4.8 Article

Finding the sources of missing heritability in a yeast cross

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NATURE
卷 494, 期 7436, 页码 234-237

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NATURE PUBLISHING GROUP
DOI: 10.1038/nature11867

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资金

  1. National Institutes of Health (NIH) [R37 MH59520, R01 GM102308]
  2. James S. McDonnell Centennial Fellowship
  3. Howard Hughes Medical Institute
  4. National Science Foundation (NSF)
  5. NIH postdoctoral fellowship [F32 HG51762]
  6. NIH grant [P50 GM071508]

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For many traits, including susceptibility to common diseases in humans, causal loci uncovered by genetic-mapping studies explain only a minority of the heritable contribution to trait variation. Multiple explanations for this 'missing heritability' have been proposed(1). Here we use a large cross between two yeast strains to accurately estimate different sources of heritable variation for 46 quantitative traits, and to detect underlying loci with high statistical power. We find that the detected loci explain nearly the entire additive contribution to heritable variation for the traits studied. We also show that the contribution to heritability of gene-gene interactions varies among traits, from near zero to approximately 50 per cent. Detected two-locus interactions explain only a minority of this contribution. These results substantially advance our understanding of the missing heritability problem and have important implications

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