Keightley P D, Hardge T, May L, Bulfield G
Institute of Cell, Animal and Population Biology, University of Edinburgh, Scotland.
Genetics. 1996 Jan;142(1):227-35. doi: 10.1093/genetics/142.1.227.
The genetic basis of body weight in the mouse was investigated by measuring frequency changes of microsatellite marker alleles in lines divergently selected for body weight from a base population of a cross between two inbred strains. In several regions of the genome, sharp peaks of frequency change at linked markers were detected, which suggested the presence of single genes of moderate effect, although in several other regions, significant frequency changes occurred over large portions of chromosomes. A method based on maximum likelihood was used to infer effects and map positions of quantitative trait loci (QTLs) based on genotype frequencies at one or more marker loci. Eleven QTLs with effects in the range 0.17-0.28 phenotypic standard deviations were detected; but under an additive model, these did not fully account for the observed selection response. Tests for the presence of more than one QTL in regions where there were large changes of marker allele frequency were mostly inconclusive.
通过测量从两个近交系杂交的基础群体中对体重进行差异选择的品系中微卫星标记等位基因的频率变化,研究了小鼠体重的遗传基础。在基因组的几个区域,检测到连锁标记处频率变化的尖锐峰值,这表明存在具有中等效应的单个基因,尽管在其他几个区域,染色体的大部分区域都发生了显著的频率变化。一种基于最大似然法的方法被用于根据一个或多个标记位点的基因型频率推断数量性状位点(QTL)的效应并定位其位置。检测到11个QTL,其效应范围为0.17 - 0.28个表型标准差;但在加性模型下,这些QTL并不能完全解释观察到的选择反应。在标记等位基因频率有较大变化的区域,对是否存在多个QTL的测试大多没有定论。