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Interactions between genetic variation and cellular environment in skeletal muscle gene expression.
Taylor, D Leland; Knowles, David A; Scott, Laura J; Ramirez, Andrea H; Casale, Francesco Paolo; Wolford, Brooke N; Guan, Li; Varshney, Arushi; Albanus, Ricardo D'Oliveira; Parker, Stephen C J; Narisu, Narisu; Chines, Peter S; Erdos, Michael R; Welch, Ryan P; Kinnunen, Leena; Saramies, Jouko; Sundvall, Jouko; Lakka, Timo A; Laakso, Markku; Tuomilehto, Jaakko; Koistinen, Heikki A; Stegle, Oliver; Boehnke, Michael; Birney, Ewan; Collins, Francis S.
Afiliação
  • Taylor DL; National Human Genome Research Institute, National Institutes of Health, Bethesda, United States of America.
  • Knowles DA; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
  • Scott LJ; Department of Computer Science, Stanford University, Stanford, California, United States of America.
  • Ramirez AH; Department of Biostatistics and Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Casale FP; Department of Medicine, Vanderbilt University Medical Center, Tennessee, United States of America.
  • Wolford BN; European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridgeshire, United Kingdom.
  • Guan L; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Varshney A; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Albanus RD; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Parker SCJ; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Narisu N; Department of Computational Medicine & Bioinformatics, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Chines PS; Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Erdos MR; National Human Genome Research Institute, National Institutes of Health, Bethesda, United States of America.
  • Welch RP; National Human Genome Research Institute, National Institutes of Health, Bethesda, United States of America.
  • Kinnunen L; National Human Genome Research Institute, National Institutes of Health, Bethesda, United States of America.
  • Saramies J; Department of Biostatistics and Center for Statistical Genetics, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Sundvall J; Department of Public Health Solutions, National Institute for Health and Welfare, Helsinki, Finland.
  • Lakka TA; South Karelia Social and Health Care District, Lappeenranta, Finland.
  • Laakso M; Department of Public Health Solutions, National Institute for Health and Welfare, Helsinki, Finland.
  • Tuomilehto J; Institute of Biomedicine/Physiology, University of Eastern Finland, Kuopio, Finland.
  • Koistinen HA; Kuopio Research Institute of Exercise Medicine, Kuopio, Finland.
  • Stegle O; Department of Clinical Physiology and Nuclear Medicine, Kuopio University Hospital, University of Eastern Finland, Kuopio, Finland.
  • Boehnke M; Department of Medicine, University of Eastern Finland, Kuopio, Finland.
  • Birney E; Kuopio University Hospital, Kuopio, Finland.
  • Collins FS; Department of Public Health Solutions, National Institute for Health and Welfare, Helsinki, Finland.
PLoS One ; 13(4): e0195788, 2018.
Article em En | MEDLINE | ID: mdl-29659628
ABSTRACT
From whole organisms to individual cells, responses to environmental conditions are influenced by genetic makeup, where the effect of genetic variation on a trait depends on the environmental context. RNA-sequencing quantifies gene expression as a molecular trait, and is capable of capturing both genetic and environmental effects. In this study, we explore opportunities of using allele-specific expression (ASE) to discover cis-acting genotype-environment interactions (GxE)-genetic effects on gene expression that depend on an environmental condition. Treating 17 common, clinical traits as approximations of the cellular environment of 267 skeletal muscle biopsies, we identify 10 candidate environmental response expression quantitative trait loci (reQTLs) across 6 traits (12 unique gene-environment trait pairs; 10% FDR per trait) including sex, systolic blood pressure, and low-density lipoprotein cholesterol. Although using ASE is in principle a promising approach to detect GxE effects, replication of such signals can be challenging as validation requires harmonization of environmental traits across cohorts and a sufficient sampling of heterozygotes for a transcribed SNP. Comprehensive discovery and replication will require large human transcriptome datasets, or the integration of multiple transcribed SNPs, coupled with standardized clinical phenotyping.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Regulação da Expressão Gênica / Músculo Esquelético / Fibras Musculares Esqueléticas / Microambiente Celular / Interação Gene-Ambiente Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Regulação da Expressão Gênica / Músculo Esquelético / Fibras Musculares Esqueléticas / Microambiente Celular / Interação Gene-Ambiente Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos