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Fitness consequences of polymorphic inversions in the zebra finch genome
BACKGROUND: Inversion polymorphisms constitute an evolutionary puzzle: they should increase embryo mortality in heterokaryotypic individuals but still they are widespread in some taxa. Some insect species have evolved mechanisms to reduce the cost of embryo mortality but humans have not. In birds, a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043542/ https://www.ncbi.nlm.nih.gov/pubmed/27687629 http://dx.doi.org/10.1186/s13059-016-1056-3 |
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author | Knief, Ulrich Hemmrich-Stanisak, Georg Wittig, Michael Franke, Andre Griffith, Simon C. Kempenaers, Bart Forstmeier, Wolfgang |
author_facet | Knief, Ulrich Hemmrich-Stanisak, Georg Wittig, Michael Franke, Andre Griffith, Simon C. Kempenaers, Bart Forstmeier, Wolfgang |
author_sort | Knief, Ulrich |
collection | PubMed |
description | BACKGROUND: Inversion polymorphisms constitute an evolutionary puzzle: they should increase embryo mortality in heterokaryotypic individuals but still they are widespread in some taxa. Some insect species have evolved mechanisms to reduce the cost of embryo mortality but humans have not. In birds, a detailed analysis is missing although intraspecific inversion polymorphisms are regarded as common. In Australian zebra finches (Taeniopygia guttata), two polymorphic inversions are known cytogenetically and we set out to detect these two and potentially additional inversions using genomic tools and study their effects on embryo mortality and other fitness-related and morphological traits. RESULTS: Using whole-genome SNP data, we screened 948 wild zebra finches for polymorphic inversions and describe four large (12–63 Mb) intraspecific inversion polymorphisms with allele frequencies close to 50 %. Using additional data from 5229 birds and 9764 eggs from wild and three captive zebra finch populations, we show that only the largest inversions increase embryo mortality in heterokaryotypic males, with surprisingly small effect sizes. We test for a heterozygote advantage on other fitness components but find no evidence for heterosis for any of the inversions. Yet, we find strong additive effects on several morphological traits. CONCLUSIONS: The mechanism that has carried the derived inversion haplotypes to such high allele frequencies remains elusive. It appears that selection has effectively minimized the costs associated with inversions in zebra finches. The highly skewed distribution of recombination events towards the chromosome ends in zebra finches and other estrildid species may function to minimize crossovers in the inverted regions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1056-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5043542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50435422016-10-05 Fitness consequences of polymorphic inversions in the zebra finch genome Knief, Ulrich Hemmrich-Stanisak, Georg Wittig, Michael Franke, Andre Griffith, Simon C. Kempenaers, Bart Forstmeier, Wolfgang Genome Biol Research BACKGROUND: Inversion polymorphisms constitute an evolutionary puzzle: they should increase embryo mortality in heterokaryotypic individuals but still they are widespread in some taxa. Some insect species have evolved mechanisms to reduce the cost of embryo mortality but humans have not. In birds, a detailed analysis is missing although intraspecific inversion polymorphisms are regarded as common. In Australian zebra finches (Taeniopygia guttata), two polymorphic inversions are known cytogenetically and we set out to detect these two and potentially additional inversions using genomic tools and study their effects on embryo mortality and other fitness-related and morphological traits. RESULTS: Using whole-genome SNP data, we screened 948 wild zebra finches for polymorphic inversions and describe four large (12–63 Mb) intraspecific inversion polymorphisms with allele frequencies close to 50 %. Using additional data from 5229 birds and 9764 eggs from wild and three captive zebra finch populations, we show that only the largest inversions increase embryo mortality in heterokaryotypic males, with surprisingly small effect sizes. We test for a heterozygote advantage on other fitness components but find no evidence for heterosis for any of the inversions. Yet, we find strong additive effects on several morphological traits. CONCLUSIONS: The mechanism that has carried the derived inversion haplotypes to such high allele frequencies remains elusive. It appears that selection has effectively minimized the costs associated with inversions in zebra finches. The highly skewed distribution of recombination events towards the chromosome ends in zebra finches and other estrildid species may function to minimize crossovers in the inverted regions. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-016-1056-3) contains supplementary material, which is available to authorized users. BioMed Central 2016-09-29 /pmc/articles/PMC5043542/ /pubmed/27687629 http://dx.doi.org/10.1186/s13059-016-1056-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Knief, Ulrich Hemmrich-Stanisak, Georg Wittig, Michael Franke, Andre Griffith, Simon C. Kempenaers, Bart Forstmeier, Wolfgang Fitness consequences of polymorphic inversions in the zebra finch genome |
title | Fitness consequences of polymorphic inversions in the zebra finch genome |
title_full | Fitness consequences of polymorphic inversions in the zebra finch genome |
title_fullStr | Fitness consequences of polymorphic inversions in the zebra finch genome |
title_full_unstemmed | Fitness consequences of polymorphic inversions in the zebra finch genome |
title_short | Fitness consequences of polymorphic inversions in the zebra finch genome |
title_sort | fitness consequences of polymorphic inversions in the zebra finch genome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043542/ https://www.ncbi.nlm.nih.gov/pubmed/27687629 http://dx.doi.org/10.1186/s13059-016-1056-3 |
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