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首页> 外文期刊>Environmental and molecular mutagenesis. >DNA damage induced by industrial solid waste leachates in Drosophila melanogaster: A mechanistic approach.
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DNA damage induced by industrial solid waste leachates in Drosophila melanogaster: A mechanistic approach.

机译:果蝇工业固体垃圾渗滤液诱导的DNA损伤:一种机械方法。

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Genomic stability requires that error-free genetic information be transmitted from generation to generation, a process that is dependent upon efficient DNA repair. Industrial leachates which contain mixtures of diverse chemicals are a major environmental concern. The interaction between these chemicals may have synergistic, antagonistic, or simply additive effects on biological systems. In the present study, the Comet assay was used to measure the DNA damage produced by leachates of solid wastes from flashlight battery, pigment, and tanning factories in the midgut cells and brain ganglia of Drosophila melanogaster mutants deficient in DNA repair proteins. Larvae were allowed to feed for 48 or 72 hr on diets containing 0.1, 0.5, and 2.0% (v/v) of the leachates. Physicochemical analysis run on the solid wastes, leachates, and treated larvae detected elevated levels of heavy metals. Leachates produced significantly greater levels of DNA damage in mutant strains mei41 (deficient in cell cycle check point protein), mus201 (deficient in excision repair protein), mus308 (deficient in postreplication repair protein), and rad54 (deficient in double strand break repair protein) than in the OregonR(+) wild-type strain. Larvae of the ligaseIV mutant (deficient in double strand break repair protein) were hypersensitive only to the pigment plant waste leachate. Conversely, the dnase2 mutant (deficient in protein responsible for degrading fragmented DNA) was more sensitive to DNA damage induction from the flashlight battery and tannery waste leachates. Our data demonstrate that repair of DNA damage in organisms exposed to leachates is dependent upon several DNA repair proteins, indicative of the involvement of multiple overlapping repair pathways. The study further suggests the usefulness of the Comet assay for studying the mechanisms of DNA repair in Drosophila. Environ. Mol. Mutagen., 2008. (c) 2008 Wiley-Liss, Inc.
机译:基因组稳定性要求无错遗传信息一代一代地传递,这一过程取决于有效的DNA修复。包含多种化学物质混合物的工业渗滤液是主要的环境问题。这些化学物质之间的相互作用可能会对生物系统产生协同,拮抗或简单的累加作用。在本研究中,彗星分析法用于测量果蝇果蝇黑色素突变体突变体中肠细胞和脑神经节中手电筒电池,色素和鞣制工厂产生的固体废物浸出液对DNA修复蛋白缺乏的DNA损伤。允许幼虫以含0.1%,0.5%和2.0%(v / v)沥滤液的日粮喂养48或72小时。对固体废物,浸出液和处理过的幼虫进行了理化分析,发现重金属含量升高。在突变株mei41(缺乏细胞周期检查点蛋白),mus201(缺乏切除修复蛋白),mus308(缺乏复制后修复蛋白)和rad54(缺乏双链断裂修复蛋白)中,渗滤液产生的DNA损伤水平明显更高。 )比OregonR(+)野生型菌株中的高。 ligaseIV突变体的幼虫(缺乏双链断裂修复蛋白)仅对色素植物废浸液敏感。相反,dnase2突变体(缺乏负责降解片段化DNA的蛋白质)对手电筒电池和制革厂垃圾渗滤液引起的DNA损伤感应更为敏感。我们的数据表明,暴露于渗滤液的生物体中DNA损伤的修复取决于几种DNA修复蛋白,这表明涉及多个重叠的修复途径。这项研究进一步表明,彗星试验对于研究果蝇中DNA修复机制的有用性。环境。大声笑Mutagen。,2008.(c)2008 Wiley-Liss,Inc.

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