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Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird

Germline mutations are the ultimate source of genetic variation and the raw material for organismal evolution. Despite their significance, the frequency and genomic locations of mutations, as well as potential sex bias, are yet to be widely investigated in most species. To address these gaps, we con...

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Autores principales: Zhang, Hongkai, Lundberg, Max, Tarka, Maja, Hasselquist, Dennis, Hansson, Bengt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10627410/
https://www.ncbi.nlm.nih.gov/pubmed/37793164
http://dx.doi.org/10.1093/gbe/evad180
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author Zhang, Hongkai
Lundberg, Max
Tarka, Maja
Hasselquist, Dennis
Hansson, Bengt
author_facet Zhang, Hongkai
Lundberg, Max
Tarka, Maja
Hasselquist, Dennis
Hansson, Bengt
author_sort Zhang, Hongkai
collection PubMed
description Germline mutations are the ultimate source of genetic variation and the raw material for organismal evolution. Despite their significance, the frequency and genomic locations of mutations, as well as potential sex bias, are yet to be widely investigated in most species. To address these gaps, we conducted whole-genome sequencing of 12 great reed warblers (Acrocephalus arundinaceus) in a pedigree spanning 3 generations to identify single-nucleotide de novo mutations (DNMs) and estimate the germline mutation rate. We detected 82 DNMs within the pedigree, primarily enriched at CpG sites but otherwise randomly located along the chromosomes. Furthermore, we observed a pronounced sex bias in DNM occurrence, with male warblers exhibiting three times more mutations than females. After correction for false negatives and adjusting for callable sites, we obtained a mutation rate of 7.16 × 10(−9) mutations per site per generation (m/s/g) for the autosomes and 5.10 × 10(−9) m/s/g for the Z chromosome. To demonstrate the utility of species-specific mutation rates, we applied our autosomal mutation rate in models reconstructing the demographic history of the great reed warbler. We uncovered signs of drastic population size reductions predating the last glacial period (LGP) and reduced gene flow between western and eastern populations during the LGP. In conclusion, our results provide one of the few direct estimates of the mutation rate in wild songbirds and evidence for male-driven mutations in accordance with theoretical expectations.
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spelling pubmed-106274102023-11-07 Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird Zhang, Hongkai Lundberg, Max Tarka, Maja Hasselquist, Dennis Hansson, Bengt Genome Biol Evol Article Germline mutations are the ultimate source of genetic variation and the raw material for organismal evolution. Despite their significance, the frequency and genomic locations of mutations, as well as potential sex bias, are yet to be widely investigated in most species. To address these gaps, we conducted whole-genome sequencing of 12 great reed warblers (Acrocephalus arundinaceus) in a pedigree spanning 3 generations to identify single-nucleotide de novo mutations (DNMs) and estimate the germline mutation rate. We detected 82 DNMs within the pedigree, primarily enriched at CpG sites but otherwise randomly located along the chromosomes. Furthermore, we observed a pronounced sex bias in DNM occurrence, with male warblers exhibiting three times more mutations than females. After correction for false negatives and adjusting for callable sites, we obtained a mutation rate of 7.16 × 10(−9) mutations per site per generation (m/s/g) for the autosomes and 5.10 × 10(−9) m/s/g for the Z chromosome. To demonstrate the utility of species-specific mutation rates, we applied our autosomal mutation rate in models reconstructing the demographic history of the great reed warbler. We uncovered signs of drastic population size reductions predating the last glacial period (LGP) and reduced gene flow between western and eastern populations during the LGP. In conclusion, our results provide one of the few direct estimates of the mutation rate in wild songbirds and evidence for male-driven mutations in accordance with theoretical expectations. Oxford University Press 2023-10-04 /pmc/articles/PMC10627410/ /pubmed/37793164 http://dx.doi.org/10.1093/gbe/evad180 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Article
Zhang, Hongkai
Lundberg, Max
Tarka, Maja
Hasselquist, Dennis
Hansson, Bengt
Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird
title Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird
title_full Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird
title_fullStr Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird
title_full_unstemmed Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird
title_short Evidence of Site-Specific and Male-Biased Germline Mutation Rate in a Wild Songbird
title_sort evidence of site-specific and male-biased germline mutation rate in a wild songbird
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10627410/
https://www.ncbi.nlm.nih.gov/pubmed/37793164
http://dx.doi.org/10.1093/gbe/evad180
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