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Functional Evolution of a cis-Regulatory Module

Lack of knowledge about how regulatory regions evolve in relation to their structure–function may limit the utility of comparative sequence analysis in deciphering cis-regulatory sequences. To address this we applied reverse genetics to carry out a functional genetic complementation analysis of a eu...

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Autores principales: Ludwig, Michael Z, Palsson, Arnar, Alekseeva, Elena, Bergman, Casey M, Nathan, Janaki, Kreitman, Martin
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064851/
https://www.ncbi.nlm.nih.gov/pubmed/15757364
http://dx.doi.org/10.1371/journal.pbio.0030093
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author Ludwig, Michael Z
Palsson, Arnar
Alekseeva, Elena
Bergman, Casey M
Nathan, Janaki
Kreitman, Martin
author_facet Ludwig, Michael Z
Palsson, Arnar
Alekseeva, Elena
Bergman, Casey M
Nathan, Janaki
Kreitman, Martin
author_sort Ludwig, Michael Z
collection PubMed
description Lack of knowledge about how regulatory regions evolve in relation to their structure–function may limit the utility of comparative sequence analysis in deciphering cis-regulatory sequences. To address this we applied reverse genetics to carry out a functional genetic complementation analysis of a eukaryotic cis-regulatory module—the even-skipped stripe 2 enhancer—from four Drosophila species. The evolution of this enhancer is non-clock-like, with important functional differences between closely related species and functional convergence between distantly related species. Functional divergence is attributable to differences in activation levels rather than spatiotemporal control of gene expression. Our findings have implications for understanding enhancer structure–function, mechanisms of speciation and computational identification of regulatory modules.
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spelling pubmed-10648512005-03-16 Functional Evolution of a cis-Regulatory Module Ludwig, Michael Z Palsson, Arnar Alekseeva, Elena Bergman, Casey M Nathan, Janaki Kreitman, Martin PLoS Biol Research Article Lack of knowledge about how regulatory regions evolve in relation to their structure–function may limit the utility of comparative sequence analysis in deciphering cis-regulatory sequences. To address this we applied reverse genetics to carry out a functional genetic complementation analysis of a eukaryotic cis-regulatory module—the even-skipped stripe 2 enhancer—from four Drosophila species. The evolution of this enhancer is non-clock-like, with important functional differences between closely related species and functional convergence between distantly related species. Functional divergence is attributable to differences in activation levels rather than spatiotemporal control of gene expression. Our findings have implications for understanding enhancer structure–function, mechanisms of speciation and computational identification of regulatory modules. Public Library of Science 2005-04 2005-03-15 /pmc/articles/PMC1064851/ /pubmed/15757364 http://dx.doi.org/10.1371/journal.pbio.0030093 Text en Copyright: © 2005 Ludwig 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
Ludwig, Michael Z
Palsson, Arnar
Alekseeva, Elena
Bergman, Casey M
Nathan, Janaki
Kreitman, Martin
Functional Evolution of a cis-Regulatory Module
title Functional Evolution of a cis-Regulatory Module
title_full Functional Evolution of a cis-Regulatory Module
title_fullStr Functional Evolution of a cis-Regulatory Module
title_full_unstemmed Functional Evolution of a cis-Regulatory Module
title_short Functional Evolution of a cis-Regulatory Module
title_sort functional evolution of a cis-regulatory module
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1064851/
https://www.ncbi.nlm.nih.gov/pubmed/15757364
http://dx.doi.org/10.1371/journal.pbio.0030093
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