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首页> 外文期刊>Radiation Research: Official Organ of the Radiation Research Society >THE INVOLVEMENT OF TOPOISOMERASE I IN THE INDUCTION OF DNA-PROTEIN CROSSLINKS AND DNA SINGLE-STRAND BREAKS IN CELLS OF ULTRAVIOLET-IRRADIATED HUMAN AND FROG CELL LINES
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THE INVOLVEMENT OF TOPOISOMERASE I IN THE INDUCTION OF DNA-PROTEIN CROSSLINKS AND DNA SINGLE-STRAND BREAKS IN CELLS OF ULTRAVIOLET-IRRADIATED HUMAN AND FROG CELL LINES

机译:拓扑异构酶I在紫外线照射的人和Frog细胞系细胞中诱导DNA-蛋白质交联和DNA单链断裂的参与

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Exposure of GM 4390 human skin fibroblasts and ICR 2A frog cells to 10 kJ m(-2) of ultraviolet B (UVB) radiation resulted in the formation of DNA-protein crosslinks (DPCs) and DNA single-strand breaks (SSBs). However, upon incubation, there were rapid increases in the yields of both DPCs and SSBs. An enhancement in these DNA alterations was detected within 12 min after irradiation and their levels continued to rise by 5-8-fold within 15 h after exposure to UV radiation. Using an antibody-based assay that measures covalent complex formation between topoisomerase (topo) I and genomic DNA, it was found that topo I is one of the proteins involved in these DPCs induced by UV radiation. The levels and rate of increase of topo I-DNA covalent complexes were similar to the UV-radiation-dependent formation of DPCs and SSBs. A UV-radiation-sensitive mutant frog cell line, DRP 153, was also examined and was found to be deficient in this induction of DPCs and SSBs by UV radiation. When these cells were transfected with the human SUVCC3 gene, the resulting transformant displayed kinetics for the induction of DPCs and SSBs similar to the human and parental frog cells. However, human topo I was not detected in the transformed frog cells, indicating that SUVCC3 does not encode topo I. It is likely that SUVCC3 encodes an associated enzymatic activity which permits normal stimulation of topo I-DNA covalent complexes in UV-irradiated cells. (C) 1997 by Radiation Research Society. [References: 30]
机译:GM 4390人皮肤成纤维细胞和ICR 2A青蛙细胞暴露于10 kJ m(-2)的紫外线B(UVB)辐射导致形成DNA-蛋白质交联(DPC)和DNA单链断裂(SSB)。但是,孵育后,DPC和SSB的产量均迅速增加。在照射后12分钟内检测到这些DNA改变的增强,并且在暴露于UV辐射后15小时内它们的水平持续升高5-8倍。使用基于抗体的检测方法来测量拓扑异构酶(拓扑)I与基因组DNA之间共价复合物的形成,发现拓扑I是紫外线辐射诱导的这些DPC中涉及的蛋白质之一。拓扑I-DNA共价复合物的水平和增加速率与DPC和SSB的紫外线辐射依赖性形成相似。还检查了对紫外线辐射敏感的突变青蛙细胞系DRP 153,发现它在通过紫外线辐射诱导DPC和SSB方面存在缺陷。当这些细胞用人SUVCC3基因转染时,所得转化体显示出与人和亲代青蛙细胞相似的DPC和SSB诱导动力学。但是,在转化的青蛙细胞中未检测到人topo I,这表明SUVCC3不编码topoI。很可能SUVCC3编码了一种相关的酶活性,可以正常刺激紫外线照射的细胞中topo I-DNA共价复合物。 (C)1997年,辐射研究学会。 [参考:30]

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