Identifying miRNA Targets Using AGO-RIPseq

Methods Mol Biol. 2018:1720:131-140. doi: 10.1007/978-1-4939-7540-2_9.

Abstract

microRNAs (miRNA) are small, noncoding RNAs that bind to messenger RNAs (mRNAs) and regulate their activity. They are, therefore, important posttranscriptional regulators. In recent years it has become clear that miRNAs regulate large genetic networks, rather than single genes, and that one gene can be targeted by several miRNAs. To understand the role of miRNAs in cells or tissues, it is therefore important to analyze the targetome of miRNAs. Here, we present a technique called Argonaute-RNA Immunoprecipitation (AGO-RIP) which takes advantages of the fact that miRNAs and their targets are directly bound by the Argonaute protein family. With this approach quantitative, genome-wide analysis of miRNA targets is possible. In this chapter we describe the RIP-methodology and provide advice for RNA sequencing and bioinformatic analyses.

Keywords: Argonaute; Immunoprecipitation; Small and total RNA sequencing; Targetome; microRNAs.

MeSH terms

  • Argonaute Proteins / metabolism*
  • Computational Biology / methods
  • Gene Library
  • Immunoprecipitation / methods*
  • MicroRNAs / genetics
  • MicroRNAs / isolation & purification
  • MicroRNAs / metabolism*
  • Protein Binding
  • RNA Interference
  • RNA, Messenger / genetics
  • RNA, Messenger / immunology
  • RNA, Messenger / isolation & purification
  • RNA, Messenger / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Analysis, RNA / methods*
  • Software

Substances

  • Argonaute Proteins
  • MicroRNAs
  • RNA, Messenger