Enhancer Runaway and the Evolution of Diploid Gene Expression.

Evidence is mounting that the evolution of gene expression plays a major role in adaptation and speciation. Understanding the evolution of gene regulatory regions is indeed an essential step in linking genotypes and phenotypes and in understanding the molecular mechanisms underlying evolutionary cha...

Full description

Bibliographic Details
Main Authors: Frédéric Fyon, Aurélie Cailleau, Thomas Lenormand
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-11-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC4642963?pdf=render
id doaj-d38755376e8c4f19be7a6e995866098c
record_format Article
spelling doaj-d38755376e8c4f19be7a6e995866098c2020-11-25T01:04:19ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042015-11-011111e100566510.1371/journal.pgen.1005665Enhancer Runaway and the Evolution of Diploid Gene Expression.Frédéric FyonAurélie CailleauThomas LenormandEvidence is mounting that the evolution of gene expression plays a major role in adaptation and speciation. Understanding the evolution of gene regulatory regions is indeed an essential step in linking genotypes and phenotypes and in understanding the molecular mechanisms underlying evolutionary change. The common view is that expression traits (protein folding, expression timing, tissue localization and concentration) are under natural selection at the individual level. Here, we use a theoretical approach to show that, in addition, in diploid organisms, enhancer strength (i.e., the ability of enhancers to activate transcription) may increase in a runaway process due to competition for expression between homologous enhancer alleles. These alleles may be viewed as self-promoting genetic elements, as they spread without conferring a benefit at the individual level. They gain a selective advantage by getting associated to better genetic backgrounds: deleterious mutations are more efficiently purged when linked to stronger enhancers. This process, which has been entirely overlooked so far, may help understand the observed overrepresentation of cis-acting regulatory changes in between-species phenotypic differences, and sheds a new light on investigating the contribution of gene expression evolution to adaptation.http://europepmc.org/articles/PMC4642963?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Frédéric Fyon
Aurélie Cailleau
Thomas Lenormand
spellingShingle Frédéric Fyon
Aurélie Cailleau
Thomas Lenormand
Enhancer Runaway and the Evolution of Diploid Gene Expression.
PLoS Genetics
author_facet Frédéric Fyon
Aurélie Cailleau
Thomas Lenormand
author_sort Frédéric Fyon
title Enhancer Runaway and the Evolution of Diploid Gene Expression.
title_short Enhancer Runaway and the Evolution of Diploid Gene Expression.
title_full Enhancer Runaway and the Evolution of Diploid Gene Expression.
title_fullStr Enhancer Runaway and the Evolution of Diploid Gene Expression.
title_full_unstemmed Enhancer Runaway and the Evolution of Diploid Gene Expression.
title_sort enhancer runaway and the evolution of diploid gene expression.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2015-11-01
description Evidence is mounting that the evolution of gene expression plays a major role in adaptation and speciation. Understanding the evolution of gene regulatory regions is indeed an essential step in linking genotypes and phenotypes and in understanding the molecular mechanisms underlying evolutionary change. The common view is that expression traits (protein folding, expression timing, tissue localization and concentration) are under natural selection at the individual level. Here, we use a theoretical approach to show that, in addition, in diploid organisms, enhancer strength (i.e., the ability of enhancers to activate transcription) may increase in a runaway process due to competition for expression between homologous enhancer alleles. These alleles may be viewed as self-promoting genetic elements, as they spread without conferring a benefit at the individual level. They gain a selective advantage by getting associated to better genetic backgrounds: deleterious mutations are more efficiently purged when linked to stronger enhancers. This process, which has been entirely overlooked so far, may help understand the observed overrepresentation of cis-acting regulatory changes in between-species phenotypic differences, and sheds a new light on investigating the contribution of gene expression evolution to adaptation.
url http://europepmc.org/articles/PMC4642963?pdf=render
work_keys_str_mv AT fredericfyon enhancerrunawayandtheevolutionofdiploidgeneexpression
AT aureliecailleau enhancerrunawayandtheevolutionofdiploidgeneexpression
AT thomaslenormand enhancerrunawayandtheevolutionofdiploidgeneexpression
_version_ 1725198881583529984