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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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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 |
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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 |
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