Quantitative trait loci mapped to single-nucleotide resolution in yeast

被引:190
作者
Deutschbauer, AM [1 ]
Davis, RW
机构
[1] Stanford Univ, Sch Med, Dept Biochem, Stanford, CA 94305 USA
[2] Stanford Genome Technol Ctr, Palo Alto, CA 94304 USA
关键词
D O I
10.1038/ng1674
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Identifying the genetic variation underlying quantitative trait loci remains problematic. Consequently, our molecular understanding of genetically complex, quantitative traits is limited. To address this issue directly, we mapped three quantitative trait loci that control yeast sporulation efficiency to single-nucleotide resolution in a noncoding regulatory region (RME1) and to two missense mutations (TAO3 and MKT1). For each quantitative trait locus, the responsible polymorphism is rare among a diverse set of 13 yeast strains, suggestive of genetic heterogeneity in the control of yeast sporulation. Additionally, under optimal conditions, we reconstituted similar to 92% of the sporulation efficiency difference between the two genetically distinct parents by engineering three nucleotide changes in the appropriate yeast genome. Our results provide the highest resolution to date of the molecular basis of a quantitative trait, showing that the interaction of a few genetic variants can have a profound phenotypic effect.
引用
收藏
页码:1333 / 1340
页数:8
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