pch2 in linking two axial element proteins Red1 and Hop1 thus coordinating their effects in meiotic recombination and the checkpoint network.

摘要

在大多数有性繁殖生物的减数分裂中,一个突出的特征是同源重组,其中相当一部分程序性减数分裂双链断裂是使用完整的同源非姐妹染色单体而不是姐妹染色单体修复的。芽殖酵母 DNA 损伤检查点激酶 Mec1 和 Tel1 与轴元件蛋白 Red1 一起作用,通过磷酸化另一个轴元件蛋白 Hop1 来促进同源重组。Mec1 和 Tel1 还独立于 Red1 磷酸化 γH2A 和联会复合体蛋白 Zip1,分别促进减数分裂前 DNA 复制和破坏同源非依赖性着丝粒配对。目前还不清楚为什么 Hop1 磷酸化依赖于 Red1。在这里,我们报告说粗线期检查点蛋白 2 (Pch2) 特异性地阻止了 Red1 非依赖性 Hop1 磷酸化。我们的发现揭示了 Pch2 在连接两个轴元件蛋白 Red1 和 Hop1 方面的新功能,从而协调它们在减数分裂重组和检查点网络中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd06/3897485/333be5ca878f/pone.0085687.g001.jpg

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