Meffert L M
Department of Biology, University of Houston, Texas 77204-5513.
Genetics. 1995 Jan;139(1):365-74. doi: 10.1093/genetics/139.1.365.
Bottleneck effects on evolutionary potential in mating behavior were addressed through assays of additive genetic variances and resulting phenotypic responses to drift in the courtship repertoires of six two-pair founder-flush lines and two control populations of the housefly. A simulation addressed the complication that an estimate of the genetic variance for a courtship trait (e.g., male performance vigor or the female requirement for copulation) must involve assays against the background behavior of the mating partners. The additive "environmental" effect of the mating partner's phenotype simply dilutes the net parent-offspring covariance for a trait. However, it there is an interaction with this "environmental" component, negative parent-offspring covariances can result under conditions of high incompatibility between the population's distributions for male performance and female choice requirements, despite high levels of genetic variance. All six bottlenecked lines exhibited significant differentiation from the controls in at least one measure of the parent-offspring covariance for male performance or female choice (estimated by 50 parent-son and 50 parent-daughter covariances for 10 courtship traits per line) which translated to significant phenotypic drift. However, the average effect across traits or across lines did not yield a significant net increase in genetic variance due to bottlenecks. Concerted phenotypic differentiation due to the founder-flush event provided indirect evidence of directional dominance in a subset of traits. Furthermore, indirect evidence of genotype-environment interactions (potentially producing genotype-genotype effects) was found in the negative parent-offspring covariances predicted by the male-female interaction simulation and by the association of the magnitude of phenotypic drift with the absolute value of the parent-offspring covariance. Hence, nonadditive genetic effects on mating behavior may be important in structuring genetic variance for courtship, although most of the increases in genetic variance would be expected to reflect inbreeding depression with relatively rare situations representing the facilitation of speciation by bottlenecks.
通过对六个两对创始-冲洗品系和两个家蝇对照种群求偶行为库中的加性遗传方差以及由此产生的对漂变的表型反应进行测定,研究了瓶颈效应在交配行为进化潜力方面的影响。一项模拟研究探讨了这样一个复杂问题:对求偶性状(例如雄性求偶活力或雌性交配需求)的遗传方差估计必须涉及针对交配伙伴背景行为的测定。交配伙伴表型的加性“环境”效应会简单地稀释一个性状的净亲子协方差。然而,如果与这个“环境”成分存在相互作用,那么在雄性求偶表现和雌性选择需求的种群分布高度不匹配的情况下,尽管遗传方差水平很高,也可能产生负的亲子协方差。所有六个瓶颈品系在雄性求偶表现或雌性选择的亲子协方差的至少一项指标上(通过对每个品系的10个求偶性状的50对父子和50对父女协方差进行估计)与对照表现出显著差异,这转化为显著的表型漂变。然而,由于瓶颈效应,跨性状或跨品系的平均效应并未产生遗传方差的显著净增加。由创始-冲洗事件导致的协同表型分化为一部分性状中的定向显性提供了间接证据。此外,在由雌雄相互作用模拟预测的负亲子协方差以及表型漂变幅度与亲子协方差绝对值的关联中,发现了基因型-环境相互作用(可能产生基因型-基因型效应)的间接证据。因此,对交配行为非加性遗传效应在构建求偶遗传方差方面可能很重要,尽管大部分遗传方差的增加预计反映的是近亲繁殖衰退,相对罕见的情况才代表瓶颈效应促进物种形成。