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Integrated miRNA and mRNA expression profiling to identify mRNA targets of dysregulated miRNAs in non-obstructive azoospermia

机译:整合的miRNA和mRNA表达谱以鉴定非阻塞性无精子症中失调的miRNA的mRNA靶标

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摘要

The aim of this study was to identify mRNA targets of dysregulated miRNAs through the integrated analysis of miRNA and mRNA expression profiling in men with normal versus impaired spermatogenesis. The expression of mRNAs and miRNAs in testicular tissues obtained from males with non-obstructive azoospermia (NOA, n = 4) or obstructive azoospermia (OA, n = 3) with normal spermatogenesis was analyzed using microarray technology. Some of the most interesting results were validated by real time PCR using samples from the same cohort. Ninety-three miRNAs and 4172 mRNAs were differentially expressed in the NOA and normozoospermic OA patients. In addition to confirming that significantly dysregulated genes and miRNAs play pivotal roles in NOA, promising correlation signatures of these miRNA/mRNA pairs were discovered in this study. The functional classification of the miRNA/mRNA pairs revealed that differentially expressed genes were most frequently associated with spermatogenesis, the cell meiosis, the cell cycle, and the development of secondary male sexual characteristics. This is the first systematic profiling of both mRNA and miRNA in testicular tissues of patients with NOA and OA. Our results indicate that the phenotypic status of NOA is characterized by the dysfunction of normal spermatogenesis when compared with OA or normozoospermic males.
机译:这项研究的目的是通过对男性精子发生正常与受损的男性中的miRNA和mRNA表达谱进行综合分析,确定失调的miRNA的mRNA靶标。使用微阵列技术分析了具有正常精子发生的非阻塞性无精子症(NOA,n = 4)或阻塞性无精子症(OA,n = 3)的男性睾丸组织中mRNA和miRNA的表达。一些最有趣的结果已通过实时PCR验证,使用的是同一队列的样本。在NOA和正常精子OA患者中,有93个miRNA和4172 mRNA差异表达。除了确认显着失调的基因和miRNA在NOA中起关键作用外,在这项研究中还发现了这些miRNA / mRNA对的有希望的相关特征。 miRNA / mRNA对的功能分类显示,差异表达的基因最常与精子发生,细胞减数分裂,细胞周期和继发男性性特征的发展有关。这是NOA和OA患者睾丸组织中mRNA和miRNA的第一个系统分析。我们的结果表明,与OA或正常精子症的男性相比,NOA的表型状态以正常精子发生功能障碍为特征。

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