Cargando…

Hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation

Estimating the complex relationship between fitness and genotype or phenotype (i.e. the adaptive landscape) is one of the central goals of evolutionary biology. However, adaptive walks connecting genotypes to organismal fitness, speciation, and novel ecological niches are still poorly understood and...

Descripción completa

Detalles Bibliográficos
Autores principales: Patton, Austin H, Richards, Emilie J, Gould, Katelyn J, Buie, Logan K, Martin, Christopher H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135402/
https://www.ncbi.nlm.nih.gov/pubmed/35616528
http://dx.doi.org/10.7554/eLife.72905
_version_ 1784713954457550848
author Patton, Austin H
Richards, Emilie J
Gould, Katelyn J
Buie, Logan K
Martin, Christopher H
author_facet Patton, Austin H
Richards, Emilie J
Gould, Katelyn J
Buie, Logan K
Martin, Christopher H
author_sort Patton, Austin H
collection PubMed
description Estimating the complex relationship between fitness and genotype or phenotype (i.e. the adaptive landscape) is one of the central goals of evolutionary biology. However, adaptive walks connecting genotypes to organismal fitness, speciation, and novel ecological niches are still poorly understood and processes for surmounting fitness valleys remain controversial. One outstanding system for addressing these connections is a recent adaptive radiation of ecologically and morphologically novel pupfishes (a generalist, molluscivore, and scale-eater) endemic to San Salvador Island, Bahamas. We leveraged whole-genome sequencing of 139 hybrids from two independent field fitness experiments to identify the genomic basis of fitness, estimate genotypic fitness networks, and measure the accessibility of adaptive walks on the fitness landscape. We identified 132 single nucleotide polymorphisms (SNPs) that were significantly associated with fitness in field enclosures. Six out of the 13 regions most strongly associated with fitness contained differentially expressed genes and fixed SNPs between trophic specialists; one gene (mettl21e) was also misexpressed in lab-reared hybrids, suggesting a potential intrinsic genetic incompatibility. We then constructed genotypic fitness networks from adaptive alleles and show that scale-eating specialists are the most isolated of the three species on these networks. Intriguingly, introgressed and de novo variants reduced fitness landscape ruggedness as compared to standing variation, increasing the accessibility of genotypic fitness paths from generalist to specialists. Our results suggest that adaptive introgression and de novo mutations alter the shape of the fitness landscape, providing key connections in adaptive walks circumventing fitness valleys and triggering the evolution of novelty during adaptive radiation.
format Online
Article
Text
id pubmed-9135402
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-91354022022-05-27 Hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation Patton, Austin H Richards, Emilie J Gould, Katelyn J Buie, Logan K Martin, Christopher H eLife Evolutionary Biology Estimating the complex relationship between fitness and genotype or phenotype (i.e. the adaptive landscape) is one of the central goals of evolutionary biology. However, adaptive walks connecting genotypes to organismal fitness, speciation, and novel ecological niches are still poorly understood and processes for surmounting fitness valleys remain controversial. One outstanding system for addressing these connections is a recent adaptive radiation of ecologically and morphologically novel pupfishes (a generalist, molluscivore, and scale-eater) endemic to San Salvador Island, Bahamas. We leveraged whole-genome sequencing of 139 hybrids from two independent field fitness experiments to identify the genomic basis of fitness, estimate genotypic fitness networks, and measure the accessibility of adaptive walks on the fitness landscape. We identified 132 single nucleotide polymorphisms (SNPs) that were significantly associated with fitness in field enclosures. Six out of the 13 regions most strongly associated with fitness contained differentially expressed genes and fixed SNPs between trophic specialists; one gene (mettl21e) was also misexpressed in lab-reared hybrids, suggesting a potential intrinsic genetic incompatibility. We then constructed genotypic fitness networks from adaptive alleles and show that scale-eating specialists are the most isolated of the three species on these networks. Intriguingly, introgressed and de novo variants reduced fitness landscape ruggedness as compared to standing variation, increasing the accessibility of genotypic fitness paths from generalist to specialists. Our results suggest that adaptive introgression and de novo mutations alter the shape of the fitness landscape, providing key connections in adaptive walks circumventing fitness valleys and triggering the evolution of novelty during adaptive radiation. eLife Sciences Publications, Ltd 2022-05-26 /pmc/articles/PMC9135402/ /pubmed/35616528 http://dx.doi.org/10.7554/eLife.72905 Text en © 2022, Patton et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Evolutionary Biology
Patton, Austin H
Richards, Emilie J
Gould, Katelyn J
Buie, Logan K
Martin, Christopher H
Hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation
title Hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation
title_full Hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation
title_fullStr Hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation
title_full_unstemmed Hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation
title_short Hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation
title_sort hybridization alters the shape of the genotypic fitness landscape, increasing access to novel fitness peaks during adaptive radiation
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9135402/
https://www.ncbi.nlm.nih.gov/pubmed/35616528
http://dx.doi.org/10.7554/eLife.72905
work_keys_str_mv AT pattonaustinh hybridizationalterstheshapeofthegenotypicfitnesslandscapeincreasingaccesstonovelfitnesspeaksduringadaptiveradiation
AT richardsemiliej hybridizationalterstheshapeofthegenotypicfitnesslandscapeincreasingaccesstonovelfitnesspeaksduringadaptiveradiation
AT gouldkatelynj hybridizationalterstheshapeofthegenotypicfitnesslandscapeincreasingaccesstonovelfitnesspeaksduringadaptiveradiation
AT buielogank hybridizationalterstheshapeofthegenotypicfitnesslandscapeincreasingaccesstonovelfitnesspeaksduringadaptiveradiation
AT martinchristopherh hybridizationalterstheshapeofthegenotypicfitnesslandscapeincreasingaccesstonovelfitnesspeaksduringadaptiveradiation