Abstract
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. © 2012 Bowers et al.
Author supplied keywords
Cite
CITATION STYLE
Kim, H. S., Huh, J., Riles, L., Reyes, A., & Fay, J. C. (2012). A noncomplementation screen for quantitative trait alleles in saccharomyces cerevisiae. G3: Genes, Genomes, Genetics, 2(7), 753–760. https://doi.org/10.1534/g3.112.002550
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.