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首页> 外文期刊>Mutagenesis >An increase of oxidised nucleotides activates DNA damage checkpoint pathway that regulates post-embryonic development in Caenorhabditis elegans
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An increase of oxidised nucleotides activates DNA damage checkpoint pathway that regulates post-embryonic development in Caenorhabditis elegans

机译:氧化核苷酸的增加激活DNA损伤检查点途径,该途径调节秀丽隐杆线虫的胚后发育。

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摘要

8-Oxo-dGTP, an oxidised form of dGTP generated in the nucleotide pool, can be incorporated opposite adenine or cytosine in template DNA, which can in turn induce mutations. In this study, we identified a novel MutT homolog (NDX-2) of Caenorhabditis elegans that hydrolyzes 8-oxo-dGDP to 8-oxo-dGMP. In addition, we found that NDX-1, NDX-2 and NDX-4 proteins have 8-oxo-GTPase or 8-oxo-GDPase activity. The sensitivity of ndx-2 knockdown C elegans worms to methyl viologen and menadione bisulphite was increased compared with that of control worms. This sensitivity was rescued by depletion of chk-2 and clk-2, suggesting that growth of the worms is regulated by the checkpoint pathway in response to the accumulation of oxidised nucleotides. Moreover, we found that the sensitivity to menadione bisulphite of ndx-1 and ndx-2-double knockdown worms was enhanced by elimination of XPA-1, a factor involved in nucleotide excision repair. The rescue effect by depletion of chk-2 and clk-2 was limited in the xpa-1 mutant, suggesting that the chk-2 and clk-2 checkpoint pathway is partially linked to the function of XPA-1.
机译:可以将8-Oxo-dGTP(一种在核苷酸库中生成的dGTP的氧化形式)掺入模板DNA中与腺嘌呤或胞嘧啶相对的位置,从而可以诱导突变。在这项研究中,我们确定了秀丽隐杆线虫的新型MutT同源物(NDX-2),它将8-氧代-dGDP水解为8-氧代-dGMP。此外,我们发现NDX-1,NDX-2和NDX-4蛋白具有8-oxo-GTPase或8-oxo-GDPase活性。与对照蠕虫相比,ndx-2敲除线虫蠕虫对甲基紫精和甲萘醌亚硫酸氢盐的敏感性增加。通过消除chk-2和clk-2可以挽救这种敏感性,这表明蠕虫的生长受检查点途径调节,以应对氧化核苷酸的积累。此外,我们发现,通过消除XPA-1(一种涉及核苷酸切除修复的因素),可以提高ndx-1和ndx-2-double敲除蠕虫对甲萘醌亚硫酸氢盐的敏感性。耗尽chk-2和clk-2的挽救作用在xpa-1突变体中受到限制,这表明chk-2和clk-2检查点途径部分与XPA-1的功能有关。

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