Evidence for a second ankylosing spondylitis-associatedRUNX3regulatory polymorphism

• DOI: 10.1136/rmdopen-2017-000628
• Publication Date: 2018-02-12T16:09:55Z
• Authors: Matteo Vecellio; Adrian Cortes; Amity R Roberts; Jonathan Ellis; Carla Jayne Cohen; Julian C Knight; Matthew A Brown; Paul Bowness; Bryan Paul Wordsw...
• Keywords: gene polymorphism; Complex Traits; Loci; Variants; Proteins; Expression; spondyloarthritis; Criteria; 03 medical and health sciences; 0302 clinical medicine; Differentiation; ankylosing spondylitis; Spondyloarthritis; Disease; epidemiology; Recruitment; Genetic Association

ObjectivesTo explore the functions ofRUNX3single nucleotide polymorphisms (SNPs) associated with ankylosing spondylitis (AS).MethodsIndividual SNP associations were evaluated in 4230 UK cases. Their effects on transcription factor (TF) binding, transcription regulation, chromatin modifications, gene expression and gene interactions were tested by database interrogation, luciferase reporter assays, electrophoretic mobility gel shifts, chromatin immunoprecipitation and real-time PCR.ResultsWe confirmed the independent association of AS withrs4265380, which was robust (P=4.7×10−6) to conditioning on another nearby AS-associatedRUNX3SNP (rs4648889). ARUNX3haplotype incorporating both SNPs was strongly associated with AS (OR 6.2; 95% CI 3.1 to 13.2, P=1.4×10−8). In a large UK cohort,rs4265380is associated with leucocyte counts (including monocytes).RUNX3expression is lower in AS peripheral blood mononuclear cells than healthy controls (P<0.002), independent ofrs4265380genotype. Enhancer function for thisRUNX3region was suggested by increased luciferase activity (approximately tenfold; P=0.005) for reporter constructs containingrs4265380. In monocytes, there was differential allelic binding of nuclear protein extracts to a 50 bp DNA probe containingrs4265380that was strongly augmented by lipopolysaccharide activation. TF binding also included the histone modifier p300. There was enrichment for histone modifications associated with active enhancer elements (H3K27Ac and H3K79Me2) that may be allele dependent. Hi-C database interrogation showed chromosome interactions of RUNX3 bait with the nearby RP4-799D16.1 lincRNA.ConclusionsThe association of AS with thisRUNX3regulatory region involves at least two SNPs apparently operating in different cell types. Monocytes may be potential therapeutic targets in AS.