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通过实时PCR定量微小RNA表达的简便方法。

Facile means for quantifying microRNA expression by real-time PCR.

作者信息

Shi Rui, Chiang Vincent L

机构信息

North Carolina State University, Raleigh, NC 27695-7247, USA.

出版信息

Biotechniques. 2005 Oct;39(4):519-25. doi: 10.2144/000112010.

Abstract

MicroRNAs (miRNAs) are 20-24 nucleotide RNAs that are predicted to play regulatory roles in animals and plants. Here we report a simple and sensitive real-time PCR method for quantifying the expression of plant miRNAs. Total RNA, including miRNAs, was polyadenylated and reverse-transcribed with a poly(T) adapter into cDNAs for real-time PCR using the miRNA-specific forward primer and the sequence complementary to the poly(T) adapter as the reverse primer. Several Arabidopsis miRNA sequences were tested using SYBR Green reagent, demonstrating that this method, using as little as 100 pg total RNA, could readily discriminate the expression of miRNAs having asfew as one nucleotide sequence difference. This method also revealed miRNA tissue-specific expression patterns that cannot be resolved by Northern blot analysis and may therefore be widely useful for characterizing miRNA expression in plants as well as in animals.

摘要

微小RNA(miRNAs)是20 - 24个核苷酸的RNA,预计在动植物中发挥调控作用。在此,我们报告一种简单且灵敏的实时PCR方法,用于定量植物miRNAs的表达。包括miRNAs在内的总RNA进行聚腺苷酸化处理,并使用带有聚(T)接头的引物逆转录成cDNA,以便使用miRNA特异性正向引物和与聚(T)接头互补的序列作为反向引物进行实时PCR。使用SYBR Green试剂对几个拟南芥miRNA序列进行了测试,结果表明该方法使用低至100 pg的总RNA,就能轻松区分仅有一个核苷酸序列差异的miRNAs的表达。该方法还揭示了miRNA组织特异性表达模式,而这是Northern印迹分析无法解析的,因此可能广泛用于表征植物以及动物中miRNA的表达。

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