Mackay Trudy F C, Lyman Richard F, Lawrence Faye
Department of Genetics, North Carolina State University, Raleigh, North Carolina 27695, USA.
Genetics. 2005 Aug;170(4):1723-35. doi: 10.1534/genetics.104.032581. Epub 2005 Jun 8.
Our ability to predict long-term responses to artificial and natural selection, and understand the mechanisms by which naturally occurring variation for quantitative traits is maintained, depends on detailed knowledge of the properties of spontaneous polygenic mutations, including the quantitative trait loci (QTL) at which mutations occur, mutation rates, and mutational effects. These parameters can be estimated by mapping QTL that cause divergence between mutation-accumulation lines that have been established from an inbred base population and selected for high and low trait values. Here, we have utilized quantitative complementation to deficiencies to map QTL at which spontaneous mutations affecting Drosophila abdominal and sternopleural bristle number have occurred in 11 replicate lines during 206 generations of divergent selection. Estimates of the numbers of mutations were consistent with diploid per-character mutation rates for bristle traits of 0.03. The ratio of the per-character mutation rate to total mutation rate (0.023) implies that >2% of the genome could affect just one bristle trait and that there must be extensive pleiotropy for quantitative phenotypes. The estimated mutational effects were not, however, additive and exhibited dependency on genetic background consistent with diminishing epistasis. However, these inferences must be tempered by the potential for epistatic interactions between spontaneous mutations and QTL affecting bristle number on the deficiency-bearing chromosomes, which could lead to overestimates in numbers of QTL and inaccurate inference of gene action.
我们预测对人工选择和自然选择的长期反应,以及理解维持数量性状自然发生变异机制的能力,取决于对自发多基因变异特性的详细了解,包括发生突变的数量性状基因座(QTL)、突变率和突变效应。这些参数可以通过对QTL进行定位来估计,这些QTL导致从近交基础群体建立并针对高、低性状值进行选择的突变积累系之间产生差异。在这里,我们利用对缺陷的定量互补来定位QTL,在206代的分歧选择过程中,11个重复系中发生了影响果蝇腹部和胸部刚毛数量的自发突变。突变数量的估计与刚毛性状的二倍体每性状突变率0.03一致。每性状突变率与总突变率的比值(0.023)意味着超过2%的基因组可能仅影响一个刚毛性状,并且数量性状必然存在广泛的多效性。然而,估计的突变效应并非累加性的,并且表现出对遗传背景的依赖性,这与上位性减弱一致。然而,这些推断必须考虑到自发突变与影响携带缺陷染色体上刚毛数量的QTL之间发生上位相互作用的可能性,这可能导致对QTL数量的高估和对基因作用的不准确推断。