UMMS Affiliation

Program in Molecular Medicine; RNA Therapeutics Institute

Date

1-9-2015

Document Type

Article

Disciplines

Biochemistry | Bioinformatics | Computational Biology | Genomics | Molecular Biology | Molecular Genetics

Abstract

The preparation and high-throughput sequencing of cDNA libraries from samples of small RNA is a powerful tool to quantify known small RNAs (such as microRNAs) and to discover novel RNA species. Interest in identifying the small RNA repertoire present in tissues and in biofluids has grown substantially with the findings that small RNAs can serve as indicators of biological conditions and disease states. Here we describe a novel and straightforward method to clone cDNA libraries from small quantities of input RNA. This method permits the generation of cDNA libraries from sub-picogram quantities of RNA robustly, efficiently and reproducibly. We demonstrate that the method provides a significant improvement in sensitivity compared to previous cloning methods while maintaining reproducible identification of diverse small RNA species. This method should have widespread applications in a variety of contexts, including biomarker discovery from scarce samples of human tissue or body fluids.

Rights and Permissions

Citation: Nucleic Acids Res. 2015 Jan 9;43(1):e1. doi: 10.1093/nar/gku637. Epub 2014 Jul 23. Link to article on publisher's site

Related Resources

Link to Article in PubMed

PubMed ID

25056322

Creative Commons License

Creative Commons Attribution 4.0 License
This work is licensed under a Creative Commons Attribution 4.0 License.

 
 

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