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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Restoration of X-ray and etoposide resistance, Ku-end binding activity and V(D) J recombination to the Chinese hamster sxi-3 mutant by a hamster Ku86 cDNA.
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Restoration of X-ray and etoposide resistance, Ku-end binding activity and V(D) J recombination to the Chinese hamster sxi-3 mutant by a hamster Ku86 cDNA.

机译:通过仓鼠Ku86 cDNA恢复对中国仓鼠sxi-3突变体的X射线和依托泊苷抗性,Ku-end结合活性和V(D)J重组。

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摘要

Ku is a heterodimeric protein composed of 86 and 70 kDa subunits that binds preferentially to the double-stranded ends of DNA. Recent molecular characterization of ionizing-radiation sensitive (IRs) mutants belonging to the XRCC5 complementation group demonstrated the involvement of Ku in DNA double-strand break (DSB) repair and lymphoid V(D)J recombination. Here, we describe the isolation of a full-length hamster cDNA encoding the large subunit of the Ku heterodimer and demonstrate that the stable expression of this cDNA can functionally restore IR, Ku DNA end-binding activity and V(D)J recombination proficiency in the Chinese hamster IRs sxi-3 mutant. Moreover, we also demonstrate that sxi-3 cells are hypersensitive to etoposide, a DNA topoisomerase II inhibitor, and that resistance to this drug was restored by the Ku86 cDNA. These experiments suggest that a defect in the large subunit of the heterodimeric Ku protein is the sole factor responsible for the known defects of sxi-3 cells and our data of further support the role of Ku in DNA DSB repair and V(D)J recombination.
机译:Ku是由86和70 kDa亚基组成的异二聚体蛋白,优先与DNA的双链末端结合。属于XRCC5互补组的电离辐射敏感(IRs)突变体的最新分子表征表明,Ku参与了DNA双链断裂(DSB)修复和淋巴样V(D)J重组。在这里,我们描述了编码仓鼠二聚体大亚基的全长仓鼠cDNA的分离,并证明了该cDNA的稳定表达可以在功能上恢复IR,Ku DNA末端结合活性和V(D)J重组能力。中国仓鼠IR sxi-3突变体。此外,我们还证明sxi-3细胞对依托泊苷(一种DNA拓扑异构酶II抑制剂)高度敏感,并且通过Ku86 cDNA恢复了对该药物的耐药性。这些实验表明异二聚体Ku蛋白大亚基的缺陷是造成sxi-3细胞已知缺陷的唯一因素,我们的数据进一步支持了Ku在DNA DSB修复和V(D)J重组中的作用。 。

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