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Hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp Nasonia
Study of genome incompatibilities in species hybrids is important for understanding the genetic basis of reproductive isolation and speciation. According to Haldane's rule hybridization affects the heterogametic sex more than the homogametic sex. Several theories have been proposed that attribu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397956/ https://www.ncbi.nlm.nih.gov/pubmed/25926847 http://dx.doi.org/10.3389/fgene.2015.00140 |
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author | Beukeboom, Leo W. Koevoets, Tosca Morales, Hernán E. Ferber, Steven van de Zande, Louis |
author_facet | Beukeboom, Leo W. Koevoets, Tosca Morales, Hernán E. Ferber, Steven van de Zande, Louis |
author_sort | Beukeboom, Leo W. |
collection | PubMed |
description | Study of genome incompatibilities in species hybrids is important for understanding the genetic basis of reproductive isolation and speciation. According to Haldane's rule hybridization affects the heterogametic sex more than the homogametic sex. Several theories have been proposed that attribute asymmetry in hybridization effects to either phenotype (sex) or genotype (heterogamety). Here we investigate the genetic basis of hybrid genome incompatibility in the haplodiploid wasp Nasonia using the powerful features of haploid males and sex reversal. We separately investigate the effects of heterozygosity (ploidy level) and sex by generating sex reversed diploid hybrid males and comparing them to genotypically similar haploid hybrid males and diploid hybrid females. Hybrid effects of sterility were more pronounced than of inviability, and were particularly strong in haploid males, but weak to absent in diploid males and females, indicating a strong ploidy level but no sex specific effect. Molecular markers identified a number of genomic regions associated with hybrid inviability in haploid males that disappeared under diploidy in both hybrid males and females. Hybrid inviability was rescued by dominance effects at some genomic regions, but aggravated or alleviated by dosage effects at other regions, consistent with cytonuclear incompatibilities. Dosage effects underlying Bateson–Dobzhansky–Muller (BDM) incompatibilities need more consideration in explaining Haldane's rule in diploid systems. |
format | Online Article Text |
id | pubmed-4397956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43979562015-04-29 Hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp Nasonia Beukeboom, Leo W. Koevoets, Tosca Morales, Hernán E. Ferber, Steven van de Zande, Louis Front Genet Genetics Study of genome incompatibilities in species hybrids is important for understanding the genetic basis of reproductive isolation and speciation. According to Haldane's rule hybridization affects the heterogametic sex more than the homogametic sex. Several theories have been proposed that attribute asymmetry in hybridization effects to either phenotype (sex) or genotype (heterogamety). Here we investigate the genetic basis of hybrid genome incompatibility in the haplodiploid wasp Nasonia using the powerful features of haploid males and sex reversal. We separately investigate the effects of heterozygosity (ploidy level) and sex by generating sex reversed diploid hybrid males and comparing them to genotypically similar haploid hybrid males and diploid hybrid females. Hybrid effects of sterility were more pronounced than of inviability, and were particularly strong in haploid males, but weak to absent in diploid males and females, indicating a strong ploidy level but no sex specific effect. Molecular markers identified a number of genomic regions associated with hybrid inviability in haploid males that disappeared under diploidy in both hybrid males and females. Hybrid inviability was rescued by dominance effects at some genomic regions, but aggravated or alleviated by dosage effects at other regions, consistent with cytonuclear incompatibilities. Dosage effects underlying Bateson–Dobzhansky–Muller (BDM) incompatibilities need more consideration in explaining Haldane's rule in diploid systems. Frontiers Media S.A. 2015-04-15 /pmc/articles/PMC4397956/ /pubmed/25926847 http://dx.doi.org/10.3389/fgene.2015.00140 Text en Copyright © 2015 Beukeboom, Koevoets, Morales, Ferber and van de Zande. 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) or licensor 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 Beukeboom, Leo W. Koevoets, Tosca Morales, Hernán E. Ferber, Steven van de Zande, Louis Hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp Nasonia |
title | Hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp Nasonia |
title_full | Hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp Nasonia |
title_fullStr | Hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp Nasonia |
title_full_unstemmed | Hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp Nasonia |
title_short | Hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp Nasonia |
title_sort | hybrid incompatibilities are affected by dominance and dosage in the haplodiploid wasp nasonia |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4397956/ https://www.ncbi.nlm.nih.gov/pubmed/25926847 http://dx.doi.org/10.3389/fgene.2015.00140 |
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