Simple and nonradioactive detection of microRNAs using digoxigenin (DIG)-labeled probes with high sensitivity
- Wei Wu1,2,
- Pengtao Gong1,2,
- Jianhua Li1,3,
- Ju Yang1,
- Guocai Zhang1,
- He Li1,
- Zhengtao Yang1 and
- Xichen Zhang1,3
- 1Key Laboratory of Zoonosis Research, Ministry of Education, College of Veterinary Medicine, Jilin University, Changchun 130062, China
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↵2 These authors contributed equally to this work.
Abstract
The discovery of microRNAs (miRNAs), which are ∼21–23 nucleotides that can regulate targeted mRNA by transcript cleavage or protein translation suppression, has changed the landscape of biomedical field greatly. At present, Northern blot analysis based on radioisotopes is still the most popular method on the detection of miRNAs for its high sensitivity. However, radioisotopes have been known for certain disadvantages, such as instability, expense, and safety; thus, developing a nonradioactive and highly sensitive method is needed. Here, we report a simple, nonradioactive, and sensitive method for miRNAs detection based on 5′-phos-3′-DIG–labeled probes prepared through splinted ligation and EDC cross-linking (DSLE). The method was more sensitive than traditional Northern blots with a DIG-labeled DNA probe and can detect as low as 2 fmol of miRNAs. The whole procedure can be completed within 6–8 h. DSLE method is very convenient, cost-effective, time-saving, and highly sensitive.
Keywords
Footnotes
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↵3 Corresponding authors
E-mail xczhang{at}jlu.edu.cn
E-mail jianhuali7207{at}163.com
- Received August 28, 2013.
- Accepted January 19, 2014.
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