Liu Z, Dekkers J C
Centre for Genetic Improvement of Livestock, Department of Animal and Poultry Science, University of Guelph, Ontario, Canada.
Genetics. 1998 Jan;148(1):495-505. doi: 10.1093/genetics/148.1.495.
Genetic marker and phenotypic data for a quantitative trait were simulated on 20 paternal half-sib families with 100 progeny to investigate properties of within-family-regression interval mapping of a postulated single quantitative trait locus (QTL) in a marker interval under the infinitesimal genetic model, which has been the basis of the application of quantitative genetics to genetic improvement programs, and to investigate use of the infinitesimal model as null hypothesis in testing for presence of a major QTL. Genetic effects on the marked chromosome were generated based on a major gene model, which simulated a central biallelic QTL, or based on 101 biallelic QTL of equal effect, which approximated the infinitesimal model. The marked chromosome contained 0, 3.3%, 13.3%, or 33.3% of genetic variance and heritability was 0.25 or 0.70. Under the polygenic model with 3.3% of genetic variance on the marked chromosome, which corresponds to the infinitesimal model for the bovine, significant QTL effects were found for individual families. Correlations between estimates of QTL effects and true chromosome substitution effects were 0.29 and 0.47 for heritabilities of 0.25 and 0.70 but up to 0.85 with 33.3% of polygenic variance on the marked chromosome. These results illustrate the potential of marker-assisted selection even under the infinitesimal genetic model. Power of tests for presence of QTL was substantially reduced when the polygenic model with 3.3% of genetic variance on the chromosome was used as a null hypothesis. The ability to determine whether genetic variance on a chromosome was contributed by a single QTL of major effect or a large number of QTL with minor effects, corresponding to the infinitesimal model, was limited.
在20个父系半同胞家系中模拟了一个数量性状的遗传标记和表型数据,每个家系有100个后代,以研究在无穷小遗传模型下,标记区间内假定的单个数量性状基因座(QTL)的家系内回归区间作图的性质,该模型一直是数量遗传学应用于遗传改良计划的基础,并研究将无穷小模型用作检验主效QTL存在的零假设。基于主基因模型生成对标记染色体的遗传效应,该模型模拟一个中心双等位基因QTL,或者基于101个等效应的双等位基因QTL,后者近似于无穷小模型。标记染色体包含0%、3.3%、13.3%或33.3%的遗传方差,遗传力为0.25或0.70。在标记染色体上具有3.3%遗传方差的多基因模型下,这对应于牛的无穷小模型,可以发现各个家系存在显著的QTL效应。对于遗传力为0.25和0.70的情况,QTL效应估计值与真实染色体替代效应之间的相关性分别为0.29和0.47,但当标记染色体上的多基因方差为33.3%时,相关性高达0.85。这些结果说明了即使在无穷小遗传模型下标记辅助选择的潜力。当将染色体上具有3.3%遗传方差的多基因模型用作零假设时,检验QTL存在的功效会大幅降低。确定染色体上的遗传方差是由一个主效单QTL还是大量微效QTL(对应于无穷小模型)贡献的能力是有限的。