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携带截短型Brca2突变的小鼠的肿瘤发生及DNA修复缺陷

Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation.

作者信息

Connor F, Bertwistle D, Mee P J, Ross G M, Swift S, Grigorieva E, Tybulewicz V L, Ashworth A

机构信息

CRC Centre for Cell and Molecular Biology, Chester Beatty Laboratories, Institute of Cancer Research, London, UK.

出版信息

Nat Genet. 1997 Dec;17(4):423-30. doi: 10.1038/ng1297-423.

Abstract

Germline mutation of the BRCA2 gene carries a high risk of developing breast cancer. To study the function of this gene, we generated a mutation in Brca2 in mice. Unlike other mutations in the Brca2 gene, which are lethal early in embryogenesis when homozygous, some of our homozygous mutant mice survive to adulthood. These animals have a wide range of defects, including small size, improper differentiation of tissues, absence of germ cells and the development of lethal thymic lymphomas. Fibroblasts cultured from BrcaZ-/-embryos have a defect in proliferation that may be mediated by over-expression of p53 and p21Waf1/CIP1. We show that Brca2 is required for efficient DNA repair, and our results suggest that loss of the p53 checkpoint may be essential for tumour progression triggered by mutations in BRCA2.

摘要

BRCA2基因的种系突变会带来患乳腺癌的高风险。为了研究该基因的功能,我们在小鼠的Brca2基因中制造了一种突变。与Brca2基因中的其他突变不同,其他突变在纯合时会在胚胎发育早期致死,而我们的一些纯合突变小鼠能存活至成年。这些动物存在广泛的缺陷,包括体型小、组织分化不当、生殖细胞缺失以及致死性胸腺淋巴瘤的发生。从Brca2基因敲除胚胎中培养的成纤维细胞存在增殖缺陷,这可能是由p53和p21Waf1/CIP1的过度表达介导的。我们发现Brca2对于有效的DNA修复是必需的,并且我们的结果表明p53检查点的缺失可能对于由BRCA2突变引发的肿瘤进展至关重要。

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