Instituto Gulbenkian de Ciência, Oeiras, Portugal.
UMR5174-CNRS, Laboratoire Évolution & Diversité Biologique, Université Paul Sabatier, Toulouse, France.
PLoS Genet. 2018 Sep 26;14(9):e1007686. doi: 10.1371/journal.pgen.1007686. eCollection 2018 Sep.
Body size is a quantitative trait that is closely associated to fitness and under the control of both genetic and environmental factors. While developmental plasticity for this and other traits is heritable and under selection, little is known about the genetic basis for variation in plasticity that can provide the raw material for its evolution. We quantified genetic variation for body size plasticity in Drosophila melanogaster by measuring thorax and abdomen length of females reared at two temperatures from a panel representing naturally segregating alleles, the Drosophila Genetic Reference Panel (DGRP). We found variation between genotypes for the levels and direction of thermal plasticity in size of both body parts. We then used a Genome-Wide Association Study (GWAS) approach to unravel the genetic basis of inter-genotype variation in body size plasticity, and used different approaches to validate selected QTLs and to explore potential pleiotropic effects. We found mostly "private QTLs", with little overlap between the candidate loci underlying variation in plasticity for thorax versus abdomen size, for different properties of the plastic response, and for size versus size plasticity. We also found that the putative functions of plasticity QTLs were diverse and that alleles for higher plasticity were found at lower frequencies in the target population. Importantly, a number of our plasticity QTLs have been targets of selection in other populations. Our data sheds light onto the genetic basis of inter-genotype variation in size plasticity that is necessary for its evolution.
体型是一个与适应度密切相关的数量性状,受遗传和环境因素的共同控制。虽然这种性状和其他性状的发育可塑性具有遗传性且受到选择的影响,但对于可塑性变异的遗传基础,即其进化的原始材料,我们知之甚少。我们通过测量代表自然分离等位基因的 Drosophila Genetic Reference Panel(DGRP)中两种温度下饲养的雌性果蝇的胸部和腹部长度,来量化黑腹果蝇体型可塑性的遗传变异。我们发现,不同基因型在两个体节大小的热可塑性水平和方向上存在差异。然后,我们使用全基因组关联研究(GWAS)方法来揭示体型可塑性的基因型间变异的遗传基础,并使用不同的方法来验证选定的 QTL 并探索潜在的多效性效应。我们发现大多数情况下是“特有 QTL”,在胸部和腹部大小的可塑性、不同的可塑性响应特性以及大小和大小可塑性之间的候选基因座之间几乎没有重叠。我们还发现,可塑性 QTL 的假定功能是多样化的,在目标群体中,较高可塑性的等位基因频率较低。重要的是,我们的一些可塑性 QTL 已经成为其他群体选择的目标。我们的数据揭示了体型可塑性的基因型间变异的遗传基础,这对于其进化是必要的。