Department of Biology, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.
PLoS Genet. 2021 Mar 18;17(3):e1009442. doi: 10.1371/journal.pgen.1009442. eCollection 2021 Mar.
DNA double-strand breaks arise in vivo when a dicentric chromosome (two centromeres on one chromosome) goes through mitosis with the two centromeres attached to opposite spindle pole bodies. Repair of the DSBs generates phenotypic diversity due to the range of monocentric derivative chromosomes that arise. To explore whether DSBs may be differentially repaired as a function of their spatial position in the chromosome, we have examined the structure of monocentric derivative chromosomes from cells containing a suite of dicentric chromosomes in which the distance between the two centromeres ranges from 6.5 kb to 57.7 kb. Two major classes of repair products, homology-based (homologous recombination (HR) and single-strand annealing (SSA)) and end-joining (non-homologous (NHEJ) and micro-homology mediated (MMEJ)) were identified. The distribution of repair products varies as a function of distance between the two centromeres. Genetic dependencies on double strand break repair (Rad52), DNA ligase (Lif1), and S phase checkpoint (Mrc1) are indicative of distinct repair pathway choices for DNA breaks in the pericentromeric chromatin versus the arms.
体内的 DNA 双链断裂是在双着丝粒染色体(一条染色体上有两个着丝粒)与附着在相反纺锤体极体上的两个着丝粒一起经历有丝分裂时产生的。由于产生的单着丝粒衍生染色体的范围,DSB 的修复会产生表型多样性。为了探究 DSB 是否可以根据其在染色体中的空间位置进行差异修复,我们检查了来自含有一系列双着丝粒染色体的细胞中单着丝粒衍生染色体的结构,其中两个着丝粒之间的距离从 6.5kb 到 57.7kb 不等。确定了两种主要的修复产物类别,基于同源性的(同源重组 (HR) 和单链退火 (SSA))和末端连接(非同源 (NHEJ) 和微同源介导 (MMEJ))。修复产物的分布随两个着丝粒之间的距离而变化。对双链断裂修复 (Rad52)、DNA 连接酶 (Lif1) 和 S 期检查点 (Mrc1) 的遗传依赖性表明,着丝粒周围染色质中的 DNA 断裂与臂部的修复途径选择不同。