A MUTANT P53 TRANSGENE ACCELERATES TUMOR-DEVELOPMENT IN HETEROZYGOUS BUT NOT NULLIZYGOUS P53 DEFICIENT MICE

被引:220
作者
HARVEY, M
VOGEL, H
MORRIS, D
BRADLEY, A
BERNSTEIN, A
DONEHOWER, LA
机构
[1] BAYLOR COLL MED,DIV MOLEC VIROL,HOUSTON,TX 77030
[2] BAYLOR COLL MED,DEPT PATHOL,HOUSTON,TX 77030
[3] BAYLOR COLL MED,DEPT HUMAN & MOLEC GENET,HOUSTON,TX 77030
[4] BAYLOR COLL MED,HOWARD HUGHES MED INST,HOUSTON,TX 77030
[5] MT SINAI HOSP,SAMUEL LUNENFELD RES INST,TORONTO,ON M5G 1X5,CANADA
[6] UNIV TORONTO,DEPT MOLEC & MED GENET,TORONTO,ON M5G 1X5,CANADA
关键词
D O I
10.1038/ng0395-305
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
To test the behaviour of a mutant form of p53 in the presence and absence of wild-type p53 in vivo, we mated p53-deficient mice containing a p53 null allele to transgenic mice containing multiple copies of a mutant p53 gene (Val 135). Animals hemizygous for the endogenous wild-type p53 gene with the mutant transgene exhibited accelerated tumour development and an altered tumour spectrum compared to their non-transgenic counterparts. In contrast, transgenic and non-transgenic animals nullizygous for endogenous p53 developed tumours at the same rate. Thus, the mutant Val-135 p53 allele may act in vivo in a dominant negative manner in the presence of wild-type p53 but does not display gain of function activity in the absence of wild-type p53.
引用
收藏
页码:305 / 311
页数:7
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