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Finding the sources of missing heritability in a yeast cross

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 be...

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Autores principales: Bloom, Joshua S., Ehrenreich, Ian M., Loo, Wesley, Võ Lite, Thúy-Lan, Kruglyak, Leonid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001867/
https://www.ncbi.nlm.nih.gov/pubmed/23376951
http://dx.doi.org/10.1038/nature11867
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author Bloom, Joshua S.
Ehrenreich, Ian M.
Loo, Wesley
Võ Lite, Thúy-Lan
Kruglyak, Leonid
author_facet Bloom, Joshua S.
Ehrenreich, Ian M.
Loo, Wesley
Võ Lite, Thúy-Lan
Kruglyak, Leonid
author_sort Bloom, Joshua S.
collection PubMed
description 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%. 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 for future studies of complex and quantitative traits.
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spelling pubmed-40018672014-04-28 Finding the sources of missing heritability in a yeast cross Bloom, Joshua S. Ehrenreich, Ian M. Loo, Wesley Võ Lite, Thúy-Lan Kruglyak, Leonid Nature Article 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%. 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 for future studies of complex and quantitative traits. 2013-02-03 2013-02-14 /pmc/articles/PMC4001867/ /pubmed/23376951 http://dx.doi.org/10.1038/nature11867 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Bloom, Joshua S.
Ehrenreich, Ian M.
Loo, Wesley
Võ Lite, Thúy-Lan
Kruglyak, Leonid
Finding the sources of missing heritability in a yeast cross
title Finding the sources of missing heritability in a yeast cross
title_full Finding the sources of missing heritability in a yeast cross
title_fullStr Finding the sources of missing heritability in a yeast cross
title_full_unstemmed Finding the sources of missing heritability in a yeast cross
title_short Finding the sources of missing heritability in a yeast cross
title_sort finding the sources of missing heritability in a yeast cross
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001867/
https://www.ncbi.nlm.nih.gov/pubmed/23376951
http://dx.doi.org/10.1038/nature11867
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