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Real-time polymerase chain reaction microRNA detection based on enzymatic stem-loop probes ligation

  • Juan Li
  • , Bo Yao
  • , Huang Huang
  • , Zhao Wang
  • , Changhong Sun
  • , Yu Fan
  • , Qing Chang
  • , Shaolu Li
  • , Xiang Wang*
  • , Jianzhong Xi
  • *此作品的通讯作者

科研成果: 期刊稿件文章同行评审

摘要

MiRNAs (microRNAs) are a group of endogenous, small noncoding RNA with the length of 18-25 nucleotides, which have recently been demonstrated to play important roles in a wide range of biological processes. In this work, we developed a simple, sensitive, specific, and inexpensive assay through the combination of enzymatic probe ligation and real-time PCR amplification for the measurement of mature miRNAs. A couple of novel DNA probes with a stem-loop structure were implemented to reduce nonspecific ligation by at least 100-fold. The assay has several remarkable features including wide dynamic range, low total RNA input (0.02-0.2 ng), distinct anti-interference from precursor miRNAs (signal-to-noise ratio > 500), and single-base mismatch discrimination among miRNA sequences. In addition, a one-tube assay could be accomplished by designing a couple of universal probes, which makes it feasible to examine the expression of a whole family of miRNA (such as let-7) at one time. Finally, we validated the method for quantifying the expression of four mature miRNAs including miR-122, miR-1, miR-34a, and let-7a across 10 mouse tissues, where U6 snRNA could be simultaneously examined as an endogenous control. Thus, this method revealed a great potential for miRNA quantitation in ordinary laboratory studies and clinical diagnoses.

源语言英语
页(从-至)5446-5451
页数6
期刊Analytical Chemistry
81
13
DOI
出版状态已出版 - 1 7月 2009

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