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Ku70/80 gene expression and DNA-dependent protein kinase (DNA-PK) activity do not correlate with double-strand break (dsb) repair capacity and cellular radiosensitivity in normal human fibroblasts

机译:Ku70 / 80基因表达和DNA依赖性蛋白激酶(DNA-PK)活性与正常人成纤维细胞的双链断裂(dsb)修复能力和细胞放射敏感性无关

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摘要

The expression of the Ku70 and Ku80 genes as well as the activity of the DNA-dependent protein kinase (DNA-PK) were studied in 11 normal human fibroblast lines. The proteins studied are known to be part of a double-strand break (dsb) repair complex involved in non-homologous recombination, as was demonstrated for the radiosensitive rodent mutant cell lines of the complementation groups 5–7. The 11 fibroblast lines used in this study represent a typical spectrum of normal human radiosensitivity with the surviving fraction measured for a dose of 3.5 Gy, SF3.5 Gy, ranging from 0.03 to 0.28. These differences in cell survival were previously shown to correlate with the number of non-repaired dsbs. We found that the mRNA signal intensities of both Ku70 and Ku80 genes were fairly similar for the 11 cell lines investigated. In addition, the DNA-PK activity determined by the pulldown assay was fairly constant in these fibroblast lines. Despite the correlation between cell survival and dsb repair capacity, there was no correlation between dsb repair capacity and DNA-PK activity in the tested normal human fibroblast lines. Obviously, in this respect, other proteins/pathways appear to be more relevant. © 1999 Cancer Research Campaign
机译:在11种正常人成纤维细胞系中研究了Ku70和Ku80基因的表达以及DNA依赖性蛋白激酶(DNA-PK)的活性。已知研究的蛋白质是参与非同源重组的双链断裂(dsb)修复复合物的一部分,这是对5-7互补组的放射敏感性啮齿动物突变细胞系的证明。本研究中使用的11个成纤维细胞系代表正常人体放射敏感性的典型光谱,其存活分数为3.5 Gy,SF3.5 Gy的剂量范围为0.03至0.28。先前已证明这些细胞存活率的差异与未修复的dsb的数量相关。我们发现Ku70和Ku80基因的mRNA信号强度对于所研究的11种细胞系都非常相似。另外,在这些成纤维细胞系中,通过下拉测定法测定的DNA-PK活性相当恒定。尽管细胞存活与dsb修复能力之间存在相关性,但在测试的正常人成纤维细胞系中dsb修复能力与DNA-PK活性之间没有相关性。显然,就此而言,其他蛋白质/途径似乎更为相关。 ©1999癌症研究运动

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