Cargando…

The Genetic Architecture of Intra-Species Hybrid Mito-Nuclear Epistasis

Genetic variants that are neutral within, but deleterious between, populations (Dobzhansky-Muller Incompatibilities) are thought to initiate hybrid dysfunction and then to accumulate and complete the speciation process. To identify the types of genetic differences that might initiate speciation, it...

Descripción completa

Detalles Bibliográficos
Autores principales: Haddad, Rania, Meter, Brandon, Ross, Joseph A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250786/
https://www.ncbi.nlm.nih.gov/pubmed/30505316
http://dx.doi.org/10.3389/fgene.2018.00481
_version_ 1783372977567432704
author Haddad, Rania
Meter, Brandon
Ross, Joseph A.
author_facet Haddad, Rania
Meter, Brandon
Ross, Joseph A.
author_sort Haddad, Rania
collection PubMed
description Genetic variants that are neutral within, but deleterious between, populations (Dobzhansky-Muller Incompatibilities) are thought to initiate hybrid dysfunction and then to accumulate and complete the speciation process. To identify the types of genetic differences that might initiate speciation, it is useful to study inter-population (intra-species) hybrids that exhibit reduced fitness. In Caenorhabditis briggsae, a close relative of the nematode C. elegans, such minor genetic incompatibilities have been identified. One incompatibility between the mitochondrial and nuclear genomes reduces the fitness of some hybrids. To understand the nuclear genetic architecture of this epistatic interaction, we constructed two sets of recombinant inbred lines by hybridizing two genetically diverse wild populations. In such lines, selection is able to eliminate deleterious combinations of alleles derived from the two parental populations. The genotypes of surviving hybrid lines thus reveal favorable allele combinations at loci experiencing selection. Our genotype data from the resulting lines are consistent with the interpretation that the X alleles participate in epistatic interactions with autosomes and the mitochondrial genome. We evaluate this possibility given predictions that mitochondria-X epistasis should be more prevalent than between mitochondria and autosomes. Our empirical identification of inter-genomic linkage disequilibrium supports the body of literature indicating that the accumulation of mito-nuclear genetic incompatibilities might initiate the speciation process through the generation of less-fit inter-population hybrids.
format Online
Article
Text
id pubmed-6250786
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-62507862018-11-30 The Genetic Architecture of Intra-Species Hybrid Mito-Nuclear Epistasis Haddad, Rania Meter, Brandon Ross, Joseph A. Front Genet Genetics Genetic variants that are neutral within, but deleterious between, populations (Dobzhansky-Muller Incompatibilities) are thought to initiate hybrid dysfunction and then to accumulate and complete the speciation process. To identify the types of genetic differences that might initiate speciation, it is useful to study inter-population (intra-species) hybrids that exhibit reduced fitness. In Caenorhabditis briggsae, a close relative of the nematode C. elegans, such minor genetic incompatibilities have been identified. One incompatibility between the mitochondrial and nuclear genomes reduces the fitness of some hybrids. To understand the nuclear genetic architecture of this epistatic interaction, we constructed two sets of recombinant inbred lines by hybridizing two genetically diverse wild populations. In such lines, selection is able to eliminate deleterious combinations of alleles derived from the two parental populations. The genotypes of surviving hybrid lines thus reveal favorable allele combinations at loci experiencing selection. Our genotype data from the resulting lines are consistent with the interpretation that the X alleles participate in epistatic interactions with autosomes and the mitochondrial genome. We evaluate this possibility given predictions that mitochondria-X epistasis should be more prevalent than between mitochondria and autosomes. Our empirical identification of inter-genomic linkage disequilibrium supports the body of literature indicating that the accumulation of mito-nuclear genetic incompatibilities might initiate the speciation process through the generation of less-fit inter-population hybrids. Frontiers Media S.A. 2018-11-16 /pmc/articles/PMC6250786/ /pubmed/30505316 http://dx.doi.org/10.3389/fgene.2018.00481 Text en Copyright © 2018 Haddad, Meter and Ross. 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
Haddad, Rania
Meter, Brandon
Ross, Joseph A.
The Genetic Architecture of Intra-Species Hybrid Mito-Nuclear Epistasis
title The Genetic Architecture of Intra-Species Hybrid Mito-Nuclear Epistasis
title_full The Genetic Architecture of Intra-Species Hybrid Mito-Nuclear Epistasis
title_fullStr The Genetic Architecture of Intra-Species Hybrid Mito-Nuclear Epistasis
title_full_unstemmed The Genetic Architecture of Intra-Species Hybrid Mito-Nuclear Epistasis
title_short The Genetic Architecture of Intra-Species Hybrid Mito-Nuclear Epistasis
title_sort genetic architecture of intra-species hybrid mito-nuclear epistasis
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250786/
https://www.ncbi.nlm.nih.gov/pubmed/30505316
http://dx.doi.org/10.3389/fgene.2018.00481
work_keys_str_mv AT haddadrania thegeneticarchitectureofintraspecieshybridmitonuclearepistasis
AT meterbrandon thegeneticarchitectureofintraspecieshybridmitonuclearepistasis
AT rossjosepha thegeneticarchitectureofintraspecieshybridmitonuclearepistasis
AT haddadrania geneticarchitectureofintraspecieshybridmitonuclearepistasis
AT meterbrandon geneticarchitectureofintraspecieshybridmitonuclearepistasis
AT rossjosepha geneticarchitectureofintraspecieshybridmitonuclearepistasis