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Brca2和p53的缺失协同促进基因组不稳定和T细胞凋亡失调。

Loss of Brca2 and p53 synergistically promotes genomic instability and deregulation of T-cell apoptosis.

作者信息

Cheung Alison M Y, Hande M Prakash, Jalali Farid, Tsao Ming-Sound, Skinnider Brian, Hirao Atsushi, McPherson J Peter, Karaskova Jana, Suzuki Akira, Wakeham Andrew, You-Ten Annick, Elia Andrew, Squire Jeremy, Bristow Rob, Hakem Razqallah, Mak Tak W

机构信息

Ontario Cancer Institute and Department of Medical Biophysics, University of Toronto, Ontario, Canada M5G 2M9.

出版信息

Cancer Res. 2002 Nov 1;62(21):6194-204.

Abstract

BRCA2 is a breast cancer susceptibility gene of which the product is thought to be involved in monitoring genome integrity and cell cycle progression. Brca2-null mice have a defect in embryonic cellular proliferation and die in utero. Here we report the generation of T-cell lineage-specific Brca2-deficient (tBrca2(-/-)) mice using the Cre-loxP system. Mice with a flanked by loxP allele of Brca2 were crossed to transgenic mice bearing Cre recombinase driven by the T cell-specific promoter Lck. Thymic cellularity and distribution of subset populations were normal in tBrca2(-/-) mutants. Thymocytes from tBrca2(-/-) mice underwent normal apoptosis in response to a variety of stimuli, and activated tBrca2(-/-) T cells had normal proliferative capacity. tBrca2(-/-) T cells were more likely than wild-type cells to undergo spontaneous apoptosis, but apoptosed normally in response to restimulation or DNA-damaging stress signals. Examination of metaphase spreads of tBrca2(-/-) T cells revealed that the chromosomes often exhibited aberrations such as breaks and tri-radial structures. The level of chromosomal abnormalities was enhanced in T cells from tBrca2(-/-); p53(-/-) double-mutant mice. However, tBrca2(-/-); p53(-/-) T cells did not show the enhanced level of spontaneous apoptosis demonstrated by tBrca2(-/-) T cells, a difference that likely accounts for an increase in cell number and (3)[H]thymidine incorporation of double-mutant T cells in culture compared with either single mutant. Despite this increased T-cell number, the onset of T-cell lymphomas was only marginally accelerated in tBrca2(-/-); p53(-/-) mice compared with p53(-/-) mice. Our results support a role for Brca2 in repairing spontaneous DNA lesions, and suggest that loss of Brca2 enhances the susceptibility of mouse T-lineage cells to chromosomal aberrations and deregulation of apoptosis in the absence of p53.

摘要

BRCA2是一种乳腺癌易感基因,其产物被认为参与监测基因组完整性和细胞周期进程。Brca2基因敲除小鼠在胚胎细胞增殖方面存在缺陷,会在子宫内死亡。在此,我们报告利用Cre-loxP系统生成T细胞谱系特异性Brca2缺陷(tBrca2(-/-))小鼠。将携带两侧有loxP位点的Brca2等位基因的小鼠与携带由T细胞特异性启动子Lck驱动的Cre重组酶的转基因小鼠杂交。tBrca2(-/-)突变体的胸腺细胞数量和亚群分布正常。来自tBrca2(-/-)小鼠的胸腺细胞在受到多种刺激时能正常凋亡,活化的tBrca2(-/-) T细胞具有正常的增殖能力。tBrca2(-/-) T细胞比野生型细胞更易发生自发凋亡,但在再次刺激或DNA损伤应激信号作用下能正常凋亡。对tBrca2(-/-) T细胞中期染色体铺展的检查显示,染色体常出现诸如断裂和三辐射结构等畸变。在tBrca2(-/-); p53(-/-)双突变小鼠的T细胞中,染色体异常水平有所增强。然而,tBrca2(-/-); p53(-/-) T细胞并未表现出tBrca2(-/-) T细胞所显示的自发凋亡增强水平,这一差异可能解释了与单突变体相比,双突变T细胞在培养中细胞数量增加以及[3H]胸腺嘧啶核苷掺入增加的现象。尽管T细胞数量增加,但与p53(-/-)小鼠相比,tBrca2(-/-); p53(-/-)小鼠中T细胞淋巴瘤的发病仅略有加速。我们的结果支持Brca2在修复自发DNA损伤中的作用,并表明在缺乏p53的情况下,Brca2的缺失会增强小鼠T谱系细胞对染色体畸变和凋亡失调的易感性。

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