Abstract

The impact of the parental origin of associated alleles in GWAS has been largely ignored. Yet sequence variants could affect traits differently depending on whether they are inherited from the mother or the father, as in imprinted regions, where identical inherited DNA sequences can have different effects based on the parental origin. To explore parent-of-origin effects (POEs), we studied 21 quantitative phenotypes in a large Hutterite pedigree to identify variants with single parent (maternal-only or paternal-only) effects, and then variants with opposite parental effects. Here we show that POEs, which can be opposite in direction, are relatively common in humans, have potentially important clinical effects, and will be missed in traditional GWAS. We identified POEs with 11 phenotypes, most of which are risk factors for cardiovascular disease. Many of the loci identified are characteristic of imprinted regions and are associated with the expression of nearby genes.

Sahar Mozaffari et al. conduct a parent of origin genome-wide association study in a large Hutterite pedigree to determine parent-of-origin effects on 21 phenotypes. They identify effects on 11 phenotypes (including single parent and opposite parental effects), most of which are associated with cardiovascular disease.

Details

Title
Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree
Author
Mozaffari, Sahar V 1   VIAFID ORCID Logo  ; DeCara, Jeanne M 2 ; Shah, Sanjiv J 3 ; Sidore Carlo 4 ; Fiorillo Edoardo 4 ; Cucca Francesco 5 ; Lang, Roberto M 2 ; Nicolae, Dan L 6 ; Ober, Carole 1 

 University of Chicago, Department of Human Genetics, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); University of Chicago, Committee on Genetics, Genomics, and Systems Biology, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822) 
 University of Chicago, Department of Medicine, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822) 
 Northwestern University Feinberg School of Medicine, Department of Medicine, Chicago, USA (GRID:grid.16753.36) (ISNI:0000 0001 2299 3507) 
 Istituto di Ricerca Genetica e Biomedica (IRGB), CNR, Monserrato, Italy (GRID:grid.428485.7) (ISNI:0000 0004 1789 9390) 
 Istituto di Ricerca Genetica e Biomedica (IRGB), CNR, Monserrato, Italy (GRID:grid.428485.7) (ISNI:0000 0004 1789 9390); Universita di Sassari, Dipartimento di Scienze Biomediche, Sassari, Italy (GRID:grid.11450.31) (ISNI:0000 0001 2097 9138) 
 University of Chicago, Department of Human Genetics, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); University of Chicago, Committee on Genetics, Genomics, and Systems Biology, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); University of Chicago, Department of Medicine, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822); University of Chicago, Department of Statistics, Chicago, USA (GRID:grid.170205.1) (ISNI:0000 0004 1936 7822) 
Publication year
2019
Publication date
2019
Publisher
Nature Publishing Group
e-ISSN
23993642
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2389676816
Copyright
© The Author(s) 2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.