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用于筛选和定量微小RNA的通用茎环引物法

Universal stem-loop primer method for screening and quantification of microRNA.

作者信息

Yang Li-hong, Wang Si-lu, Tang Li-li, Liu Biao, Ye Wen-le, Wang Ling-ling, Wang Zhang-yang, Zhou Meng-tao, Chen Bi-cheng

机构信息

Clinical Laboratory Diagnostic Centre, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, 325000, Peoples Republic of China.

Wenzhou Key Laboratory of Surgery, Department of Surgery, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, 325000, Peoples Republic of China.

出版信息

PLoS One. 2014 Dec 30;9(12):e115293. doi: 10.1371/journal.pone.0115293. eCollection 2014.

Abstract

RT-qPCR is the accepted technique for the quantification of microRNA (miR) expression: however, stem-loop RT-PCR, the most frequently used method for quantification of miRs, is time- and reagent-consuming as well as inconvenient for scanning. We established a new method called 'universal stem-loop primer' (USLP) with 8 random nucleotides instead of a specific sequence at the 3' end of the traditional stem-loop primer (TSLP), for screening miR profile and to semi-quantify expression of miRs. Peripheral blood samples were cultured with phytohaemagglutinin (PHA), and then 87 candidate miRs were scanned in cultured T cells. By USLP, our study revealed that the expression of miR-150-5p (miR-150) decreased nearly 10-fold, and miR-155-5p (miR-155) increased more than 7-fold after treated with PHA. The results of the dissociation curve and gel electrophoresis showed that the PCR production of the USLP and TSLP were specificity. The USLP method has high precision because of its low ICV (ICV<2.5%). The sensitivity of the USLP is up to 103 copies/µl miR. As compared with the TSLP, USLP saved 75% the cost of primers and 60% of the test time. The USLP method is a simple, rapid, precise, sensitive, and cost-effective approach that is suitable for screening miR profiles.

摘要

逆转录定量聚合酶链反应(RT-qPCR)是用于定量微小RNA(miR)表达的公认技术:然而,茎环RT-PCR作为最常用的miR定量方法,既耗时又耗试剂,而且不利于扫描。我们建立了一种名为“通用茎环引物”(USLP)的新方法,在传统茎环引物(TSLP)的3'端用8个随机核苷酸代替特定序列,用于筛选miR谱并半定量miR的表达。外周血样本用植物血凝素(PHA)培养,然后在培养的T细胞中扫描87个候选miR。通过USLP,我们的研究表明,用PHA处理后,miR-150-5p(miR-150)的表达下降了近10倍,而miR-155-5p(miR-155)的表达增加了7倍多。解离曲线和凝胶电泳结果表明,USLP和TSLP的PCR产物具有特异性。USLP方法因其低组内变异系数(ICV<2.5%)而具有高精度。USLP的灵敏度高达103拷贝/μl miR。与TSLP相比,USLP节省了75%的引物成本和60%的检测时间。USLP方法是一种简单、快速、精确、灵敏且经济高效的方法,适用于筛选miR谱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19b6/4280144/6e54fc172c8c/pone.0115293.g001.jpg

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