Muralidhar Pavitra, Coop Graham
Center for Population Biology, University of California, Davis, CA, United States.
Department of Evolution and Ecology, University of California, Davis, CA, United States.
Evolution. 2024 Feb 29;78(3):539-554. doi: 10.1093/evolut/qpad231.
Sexual antagonism occurs when males and females differ in their phenotypic fitness optima but are constrained in their evolution to these optima because of their shared genome. The sex chromosomes, which have distinct evolutionary "interests" relative to the autosomes, are theorized to play an important role in sexually antagonistic conflict. However, the evolutionary responses of sex chromosomes and autosomes have usually been considered independently, that is, via contrasting the response of a gene located on either an X chromosome or an autosome. Here, we study the coevolutionary response of the X chromosome and autosomes to sexually antagonistic selection acting on a polygenic phenotype. We model a phenotype initially under stabilizing selection around a single optimum, followed by a sudden divergence of the male and female optima. We find that, in the absence of dosage compensation, the X chromosome promotes evolution toward the female optimum, inducing coevolutionary male-biased responses on the autosomes. Dosage compensation obscures the female-biased interests of the X, causing it to contribute equally to male and female phenotypic change. We further demonstrate that fluctuations in an adaptive landscape can generate prolonged intragenomic conflict and accentuate the differential responses of the X and autosomes to this conflict.
当雄性和雌性在表型适合度最优值上存在差异,但由于共享基因组而在进化上受到这些最优值的限制时,就会出现性拮抗。相对于常染色体,性染色体具有独特的进化“利益”,理论上在性拮抗冲突中发挥重要作用。然而,性染色体和常染色体的进化反应通常被独立考虑,即通过对比位于X染色体或常染色体上的基因的反应。在这里,我们研究了X染色体和常染色体对作用于多基因表型的性拮抗选择的共同进化反应。我们构建了一个模型,该模型中的表型最初在围绕单一最优值的稳定选择下,随后雄性和雌性最优值突然出现分歧。我们发现,在没有剂量补偿的情况下,X染色体促进向雌性最优值的进化,在常染色体上诱导共同进化的雄性偏向反应。剂量补偿掩盖了X染色体偏向雌性的利益,使其对雄性和雌性表型变化的贡献相等。我们进一步证明,适应性景观的波动会产生长期的基因组内冲突,并加剧X染色体和常染色体对这种冲突的不同反应。