TY - JOUR
T1 - Sexual antagonism drives the displacement of polymorphism across gene regulatory cascades
AU - Hill, Mark S
AU - Reuter, Max
AU - Stewart, Alexander J
N1 - This work was supported by a UCL IMPACT PhD Studentship to M.S.H. and a Royal Society University Research Fellowship to A.J.S.
PY - 2019/6/12
Y1 - 2019/6/12
N2 - Males and females have different reproductive roles and are often subject to contrasting selection pressures. This sexual antagonism can lead, at a given locus, to different alleles being favoured in each sex and, consequently, to genetic variation being maintained in a population. Although the presence of sexually antagonistic (SA) polymorphisms has been documented across a range of species, their evolutionary dynamics remain poorly understood. Here, we study SA selection on gene expression, which is fundamental to sexual dimorphism, via the evolution of regulatory binding sites. We show that for sites longer than 1 nucleotide, expression polymorphism is maintained only when intermediate expression levels are deleterious to both sexes. We then show that, in a regulatory cascade, expression polymorphism tends to become displaced over evolutionary time from the target of SA selection to upstream regulators. Our results have consequences for understanding the evolution of sexual dimorphism, and provide specific empirical predictions for the regulatory architecture of genes under SA selection.
AB - Males and females have different reproductive roles and are often subject to contrasting selection pressures. This sexual antagonism can lead, at a given locus, to different alleles being favoured in each sex and, consequently, to genetic variation being maintained in a population. Although the presence of sexually antagonistic (SA) polymorphisms has been documented across a range of species, their evolutionary dynamics remain poorly understood. Here, we study SA selection on gene expression, which is fundamental to sexual dimorphism, via the evolution of regulatory binding sites. We show that for sites longer than 1 nucleotide, expression polymorphism is maintained only when intermediate expression levels are deleterious to both sexes. We then show that, in a regulatory cascade, expression polymorphism tends to become displaced over evolutionary time from the target of SA selection to upstream regulators. Our results have consequences for understanding the evolution of sexual dimorphism, and provide specific empirical predictions for the regulatory architecture of genes under SA selection.
KW - Adaptation, Physiological
KW - Animals
KW - Binding Sites/genetics
KW - Female
KW - Gene Regulatory Networks/genetics
KW - Male
KW - Mating Preference, Animal
KW - Polymorphism, Genetic
KW - Reproduction
KW - Sex Characteristics
U2 - 10.1098/rspb.2019.0660
DO - 10.1098/rspb.2019.0660
M3 - Article
C2 - 31161912
SN - 0962-8452
VL - 286
JO - Proceedings. Biological sciences
JF - Proceedings. Biological sciences
IS - 1904
M1 - 20190660
ER -