Cargando…

Admixture Effects on Coevolved Metabolic Systems

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....

Descripción completa

Detalles Bibliográficos
Autores principales: Zascavage, Roxanne R., Planz, John V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299042/
https://www.ncbi.nlm.nih.gov/pubmed/30619461
http://dx.doi.org/10.3389/fgene.2018.00634
_version_ 1783381403956674560
author Zascavage, Roxanne R.
Planz, John V.
author_facet Zascavage, Roxanne R.
Planz, John V.
author_sort Zascavage, Roxanne R.
collection PubMed
description 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 Mus musculus 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.
format Online
Article
Text
id pubmed-6299042
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-62990422019-01-07 Admixture Effects on Coevolved Metabolic Systems Zascavage, Roxanne R. Planz, John V. Front Genet Genetics 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 Mus musculus 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. Frontiers Media S.A. 2018-12-12 /pmc/articles/PMC6299042/ /pubmed/30619461 http://dx.doi.org/10.3389/fgene.2018.00634 Text en Copyright © 2018 Zascavage and Planz. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Zascavage, Roxanne R.
Planz, John V.
Admixture Effects on Coevolved Metabolic Systems
title Admixture Effects on Coevolved Metabolic Systems
title_full Admixture Effects on Coevolved Metabolic Systems
title_fullStr Admixture Effects on Coevolved Metabolic Systems
title_full_unstemmed Admixture Effects on Coevolved Metabolic Systems
title_short Admixture Effects on Coevolved Metabolic Systems
title_sort admixture effects on coevolved metabolic systems
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299042/
https://www.ncbi.nlm.nih.gov/pubmed/30619461
http://dx.doi.org/10.3389/fgene.2018.00634
work_keys_str_mv AT zascavageroxanner admixtureeffectsoncoevolvedmetabolicsystems
AT planzjohnv admixtureeffectsoncoevolvedmetabolicsystems