首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >CHROMOSOMAL DOUBLE-STRAND BREAK REPAIR IN KU80-DEFICIENT CELLS
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CHROMOSOMAL DOUBLE-STRAND BREAK REPAIR IN KU80-DEFICIENT CELLS

机译:KU80缺失细胞的染色体双链断裂修复

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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 endonu clease 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. [References: 37]
机译:X射线敏感的仓鼠细胞系xrs-6缺乏DNA双链断裂(DSB)修复,并且显示出受损的V(D)J重组。该细胞系中的分子缺陷位于Ku自身抗原的80 kDa亚基中,该蛋白与DNA末端结合,并将依赖DNA的蛋白激酶募集到DNA。使用I-SceI核酸内切酶表达系统,检查了xrs-6和亲代CHO-K1细胞系中的染色体DSB修复,染色体DNA中的DSB使得重组子的产量比xrs-6和xrs-6中的背景高数千倍。在用内切核酸酶表达载体电穿孔的100个细胞中,有多达1个发生了CHO-K1细胞的DSB重组修复。因此,染色体DSB的重组修复可以在哺乳动物细胞中大量发生,并且在我们的测定中不会因Ku自身抗原的缺乏而受到重大影响。还检查了DSB部位附近断裂的染色体末端的重新结合(末端结合)。与重组修复相反,发现末端连接在xrs-6细胞中受到严重破坏,因此,Ku蛋白似乎仅在一种染色体DSB修复途径中起关键作用。 [参考:37]

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