scholarly journals Evolutionary inevitability of sexual antagonism

2014 ◽  
Vol 281 (1776) ◽  
pp. 20132123 ◽  
Author(s):  
Tim Connallon ◽  
Andrew G. Clark
Keyword(s):  
Sex Differences ◽  
Natural Populations ◽  
Evolutionary Divergence ◽  
Sexual Antagonism ◽  
Evolutionary Theories ◽  
Sex Effects ◽  
Evolutionary Trajectories ◽  
Males And Females ◽  
Evolutionary Consequences

Sexual antagonism, whereby mutations are favourable in one sex and disfavourable in the other, is common in natural populations, yet the root causes of sexual antagonism are rarely considered in evolutionary theories of adaptation. Here, we explore the evolutionary consequences of sex-differential selection and genotype-by-sex interactions for adaptation in species with separate sexes. We show that sexual antagonism emerges naturally from sex differences in the direction of selection on phenotypes expressed by both sexes or from sex-by-genotype interactions affecting the expression of such phenotypes. Moreover, modest sex differences in selection or genotype-by-sex effects profoundly influence the long-term evolutionary trajectories of populations with separate sexes, as these conditions trigger the evolution of strong sexual antagonism as a by-product of adaptively driven evolutionary change. The theory demonstrates that sexual antagonism is an inescapable by-product of adaptation in species with separate sexes, whether or not selection favours evolutionary divergence between males and females.

scholarly journals No sex differences in learning in wild bumblebees

2021 ◽  
Author(s):  
Felicity Muth ◽  
Amber D Tripodi ◽  
Rene Bonilla ◽  
James P Strange ◽  
Anne S Leonard
Keyword(s):  
Sex Differences ◽  
Associative Learning ◽  
Sierra Nevada ◽  
Comparative Cognition ◽  
Natural Populations ◽  
Interspecific Variation ◽  
Learning Task ◽  
Learning Ability ◽  
Learning Performance ◽  
Males And Females

Abstract Females and males often face different sources of selection, resulting in dimorphism in morphological, physiological, and even cognitive traits. Sex differences are often studied in respect to spatial cognition, yet the different ecological roles of males and females might shape cognition in multiple ways. For example, in dietary generalist bumblebees (Bombus), the ability to learn associations is critical to female workers, who face informationally rich foraging scenarios as they collect nectar and pollen from thousands of flowers over a period of weeks to months to feed the colony. While male bumblebees likely need to learn associations as well, they only forage for themselves while searching for potential mates. It is thus less clear whether foraging males would benefit from the same associative learning performance as foraging females. In this system, as in others, cognitive performance is typically studied in lab-reared animals under captive conditions, which may not be representative of patterns in the wild. In the first test of sex and species differences in cognition using wild bumblebees, we compared the performance of Bombus vancouverensis nearcticus (formerly bifarius) and Bombus vosnesenskii of both sexes on an associative learning task at Sierra Nevada (CA) field sites. Across both species, we found that males and females did not differ in their ability to learn, although males were slower to respond to the sucrose reward. These results offer the first evidence from natural populations that male bumblebees may be equally as able to learn associations as females, supporting findings from captive colonies of commercial bees. The observed interspecific variation in learning ability opens the door to using the Bombus system to test hypotheses about comparative cognition.

scholarly journals Linking sex differences to the evolution of infectious disease life-histories

2018 ◽  
Vol 373 (1757) ◽  
pp. 20170431 ◽  
Author(s):  
Matthew D. Hall ◽  
Nicole Mideo
Keyword(s):  
Infectious Disease ◽  
Sex Differences ◽  
Life Histories ◽  
Test Case ◽  
Theme Issue ◽  
Genetic Covariance ◽  
Covariance Functions ◽  
Genetic Constraint ◽  
Males And Females ◽  
Evolutionary Consequences

Sex differences in the prevalence, course and severity of infection are widespread, yet the evolutionary consequences of these differences remain unclear. Understanding how male–female differences affect the trajectory of infectious disease requires connecting the contrasting dynamics that pathogens might experience within each sex to the number of susceptible and infected individuals that are circulating in a population. In this study, we build on theory using genetic covariance functions to link the growth of a pathogen within a host to the evolution and spread of disease between individuals. Using the Daphnia–Pasteuria system as a test case, we show that on the basis of within-host dynamics alone, females seem to be more evolutionarily liable for the pathogen, with higher spore loads and greater divergence among pathogen genotypes as infection progresses. Between-host transmission, however, appears to offset the lower performance of a pathogen within a male host, making even subtle differences between the sexes evolutionarily relevant, as long as the selection generated by the between-host dynamics is sufficiently strong. Our model suggests that relatively simple differences in within-host processes occurring in males and females can lead to complex patterns of genetic constraint on pathogen evolution, particularly during an expanding epidemic. This article is part of the theme issue ‘Linking local adaptation with the evolution of sex differences’.

scholarly journals Macroevolutionary consequences of sexual conflict

2018 ◽  
Vol 14 (6) ◽  
pp. 20180186
Author(s):  
Jo S. Hermansen ◽  
Jostein Starrfelt ◽  
Kjetil L. Voje ◽  
Nils C. Stenseth
Keyword(s):  
Sexual Selection ◽  
Genetic Architecture ◽  
Time Frame ◽  
Sexual Conflicts ◽  
Males And Females ◽  
Selection For ◽  
Evolutionary Consequences ◽  
Future Work ◽  
Shared Genetic

Intralocus sexual conflicts arise whenever the fitness optima for a trait expressed in both males and females differ between the sexes and shared genetic architecture constrains the sexes from evolving independently towards their respective optima. Such sexual conflicts are commonplace in nature, yet their long-term evolutionary consequences remain unexplored. Using a Bayesian phylogenetic comparative framework, we studied the macroevolutionary dynamics of intersexual trait integration in stalk-eyed flies (Diopsidae) spanning a time frame of more than 25 Myr. We report that increased intensity of sexual selection on male eyestalks is associated with reduced intersexual eyestalk integration, as well as sex-specific rates of eyestalk evolution. Despite this, lineages where males have been under strong sexual selection for millions of years still exhibit high levels of intersexual trait integration. This low level of decoupling between the sexes may indicate that exaggerated female eyestalks are in fact adaptive—or alternatively, that there are strong constraints on reducing trait integration between the sexes. Future work should seek to clarify the relative roles of constraints and selection in contributing to the varying levels of intersexual trait integration in stalk-eyed flies, and in this way clarify whether sexual conflicts can act as constraints on adaptive evolution even on macroevolutionary time scales.

scholarly journals Immune Cells Have Sex and So Should Journal Articles

Endocrinology ◽  
2012 ◽  
Vol 153 (6) ◽  
pp. 2544-2550 ◽  
Author(s):  
Sabra L. Klein
Keyword(s):  
Sex Differences ◽  
Immune Function ◽  
Immune Cells ◽  
Hormone Receptors ◽  
Journal Articles ◽  
Immune Mediated ◽  
Males And Females ◽  
Journal Policies ◽  
Increased Susceptibility

Males and females have the same immunological cells, proteins, and pathways in place to protect against the development of disease. The kinetics, magnitude, and skewing of the responses mounted against pathogens, allergens, toxins, or self-antigens, however, can differ dramatically between the sexes. Generally, females mount higher innate and adaptive immune responses than males, which can result in faster clearance of pathogens but also contributes to increased susceptibility to inflammatory and autoimmune diseases in females compared with males. Hormonal and genetic factors contribute significantly to sex differences in immune function and disease pathogenesis. In particular, the expression of X-linked genes and microRNA as well as sex steroid hormones signaling through hormone receptors in immune cells can affect responses to immunological stimuli differently in males and females. Despite data illustrating profound differences between the sexes in immune function, sex differences in the pathogenesis of disease are often overlooked in biomedical research. Establishing journal policies that require authors to report the sex of their cells, animals, and subjects will improve our understanding of the pathogenesis of diseases, with the long-term goal of personalizing treatments for immune-mediated diseases differently for males and females in an effort to protect us equally.

Sex Differences in Patterns of Association Among Indian Ocean Bottlenose Dolphins

Behaviour ◽  
1992 ◽  
Vol 123 (1-2) ◽  
pp. 38-69 ◽  
Author(s):  
Rachel A. Smolker ◽  
Andrew F. Richards ◽  
Richard C. Connor ◽  
John W. Pepper
Keyword(s):  
Sex Differences ◽  
Bottlenose Dolphins ◽  
Same Sex ◽  
Reproductive State ◽  
Discrete Subgroups ◽  
Party Size ◽  
Shark Bay ◽  
Association Coefficients ◽  
Males And Females

AbstractPatterns of association among bottlenose dolphins resident in Shark Bay, Western Australia were analyzed using party membership data. Parties contained an average of 4.8 individuals, but party size and composition were unstable. While these temporary parties often contained both males and females, long term consistent associations generally were between members of the same sex. The highest association coefficients, resulting from very frequent co-occurrence within parties were between males and between mothers and offspring. Males formed subgroups of two or three individuals who consistently associated with each other, and these were stable over periods of at least seven years in some cases. Male subgroups preferentially associated with particular other male subgroups. Females associated most consistently with other females, although not to the same extent as some males. Female associations were better described as a network rather than discrete subgroups. Male-female associations were generally inconsistent and depended in part on female reproductive state. Mothers and their offspring associated very consistently for at least 4 years.

scholarly journals Self-fertilization and inbreeding limit the scope for sexual antagonism

2014 ◽  
Author(s):  
Samuel J. Tazzyman ◽  
Jessica K. Abbott
Keyword(s):  
Genetic Variation ◽  
A Priori ◽  
Interactive Effect ◽  
Natural Populations ◽  
Sexual Antagonism ◽  
Considerable Evidence ◽  
Fitness Effects ◽  
Genomic Location ◽  
Self Fertilization ◽  
Males And Females

Sexual antagonism occurs when there is a positive intersexual genetic correlation in trait expression but opposite fitness effects of the trait(s) in males and females. As such, it constrains the evolution of sexual dimorphism and may therefore have implications for adaptive evolution. There is currently considerable evidence for the existence of sexually antagonistic genetic variation in laboratory and natural populations, but how sexual antagonism interacts with other evolutionary phenomena is still poorly understood in many cases. Here we explore how self-fertilization and inbreeding affect the maintenance of polymorphism for sexually antagonistic loci. We expected a priori that selfing should reduce the region of polymorphism, since inbreeding reduces the frequency of heterozygotes and speeds fixation. Although this expectation was supported, our results show that there is an interactive effect between the degree of selfing and dominance such that those segregating sexually antagonistic loci that do exist are more likely to be partially dominant. In addition, inbreeding effects may influence population persistence and genomic location of sexually antagonistic loci in separate-sexed organisms.

scholarly journals Stable linkage disequilibrium owing to sexual antagonism

2010 ◽  
Vol 278 (1707) ◽  
pp. 855-862 ◽  
Author(s):  
Francisco Úbeda ◽  
David Haig ◽  
Manus M. Patten
Keyword(s):  
Linkage Disequilibrium ◽  
Genomic Structure ◽  
Natural Populations ◽  
Allele Frequencies ◽  
Population Subdivision ◽  
Sexual Antagonism ◽  
Antagonistic Selection ◽  
Sexually Antagonistic Selection ◽  
Males And Females ◽  
Frequent Observation

Linkage disequilibrium (LD) is an association between genetic loci that is typically transient. Here, we identify a previously overlooked cause of stable LD that may be pervasive: sexual antagonism. This form of selection produces unequal allele frequencies in males and females each generation, which upon admixture at fertilization give rise to an excess of haplotypes that couple male-beneficial with male-beneficial and female-beneficial with female-beneficial alleles. Under sexual antagonism, LD is obtained for all recombination frequencies in the absence of epistasis. The extent of LD is highest at low recombination and for stronger selection. We provide a partition of the total LD into distinct components and compare our result for sexual antagonism with Li and Nei's model of LD owing to population subdivision. Given the frequent observation of sexually antagonistic selection in natural populations and the number of traits that are often involved, these results suggest a major contribution of sexual antagonism to genomic structure.

Sex differences in temporal parameters of partner preference in prairie voles (Microtus ochrogaster)

1999 ◽  
Vol 77 (6) ◽  
pp. 885-889 ◽  
Author(s):  
A Courtney DeVries ◽  
C Sue Carter
Keyword(s):  
Sex Differences ◽  
Reproductive Strategies ◽  
Social Preferences ◽  
Mate Guarding ◽  
Microtus Ochrogaster ◽  
Prairie Voles ◽  
Temporal Parameters ◽  
Partner Preferences ◽  
Males And Females

Prairie voles (Microtus ochrogaster) are monogamous rodents in which both sexes form social preferences for a familiar partner. This species exhibits many of the characteristics of monogamy, including long-term social bonds, mate guarding, and biparental care. Although the behaviors associated with the development of partner preferences are superficially similar in males and females, the present study documents sex differences in the temporal parameters of partner preferences in prairie voles. Following nonsexual cohabitation, female prairie voles formed partner preferences more quickly and these preferences lasted longer than in males. These data indicate that sex differences exist in the development and maintenance of social preferences and may reflect differences in the reproductive strategies of male and female prairie voles.

scholarly journals The many nuanced evolutionary consequences of duplicated genes

2018 ◽  
Author(s):  
Ashley I. Teufel ◽  
Mackenzie M. Johnson ◽  
Jon M. Laurent ◽  
Aashiq H. Kachroo ◽  
Edward M. Marcotte ◽  
...  
Keyword(s):  
Functional Divergence ◽  
Protein Structures ◽  
Evolutionary Divergence ◽  
Functional Changes ◽  
Binding Interface ◽  
Evolutionary Trajectories ◽  
Conventional Models ◽  
The Many ◽  
Evolutionary Consequences ◽  
Dosage Imbalance

AbstractGene duplication is seen as a major source of structural and functional divergence in genome evolution. Under the conventional models of sub- or neofunctionalizaton, functional changes arise in one of the duplicates after duplication. However, we suggest here that the presence of a duplicated gene can result in functional changes to its interacting partners. We explore this hypothesis by in-silico evolution of a heterodimer when one member of the interacting pair is duplicated. We examine how a range of selection pressures and protein structures leads to differential patterns of evolutionary divergence. We find that a surprising number of distinct evolutionary trajectories can be observed even in a simple three member system. Further, we observe that selection to correct dosage imbalance can affect the evolution of the initial function in several unexpected ways. For example, if a duplicate is under selective pressure to avoid binding its original binding partner, this can lead to changes in the binding interface of a non-duplicated interacting partner to exclude the duplicate. Hence, independent of the fate of the duplicate, its presence can impact how the original function operates. Additionally, we introduce a conceptual framework to describe how interacting partners cope with dosage imbalance after duplication. Contextualizing our results within this framework reveals that the evolutionary path taken by a duplicate’s interacting partners is highly stochastic in nature. Consequently, the fate of duplicate genes may not only be controlled by their own ability to accumulate mutations but also by how interacting partners cope with them.

scholarly journals The Many Nuanced Evolutionary Consequences of Duplicated Genes

2018 ◽  
Vol 36 (2) ◽  
pp. 304-314 ◽  
Author(s):  
Ashley I Teufel ◽  
Mackenzie M Johnson ◽  
Jon M Laurent ◽  
Aashiq H Kachroo ◽  
Edward M Marcotte ◽  
...  
Keyword(s):  
Functional Divergence ◽  
Protein Structures ◽  
Evolutionary Divergence ◽  
Functional Changes ◽  
Binding Interface ◽  
Evolutionary Trajectories ◽  
Conventional Models ◽  
The Many ◽  
Evolutionary Consequences ◽  
Dosage Imbalance

Abstract Gene duplication is seen as a major source of structural and functional divergence in genome evolution. Under the conventional models of sub or neofunctionalization, functional changes arise in one of the duplicates after duplication. However, we suggest here that the presence of a duplicated gene can result in functional changes to its interacting partners. We explore this hypothesis by in silico evolution of a heterodimer when one member of the interacting pair is duplicated. We examine how a range of selection pressures and protein structures leads to differential patterns of evolutionary divergence. We find that a surprising number of distinct evolutionary trajectories can be observed even in a simple three member system. Further, we observe that selection to correct dosage imbalance can affect the evolution of the initial function in several unexpected ways. For example, if a duplicate is under selective pressure to avoid binding its original binding partner, this can lead to changes in the binding interface of a nonduplicated interacting partner to exclude the duplicate. Hence, independent of the fate of the duplicate, its presence can impact how the original function operates. Additionally, we introduce a conceptual framework to describe how interacting partners cope with dosage imbalance after duplication. Contextualizing our results within this framework reveals that the evolutionary path taken by a duplicate’s interacting partners is highly stochastic in nature. Consequently, the fate of duplicate genes may not only be controlled by their own ability to accumulate mutations but also by how interacting partners cope with them.

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