Nuzhdin S V, Harshman L G, Zhou M, Harmon K
Department of Evolution and Ecology, University of California at Davis, Davis, CA 95616, USA.
Heredity (Edinb). 2007 Sep;99(3):313-21. doi: 10.1038/sj.hdy.6801003. Epub 2007 Jun 27.
Identification of genes underlying complex traits is an important problem. Quantitative trait loci (QTL) are mapped using marker-trait co-segregation in large panels of recombinant genotypes. Most frequently, recombinant inbred lines derived from two isogenic parents are used. Segregation patterns are also studied in pedigrees from multiple families. Great advances have been made through creative use of these techniques, but narrow sampling and inadequate power represent strong limitations. Here, we propose an approach combining the strengths of both techniques. We established a mapping population from a sample of natural genotypes, and applied artificial selection for a complex character. Selection changed the frequencies of alleles in QTLs contributing to the selection response. We infer QTLs with dense genotyping microarrays by identifying blocks of linked markers undergoing selective changes in allele frequency. We demonstrated this approach with an experimental population composed from 20 isogenic strains. Selection for starvation survival was executed in three replicated populations with three control non-selected populations. Three individuals per population were genotyped using Affymetrix GeneChips. Two regions of the genome, one each on the left arms of the second and third chromosomes, showed significant divergence between control and selected populations. For the former region, we inferred allele frequencies in selected and control populations by pyrosequencing. We conclude that the allele frequency difference, averaging approximately 40% between selected and control lines, contributed to selection response. Our approach can contribute to the fine scale decomposition of the genetics of direct and indirect selection responses, and genotype by environment interactions.
鉴定复杂性状背后的基因是一个重要问题。数量性状位点(QTL)通过在大量重组基因型面板中利用标记 - 性状共分离来进行定位。最常用的是使用源自两个同基因亲本的重组自交系。在多个家族的谱系中也会研究分离模式。通过创造性地运用这些技术已经取得了巨大进展,但抽样范围狭窄和统计功效不足是严重的限制因素。在此,我们提出一种结合这两种技术优势的方法。我们从自然基因型样本中建立了一个定位群体,并针对一个复杂性状进行人工选择。选择改变了对选择反应有贡献的QTL中等位基因的频率。我们通过识别等位基因频率发生选择性变化的连锁标记块,利用高密度基因分型微阵列推断QTL。我们用由20个同基因品系组成的实验群体证明了这种方法。在三个重复群体中进行饥饿存活选择,同时设置三个未选择的对照群体。每个群体选取三个个体使用Affymetrix基因芯片进行基因分型。基因组的两个区域,分别位于第二条和第三条染色体的左臂上,在对照群体和选择群体之间表现出显著差异。对于前一个区域,我们通过焦磷酸测序推断选择群体和对照群体中的等位基因频率。我们得出结论,选择群体和对照品系之间的等位基因频率差异平均约为40%,这对选择反应有贡献。我们的方法有助于对直接和间接选择反应的遗传学以及基因型与环境相互作用进行精细分解。