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Role of repair mechanisms in the variations of ultraviolet and $gamma$- radiation sensitivity during the cell cycle of Schizosaccharomyces pombe

Journal Article · · Radiat. Res., v. 56, no. 3, pp. 528-539
OSTI ID:4358394
The lethal effects of uv and gamma rays were studied on synchronized cells of S. pombe with different defects in their repair pathways: UVS A cells do not excise pyrimidine dimers; UVS 1 cells are probably deficient in a repair mechanism related to recombination. UVS/sup +/ (wild-type) cells, after uv and gamma -irradiation, and UVS A cells after gamma -irradiation, are the most resistant in the G2 phase of the mitotic cycle. These observations support the existence of a repair mecharism, which acts on uv- and gamma -induced lesions before DNA replication and is different from that of excision-resynthesis. After uv irradiation, it requires the participation of an incision enzyme also involved for excision repair. The uv response of UVS A cells is constant during the cycle, suggesting the presence of a repair mechanism acting during or after DNA replication. The uv resistance of UVS 1 cells decreases progressively from the beginning of the G2 to the end of the S period. This is interpreted in terms of delay available for excision repair. The practically constant response to uv of UVS A and of the double mutant UVS 1A, and to gamma -rays of UVS 1A cells indicates that when variations occur, they are mainly due to diffurential repair abilities within the cycle. (auth)
Research Organization:
Institut du Radium, Orsay, France
NSA Number:
NSA-29-015872
OSTI ID:
4358394
Journal Information:
Radiat. Res., v. 56, no. 3, pp. 528-539, Journal Name: Radiat. Res., v. 56, no. 3, pp. 528-539; ISSN RAREA
Country of Publication:
Country unknown/Code not available
Language:
English