A Noncomplementation Screen for Quantitative Trait Alleles in Saccharomyces cerevisiae

被引:12
作者
Kim, Hyun Seok [1 ,2 ]
Huh, Juyoung [1 ]
Riles, Linda [1 ]
Reyes, Alejandro [2 ]
Fay, Justin C. [1 ,2 ,3 ]
机构
[1] Washington Univ, Dept Genet, St Louis, MO 63108 USA
[2] Washington Univ, Computat Biol Program, St Louis, MO 63108 USA
[3] Washington Univ, Ctr Genome Sci & Syst Biol, St Louis, MO 63108 USA
基金
美国国家卫生研究院;
关键词
complex trait; copper sulfate; hydrogen sulfide; DROSOPHILA-MELANOGASTER; GENETIC INTERACTIONS; RARE VARIANTS; YEAST; GENOME; NUCLEOTIDE; SUSCEPTIBILITY; ARCHITECTURE; DISRUPTION; RESOLUTION;
D O I
10.1534/g3.112.002550
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Both linkage and linkage disequilibrium mapping provide well-defined approaches to mapping quantitative trait alleles. However, alleles of small effect are particularly difficult to refine to individual genes and causative mutations. Quantitative noncomplementation provides a means of directly testing individual genes for quantitative trait alleles in a fixed genetic background. Here, we implement a genome-wide noncomplementation screen for quantitative trait alleles that affect colony color or size by using the yeast deletion collection. As proof of principle, we find a previously known allele of CYS4 that affects colony color and a novel allele of CTT1 that affects resistance to hydrogen peroxide. To screen nearly 4700 genes in nine diverse yeast strains, we developed a high-throughput robotic plating assay to quantify colony color and size. Although we found hundreds of candidate alleles, reciprocal hemizygosity analysis of a select subset revealed that many of the candidates were false positives, in part the result of background-dependent haploinsufficiency or second-site mutations within the yeast deletion collection. Our results highlight the difficulty of identifying small-effect alleles but support the use of noncomplementation as a rapid means of identifying quantitative trait alleles of large effect.
引用
收藏
页码:753 / 760
页数:8
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