IDEAS home Printed from https://ideas.repec.org/a/plo/pone00/0114128.html
   My bibliography  Save this article

Association between Expression Quantitative Trait Loci and Metabolic Traits in Two Korean Populations

Author

Listed:
  • Kyung-Won Hong
  • Seok Won Jeong
  • Myungguen Chung
  • Seong Beom Cho

Abstract

Most genome-wide association studies consider genes that are located closest to single nucleotide polymorphisms (SNPs) that are highly significant for those studies. However, the significance of the associations between SNPs and candidate genes has not been fully determined. An alternative approach that used SNPs in expression quantitative trait loci (eQTL) was reported previously for Crohn’s disease; it was shown that eQTL-based preselection for follow-up studies was a useful approach for identifying risk loci from the results of moderately sized GWAS. In this study, we propose an approach that uses eQTL SNPs to support the functional relationships between an SNP and a candidate gene in a genome-wide association study. The genome-wide SNP genotypes and 10 biochemical measures (fasting glucose levels, BUN, serum albumin levels, AST, ALT, gamma GTP, total cholesterol, HDL cholesterol, triglycerides, and LDL cholesterol) were obtained from the Korean Association Resource (KARE) consortium. The eQTL SNPs were isolated from the SNP dataset based on the RegulomeDB eQTL-SNP data from the ENCODE projects and two recent eQTL reports. A total of 25,658 eQTL SNPs were tested for their association with the 10 metabolic traits in 2 Korean populations (Ansung and Ansan). The proportion of phenotypic variance explained by eQTL and non-eQTL SNPs showed that eQTL SNPs were more likely to be associated with the metabolic traits genetically compared with non-eQTL SNPs. Finally, via a meta-analysis of the two Korean populations, we identified 14 eQTL SNPs that were significantly associated with metabolic traits. These results suggest that our approach can be expanded to other genome-wide association studies.

Suggested Citation

  • Kyung-Won Hong & Seok Won Jeong & Myungguen Chung & Seong Beom Cho, 2014. "Association between Expression Quantitative Trait Loci and Metabolic Traits in Two Korean Populations," PLOS ONE, Public Library of Science, vol. 9(12), pages 1-13, December.
  • Handle: RePEc:plo:pone00:0114128
    DOI: 10.1371/journal.pone.0114128
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0114128
    Download Restriction: no

    File URL: https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0114128&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pone.0114128?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. John PA Ioannidis & Nikolaos A Patsopoulos & Evangelos Evangelou, 2007. "Heterogeneity in Meta-Analyses of Genome-Wide Association Investigations," PLOS ONE, Public Library of Science, vol. 2(9), pages 1-7, September.
    2. Stephen B. Montgomery & Micha Sammeth & Maria Gutierrez-Arcelus & Radoslaw P. Lach & Catherine Ingle & James Nisbett & Roderic Guigo & Emmanouil T. Dermitzakis, 2010. "Transcriptome genetics using second generation sequencing in a Caucasian population," Nature, Nature, vol. 464(7289), pages 773-777, April.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Coren L Apicella & David Cesarini & Magnus Johannesson & Christopher T Dawes & Paul Lichtenstein & Björn Wallace & Jonathan Beauchamp & Lars Westberg, 2010. "No Association between Oxytocin Receptor (OXTR) Gene Polymorphisms and Experimentally Elicited Social Preferences," PLOS ONE, Public Library of Science, vol. 5(6), pages 1-8, June.
    2. Zhao-Yang Wang & Keke Zhao & Jingwei Zheng & Brian Rossmiller & Cristhian Ildefonso & Manas Biswal & Pei-quan Zhao, 2014. "Systematic Review and Meta-Analysis of the Association between Complement Factor H I62V Polymorphism and Risk of Polypoidal Choroidal Vasculopathy in Asian Populations," PLOS ONE, Public Library of Science, vol. 9(2), pages 1-8, February.
    3. Barbara E Stranger & Stephen B Montgomery & Antigone S Dimas & Leopold Parts & Oliver Stegle & Catherine E Ingle & Magda Sekowska & George Davey Smith & David Evans & Maria Gutierrez-Arcelus & Alkes P, 2012. "Patterns of Cis Regulatory Variation in Diverse Human Populations," PLOS Genetics, Public Library of Science, vol. 8(4), pages 1-13, April.
    4. Lebrec Jeremie J & Stijnen Theo & van Houwelingen Hans C, 2010. "Dealing with Heterogeneity between Cohorts in Genomewide SNP Association Studies," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 9(1), pages 1-22, January.
    5. Thomas R Roos & Andrew K Roos & Andrew L Avins & Marwa A Ahmed & John P Kleimeyer & Michael Fredericson & John P A Ioannidis & Jason L Dragoo & Stuart K Kim, 2017. "Genome-wide association study identifies a locus associated with rotator cuff injury," PLOS ONE, Public Library of Science, vol. 12(12), pages 1-15, December.
    6. Marilyn C Cornelis & Keri L Monda & Kai Yu & Nina Paynter & Elizabeth M Azzato & Siiri N Bennett & Sonja I Berndt & Eric Boerwinkle & Stephen Chanock & Nilanjan Chatterjee & David Couper & Gary Curhan, 2011. "Genome-Wide Meta-Analysis Identifies Regions on 7p21 (AHR) and 15q24 (CYP1A2) As Determinants of Habitual Caffeine Consumption," PLOS Genetics, Public Library of Science, vol. 7(4), pages 1-9, April.
    7. Jungsoo Gim & Sungho Won & Taesung Park, 2016. "LPEseq: Local-Pooled-Error Test for RNA Sequencing Experiments with a Small Number of Replicates," PLOS ONE, Public Library of Science, vol. 11(8), pages 1-15, August.
    8. Ping-Yu Wang & Zong-Hua Gao & Zhong-Hua Jiang & Xin-Xin Li & Bao-Fa Jiang & Shu-Yang Xie, 2013. "The Associations of Single Nucleotide Polymorphisms in miR-146a, miR-196a and miR-499 with Breast Cancer Susceptibility," PLOS ONE, Public Library of Science, vol. 8(9), pages 1-7, September.
    9. Faisal Shahla & Tutz Gerhard, 2017. "Missing value imputation for gene expression data by tailored nearest neighbors," Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 16(2), pages 95-106, April.
    10. Eric O Johnson & Dana B Hancock & Nathan C Gaddis & Joshua L Levy & Grier Page & Scott P Novak & Cristie Glasheen & Nancy L Saccone & John P Rice & Michael P Moreau & Kimberly F Doheny & Jane M Romm &, 2015. "Novel Genetic Locus Implicated for HIV-1 Acquisition with Putative Regulatory Links to HIV Replication and Infectivity: A Genome-Wide Association Study," PLOS ONE, Public Library of Science, vol. 10(3), pages 1-15, March.
    11. Thanh Nguyen & Asim Bhatti & Samuel Yang & Saeid Nahavandi, 2016. "RNA-Seq Count Data Modelling by Grey Relational Analysis and Nonparametric Gaussian Process," PLOS ONE, Public Library of Science, vol. 11(10), pages 1-18, October.
    12. Farnoosh Abbas-Aghababazadeh & Qian Li & Brooke L Fridley, 2018. "Comparison of normalization approaches for gene expression studies completed with high-throughput sequencing," PLOS ONE, Public Library of Science, vol. 13(10), pages 1-21, October.
    13. Kensuke Yamaguchi & Kazuyoshi Ishigaki & Akari Suzuki & Yumi Tsuchida & Haruka Tsuchiya & Shuji Sumitomo & Yasuo Nagafuchi & Fuyuki Miya & Tatsuhiko Tsunoda & Hirofumi Shoda & Keishi Fujio & Kazuhiko , 2022. "Splicing QTL analysis focusing on coding sequences reveals mechanisms for disease susceptibility loci," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    14. Alexandra C Nica & Leopold Parts & Daniel Glass & James Nisbet & Amy Barrett & Magdalena Sekowska & Mary Travers & Simon Potter & Elin Grundberg & Kerrin Small & Åsa K Hedman & Veronique Bataille & Jo, 2011. "The Architecture of Gene Regulatory Variation across Multiple Human Tissues: The MuTHER Study," PLOS Genetics, Public Library of Science, vol. 7(2), pages 1-9, February.
    15. Jean Francois Lefebvre & Emilio Vello & Bing Ge & Stephen B Montgomery & Emmanouil T Dermitzakis & Tomi Pastinen & Damian Labuda, 2012. "Genotype-Based Test in Mapping Cis-Regulatory Variants from Allele-Specific Expression Data," PLOS ONE, Public Library of Science, vol. 7(6), pages 1-15, June.
    16. Hélène Choquet & Jay Kasberger & Ajna Hamidovic & Eric Jorgenson, 2013. "Contribution of Common PCSK1 Genetic Variants to Obesity in 8,359 Subjects from Multi-Ethnic American Population," PLOS ONE, Public Library of Science, vol. 8(2), pages 1-7, February.
    17. John Platig & Peter J Castaldi & Dawn DeMeo & John Quackenbush, 2016. "Bipartite Community Structure of eQTLs," PLOS Computational Biology, Public Library of Science, vol. 12(9), pages 1-17, September.
    18. Elie Aoun & Chung-Chou H Chang & Julia B Greer & Georgios I Papachristou & M Michael Barmada & David C Whitcomb, 2008. "Pathways to Injury in Chronic Pancreatitis: Decoding the Role of the High-Risk SPINK1 N34S Haplotype Using Meta-Analysis," PLOS ONE, Public Library of Science, vol. 3(4), pages 1-8, April.
    19. Daria V Zhernakova & Eleonora de Klerk & Harm-Jan Westra & Anastasios Mastrokolias & Shoaib Amini & Yavuz Ariyurek & Rick Jansen & Brenda W Penninx & Jouke J Hottenga & Gonneke Willemsen & Eco J de Ge, 2013. "DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts," PLOS Genetics, Public Library of Science, vol. 9(6), pages 1-15, June.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pone00:0114128. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosone (email available below). General contact details of provider: https://journals.plos.org/plosone/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.