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Circulating microRNA profiles and the identification of miR-593 and miR-511 which directly target the PROP1 gene in children with combined pituitary hormone deficiency

机译:垂体激素缺乏症患儿的循环microRNA谱及直接靶向PROP1基因的miR-593和miR-511的鉴定

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摘要

Since the tissue of children with combined pituitary hormone deficiency (CPHD) is not readily accessible, a new focus in children with CPHD is the blood-based expression profiling of non-protein coding genes, such as microRNAs (miRNAs or miRs), which regulate gene expression by inhibiting the translation of mRNAs. In this study, to address this, we identified potential miRNA signatures for CPHD by comparing genome-wide miRNA expression profiles in the serum of children with CPHD vs. normal (healthy) controls. Human embryonic kidney 293T cells were transfected with miR-593 or miR-511 oligonucleotides. Potential target gene expression was validated by western blot analysis for proteins and by miR-593 or miR-511 reporter assay using PROP1 gene 3′-untranslated region (3′-UTR) reporter. The miR-593 and miR-511 levels in the serum of 103 children with CPHD were assessed using the reverse transcription-quantitative polymerase chain reaction (RT-qPCR) method. We found 23 upregulated and 19 down-regulated miRNAs with abnormal expression in children with CPHD compared with the normal controls using miRNA microarray analysis and RT-qPCR. miR-593 and miR-511 targeted the 3′-UTR of the PROP1 gene and attenuated the expression of PROP1. The levels of miR-593 and miR-511 in the serum of children with CPHD were increased compared with those in the control subjects. According to Youden’s index, the sensitivity was 82.54 and 84.86%, and the specificity was 98.15 and 91.36% for miR-593 and miR-511, respectively. The various levels of specific miRNAs, particularly miR-593 and miR-511 whose direct target is the PROP1 gene, may serve as a non-invasive diagnostic biomarkers for children with CPHD.
机译:由于合并垂体激素缺乏症(CPHD)的儿童的组织不易获得,因此CPHD儿童的新焦点是非蛋白质编码基因(如microRNA(miRNA或miRs))的基于血液的表达谱分析,该基因可调节通过抑制mRNA的翻译来表达基因。在这项研究中,为了解决这个问题,我们通过比较CPHD儿童与正常(健康)对照者血清中的全基因组miRNA表达谱,确定了CPHD的潜在miRNA特征。用miR-593或miR-511寡核苷酸转染人胚胎肾293T细胞。通过蛋白质的蛋白质印迹分析以及使用PROP1基因3'-非翻译区(3'-UTR)报告基因的miR-593或miR-511报告基因分析,验证了潜在的靶基因表达。采用逆转录定量聚合酶链反应(RT-qPCR)方法评估103名CPHD儿童血清中的miR-593和miR-511水平。使用miRNA芯片分析和RT-qPCR,与正常对照组相比,我们发现CPHD儿童中有23种表达异常的miRNA和19种表达异常的miRNA。 miR-593和miR-511靶向PROP1基因的3'-UTR,并减弱了PROP1的表达。与对照组相比,CPHD患儿血清中的miR-593和miR-511水平升高。根据尤登指数,miR-593和miR-511的敏感性分别为82.54和84.86%,特异性为98.15和91.36%。各种水平的特定miRNA,尤其是miR-593和miR-511(其直接靶标是PROP1基因),可以作为CPHD儿童的非侵入性诊断生物标志物。

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