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Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

  • Generation Scotland Consortium
  • , The LifeLines Cohort Study
  • , The GIANT Consortium
  • Centre for Genomics and Experimental Medicine
  • University of Edinburgh
  • University of Groningen
  • Divisions of Endocrinology and Genetics and Center for Basic and Translational Obesity Research
  • Children's Hospital Boston
  • Imperial College London
  • University of Lausanne
  • King's College London
  • Washington University in St. Louis
  • University of Cambridge
  • University of Greifswald
  • University of Tartu
  • Estonian Biocenter
  • Johns Hopkins University
  • Broad Institute
  • Harvard University
  • University of Milan
  • Hopital Gui de Chauliac
  • The University of Queensland
  • University of Turin
  • University of Regensburg
  • Helmholtz Zentrum München - Deutsches Forschungszentrum für Gesundheit und Umwelt
  • Human Genetics Foundation
  • Service of Gastroenterology and Hepatology
  • Hospital Clinic
  • University of Duisburg-Essen
  • University of Bristol
  • Leiden University
  • Epilepsy Institutes of the Netherlands Foundation
  • University of Basel
  • QIMR Berghofer Medical Research Institute

Abstract

The phenotypic effect of some single nucleotide polymorphisms (SNPs) depends on their parental origin. We present a novel approach to detect parent-of-origin effects (POEs) in genome-wide genotype data of unrelated individuals. The method exploits increased phenotypic variance in the heterozygous genotype group relative to the homozygous groups. We applied the method to >56,000 unrelated individuals to search for POEs influencing body mass index (BMI). Six lead SNPs were carried forward for replication in five family-based studies (of ∼4,000 trios). Two SNPs replicated: the paternal rs2471083-C allele (located near the imprinted KCNK9 gene) and the paternal rs3091869-T allele (located near the SLC2A10 gene) increased BMI equally (beta = 0.11 (SD), P<0.0027) compared to the respective maternal alleles. Real-time PCR experiments of lymphoblastoid cell lines from the CEPH families showed that expression of both genes was dependent on parental origin of the SNPs alleles (P<0.01). Our scheme opens new opportunities to exploit GWAS data of unrelated individuals to identify POEs and demonstrates that they play an important role in adult obesity.

Original languageEnglish
Article numbere1004508
JournalPLOS Genetics
Volume10
Issue number7
Pages (from-to)1-12
Number of pages12
ISSN1553-7390
DOIs
Publication statusPublished - 01.01.2014

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being
  2. SDG 5 - Gender Equality
    SDG 5 Gender Equality

Research Areas and Centers

  • Research Area: Medical Genetics

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