Rai Ragini, Laloraya Shikha
Department of Biochemistry, Indian Institute of Science, C. V. Raman Avenue, Bangalore, Karnataka, 560012, India.
Curr Genet. 2017 Aug;63(4):765-776. doi: 10.1007/s00294-017-0680-0. Epub 2017 Feb 16.
Replication of linear chromosomes is facilitated by firing of multiple replication origins that ensures timely duplication of the entire chromosome. The Smc5/6 complex is thought to play an important role in replication by its involvement in the restart of collapsed replication forks. Here, we present genetic evidence for functional interaction between replication origin distribution and two subunits of the Smc5/6 complex, Smc6 and Mms21, as well as Top1. An artificial chromosome that has a long arm having low origin density (5ori∆YAC) is relatively unstable compared to the YAC having normal origin distribution in wild-type cells, but is partially stabilized in smc6-56 and top1∆ mutants. While a SUMO-ligase-deficient mutant of Mms21 does not affect stability of the 5ori∆YAC by itself, in combination with top1∆, the 5ori∆YAC is destabilized as evidenced by increased chromosome loss frequency in the mms21∆sl top1∆ double mutant. Likewise, the smc6-56 top1∆ double mutant also exhibits enhanced destabilization of the 5ori∆YAC compared to either single mutant. Such an increase in chromosome loss is not observed for a similar YAC that retains the original replication origins and normal origin distribution on the long arm, in either double mutant having the mms21∆sl or smc6-56 mutations in combination with top1∆. Our findings reveal a requirement for the Smc5/6 complex, including Mms21/Nse2 mediated sumoylation, and topoisomerase-1 (Top1), for maintaining stability of a chromosome having low origin density and suggest a functional cooperation between the Smc5/6 complex and Top1 in maintenance of topologically challenged chromosomes prone to replication fork collapse or accumulation of torsional stress.
多个复制起点的启动促进了线性染色体的复制,从而确保整个染色体的及时复制。Smc5/6复合体被认为通过参与崩溃的复制叉的重启在复制过程中发挥重要作用。在此,我们提供了遗传证据,证明复制起点分布与Smc5/6复合体的两个亚基Smc6和Mms21以及拓扑异构酶1(Top1)之间存在功能相互作用。与野生型细胞中具有正常复制起点分布的酵母人工染色体(YAC)相比,具有低起点密度长臂的人工染色体(5ori∆YAC)相对不稳定,但在smc6 - 56和top1∆突变体中部分稳定。虽然Mms21的SUMO连接酶缺陷型突变体本身不影响5ori∆YAC的稳定性,但与top1∆结合时,5ori∆YAC会不稳定,这在mms21∆sl top1∆双突变体中染色体丢失频率增加得到证明。同样,与任何一个单突变体相比,smc6 - 56 top1∆双突变体也表现出5ori∆YAC的不稳定增强。对于在长臂上保留原始复制起点和正常起点分布的类似YAC,在具有mms21∆sl或smc6 - 56突变与top1∆组合的双突变体中均未观察到这种染色体丢失的增加。我们的研究结果揭示了Smc5/6复合体(包括Mms21/Nse2介导的SUMO化)和拓扑异构酶1(Top1)对于维持低起点密度染色体稳定性的必要性,并表明Smc5/6复合体与Top1在维持易发生复制叉崩溃或扭转应力积累的拓扑挑战性染色体方面存在功能协作。