The pdm3 locus is a hotspot for recurrent evolution of female-limited color dimorphism in Drosophila
Identifieur interne : 001646 ( Main/Merge ); précédent : 001645; suivant : 001647The pdm3 locus is a hotspot for recurrent evolution of female-limited color dimorphism in Drosophila
Auteurs : Amir Yassin [États-Unis] ; Emily K. Delaney [États-Unis] ; Adam J. Reddiex [Australie] ; Thaddeus D. Seher [États-Unis] ; Héloïse Bastide [États-Unis] ; Nicholas C. Appleton [Australie] ; Justin B. Lack [États-Unis] ; Jean R. David [France] ; Stephen F. Chenoweth [Australie] ; John E. Pool [États-Unis] ; Artyom Kopp [États-Unis]Source :
- Current biology : CB [ 0960-9822 ] ; 2016.
Abstract
Sex-limited polymorphisms are an intriguing form of sexual dimorphism that offer unique opportunities to reconstruct the evolutionary changes that decouple male and female traits encoded by a shared genome. We investigated the genetic basis of a Mendelian female-limited color dimorphism (FLCD) that segregates in natural populations of more than 20 species of the
Url:
DOI: 10.1016/j.cub.2016.07.016
PubMed: 27546577
PubMed Central: 5450831
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locus is a hotspot for recurrent evolution of female-limited color dimorphism in <italic>Drosophila</italic>
</title>
<author><name sortKey="Yassin, Amir" sort="Yassin, Amir" uniqKey="Yassin A" first="Amir" last="Yassin">Amir Yassin</name>
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<author><name sortKey="Seher, Thaddeus D" sort="Seher, Thaddeus D" uniqKey="Seher T" first="Thaddeus D." last="Seher">Thaddeus D. Seher</name>
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<author><name sortKey="Lack, Justin B" sort="Lack, Justin B" uniqKey="Lack J" first="Justin B." last="Lack">Justin B. Lack</name>
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<front><div type="abstract" xml:lang="en"><title>Summary</title>
<p id="P1">Sex-limited polymorphisms are an intriguing form of sexual dimorphism that offer unique opportunities to reconstruct the evolutionary changes that decouple male and female traits encoded by a shared genome. We investigated the genetic basis of a Mendelian female-limited color dimorphism (FLCD) that segregates in natural populations of more than 20 species of the <italic>Drosophila montium</italic>
subgroup. In these species, females have alternative abdominal color morphs, light and dark, whereas males have only one color morph in each species. A comprehensive molecular phylogeny of the <italic>montium</italic>
subgroup supports multiple origins of FLCD. Despite this, we mapped FLCD to the same locus in four distantly related species – the transcription factor <italic>POU domain motif 3</italic>
(<italic>pdm3</italic>
), which acts as a repressor of abdominal pigmentation in <italic>D. melanogaster</italic>
. In <italic>D. serrata,</italic>
FLCD maps to a structural variant in the first intron of <italic>pdm3</italic>
; however, this variant is not found in the three other species – <italic>D. kikkawai</italic>
, <italic>D. leontia,</italic>
and <italic>D. burlai</italic>
– and sequence analysis strongly suggests the <italic>pdm3</italic>
alleles responsible for FLCD originated independently at least three times. We propose that <italic>cis</italic>
-regulatory changes in <italic>pdm3</italic>
form sexually dimorphic and monomorphic alleles that segregate within species and are preserved, at least in one species, by structural variation. Surprisingly, <italic>pdm3</italic>
has not been implicated in the evolution of sex-specific pigmentation outside the <italic>montium</italic>
subgroup, suggesting that the genetic paths to sexual dimorphism may be constrained within a clade, but variable across clades.</p>
</div>
</front>
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