首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Mitochondrial DNA mutations in the parotid gland of cigarette smokers and non-smokers.
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Mitochondrial DNA mutations in the parotid gland of cigarette smokers and non-smokers.

机译:吸烟者和非吸烟者腮腺中的线粒体DNA突变。

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摘要

It has previously been demonstrated that mitochondrial DNA (mtDNA) mutations accumulate in the lung and increase in frequency with age. It has also been shown that the level of mtDNA mutations including deletions and base substitutions are elevated in lung tissue of smokers relative to non-smokers. We have previously shown that the 'common' 4977bp mtDNA deletion is present in the parotid (salivary) gland of smokers and non-smokers and that there is a significant increase in the level of this deletion in Warthins tumour, an oncocytoma of the parotid gland. In this study we used semi-quantitative PCR to confirm the presence of 4977bp mtDNA deletion in the parotid gland of non-smokers and smokers. Importantly, we show that the deletion accumulates with age regardless of smoking status and that there was no significant difference in the level of the 4977bp deletion in parotid tissue of smokers and non-smokers. Using strand conformational polymorphism (SSCP) and direct sequencing we also found 5/23 smokers had parotid tissue specific base substitutions: either an A/T to G/C transition at A4767 or a G/C to A/T transition at G4853. These results are evidence of age related increase in the 4977bp deletion and a higher level of mutations, probably due to oxidative damage, in the parotid gland of smokers.
机译:先前已证明线粒体DNA(mtDNA)突变在肺中积累,并随着年龄的增长而增加。还已经显示,相对于不吸烟者,吸烟者的肺组织中包括缺失和碱基取代在内的mtDNA突变水平升高。先前我们已经证明,吸烟者和非吸烟者的腮腺(唾液腺)中存在“常见” 4977bp mtDNA缺失,并且在Warthins肿瘤(腮腺的肿瘤细胞瘤)中这种缺失的水平显着增加。在这项研究中,我们使用半定量PCR来确认非吸烟者和吸烟者腮腺中存在4977bp mtDNA缺失。重要的是,我们表明,无论吸烟状况如何,该缺失会随着年龄的增长而累积,并且吸烟者和非吸烟者腮腺组织中4977bp缺失的水平没有显着差异。使用链构象多态性(SSCP)和直接测序,我们还发现5/23吸烟者具有腮腺组织特异性碱基取代:在A4767处从A / T到G / C转变或在G4853处从G / C到A / T转变。这些结果证明了吸烟者腮腺中4977bp缺失与年龄相关的增加以及突变水平较高,可能是由于氧化损伤所致。

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