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有缺陷的依赖DNA的蛋白激酶活性与V(D)J重组以及与小鼠严重联合免疫缺陷(scid)突变相关的DNA修复缺陷有关。

Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation.

作者信息

Blunt T, Finnie N J, Taccioli G E, Smith G C, Demengeot J, Gottlieb T M, Mizuta R, Varghese A J, Alt F W, Jeggo P A, Jackson S P

机构信息

Wellcome/Cancer Research Campaign Institute, Cambridge University, England.

出版信息

Cell. 1995 Mar 10;80(5):813-23. doi: 10.1016/0092-8674(95)90360-7.

Abstract

Murine cells homozygous for the severe combined immune deficiency mutation (scid) and V3 mutant hamster cells fall into the same complementation group and show similar defects in V(D)J recombination and DNA double-stranded break repair. Here we show that both cell types lack DNA-dependent protein kinase (DNA-PK) activity owing to defects in DNA-PKcs, the catalytic subunit of this enzyme. Furthermore, we demonstrate that yeast artificial chromosomes containing the DNA-PKcs gene complement both the DNA repair and recombination deficiencies of V3 cells, and we conclude that DNA-PKcs is encoded by the XRCC7 gene. As DNA-PK binds to DNA ends and is activated by these structures, our findings provide novel insights into V(D)J recombination and DNA repair processes.

摘要

严重联合免疫缺陷突变(scid)纯合的小鼠细胞和V3突变仓鼠细胞属于同一互补群,并且在V(D)J重组和DNA双链断裂修复方面表现出相似的缺陷。我们在此表明,由于该酶的催化亚基DNA-PKcs存在缺陷,这两种细胞类型均缺乏DNA依赖性蛋白激酶(DNA-PK)活性。此外,我们证明含有DNA-PKcs基因的酵母人工染色体可弥补V3细胞的DNA修复和重组缺陷,并且我们得出结论,DNA-PKcs由XRCC7基因编码。由于DNA-PK与DNA末端结合并被这些结构激活,我们的发现为V(D)J重组和DNA修复过程提供了新的见解。

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