Coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.

Phenotypes that appear to be conserved could be maintained not only by strong purifying selection on the underlying genetic systems, but also by stabilizing selection acting via compensatory mutations with balanced effects. Such coevolution has been invoked to explain experimental results, but has r...

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Main Authors: Antoine Barrière, Kacy L Gordon, Ilya Ruvinsky
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-09-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC3447958?pdf=render
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spelling doaj-ec15537ca3ac4d9da1bd75b1362b2fb12020-11-25T00:15:14ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042012-09-0189e100296110.1371/journal.pgen.1002961Coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.Antoine BarrièreKacy L GordonIlya RuvinskyPhenotypes that appear to be conserved could be maintained not only by strong purifying selection on the underlying genetic systems, but also by stabilizing selection acting via compensatory mutations with balanced effects. Such coevolution has been invoked to explain experimental results, but has rarely been the focus of study. Conserved expression driven by the unc-47 promoters of Caenorhabditis elegans and C. briggsae persists despite divergence within a cis-regulatory element and between this element and the trans-regulatory environment. Compensatory changes in cis and trans are revealed when these promoters are used to drive expression in the other species. Functional changes in the C. briggsae promoter, which has experienced accelerated sequence evolution, did not lead to alteration of gene expression in its endogenous environment. Coevolution among promoter elements suggests that complex epistatic interactions within cis-regulatory elements may facilitate their divergence. Our results offer a detailed picture of regulatory evolution in which subtle, lineage-specific, and compensatory modifications of interacting cis and trans regulators together maintain conserved gene expression patterns.http://europepmc.org/articles/PMC3447958?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Antoine Barrière
Kacy L Gordon
Ilya Ruvinsky
spellingShingle Antoine Barrière
Kacy L Gordon
Ilya Ruvinsky
Coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.
PLoS Genetics
author_facet Antoine Barrière
Kacy L Gordon
Ilya Ruvinsky
author_sort Antoine Barrière
title Coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.
title_short Coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.
title_full Coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.
title_fullStr Coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.
title_full_unstemmed Coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.
title_sort coevolution within and between regulatory loci can preserve promoter function despite evolutionary rate acceleration.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2012-09-01
description Phenotypes that appear to be conserved could be maintained not only by strong purifying selection on the underlying genetic systems, but also by stabilizing selection acting via compensatory mutations with balanced effects. Such coevolution has been invoked to explain experimental results, but has rarely been the focus of study. Conserved expression driven by the unc-47 promoters of Caenorhabditis elegans and C. briggsae persists despite divergence within a cis-regulatory element and between this element and the trans-regulatory environment. Compensatory changes in cis and trans are revealed when these promoters are used to drive expression in the other species. Functional changes in the C. briggsae promoter, which has experienced accelerated sequence evolution, did not lead to alteration of gene expression in its endogenous environment. Coevolution among promoter elements suggests that complex epistatic interactions within cis-regulatory elements may facilitate their divergence. Our results offer a detailed picture of regulatory evolution in which subtle, lineage-specific, and compensatory modifications of interacting cis and trans regulators together maintain conserved gene expression patterns.
url http://europepmc.org/articles/PMC3447958?pdf=render
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AT ilyaruvinsky coevolutionwithinandbetweenregulatorylocicanpreservepromoterfunctiondespiteevolutionaryrateacceleration
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