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OALib Journal期刊
ISSN: 2333-9721
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Allelic expression analysis of the osteoarthritis susceptibility locus that maps to MICAL3

DOI: 10.1186/1471-2350-13-12

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Abstract:

We used total and allelic expression analysis to assess whether the OA association to rs2277831 is mediated by an influence on MICAL3, BCL2L13 or BID expression. Using RNA extracted from joint tissues of 60 patients who had undergone elective joint replacement surgery, we assessed whether rs2277831 correlated with allelic expression of either of the three genes by: 1) measuring the expression of each gene by quantitative PCR and then stratifying the data by genotype at rs2277831 and 2) accurately discriminating and quantifying the mRNA synthesised from the alleles of OA patients using allelic-quantitative PCR.We found no evidence for a correlation between gene expression and genotype at rs2277831, with P-values of 0.09 for BCL2L13, 0.07 for BID and 0.33 for MICAL3. In the allelic expression analysis we observed several examples of significant (p < 0.05) allelic imbalances, with an allelic expression ratio of 2.82 observed in BCL2L13 (P = 0.004), 2.09 at BID (P = 0.001) and the most extreme case being at MICAL3, with an allelic expression ratio of 5.47 (P = 0.001). However, there was no correlation observed between the pattern of allelic expression and the genotype at rs2277831.In the tissues that we have studied, our data do not support our hypothesis that the association between rs2277831 and OA is due to the effect this SNP has on MICAL3, BCL2L13 or BID gene expression. Instead, our data point towards other functional effects accounting for the OA associated signal.Osteoarthritis (OA) is a common disease of the synovial joint characterized by cartilage loss and is often accompanied by alteration in the normal function of other tissues of the articulating joint [1]. Based on epidemiological studies, the disease is known to have a major genetic component, although elucidating this has proven challenging [2]. This is a reflection of the heterogeneity associated with the disease, with severe OA being a clinical end-point reached from a multitude of starting points. Ge

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