p53-independent DNA repair and cell cycle arrest in embryonic stem cells

被引:40
作者
Prost, S [1 ]
Bellamy, COC [1 ]
Clarke, AR [1 ]
Wyllie, AH [1 ]
Harrison, DJ [1 ]
机构
[1] Univ Edinburgh, Dept Pathol, Sch Med, Canc Res Campaign Labs, Edinburgh EH8 9AG, Midlothian, Scotland
关键词
embryonic stem cell; p53; cell cycle; DNA repair; UV; DNA damage;
D O I
10.1016/S0014-5793(98)00296-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The role of p53 in DNA repair and cell cycle checkpoint after ultraviolet irradiation was investigated in an embryonic stem cell line homozygous for a targeted deletion of p53, Results indicate that loss of p53 does not alter the capacity of ES cells to respond to DNA damage. wild-type and p53-deficient cells showed similar cessation of DNA synthesis after UV damage and similar ultimate capacity to repair a transiently transfected reporter plasmid, Interestingly, in the absence of DNA damaging treatment, the transit of p53-deficient cells through S phase mas slower than wild-type cells. We suggest that this may result from the absence of a p53-dependent response to endogenous DNA damage: without p53 sensing endogenous damage leading to immediate repair, such damage may persist and thus delay DNA synthesis. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:499 / 504
页数:6
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