Suppr超能文献

线粒体 tRNA 的补偿进化在低适应性的山谷中进行。

Compensatory evolution in mitochondrial tRNAs navigates valleys of low fitness.

机构信息

Bioinformatics and Genomics Programme, Centre for Genomic Regulation, C/Dr Aiguader 88, Barcelona Biomedical Research Park Building, 08003 Barcelona, Spain.

出版信息

Nature. 2010 Mar 11;464(7286):279-82. doi: 10.1038/nature08691. Epub 2010 Feb 24.

Abstract

A long-standing controversy in evolutionary biology is whether or not evolving lineages can cross valleys on the fitness landscape that correspond to low-fitness genotypes, which can eventually enable them to reach isolated fitness peaks. Here we study the fitness landscapes traversed by switches between different AU and GC Watson-Crick nucleotide pairs at complementary sites of mitochondrial transfer RNA stem regions in 83 mammalian species. We find that such Watson-Crick switches occur 30-40 times more slowly than pairs of neutral substitutions, and that alleles corresponding to GU and AC non-Watson-Crick intermediate states segregate within human populations at low frequencies, similar to those of non-synonymous alleles. Substitutions leading to a Watson-Crick switch are strongly correlated, especially in mitochondrial tRNAs encoded on the GT-nucleotide-rich strand of the mitochondrial genome. Using these data we estimate that a typical Watson-Crick switch involves crossing a fitness valley of a depth of about 10(-3) or even about 10(-2), with AC intermediates being slightly more deleterious than GU intermediates. This compensatory evolution must proceed through rare intermediate variants that never reach fixation. The ubiquitous nature of compensatory evolution in mammalian mitochondrial tRNAs and other molecules implies that simultaneous fixation of two alleles that are individually deleterious may be a common phenomenon at the molecular level.

摘要

进化生物学中长期存在的一个争议是,进化谱系是否能够跨越适应度景观中的低谷,这些低谷对应着低适应度基因型,最终使它们能够到达孤立的适应度高峰。在这里,我们研究了在 83 种哺乳动物的线粒体转移 RNA 茎区域互补位点之间不同 AU 和 GC Watson-Crick 核苷酸对之间的转换所经历的适应度景观。我们发现,这种 Watson-Crick 转换比中性替换对发生的速度慢 30-40 倍,并且对应于 GU 和 AC 非 Watson-Crick 中间状态的等位基因在人类群体中以低频率分离,类似于非同义等位基因。导致 Watson-Crick 转换的取代与高度相关,尤其是在线粒体基因组 GT-核苷酸丰富链上编码的线粒体转移 RNA 中。使用这些数据,我们估计典型的 Watson-Crick 转换涉及跨越深度约为 10(-3)甚至约 10(-2)的适应度低谷,AC 中间状态比 GU 中间状态略具危害性。这种补偿性进化必须通过从未达到固定状态的罕见中间变体进行。哺乳动物线粒体转移 RNA 和其他分子中补偿性进化的普遍存在意味着,两个单独有害的等位基因同时固定可能是分子水平上的常见现象。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验