Eck Institute for Global Health, University of Notre Dame, Notre Dame, IN 46556.
Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556.
Proc Natl Acad Sci U S A. 2018 Jul 24;115(30):E7005-E7014. doi: 10.1073/pnas.1806760115. Epub 2018 Jul 9.
Inversion polymorphisms in the African malaria vector segregate along climatic gradients of aridity. Despite indirect evidence of their adaptive significance, little is known of the phenotypic targets of selection or the underlying genetic mechanisms. Here we adopt a systems genetics approach to explore the interaction of two inversions on opposite arms of chromosome 2 with gender, climatic conditions, and one another. We measure organismal traits and transcriptional profiles in 8-d-old adults of both sexes and four alternative homokaryotypic classes reared under two alternative climatic regimes. We show that karyotype strongly influences both organismal traits and transcriptional profiles but that the strength and direction of the effects depend upon complex interactions with gender and environmental conditions and between inversions on independent arms. Our data support the suppressed recombination model for the role of inversions in local adaptation, and-supported by transcriptional and physiological measurements following perturbation with the drug rapamycin-suggest that one mechanism underlying their adaptive role may be the maintenance of energy homeostasis.
在非洲疟疾媒介中,倒位多态性沿着干旱气候梯度分离。尽管有间接证据表明它们具有适应性意义,但对选择的表型靶标或潜在的遗传机制知之甚少。在这里,我们采用系统遗传学的方法来探索两条位于染色体 2 相对臂上的倒位与性别、气候条件以及彼此之间的相互作用。我们在两个不同气候条件下培养的 8 天大的雌雄两性和四种不同的同核型个体中测量了生物体的特征和转录谱。我们表明,核型强烈影响生物体的特征和转录谱,但影响的强度和方向取决于与性别和环境条件的复杂相互作用,以及独立臂上的倒位之间的相互作用。我们的数据支持倒位在局部适应中起抑制重组作用的模型,并且——在使用药物雷帕霉素进行扰动后的转录和生理测量支持下——表明它们适应作用的一个潜在机制可能是维持能量平衡。