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Rapid adaptive radiation of Darwin’s finches depends on ancestral genetic modules

Recent adaptive radiations are models for investigating mechanisms contributing to the evolution of biodiversity. An unresolved question is the relative importance of new mutations, ancestral variants, and introgressive hybridization for phenotypic evolution and speciation. Here, we address this iss...

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Autores principales: Rubin, Carl-Johan, Enbody, Erik D., Dobreva, Mariya P., Abzhanov, Arhat, Davis, Brian W., Lamichhaney, Sangeet, Pettersson, Mats, Sendell-Price, Ashley T., Sprehn, C. Grace, Valle, Carlos A., Vasco, Karla, Wallerman, Ola, Grant, B. Rosemary, Grant, Peter R., Andersson, Leif
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269886/
https://www.ncbi.nlm.nih.gov/pubmed/35857449
http://dx.doi.org/10.1126/sciadv.abm5982
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author Rubin, Carl-Johan
Enbody, Erik D.
Dobreva, Mariya P.
Abzhanov, Arhat
Davis, Brian W.
Lamichhaney, Sangeet
Pettersson, Mats
Sendell-Price, Ashley T.
Sprehn, C. Grace
Valle, Carlos A.
Vasco, Karla
Wallerman, Ola
Grant, B. Rosemary
Grant, Peter R.
Andersson, Leif
author_facet Rubin, Carl-Johan
Enbody, Erik D.
Dobreva, Mariya P.
Abzhanov, Arhat
Davis, Brian W.
Lamichhaney, Sangeet
Pettersson, Mats
Sendell-Price, Ashley T.
Sprehn, C. Grace
Valle, Carlos A.
Vasco, Karla
Wallerman, Ola
Grant, B. Rosemary
Grant, Peter R.
Andersson, Leif
author_sort Rubin, Carl-Johan
collection PubMed
description Recent adaptive radiations are models for investigating mechanisms contributing to the evolution of biodiversity. An unresolved question is the relative importance of new mutations, ancestral variants, and introgressive hybridization for phenotypic evolution and speciation. Here, we address this issue using Darwin’s finches and investigate the genomic architecture underlying their phenotypic diversity. Admixture mapping for beak and body size in the small, medium, and large ground finches revealed 28 loci showing strong genetic differentiation. These loci represent ancestral haplotype blocks with origins predating speciation events during the Darwin’s finch radiation. Genes expressed in the developing beak are overrepresented in these genomic regions. Ancestral haplotypes constitute genetic modules for selection and act as key determinants of the unusual phenotypic diversity of Darwin’s finches. Such ancestral haplotype blocks can be critical for how species adapt to environmental variability and change.
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spelling pubmed-92698862022-07-20 Rapid adaptive radiation of Darwin’s finches depends on ancestral genetic modules Rubin, Carl-Johan Enbody, Erik D. Dobreva, Mariya P. Abzhanov, Arhat Davis, Brian W. Lamichhaney, Sangeet Pettersson, Mats Sendell-Price, Ashley T. Sprehn, C. Grace Valle, Carlos A. Vasco, Karla Wallerman, Ola Grant, B. Rosemary Grant, Peter R. Andersson, Leif Sci Adv Biomedicine and Life Sciences Recent adaptive radiations are models for investigating mechanisms contributing to the evolution of biodiversity. An unresolved question is the relative importance of new mutations, ancestral variants, and introgressive hybridization for phenotypic evolution and speciation. Here, we address this issue using Darwin’s finches and investigate the genomic architecture underlying their phenotypic diversity. Admixture mapping for beak and body size in the small, medium, and large ground finches revealed 28 loci showing strong genetic differentiation. These loci represent ancestral haplotype blocks with origins predating speciation events during the Darwin’s finch radiation. Genes expressed in the developing beak are overrepresented in these genomic regions. Ancestral haplotypes constitute genetic modules for selection and act as key determinants of the unusual phenotypic diversity of Darwin’s finches. Such ancestral haplotype blocks can be critical for how species adapt to environmental variability and change. American Association for the Advancement of Science 2022-07-08 /pmc/articles/PMC9269886/ /pubmed/35857449 http://dx.doi.org/10.1126/sciadv.abm5982 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). 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 use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Biomedicine and Life Sciences
Rubin, Carl-Johan
Enbody, Erik D.
Dobreva, Mariya P.
Abzhanov, Arhat
Davis, Brian W.
Lamichhaney, Sangeet
Pettersson, Mats
Sendell-Price, Ashley T.
Sprehn, C. Grace
Valle, Carlos A.
Vasco, Karla
Wallerman, Ola
Grant, B. Rosemary
Grant, Peter R.
Andersson, Leif
Rapid adaptive radiation of Darwin’s finches depends on ancestral genetic modules
title Rapid adaptive radiation of Darwin’s finches depends on ancestral genetic modules
title_full Rapid adaptive radiation of Darwin’s finches depends on ancestral genetic modules
title_fullStr Rapid adaptive radiation of Darwin’s finches depends on ancestral genetic modules
title_full_unstemmed Rapid adaptive radiation of Darwin’s finches depends on ancestral genetic modules
title_short Rapid adaptive radiation of Darwin’s finches depends on ancestral genetic modules
title_sort rapid adaptive radiation of darwin’s finches depends on ancestral genetic modules
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269886/
https://www.ncbi.nlm.nih.gov/pubmed/35857449
http://dx.doi.org/10.1126/sciadv.abm5982
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