DNA双链断裂调节酵母减数分裂过程中re8 -黏结蛋白的非分裂释放。

IF 1.3 4区 生物学 Q4 CELL BIOLOGY
Genes to Cells Pub Date : 2023-11-15 DOI:10.1111/gtc.13081
Ghanim Fajish V, Kiran Challa, Sagar Salim, Ajith VP, Stephen Mwaniki, Ruihao Zhang, Yurika Fujita, Masaru Ito, Koodali T. Nishant, Akira Shinohara
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引用次数: 0

摘要

姐妹染色单体内聚和染色质环形成所必需的有丝分裂内聚复合体在DNA双链断裂(DSBs)的反应中显示出与染色体的局部和全局关联。通过对减数分裂内聚蛋白与Rec8的全基因组结合分析,我们发现染色体上的Rec8定位谱在减数分裂前期I中期到后期发生了变化,发生了分裂不依赖于分裂的解离。染色体轴上的每个rec8结合位点都遵循独特的分离和可能结合的交替模式。与I前期中期相比,着丝粒在I前期晚期的Rec8结合发生了改变,这表明该区域发生了染色体重塑。每条染色体Rec8解离率与减数分裂DSB密度密切相关。事实上,减数分裂DSB形成缺陷的spo11突变体并没有改变减数分裂末期i期Rec8沿染色体的分布。这表明存在减数分裂特异性调控途径,以响应DSB对Rec8-粘聚蛋白的全球结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

DNA double-strand breaks regulate the cleavage-independent release of Rec8-cohesin during yeast meiosis

DNA double-strand breaks regulate the cleavage-independent release of Rec8-cohesin during yeast meiosis

The mitotic cohesin complex necessary for sister chromatid cohesion and chromatin loop formation shows local and global association to chromosomes in response to DNA double-strand breaks (DSBs). Here, by genome-wide binding analysis of the meiotic cohesin with Rec8, we found that the Rec8-localization profile along chromosomes is altered from middle to late meiotic prophase I with cleavage-independent dissociation. Each Rec8-binding site on the chromosome axis follows a unique alternation pattern with dissociation and probably association. Centromeres showed altered Rec8 binding in late prophase I relative to mid-prophase I, implying chromosome remodeling of the regions. Rec8 dissociation ratio per chromosome is correlated well with meiotic DSB density. Indeed, the spo11 mutant deficient in meiotic DSB formation did not change the distribution of Rec8 along chromosomes in late meiotic prophase I. These suggest the presence of a meiosis-specific regulatory pathway for the global binding of Rec8-cohesin in response to DSBs.

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来源期刊
Genes to Cells
Genes to Cells 生物-细胞生物学
CiteScore
3.40
自引率
0.00%
发文量
71
审稿时长
3 months
期刊介绍: Genes to Cells provides an international forum for the publication of papers describing important aspects of molecular and cellular biology. The journal aims to present papers that provide conceptual advance in the relevant field. Particular emphasis will be placed on work aimed at understanding the basic mechanisms underlying biological events.
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