Rad18 is required for DNA repair and checkpoint responses in fission yeast

被引:120
作者
Verkade, HM
Bugg, SJ
Lindsay, HD
Carr, AM
O'Connell, MJ [1 ]
机构
[1] Peter MacCallum Canc Inst, Trescowthick Res Labs, Melbourne, Vic 8006, Australia
[2] Univ Melbourne, Dept Genet, Parkville, Vic 3052, Australia
[3] Univ Sussex, MRC, Cell Mutat Unit, Brighton BN1 9RR, E Sussex, England
关键词
D O I
10.1091/mbc.10.9.2905
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
To survive damage to the genome, cells must respond by activating both DNA repair and checkpoint responses. Using genetic screens in the fission yeast Schizosaccharomyces pombe, we recently isolated new genes required for DNA damage checkpoint control. We show here that one of these strains defines a new allele of the previously described rad18 gene, rad18-74. rad18 is an essential gene, even in the absence of extrinsic DNA damage. It encodes a conserved protein related to the structural maintenance of chromosomes proteins. Point mutations in rad18 lead to defective DNA repair pathways responding to both UV-induced lesions and, as we show here, double-stranded breaks. Furthermore, rad18p is required to maintain cell cycle arrest in the presence of DNA damage, and failure of this leads to highly aberrant mitoses. A gene encoding a BRCT-containing protein, bud, was isolated as an allele-specific high-copy suppressor of rad18-74. bud is required for mitotic fidelity and for cellular viability in strains with rad18 mutations but is not essential for DNA damage responses. Mutations in rad18 and brc1 are synthetically lethal with a topoisomerase II mutant (top2-191), indicating that these proteins play a role in chromatin organization. These studies show a role for chromatin organization in the maintenance or activation of responses to DNA damage.
引用
收藏
页码:2905 / 2918
页数:14
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