Wittman Tyler N, Robinson Christopher D, McGlothlin Joel W, Cox Robert M
Department of Biology University of Virginia Charlottesville Virginia 22904.
Department of Biological Sciences Virginia Tech Blacksburg Virginia 24061.
Evol Lett. 2021 Jun 13;5(4):397-407. doi: 10.1002/evl3.240. eCollection 2021 Aug.
Quantitative genetic theory proposes that phenotypic evolution is shaped by , the matrix of genetic variances and covariances among traits. In species with separate sexes, the evolution of sexual dimorphism is also shaped by , the matrix of between-sex genetic variances and covariances. Despite considerable focus on estimating these matrices, their underlying biological mechanisms are largely speculative. We experimentally tested the hypothesis that and are structured by hormonal pleiotropy, which occurs when one hormone influences multiple phenotypes. Using juvenile brown anole lizards () bred in a paternal half-sibling design, we elevated the steroid hormone testosterone with slow-release implants while administering empty implants to siblings as a control. We quantified the effects of this manipulation on the genetic architecture of a suite of sexually dimorphic traits, including body size (males are larger than females) and the area, hue, saturation, and brightness of the dewlap (a colorful ornament that is larger in males than in females). Testosterone masculinized females by increasing body size and dewlap area, hue, and saturation, while reducing dewlap brightness. Control females and males differed significantly in , but treatment of females with testosterone rendered statistically indistinguishable from males. Whereas was characterized by low between-sex genetic correlations when estimated between control females and males, these same correlations increased significantly when estimated between testosterone females and either control or testosterone males. The full matrix (including ) for testosterone females and either control or testosterone males was significantly less permissive of sexually dimorphic evolution than was estimated between control females and males, suggesting that natural sex differences in testosterone help decouple genetic variance between the sexes. Our results confirm that hormonal pleiotropy structures genetic covariance, implying that hormones play an important yet overlooked role in mediating evolutionary responses to selection.
数量遗传学理论认为,表型进化受性状间遗传方差和协方差矩阵的影响。在两性分离的物种中,两性异形的进化也受两性间遗传方差和协方差矩阵的影响。尽管人们相当关注对这些矩阵的估计,但其潜在的生物学机制在很大程度上仍是推测性的。我们通过实验检验了一个假设,即这些矩阵是由激素多效性构建的,当一种激素影响多种表型时就会发生激素多效性。我们使用在父本半同胞设计中培育的幼年棕色安乐蜥,用缓释植入物提高类固醇激素睾酮水平,同时给其同胞植入空植入物作为对照。我们量化了这种操作对一系列两性异形性状的遗传结构的影响,包括体型(雄性比雌性大)以及喉扇的面积、色调、饱和度和亮度(喉扇是一种色彩鲜艳的装饰,雄性比雌性大)。睾酮通过增加体型、喉扇面积、色调和饱和度,同时降低喉扇亮度,使雌性雄性化。对照雌性和雄性在(相关矩阵)上有显著差异,但用睾酮处理雌性后,使其(相关矩阵)在统计学上与雄性无法区分。当在对照雌性和雄性之间估计时,(相关矩阵)的特征是两性间遗传相关性较低,而当在睾酮处理的雌性与对照或睾酮处理的雄性之间估计时,这些相同的相关性显著增加。与在对照雌性和雄性之间估计的(相关矩阵)相比,睾酮处理的雌性与对照或睾酮处理的雄性的完整(相关矩阵,包括……)对两性异形进化的允许程度显著降低,这表明睾酮的自然性别差异有助于使两性间的遗传方差解耦。我们的结果证实,激素多效性构建了遗传协方差,这意味着激素在介导对选择的进化反应中发挥了重要但被忽视的作用。