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Are mutagenic non D-loop direct repeat motifs in mitochondrial DNA under a negative selection pressure?

机译:负选择压力下线粒体DNA中的诱变非D环直接重复基序吗?

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摘要

Non D-loop direct repeats (DRs) in mitochondrial DNA (mtDNA) have been commonly implicated in the mutagenesis of mtDNA deletions associated with neuromuscular disease and ageing. Further, these DRs have been hypothesized to put a constraint on the lifespan of mammals and are under a negative selection pressure. Using a compendium of 294 mammalian mtDNA, we re-examined the relationship between species lifespan and the mutagenicity of such DRs. Contradicting the prevailing hypotheses, we found no significant evidence that long-lived mammals possess fewer mutagenic DRs than short-lived mammals. By comparing DR counts in human mtDNA with those in selectively randomized sequences, we also showed that the number of DRs in human mtDNA is primarily determined by global mtDNA properties, such as the bias in synonymous codon usage (SCU) and nucleotide composition. We found that SCU bias in mtDNA positively correlates with DR counts, where repeated usage of a subset of codons leads to more frequent DR occurrences. While bias in SCU and nucleotide composition has been attributed to nucleotide mutational bias, mammalian mtDNA still exhibit higher SCU bias and DR counts than expected from such mutational bias, suggesting a lack of negative selection against non D-loop DRs.
机译:线粒体DNA(mtDNA)中的非D环直接重复(DRs)通常涉及与神经肌肉疾病和衰老相关的mtDNA缺失诱变。此外,已经假设这些DR会限制哺乳动物的寿命,并且处于负选择压力下。我们使用了294种哺乳动物mtDNA纲要,重新审查了物种寿命与此类DR致突变性之间的关系。与普遍的假设相反,我们没有发现重要证据表明长寿哺乳动物比短寿哺乳动物具有更少的致突变性DR。通过比较人类mtDNA中的DR计数与选择性随机序列中的DR计数,我们还表明,人类mtDNA中的DR数量主要由全局mtDNA属性决定,例如同义密码子使用(SCU)和核苷酸组成的偏倚。我们发现,mtDNA中的SCU偏倚与DR计数呈正相关,其中重复使用密码子子集会导致更频繁的DR发生。虽然SCU和核苷酸组成的偏倚已归因于核苷酸突变偏倚,但哺乳动物mtDNA仍显示出比此类突变偏倚所预期的更高的SCU偏倚和DR计数,表明缺乏针对非D环DR的负选择。

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