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The architecture of parent-of-origin effects in mice.

Abstract:
The number of imprinted genes in the mammalian genome is predicted to be small, yet we show here, in a survey of 97 traits measured in outbred mice, that most phenotypes display parent-of-origin effects that are partially confounded with family structure. To address this contradiction, using reciprocal F1 crosses, we investigated the effects of knocking out two nonimprinted candidate genes, Man1a2 and H2-ab1, that reside at nonimprinted loci but that show parent-of-origin effects. We show that expression of multiple genes becomes dysregulated in a sex-, tissue-, and parent-of-origin-dependent manner. We provide evidence that nonimprinted genes can generate parent-of-origin effects by interaction with imprinted loci and deduce that the importance of the number of imprinted genes is secondary to their interactions. We propose that this gene network effect may account for some of the missing heritability seen when comparing sibling-based to population-based studies of the phenotypic effects of genetic variants.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.cell.2013.11.043

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author



Publisher:
Cell Press
Journal:
Cell More from this journal
Volume:
156
Issue:
1-2
Pages:
332-342
Publication date:
2014-01-01
DOI:
EISSN:
1097-4172
ISSN:
0092-8674


Language:
English
Keywords:
Pubs id:
446708
UUID:
uuid:d7c706e7-3fe6-45e1-bfee-c9bc2b53b642
Local pid:
pubs:446708
Source identifiers:
446708
Deposit date:
2014-01-30
ARK identifier:

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