Hartsuiker E, Vaessen E, Carr A M, Kohli J
Genome Damage and Stability Centre, University of Sussex, Falmer, Brighton BN1 9RR, UK.
EMBO J. 2001 Dec 3;20(23):6660-71. doi: 10.1093/emboj/20.23.6660.
To study the role of Rad50 in the DNA damage response, we cloned and deleted the Schizosaccharomyces pombe RAD50 homologue. The deletion is sensitive to a range of DNA-damaging agents and shows dynamic epistatic interactions with other recombination-repair genes. We show that Rad50 is necessary for recombinational repair of the DNA lesion at the mating-type locus and that rad50Delta shows slow DNA replication. We also find that Rad50 is not required for slowing down S phase in response to hydroxy urea or methyl methanesulfonate (MMS) treatment. Interestingly, in rad50Delta cells, the recombination frequency between two homologous chromosomes is increased at the expense of sister chromatid recombination. We propose that Rad50, an SMC-like protein, promotes the use of the sister chromatid as the template for homologous recombinational repair. In support of this, we found that Rad50 functions in the same pathway for the repair of MMS-induced damage as Rad21, the homologue of the Saccharomyces cerevisiae Scc1 cohesin protein. We speculate that Rad50 interacts with the cohesin complex during S phase to assist repair and possibly re-initiation of replication after replication fork collapse.
为了研究Rad50在DNA损伤应答中的作用,我们克隆并缺失了粟酒裂殖酵母RAD50的同源物。该缺失对一系列DNA损伤剂敏感,并与其他重组修复基因表现出动态上位相互作用。我们发现Rad50对于交配型位点处DNA损伤的重组修复是必需的,并且rad50Δ表现出缓慢的DNA复制。我们还发现,响应羟基脲或甲磺酸甲酯(MMS)处理时,减慢S期并不需要Rad50。有趣的是,在rad50Δ细胞中,两条同源染色体之间的重组频率增加,代价是姐妹染色单体重组。我们提出,Rad50,一种SMC样蛋白,促进使用姐妹染色单体作为同源重组修复的模板。为此,我们发现Rad50在修复MMS诱导的损伤中与酿酒酵母Scc1黏连蛋白的同源物Rad21处于相同的途径。我们推测Rad50在S期与黏连蛋白复合物相互作用,以协助修复,并可能在复制叉坍塌后重新启动复制。