Functional characterisation of ADIPOQ variants using individuals recruited by genotype

Mol Cell Endocrinol. 2016 Jun 15:428:49-57. doi: 10.1016/j.mce.2016.03.020. Epub 2016 Mar 17.

Abstract

Four non-coding GWAS variants in or near the ADIPOQ gene (rs17300539, rs17366653, rs3821799 and rs56354395) together explain 4% of the variation in circulating adiponectin. The functional basis for this is unknown. We tested the effect of these variants on ADIPOQ transcription, splicing and stability respectively in adipose tissue samples from participants recruited by rs17366653 genotype. Transcripts carrying rs17300539 demonstrated a 17% increase in expression (p = 0.001). Variant rs17366653 was associated with disruption of ADIPOQ splicing leading to a 7 fold increase in levels of a non-functional transcript (p = 0.002). Transcripts carrying rs56354395 demonstrated a 59% decrease in expression (p = <0.0001). No effects of rs3821799 genotype on expression was observed. Association between variation in the ADIPOQ gene and serum adiponectin may arise from effects on mRNA transcription, splicing or stability. These studies illustrate the utility of recruit-by-genotype studies in relevant human tissues in functional interpretation of GWAS signals.

Keywords: ADIPOQ; Adiponectin; Functional studies; Genetic variation; mRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / blood
  • Adiponectin / genetics*
  • Adipose Tissue / metabolism
  • Alleles
  • Base Sequence
  • Computational Biology
  • Female
  • Gene Expression Regulation
  • Gene Frequency / genetics
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide / genetics*
  • RNA Precursors / genetics
  • RNA Splicing / genetics
  • RNA, Long Noncoding / genetics
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism

Substances

  • ADIPOQ protein, human
  • Adiponectin
  • RNA Precursors
  • RNA, Long Noncoding
  • RNA, Messenger