DNA hypomethylation of a transcription factor binding site within the promoter of a gout risk gene NRBP1 upregulates its expression by inhibition of TFAP2A binding

Clin Epigenetics. 2017 Sep 15:9:99. doi: 10.1186/s13148-017-0401-z. eCollection 2017.

Abstract

Background: Genome-wide association studies (GWASs) have identified dozens of loci associated with gout, but for most cases, the risk genes and the underlying molecular mechanisms contributing to these associations are unknown. This study sought to understand the molecular mechanism of a common genetic variant, rs780093, in the development of gout, both in vitro and in vivo.

Results: Nuclear receptor binding protein 1 (NRBP1), as a gout risk gene, and its regulatory region, 72 bp upstream of the transcription start site, designated as B1, were identified through integrative analyses of genome-wide genotype and DNA methylation data. We observed elevated NRBP1 expression in human peripheral blood mononuclear cells (PBMCs) from gout patients. In vitro luciferase reporter and protein pulldown assay results showed that DNA methylation could increase the binding of the transcription factor TFAP2A to B1, leading to suppressed gene expression. There results were further confirmed by in vivo bisulfite pyrosequencing showing that hypomethylation on B1 is associated with increased NRBP1 expression in gout patients.

Conclusions: Hypomethylation at the promoter region of NRBP1 reduces the binding of TFAP2A and thus leads to elevated NRBP1 expression, which might contribute to the development of gout.

Keywords: DNA methylation; Gout; NRBP1; TFAP2A; Uric acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • DNA Methylation
  • Genome-Wide Association Study
  • Gout / genetics*
  • Gout / metabolism
  • HEK293 Cells
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Promoter Regions, Genetic
  • Protein Binding
  • Receptors, Cytoplasmic and Nuclear / blood
  • Receptors, Cytoplasmic and Nuclear / genetics*
  • Sequence Analysis, DNA
  • Transcription Factor AP-2 / metabolism*
  • Up-Regulation*
  • Vesicular Transport Proteins / blood
  • Vesicular Transport Proteins / genetics*

Substances

  • NRBP1 protein, human
  • Receptors, Cytoplasmic and Nuclear
  • TFAP2A protein, human
  • Transcription Factor AP-2
  • Vesicular Transport Proteins