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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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 |
work_keys_str_mv |
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