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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
  • Imperial College London
  • University of Lausanne
  • King's College London
  • Boston Children's Hospital
  • Washington University St. Louis
  • University of Cambridge
  • University of Greifswald
  • University of Regensburg
  • University of Tartu
  • University of Tartu
  • Johns Hopkins University
  • University of Geneva
  • Swiss Institute of Bioinformatics
  • Broad Institute
  • Harvard University
  • University of Milan
  • Institut national de la santé et de la recherche médicale
  • CHU Montpellier
  • University of Queensland
  • Queensland Institute of Medical Research
  • University of Bristol
  • University of Edinburgh
  • University of Groningen
  • University of Turin
  • Human Genetics Center
  • Helmholtz Zentrum München - German Research Center for Environmental Health
  • Human Genetics Foundation
  • Service of Gastroenterology and Hepatology
  • Hospital Clinic de Barcelona
  • University of Duisburg-Essen
  • Leiden University
  • Epilepsy Institutes of the Netherlands Foundation
  • University of Basel
  • Hospital General Universitario Gregorio Marañon
  • Service of Clinical Pathology
  • Ludwig Maximilian University of Munich
  • Deutsches Zentrum für Diabetes
  • University of Exeter
  • University of Oulu
  • National Institute for Health and Welfare
  • Friedrich Schiller University Jena
  • Icahn School of Medicine at Mount Sinai

Research output: Contribution to journalArticlepeer-review

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
Pages (from-to)1-12
Number of pages12
JournalPLoS Genetics
Volume10
Issue number7
DOIs
Publication statusPublished - 1 Jan 2014
Externally publishedYes

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