Cargando…
The Eyes Have It: Regulatory and Structural Changes Both Underlie Cichlid Visual Pigment Diversity
A major goal of evolutionary biology is to unravel the molecular genetic mechanisms that underlie functional diversification and adaptation. We investigated how changes in gene regulation and coding sequence contribute to sensory diversification in two replicate radiations of cichlid fishes. In the...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2790343/ https://www.ncbi.nlm.nih.gov/pubmed/20027211 http://dx.doi.org/10.1371/journal.pbio.1000266 |
_version_ | 1782175103242469376 |
---|---|
author | Hofmann, Christopher M. O'Quin, Kelly E. Marshall, N. Justin Cronin, Thomas W. Seehausen, Ole Carleton, Karen L. |
author_facet | Hofmann, Christopher M. O'Quin, Kelly E. Marshall, N. Justin Cronin, Thomas W. Seehausen, Ole Carleton, Karen L. |
author_sort | Hofmann, Christopher M. |
collection | PubMed |
description | A major goal of evolutionary biology is to unravel the molecular genetic mechanisms that underlie functional diversification and adaptation. We investigated how changes in gene regulation and coding sequence contribute to sensory diversification in two replicate radiations of cichlid fishes. In the clear waters of Lake Malawi, differential opsin expression generates diverse visual systems, with sensitivities extending from the ultraviolet to the red regions of the spectrum. These sensitivities fall into three distinct clusters and are correlated with foraging habits. In the turbid waters of Lake Victoria, visual sensitivity is constrained to longer wavelengths, and opsin expression is correlated with ambient light. In addition to regulatory changes, we found that the opsins coding for the shortest- and longest-wavelength visual pigments have elevated numbers of potentially functional substitutions. Thus, we present a model of sensory evolution in which both molecular genetic mechanisms work in concert. Changes in gene expression generate large shifts in visual pigment sensitivity across the collective opsin spectral range, but changes in coding sequence appear to fine-tune visual pigment sensitivity at the short- and long-wavelength ends of this range, where differential opsin expression can no longer extend visual pigment sensitivity. |
format | Text |
id | pubmed-2790343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-27903432009-12-22 The Eyes Have It: Regulatory and Structural Changes Both Underlie Cichlid Visual Pigment Diversity Hofmann, Christopher M. O'Quin, Kelly E. Marshall, N. Justin Cronin, Thomas W. Seehausen, Ole Carleton, Karen L. PLoS Biol Research Article A major goal of evolutionary biology is to unravel the molecular genetic mechanisms that underlie functional diversification and adaptation. We investigated how changes in gene regulation and coding sequence contribute to sensory diversification in two replicate radiations of cichlid fishes. In the clear waters of Lake Malawi, differential opsin expression generates diverse visual systems, with sensitivities extending from the ultraviolet to the red regions of the spectrum. These sensitivities fall into three distinct clusters and are correlated with foraging habits. In the turbid waters of Lake Victoria, visual sensitivity is constrained to longer wavelengths, and opsin expression is correlated with ambient light. In addition to regulatory changes, we found that the opsins coding for the shortest- and longest-wavelength visual pigments have elevated numbers of potentially functional substitutions. Thus, we present a model of sensory evolution in which both molecular genetic mechanisms work in concert. Changes in gene expression generate large shifts in visual pigment sensitivity across the collective opsin spectral range, but changes in coding sequence appear to fine-tune visual pigment sensitivity at the short- and long-wavelength ends of this range, where differential opsin expression can no longer extend visual pigment sensitivity. Public Library of Science 2009-12-22 /pmc/articles/PMC2790343/ /pubmed/20027211 http://dx.doi.org/10.1371/journal.pbio.1000266 Text en Hofmann et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hofmann, Christopher M. O'Quin, Kelly E. Marshall, N. Justin Cronin, Thomas W. Seehausen, Ole Carleton, Karen L. The Eyes Have It: Regulatory and Structural Changes Both Underlie Cichlid Visual Pigment Diversity |
title | The Eyes Have It: Regulatory and Structural Changes Both Underlie Cichlid Visual Pigment Diversity |
title_full | The Eyes Have It: Regulatory and Structural Changes Both Underlie Cichlid Visual Pigment Diversity |
title_fullStr | The Eyes Have It: Regulatory and Structural Changes Both Underlie Cichlid Visual Pigment Diversity |
title_full_unstemmed | The Eyes Have It: Regulatory and Structural Changes Both Underlie Cichlid Visual Pigment Diversity |
title_short | The Eyes Have It: Regulatory and Structural Changes Both Underlie Cichlid Visual Pigment Diversity |
title_sort | eyes have it: regulatory and structural changes both underlie cichlid visual pigment diversity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2790343/ https://www.ncbi.nlm.nih.gov/pubmed/20027211 http://dx.doi.org/10.1371/journal.pbio.1000266 |
work_keys_str_mv | AT hofmannchristopherm theeyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT oquinkellye theeyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT marshallnjustin theeyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT croninthomasw theeyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT seehausenole theeyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT carletonkarenl theeyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT hofmannchristopherm eyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT oquinkellye eyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT marshallnjustin eyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT croninthomasw eyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT seehausenole eyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity AT carletonkarenl eyeshaveitregulatoryandstructuralchangesbothunderliecichlidvisualpigmentdiversity |