首页> 外文期刊>Nucleic Acids Research >MAPPING FREQUENCIES OF ENDOGENOUS OXIDATIVE DAMAGE AND THE KINETIC RESPONSE TO OXIDATIVE STRESS IN A REGION OF RAT MTDNA
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MAPPING FREQUENCIES OF ENDOGENOUS OXIDATIVE DAMAGE AND THE KINETIC RESPONSE TO OXIDATIVE STRESS IN A REGION OF RAT MTDNA

机译:大鼠MTDNA区域内源性氧化损伤的映射频率及对应激的运动反应

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摘要

Genomic DNA is constantly being damaged and repaired and our genomes exist at lesion equilibrium for damage created by endogenous mutagens, Mitochondrial DNA (mtDNA) has the highest lesion equilibrium frequency recorded; presumably due to damage by H2O2 and free radicals generated during oxidative phosphorylation processes, We measured the frequencies of single strand breaks and oxidative base damage in mtDNA by ligation-mediated PCR and a quantitative Southern blot technique coupled with digestion by the enzymes endonuclease III and formamidopyrimidine DNA glycosylase, Addition of 5 mM alloxan to cultured rat cells increased the rate of oxidative base damage and, by several fold, the lesion frequency in mtDNA. After removal of this DNA damaging agent from culture, the single strand breaks and oxidative base damage frequency decreased to levels slightly below normal at 4 h and returned to normal levels at 8 h, the overshoot at 4 h being attributed to an adaptive up-regulation of mitochondrial excision repair activity, Guanine positions showed the highest endogenous lesion frequencies and were the most responsive positions to alloxan-induced oxidative stress, Although specific bases were consistently hot spots for damage, there was no evidence that removal of these lesions occurred in a strand-specific manner, The data reveal non-random oxidative damage to several nucleotides in mtDNA and an apparent adaptive, non-strand selective response for removal of such damage. These are the first studies to characterize oxidative damage and its subsequent removal at the nucleotide level in mtDNA.
机译:基因组DNA不断受到破坏和修复,我们的基因组处于病变平衡状态,以应对内源性诱变剂造成的破坏。线粒体DNA(mtDNA)记录的病变平衡频率最高;大概是由于H2O2的破坏和在氧化磷酸化过程中产生的自由基的影响,我们通过连接介导的PCR和定量Southern印迹技术结合酶内切酶III和甲酰胺基嘧啶的消化,测量了mtDNA中单链断裂和氧化碱基损伤的频率。 DNA糖基化酶,在培养的大鼠细胞中加入5 mM的四氧嘧啶可增加氧化性碱基的损伤率,并增加mtDNA的损伤频率几倍。从培养物中除去该DNA破坏剂后,单链断裂,氧化性碱基破坏频率在4 h降至略低于正常水平,并在8 h恢复至正常水平,4 h的过冲归因于适应性上调在线粒体切除修复活动中,鸟嘌呤位点显示出最高的内源性病变频率,并且是对四氧嘧啶诱导的氧化应激反应最敏感的位置。尽管特定碱基始终是损伤的热点,但没有证据表明这些损伤的清除发生在链中-特异性方式,数据揭示了对mtDNA中几个核苷酸的非随机氧化损伤,以及去除这种损伤的明显的适应性,非链选择性反应。这些是表征氧化损伤及其随后在mtDNA核苷酸水平去除的第一项研究。

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