Lee Phoebe S, Greenwell Patricia W, Dominska Margaret, Gawel Malgorzata, Hamilton Monica, Petes Thomas D
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America.
PLoS Genet. 2009 Mar;5(3):e1000410. doi: 10.1371/journal.pgen.1000410. Epub 2009 Mar 13.
Homologous recombination is an important mechanism for the repair of DNA damage in mitotically dividing cells. Mitotic crossovers between homologues with heterozygous alleles can produce two homozygous daughter cells (loss of heterozygosity), whereas crossovers between repeated genes on non-homologous chromosomes can result in translocations. Using a genetic system that allows selection of daughter cells that contain the reciprocal products of mitotic crossing over, we mapped crossovers and gene conversion events at a resolution of about 4 kb in a 120-kb region of chromosome V of Saccharomyces cerevisiae. The gene conversion tracts associated with mitotic crossovers are much longer (averaging about 12 kb) than the conversion tracts associated with meiotic recombination and are non-randomly distributed along the chromosome. In addition, about 40% of the conversion events have patterns of marker segregation that are most simply explained as reflecting the repair of a chromosome that was broken in G1 of the cell cycle.
同源重组是有丝分裂细胞中DNA损伤修复的重要机制。具有杂合等位基因的同源染色体之间的有丝分裂交换可产生两个纯合子细胞(杂合性丧失),而非同源染色体上重复基因之间的交换可导致易位。利用一种遗传系统,可选择含有有丝分裂交换的相互产物的子细胞,我们在酿酒酵母V号染色体120 kb区域内以约4 kb的分辨率绘制了交换和基因转换事件。与有丝分裂交换相关的基因转换片段比与减数分裂重组相关的转换片段长得多(平均约12 kb),并且沿染色体非随机分布。此外,约40%的转换事件具有标记分离模式,最简单的解释是反映了在细胞周期G1期断裂的染色体的修复。