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混合对协同进化代谢系统的影响。

Admixture Effects on Coevolved Metabolic Systems.

作者信息

Zascavage Roxanne R, Planz John V

机构信息

Department of Microbiology, Immunology and Genetics, Graduate School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX, United States.

Department of Criminology and Criminal Justice, University of Texas at Arlington, Arlington, TX, United States.

出版信息

Front Genet. 2018 Dec 12;9:634. doi: 10.3389/fgene.2018.00634. eCollection 2018.

DOI:10.3389/fgene.2018.00634
PMID:30619461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6299042/
Abstract

Oxidative phosphorylation (OXPHOS) is the primary energy generating system in eukaryotic organisms. The complexes within the OXPHOS pathway are of mixed genomic origin. Although most subunit-coding genes are located within the nuclear genome, several genes are coded for in the mitochondrial genome. There is strong evidence to support coadaptation between the two genomes in these OXPHOS gene regions in order to create tight protein interactions necessary for a functional energetics system. In this study, we begin to assess the physiological impact of separating coevolved protein motifs that make up the highly conserved energy production pathway, as we hypothesize that divergent matings will significantly diminish the protein interactions and therefore hinder efficient OXPHOS activity We measured mitochondrial activity in high energy-demanding tissues from six strains of with varying degrees of mixed ancestral background. Mice with divergent mitochondrial and nuclear backgrounds consistently yielded lower mitochondrial activity. Bioinformatic analysis of common single nucleotide variants across the nuclear and mitochondrial genomes failed to identify any non-synonymous variants that could account for the energetic differences, suggesting that interpopulational mating between ancestrally distinct groups influences energy production efficiency.

摘要

氧化磷酸化(OXPHOS)是真核生物中主要的能量产生系统。氧化磷酸化途径中的复合物具有混合的基因组起源。尽管大多数亚基编码基因位于核基因组内,但有几个基因是由线粒体基因组编码的。有强有力的证据支持这两个基因组在这些氧化磷酸化基因区域之间的共同适应,以便创建一个功能正常的能量系统所需的紧密蛋白质相互作用。在本研究中,我们开始评估分离构成高度保守的能量产生途径的共同进化蛋白质基序的生理影响,因为我们假设不同的交配方式将显著减少蛋白质相互作用,从而阻碍有效的氧化磷酸化活性。我们测量了来自六个具有不同程度混合祖先背景品系的高能量需求组织中的线粒体活性。线粒体和核背景不同的小鼠始终产生较低的线粒体活性。对核基因组和线粒体基因组中常见单核苷酸变异的生物信息学分析未能识别出任何可解释能量差异的非同义变异,这表明祖先不同群体之间的群体间交配会影响能量产生效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a6/6299042/f9d0107a8086/fgene-09-00634-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a6/6299042/bd34b0ad6ce6/fgene-09-00634-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a6/6299042/cd61f0589f4f/fgene-09-00634-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a6/6299042/f9d0107a8086/fgene-09-00634-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a6/6299042/bd34b0ad6ce6/fgene-09-00634-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a6/6299042/cd61f0589f4f/fgene-09-00634-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0a6/6299042/f9d0107a8086/fgene-09-00634-g0003.jpg

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Coadaptation of mitochondrial and nuclear genes, and the cost of mother's curse.线粒体和核基因的共适应,以及母性诅咒的代价。
Proc Biol Sci. 2018 Jan 31;285(1871). doi: 10.1098/rspb.2017.2257.
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Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing.线粒体和核 DNA 匹配塑造代谢和健康衰老。
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