Abstract

BackgroundThe arcOGEN genome-wide association study reported the rs9350591 C/T single nucleotide polymorphism (SNP) as marking a region on chromosome 6q14.1 that is associated with hip osteoarthritis (OA) in Europeans, with an odds ratio (OR) of 1.18 and a p-value of 2.42 × 10−9. rs9350591 is an intergenic SNP surrounded by seven genes within 1 Mb. Six of the genes are expressed in cartilage. We sought to characterise this signal to assess whether the association of rs9350591 with OA is mediated by modulating gene expression.MethodsTotal RNA was extracted from hip or knee cartilage of 161 OA patients and from hip cartilage of 29 non-OA patients who had undergone hip replacements as a result of neck-of-femur (NOF) fractures. We used quantitative PCR (qPCR) to measure overall gene expression, and pyrosequencing to assess allelic expression of the genes. A mesenchymal stem cell (MSC) differentiation model was used to assess gene expression during chondrogenesis.ResultsWe identified a significant decrease in the expression of SENP6 (p = 0.005) and MYO6 (p = 0.026) in OA hip cartilage relative to the non-OA hip control cartilage. However, we found no evidence for a correlation between gene expression and rs9350591 genotype for any of the six genes. In addition, we identified expression quantitative trait loci (eQTLs) operating on COL12A1, TMEM30A, SENP6 and MYO6, although these were not relevant to the OA associated signal. Finally, all genes were dynamically expressed during chondrogenesis.ConclusionsThe regulation of gene expression at this locus is complex, highlighted by the down-regulation of SENP6 and MYO6 in OA hip cartilage and by eQTLs operating on four of the genes at the locus. However, modulation of gene expression in the end-stage OA cartilage that we have investigated is not the mechanism by which this association signal is operating. As implied by the dynamic patterns of gene expression throughout chondrogenesis, the association signal marked by rs9350591 could instead be exerting its effects during joint development.Electronic supplementary materialThe online version of this article (doi:10.1186/s12881-015-0215-9) contains supplementary material, which is available to authorized users.

Highlights

  • The arcOGEN genome-wide association study reported the rs9350591 C/T single nucleotide polymorphism (SNP) as marking a region on chromosome 6q14.1 that is associated with hip osteoarthritis (OA) in Europeans, with an odds ratio (OR) of 1.18 and a p-value of 2.42 × 10−9. rs9350591 is an intergenic single nucleotide polymorphisms (SNPs) surrounded by seven genes within 1 Mb

  • The association signal encompasses six genes that are expressed in cartilage [4]: COL12A1 coding for the α1 polypeptide chain of type XII collagen, COX7A2 coding for cytochrome c oxidase 7A2, TMEM30A coding for transmembrane

  • We found evidence of functionality, including transcription factor binding and regions with regulatory activity, for SNPs in perfect or high linkage disequilibrium (LD) with rs9350591 (Additional file 7)

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Summary

Introduction

The arcOGEN genome-wide association study reported the rs9350591 C/T single nucleotide polymorphism (SNP) as marking a region on chromosome 6q14.1 that is associated with hip osteoarthritis (OA) in Europeans, with an odds ratio (OR) of 1.18 and a p-value of 2.42 × 10−9. rs9350591 is an intergenic SNP surrounded by seven genes within 1 Mb. The arcOGEN genome-wide association study reported the rs9350591 C/T single nucleotide polymorphism (SNP) as marking a region on chromosome 6q14.1 that is associated with hip osteoarthritis (OA) in Europeans, with an odds ratio (OR) of 1.18 and a p-value of 2.42 × 10−9. In 2012, the arcOGEN GWAS reported five genomewide significant OA association signals in Europeans [4] These resulted from the genotyping of almost 1.4 million single nucleotide polymorphisms (SNPs) in a discovery sample of 7,410 cases and 11,009 controls, with replication in 14,883 cases and 53,947 controls. One of the five signals was to the intergenic SNP rs9350591 on chromosome 6q14.1, with an odds ratio (OR) of 1.18 for the minor T allele and a p-value of 2.42 × 10−9 in the hip stratum. The association signal encompasses six genes that are expressed in cartilage [4]: COL12A1 coding for the α1 polypeptide chain of type XII collagen, COX7A2 coding for cytochrome c oxidase 7A2, TMEM30A coding for transmembrane

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