The Shmunis School of Biomedicine and Cancer Research, Tel Aviv Universitygrid.12136.37, Ramat Aviv, Israel.
Departments of Genetics, Stanford Universitygrid.168010.e, Stanford, California, USA.
mBio. 2022 Aug 30;13(4):e0142022. doi: 10.1128/mbio.01420-22. Epub 2022 Jun 16.
During DNA replication, the newly created sister chromatids are held together until their separation at anaphase. The cohesin complex is in charge of creating and maintaining sister chromatid cohesion (SCC) in all eukaryotes. In Saccharomyces cerevisiae cells, cohesin is composed of two elongated proteins, Smc1 and Smc3, bridged by the kleisin Mcd1/Scc1. The latter also acts as a scaffold for three additional proteins, Scc3/Irr1, Wpl1/Rad61, and Pds5. Although the HEAT-repeat protein Pds5 is essential for cohesion, its precise function is still debated. Deletion of the gene, encoding a PCNA unloader, can partially suppress the temperature-sensitive allele, but not a complete deletion of We carried out a genetic screen for high-copy-number suppressors and another for spontaneously arising mutants, allowing the survival of a Δ Δ strain. Our results show that cells remain viable in the absence of Pds5 provided that there is both an elevation in the level of Mcd1 (which can be due to mutations in the gene, encoding a G cyclin), and an increase in the level of SUMO-modified PCNA on chromatin (caused by lack of PCNA unloading in Δ mutants). The elevated SUMO-PCNA levels increase the recruitment of the Srs2 helicase, which evicts Rad51 molecules from the moving fork, creating single-stranded DNA (ssDNA) regions that serve as sites for increased cohesin loading and SCC establishment. Thus, our results delineate a double role for Pds5 in protecting the cohesin ring and interacting with the DNA replication machinery. Sister chromatid cohesion is vital for faithful chromosome segregation, chromosome folding into loops, and gene expression. A multisubunit protein complex known as cohesin holds the sister chromatids from S phase until the anaphase stage. In this study, we explore the function of the essential cohesin subunit Pds5 in the regulation of sister chromatid cohesion. We performed two independent genetic screens to bypass the function of the Pds5 protein. We observe that Pds5 protein is a cohesin stabilizer, and elevating the levels of Mcd1 protein along with SUMO-PCNA accumulation on chromatin can compensate for the loss of the gene. In addition, Pds5 plays a role in coordinating the DNA replication and sister chromatid cohesion establishment. This work elucidates the function of cohesin subunit Pds5, the G cyclin Cln2, and replication factors PCNA, Elg1, and Srs2 in the proper regulation of sister chromatid cohesion.
在 DNA 复制过程中,新合成的姐妹染色单体在后期被分离之前一直保持在一起。黏合蛋白复合物负责在所有真核生物中形成和维持姐妹染色单体黏合(SCC)。在酿酒酵母细胞中,黏合蛋白由两个长的蛋白质 Smc1 和 Smc3 组成,由 kleisin Mcd1/Scc1 桥接。后者还作为另外三个蛋白质 Scc3/Irr1、Wpl1/Rad61 和 Pds5 的支架。尽管 HEAT 重复蛋白 Pds5 对于黏合是必不可少的,但它的确切功能仍存在争议。编码 PCNA 卸 loader 的 基因缺失可以部分抑制温度敏感的 等位基因,但不能完全缺失 我们进行了高拷贝数抑制子的遗传筛选和自发突变体的遗传筛选,使 Δ Δ 菌株得以存活。我们的结果表明,只要 Mcd1 水平升高(可能是由于编码 G 周期蛋白的 基因发生突变),并且染色质上 SUMO 修饰的 PCNA 水平增加(由于 Δ 突变体中 PCNA 卸 loader 的缺乏),那么在没有 Pds5 的情况下,细胞仍然具有活力。升高的 SUMO-PCNA 水平增加了 Srs2 解旋酶的募集,该酶将 Rad51 分子从移动叉上逐出,形成单链 DNA(ssDNA)区域,作为增加黏合蛋白加载和 SCC 建立的位点。因此,我们的结果描绘了 Pds5 在保护黏合蛋白环和与 DNA 复制机制相互作用方面的双重作用。姐妹染色单体黏合对于忠实的染色体分离、染色体折叠成环和基因表达至关重要。一种称为黏合蛋白的多亚基蛋白复合物将姐妹染色单体从 S 期保留到后期阶段。在这项研究中,我们探索了必需的黏合蛋白亚基 Pds5 在调节姐妹染色单体黏合中的功能。我们进行了两次独立的遗传筛选,以绕过 Pds5 蛋白的功能。我们观察到 Pds5 蛋白是黏合蛋白稳定剂,并且 Mcd1 蛋白水平升高以及染色质上 SUMO-PCNA 积累可以补偿 基因的缺失。此外,Pds5 在协调 DNA 复制和姐妹染色单体黏合建立方面发挥作用。这项工作阐明了黏合蛋白亚基 Pds5、G 周期蛋白 Cln2 以及复制因子 PCNA、Elg1 和 Srs2 在正确调节姐妹染色单体黏合中的功能。