Institute of Cellular Medicine, Musculoskeletal Research Group, Newcastle University, Newcastle-upon-Tyne, UK.
BMC Med Genet. 2014 May 4;15:53. doi: 10.1186/1471-2350-15-53.
An osteoarthritis (OA) susceptibility locus has been mapped to chromosome 3p21, to a region of high linkage disequilibrium encompassing twelve genes. Six of these genes are expressed in joint tissues and we therefore assessed whether any of the six were subject to cis-acting regulatory polymorphisms active in these tissues and which could therefore account for the association signal.
We measured allelic expression using pyrosequencing assays that can distinguish mRNA output from each allele of a transcript single nucleotide polymorphism. We assessed RNA extracted from the cartilage and other joint tissues of OA patients who had undergone elective joint replacement surgery. A two-tailed Mann-Whitney exact test was used to test the significance of any allelic differences.
GNL3 and SPCS1 demonstrated significant allelic expression imbalance (AEI) in OA cartilage (GNL3, mean AEI = 1.04, p = 0.0002; SPCS1, mean AEI = 1.07, p < 0.0001). Similar results were observed in other tissues. Expression of the OA-associated allele was lower than that of the non-associated allele for both genes.
cis-acting regulatory polymorphisms acting on GNL3 and SPCS1 contribute to the OA association signal at chromosome 3p21, and these genes therefore merit further investigation.
骨关节炎(OA)易感性位点已被映射到染色体 3p21,到一个包含十二个基因的高度连锁不平衡区域。其中六个基因在关节组织中表达,因此我们评估了这些基因中的任何一个是否受到顺式作用调节多态性的影响,这些多态性在这些组织中是活跃的,并且可以解释关联信号。
我们使用焦磷酸测序测定来测量等位基因表达,该方法可以区分转录单核苷酸多态性的每个等位基因的 mRNA 输出。我们评估了接受选择性关节置换手术的 OA 患者的软骨和其他关节组织中提取的 RNA。使用双尾曼-惠特尼精确检验来检验任何等位基因差异的显著性。
GNL3 和 SPCS1 在 OA 软骨中表现出显著的等位基因表达不平衡(AEI)(GNL3,平均 AEI=1.04,p=0.0002;SPCS1,平均 AEI=1.07,p<0.0001)。在其他组织中也观察到类似的结果。对于这两个基因,OA 相关等位基因的表达低于非相关等位基因。
作用于 GNL3 和 SPCS1 的顺式作用调节多态性导致染色体 3p21 上的 OA 关联信号,因此这些基因值得进一步研究。