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由多态性rs9350591标记的6号染色体q14.1上骨关节炎易感位点的功能特征分析

Functional characterisation of the osteoarthritis susceptibility locus at chromosome 6q14.1 marked by the polymorphism rs9350591.

作者信息

Johnson Katherine, Reynard Louise N, Loughlin John

机构信息

Musculoskeletal Research Group, Institute of Cellular Medicine, 4th Floor Catherine Cookson Building, Framlington Place, Newcastle University, Newcastle-upon-Tyne, NE2 4HH, UK.

出版信息

BMC Med Genet. 2015 Sep 7;16:81. doi: 10.1186/s12881-015-0215-9.

Abstract

BACKGROUND

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. 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.

METHODS

Total 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.

RESULTS

We 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.

CONCLUSIONS

The 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.

摘要

背景

arcOGEN全基因组关联研究报告称,rs9350591 C/T单核苷酸多态性(SNP)标记了6号染色体14.1区域,该区域与欧洲人的髋骨关节炎(OA)相关,优势比(OR)为1.18,p值为2.42×10⁻⁹。rs9350591是一个基因间SNP,在1兆碱基范围内被7个基因包围。其中6个基因在软骨中表达。我们试图对这一信号进行表征,以评估rs9350591与OA的关联是否通过调节基因表达来介导。

方法

从161例OA患者的髋或膝关节软骨以及29例因股骨颈(NOF)骨折接受髋关节置换的非OA患者的髋部软骨中提取总RNA。我们使用定量PCR(qPCR)来测量总体基因表达,并使用焦磷酸测序来评估基因的等位基因表达。使用间充质干细胞(MSC)分化模型来评估软骨形成过程中的基因表达。

结果

我们发现,与非OA髋部对照软骨相比,OA髋部软骨中SENP6(p = 0.005)和MYO6(p = 0.026)的表达显著降低。然而,我们没有发现这六个基因中的任何一个基因表达与rs9350591基因型之间存在相关性的证据。此外,我们确定了作用于COL12A1、TMEM30A、SENP6和MYO6的表达定量性状位点(eQTL),尽管这些与OA相关信号无关。最后,所有基因在软骨形成过程中均动态表达。

结论

该位点的基因表达调控很复杂,OA髋部软骨中SENP6和MYO6的下调以及该位点四个基因上的eQTL均突出了这一点。然而,我们所研究的终末期OA软骨中的基因表达调节并非该关联信号起作用的机制。正如整个软骨形成过程中基因表达的动态模式所暗示的,rs9350591标记的关联信号可能在关节发育过程中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4da/4562116/9873b49f3ca8/12881_2015_215_Fig1_HTML.jpg

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