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Comprehensive identification of miRNA target sites in live animals.

Methods in molecular biology (Clifton, N.J.) · 2011 · Vol. 732 · pp. 169-85

Abstract

MicroRNAs (miRNAs) are small RNA molecules that posttranscriptionally regulate the expression of protein-coding genes. The mature miRNAs are loaded into Argonaute-containing protein complexes (miRISC, miRNA Induced S  ilencing Complex), and guide these complexes to the 3' UTR of targeted mRNA transcripts via base-pairing interactions. However, the imperfect complementarity that characterizes the interactions between animal miRNAs and target sites complicates the identification of direct target genes. We developed a biochemical method to identify on a large scale the target sequences recognized by miRISC in vivo. The mRNA sites bound by miRISC are stabilized by cross-linking and isolated by immunoprecipitation of Argonaute-containing complexes. The bound RNA molecules are trimmed to the regions protected by Argonaute, subjected to a series of isolation and linker ligation steps and identified by high-throughput sequencing methods.

Publication Types

["Journal Article"]

Keywords

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MeSH Terms

["Animals", "Caenorhabditis elegans", "Caenorhabditis elegans Proteins", "High-Throughput Nucleotide Sequencing", "Immunoprecipitation", "MicroRNAs", "RNA, Messenger", "RNA-Binding Proteins"]

Funding

R01 GM071654 NIGMS NIH HHS (United States)