Unit

UNIT 12.14 DIANA-TarBase and DIANA Suite Tools: Studying Experimentally Supported microRNA Targets

  1. Maria D. Paraskevopoulou1,2,†,
  2. Ioannis S. Vlachos1,2,†,
  3. Artemis G. Hatzigeorgiou1,2

Published Online: 7 SEP 2016

DOI: 10.1002/cpbi.12

Current Protocols in Bioinformatics

Current Protocols in Bioinformatics

How to Cite

Paraskevopoulou, M.D., Vlachos, I.S., and Hatzigeorgiou, A.G. 2016. DIANA-TarBase and DIANA suite tools: studying experimentally supported microRNA targets. Curr. Protoc. Bioinform. 55:12.14.1-12.14.18. doi: 10.1002/cpbi.12

Author Information

  1. 1

    DIANA-Lab, Department of Electrical & Computer Engineering, University of Thessaly, Volos, Greece

  2. 2

    Hellenic Pasteur Institute, Athens, Greece

  1. These authors contributed equally to this work.

Publication History

  1. Published Online: 7 SEP 2016

Abstract

microRNAs (miRNAs) are short non-coding RNAs (∼22 nts) present in animals, plants, and viruses. They are considered central post-transcriptional regulators of gene expression and are key components in a great number of physiological and pathological conditions. The accurate characterization of their targets is considered essential to a series of applications and basic or applied research settings. DIANA-TarBase (http://www.microrna.gr/tarbase) was initially launched in 2006. It is a reference repository indexing experimentally derived miRNA-gene interactions in different cell types, tissues, and conditions across numerous species. This unit focuses on the study of experimentally supported miRNA-gene interactions, as well as their functional interpretation through the use of available tools in the DIANA suite (http://www.microrna.gr). The proposed use-case scenarios are presented in protocols, describing how to utilize the DIANA-TarBase database and DIANA-microT-CDS server and perform miRNA-targeted pathway analysis with DIANA-miRPath-v3. All analyses are directly invoked or initiated from DIANA-TarBase. © 2016 by John Wiley & Sons, Inc.

Keywords:

  • microRNA;
  • target;
  • interaction;
  • experimental methodology;
  • high-throughput;
  • pathway;
  • in silico predictions;
  • RNAi;
  • miRNA interactome