Genetic analysis of the yeast NUD1 endo-exonuclease:: a role in the repair of DNA double-strand breaks

被引:11
作者
Asefa, B
Kauler, P
Cournoyer, D
Lehnert, S
Chow, TYK
机构
[1] McGill Univ, Fac Med, Dept Oncol, Montreal Gen Hosp, Montreal, PQ H3G 1A4, Canada
[2] McGill Univ, Fac Med, Dept Med & Oncol, Montreal Gen Hosp, Montreal, PQ H3G 1A4, Canada
关键词
endo-exonuclease; NUDl; DNA recombination; DNA repair; non-homologous end-joining;
D O I
10.1007/s002940050407
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The deoxyribonucleases (DNases) have been shown genetically to be important in the vital processes of DNA repair and recombination, The NUD1 gent, which codes for an endo-exonuclease of Saccharomyces cerevisiae. was analyzed for its role in the DNA double-strand break (DSB) repair processes, While the nud1 strain is only slightly sensitive to ionizing radiation, expression of the HO-endonuclease to introduce a DSB at the MAT locus in that strain results in cell death. Cell survival is inversely proportional to the duration of HO-endonuclease expression. Analysis of the surviving colonies from the nud1 strain indicated that many of the survivors an sterile and that the proportion Of these sterile survivors increases with the time of HO-endonuclease expression. On the other hand, the surviving, colonies from the isogenic NUD1 strain are mating-proficient:. interestingly, double mutants of nud1 rad52 are more resistant to ionizing irradiation than the rad52 strain and have a cell-survival fraction of 32% for rad52-1 nud1 and 9% for rad52::URA3 nud1 following prolonged HO-endonuclease expression, indicating that nud1 has a suppressor effect on the DSB-induced lethality in rad52. Polymerase chain reaction analysis show;ed that many of the nud1 survivors contained small,alternations within the,the Mat locus. suggesting that the survivors arose through the process of non-homologous end-joining. These results suggest that the endo-exonuclease acts at a DSB to promote DNA repair via the homologous recombination pathway.
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页码:360 / 367
页数:8
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