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Genome-enabled discovery of evolutionary divergence in brains and behavior
Lake Malawi cichlid fishes exhibit extensive divergence in form and function built from a relatively small number of genetic changes. We compared the genomes of rock- and sand-dwelling species and asked which genetic variants differed among the groups. We found that 96% of differentiated variants re...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217251/ https://www.ncbi.nlm.nih.gov/pubmed/34155279 http://dx.doi.org/10.1038/s41598-021-92385-8 |
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author | Patil, Chinar Sylvester, Jonathan B. Abdilleh, Kawther Norsworthy, Michael W. Pottin, Karen Malinsky, Milan Bloomquist, Ryan F. Johnson, Zachary V. McGrath, Patrick T. Streelman, Jeffrey T. |
author_facet | Patil, Chinar Sylvester, Jonathan B. Abdilleh, Kawther Norsworthy, Michael W. Pottin, Karen Malinsky, Milan Bloomquist, Ryan F. Johnson, Zachary V. McGrath, Patrick T. Streelman, Jeffrey T. |
author_sort | Patil, Chinar |
collection | PubMed |
description | Lake Malawi cichlid fishes exhibit extensive divergence in form and function built from a relatively small number of genetic changes. We compared the genomes of rock- and sand-dwelling species and asked which genetic variants differed among the groups. We found that 96% of differentiated variants reside in non-coding sequence but these non-coding diverged variants are evolutionarily conserved. Genome regions near differentiated variants are enriched for craniofacial, neural and behavioral categories. Following leads from genome sequence, we used rock- vs. sand-species and their hybrids to (i) delineate the push–pull roles of BMP signaling and irx1b in the specification of forebrain territories during gastrulation and (ii) reveal striking context-dependent brain gene expression during adult social behavior. Our results demonstrate how divergent genome sequences can predict differences in key evolutionary traits. We highlight the promise of evolutionary reverse genetics—the inference of phenotypic divergence from unbiased genome sequencing and then empirical validation in natural populations. |
format | Online Article Text |
id | pubmed-8217251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82172512021-06-22 Genome-enabled discovery of evolutionary divergence in brains and behavior Patil, Chinar Sylvester, Jonathan B. Abdilleh, Kawther Norsworthy, Michael W. Pottin, Karen Malinsky, Milan Bloomquist, Ryan F. Johnson, Zachary V. McGrath, Patrick T. Streelman, Jeffrey T. Sci Rep Article Lake Malawi cichlid fishes exhibit extensive divergence in form and function built from a relatively small number of genetic changes. We compared the genomes of rock- and sand-dwelling species and asked which genetic variants differed among the groups. We found that 96% of differentiated variants reside in non-coding sequence but these non-coding diverged variants are evolutionarily conserved. Genome regions near differentiated variants are enriched for craniofacial, neural and behavioral categories. Following leads from genome sequence, we used rock- vs. sand-species and their hybrids to (i) delineate the push–pull roles of BMP signaling and irx1b in the specification of forebrain territories during gastrulation and (ii) reveal striking context-dependent brain gene expression during adult social behavior. Our results demonstrate how divergent genome sequences can predict differences in key evolutionary traits. We highlight the promise of evolutionary reverse genetics—the inference of phenotypic divergence from unbiased genome sequencing and then empirical validation in natural populations. Nature Publishing Group UK 2021-06-21 /pmc/articles/PMC8217251/ /pubmed/34155279 http://dx.doi.org/10.1038/s41598-021-92385-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Patil, Chinar Sylvester, Jonathan B. Abdilleh, Kawther Norsworthy, Michael W. Pottin, Karen Malinsky, Milan Bloomquist, Ryan F. Johnson, Zachary V. McGrath, Patrick T. Streelman, Jeffrey T. Genome-enabled discovery of evolutionary divergence in brains and behavior |
title | Genome-enabled discovery of evolutionary divergence in brains and behavior |
title_full | Genome-enabled discovery of evolutionary divergence in brains and behavior |
title_fullStr | Genome-enabled discovery of evolutionary divergence in brains and behavior |
title_full_unstemmed | Genome-enabled discovery of evolutionary divergence in brains and behavior |
title_short | Genome-enabled discovery of evolutionary divergence in brains and behavior |
title_sort | genome-enabled discovery of evolutionary divergence in brains and behavior |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217251/ https://www.ncbi.nlm.nih.gov/pubmed/34155279 http://dx.doi.org/10.1038/s41598-021-92385-8 |
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