Dissecting the architecture of a quantitative trait locus in yeast

Lars M. Steinmetz (), Himanshu Sinha, Dan R. Richards, Jamie I. Spiegelman, Peter J. Oefner, John H. McCusker () and Ronald W. Davis
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Lars M. Steinmetz: Stanford University School of Medicine
Himanshu Sinha: Duke University Medical Center
Dan R. Richards: Stanford University School of Medicine
Jamie I. Spiegelman: Stanford Genome Technology Center
Peter J. Oefner: Stanford University School of Medicine
John H. McCusker: Duke University Medical Center
Ronald W. Davis: Stanford University School of Medicine

Nature, 2002, vol. 416, issue 6878, 326-330

Abstract: Abstract Most phenotypic diversity in natural populations is characterized by differences in degree rather than in kind. Identification of the actual genes underlying these quantitative traits has proved difficult1,2,3,4,5. As a result, little is known about their genetic architecture. The failures are thought to be due to the different contributions of many underlying genes to the phenotype and the ability of different combinations of genes and environmental factors to produce similar phenotypes6,7. This study combined genome-wide mapping and a new genetic technique named reciprocal-hemizygosity analysis to achieve the complete dissection of a quantitative trait locus (QTL) in Saccharomyces cerevisiae. A QTL architecture was uncovered that was more complex than expected. Functional linkages both in cis and in trans were found between three tightly linked quantitative trait genes that are neither necessary nor sufficient in isolation. This arrangement of alleles explains heterosis (hybrid vigour), the increased fitness of the heterozygote compared with homozygotes. It also demonstrates a deficiency in current approaches to QTL dissection with implications extending to traits in other organisms, including human genetic diseases.

Date: 2002
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DOI: 10.1038/416326a

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