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人类线粒体DNA中的重组或突变热点?

Recombination or mutational hot spots in human mtDNA?

作者信息

Innan Hideki, Nordborg Magnus

机构信息

Molecular and Computational Biology, University of Southern California, CA 90089-1340, USA.

出版信息

Mol Biol Evol. 2002 Jul;19(7):1122-7. doi: 10.1093/oxfordjournals.molbev.a004170.

Abstract

Awadalla, Eyre-Walker, and Maynard Smith (1999) recently argued that there might be recombination in human mitochondrial DNA (mtDNA). Their claim was based on their observation of decaying linkage disequilibrium (LD) as a function of physical distance. Their study was much criticized, and follow-up studies have failed to find any evidence for recombination. We argue that the criticisms levied, even if correct, could not possibly explain the findings of Awadalla, Eyre-Walker, and Maynard Smith (1999). Nonetheless, the test proposed by Awadalla, Eyre-Walker, and Maynard Smith (1999 ) is not robust because recombination is not the only explanation for decay of LD. We show that such a pattern can be caused by mutational hot spots as well. However, a closer look at the data suggests that the pattern observed was not caused by mutational hot spots but rather by chance. Thus, there appears to be no evidence for recombination in the mtDNA polymorphism data. In conclusion, we discuss the possibility of detecting recombination in mtDNA and the implications of its existence.

摘要

阿瓦达拉、艾尔-沃克和梅纳德·史密斯(1999年)最近提出,人类线粒体DNA(mtDNA)中可能存在重组现象。他们的这一主张基于对连锁不平衡(LD)随物理距离衰减的观察。他们的研究受到了诸多批评,后续研究也未能找到任何重组的证据。我们认为,即便所提出的批评是正确的,也无法解释阿瓦达拉、艾尔-沃克和梅纳德·史密斯(1999年)的研究结果。尽管如此,阿瓦达拉、艾尔-沃克和梅纳德·史密斯(1999年)提出的检验方法并不稳健,因为重组并非LD衰减的唯一解释。我们表明,这种模式也可能由突变热点导致。然而,对数据的进一步审视表明,所观察到的模式并非由突变热点引起,而是出于偶然。因此,在mtDNA多态性数据中似乎没有重组的证据。总之,我们讨论了检测mtDNA中重组的可能性及其存在的影响。

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