Meuwissen Theo H E, Karlsen Astrid, Lien Sigbjørn, Olsaker Ingrid, Goddard Mike E
Institute for Animal Science and Health, Lelystad, 8200 AB The Netherlands.
Genetics. 2002 May;161(1):373-9. doi: 10.1093/genetics/161.1.373.
A novel and robust method for the fine-scale mapping of genes affecting complex traits, which combines linkage and linkage-disequilibrium information, is proposed. Linkage information refers to recombinations within the marker-genotyped generations and linkage disequilibrium to historical recombinations before genotyping started. The identity-by-descent (IBD) probabilities at the quantitative trait locus (QTL) between first generation haplotypes were obtained from the similarity of the marker alleles surrounding the QTL, whereas IBD probabilities at the QTL between later generation haplotypes were obtained by using the markers to trace the inheritance of the QTL. The variance explained by the QTL is estimated by residual maximum likelihood using the correlation structure defined by the IBD probabilities. Unlinked background genes were accounted for by fitting a polygenic variance component. The method was used to fine map a QTL for twinning rate in cattle, previously mapped on chromosome 5 by linkage analysis. The data consisted of large half-sib families, but the method could also handle more complex pedigrees. The likelihood of the putative QTL was very small along most of the chromosome, except for a sharp likelihood peak in the ninth marker bracket, which positioned the QTL within a region <1 cM in the middle part of bovine chromosome 5. The method was expected to be robust against multiple genes affecting the trait, multiple mutations at the QTL, and relatively low marker density.
提出了一种结合连锁和连锁不平衡信息进行影响复杂性状基因精细定位的新颖且稳健的方法。连锁信息指标记基因分型世代内的重组,连锁不平衡指基因分型开始前的历史重组。通过数量性状位点(QTL)周围标记等位基因的相似性获得第一代单倍型在QTL处的同源相同(IBD)概率,而通过使用标记追踪QTL的遗传来获得后代单倍型在QTL处的IBD概率。利用由IBD概率定义的相关结构,通过残差最大似然估计QTL解释的方差。通过拟合多基因方差成分来考虑不连锁的背景基因。该方法用于对牛双胎率的QTL进行精细定位,该QTL先前通过连锁分析定位在5号染色体上。数据由大型半同胞家系组成,但该方法也可处理更复杂的谱系。除了在第九个标记区间有一个尖锐的似然峰外,假定QTL在大部分染色体上的似然性都非常小,该似然峰将QTL定位在牛5号染色体中部小于1厘摩的区域内。预计该方法对影响性状的多个基因、QTL处的多个突变以及相对较低的标记密度具有稳健性。