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一个突变型p53转基因在杂合型而非纯合型p53缺陷小鼠中加速肿瘤发展。

A mutant p53 transgene accelerates tumour development in heterozygous but not nullizygous p53-deficient mice.

作者信息

Harvey M, Vogel H, Morris D, Bradley A, Bernstein A, Donehower L A

机构信息

Division of Molecular Virology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Nat Genet. 1995 Mar;9(3):305-11. doi: 10.1038/ng0395-305.

Abstract

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.

摘要

为了在体内检测野生型p53存在和不存在时p53突变体形式的行为,我们将含有p53无效等位基因的p53缺陷小鼠与含有多个突变p53基因(Val 135)拷贝的转基因小鼠进行交配。与非转基因同窝小鼠相比,携带突变转基因的内源性野生型p53基因半合子动物表现出加速的肿瘤发展和改变的肿瘤谱。相反,内源性p53纯合缺失的转基因和非转基因动物以相同的速率发生肿瘤。因此,突变的Val-135 p53等位基因在野生型p53存在时可能在体内以显性负性方式起作用,但在没有野生型p53时不表现出功能获得活性。

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