Liang F, Romanienko P J, Weaver D T, Jeggo P A, Jasin M
Program of Molecular Biology, Sloan-Kettering Institute, New York, NY 10021, USA.
Proc Natl Acad Sci U S A. 1996 Aug 20;93(17):8929-33. doi: 10.1073/pnas.93.17.8929.
The x-ray sensitive hamster cell line xrs-6 is deficient in DNA double-strand break (DSB) repair and exhibits impaired V(D)J recombination. The molecular defect in this line is in the 80-kDa subunit of the Ku autoantigen, a protein that binds to DNA ends and recruits the DNA-dependent protein kinase to DNA. Using an I-SceI endonuclease expression system, chromosomal DSB repair was examined in xrs-6 and parental CHO-K1 cell lines. A DSB in chromosomal DNA increased the yield of recombinants several thousand-fold above background in both the xrs-6 and CHO-K1 cells, with recombinational repair of DSBs occurring in as many as 1 of 100 cells electroporated with the endonuclease expression vector. Thus, recombinational repair of chromosomal DSBs can occur at substantial levels in mammalian cells and it is not grossly affected in our assay by a deficiency of the Ku autoantigen. Rejoining of broken chromosome ends (end-joining) near the site of the DSB was also examined. In contrast to recombinational repair, end-joining was found to be severely impaired in the xrs-6 cells. Thus, the Ku protein appears to play a critical role in only one of the chromosomal DSB repair pathways.
对X射线敏感的仓鼠细胞系xrs - 6在DNA双链断裂(DSB)修复方面存在缺陷,并且其V(D)J重组功能受损。该细胞系的分子缺陷在于Ku自身抗原的80 kDa亚基,Ku是一种能与DNA末端结合并将DNA依赖性蛋白激酶招募至DNA的蛋白质。利用I - SceI核酸内切酶表达系统,在xrs - 6和亲本CHO - K1细胞系中检测了染色体DSB修复情况。染色体DNA中的DSB使xrs - 6和CHO - K1细胞中的重组体产量比背景水平提高了数千倍,用核酸内切酶表达载体电穿孔处理的细胞中,多达1/100的细胞发生了DSB的重组修复。因此,染色体DSB的重组修复在哺乳动物细胞中能以相当高的水平发生,并且在我们的检测中,它并未因Ku自身抗原的缺陷而受到严重影响。还检测了DSB位点附近断裂染色体末端的重新连接(末端连接)情况。与重组修复相反,发现xrs - 6细胞中的末端连接严重受损。因此,Ku蛋白似乎仅在染色体DSB修复途径之一中起关键作用。