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A non-radioactive method for small RNA detection by northern blotting

BACKGROUND: Small non-coding RNAs are essential regulators of gene expression at the transcriptional and posttranscriptional levels. High-throughput sequencing has revealed thousands of predicted small RNAs; however, only a few of these have been well characterized. Northern blotting is the most con...

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Detalles Bibliográficos
Autores principales: Huang, Qi, Mao, Zhinang, Li, Shaoqing, Hu, Jun, Zhu, Yingguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer New York 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4884002/
https://www.ncbi.nlm.nih.gov/pubmed/26224555
http://dx.doi.org/10.1186/s12284-014-0026-1
Descripción
Sumario:BACKGROUND: Small non-coding RNAs are essential regulators of gene expression at the transcriptional and posttranscriptional levels. High-throughput sequencing has revealed thousands of predicted small RNAs; however, only a few of these have been well characterized. Northern blotting is the most convincing method for small RNA validation. FINDINGS: In this study, we improved the Northern blot method by using biotin-labeled probes. miRNAs and siRNAs derived from both Arabidopsis thaliana and Oryza sativa were investigated. The results suggest that this improved method is sensitive and efficient, with approximately 5 μg of total RNA being sufficient for detection. Furthermore, long-term storage of probes labeled in this manner is more convenient, less contaminative and degradative compared with traditional probes. CONCLUSIONS: This protocol is an alternative strategy for small RNA detection and represents an efficient means of researching small RNAs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12284-014-0026-1) contains supplementary material, which is available to authorized users.