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Reconstitution Assay of miRNA Biogenesis by Arabidopsis DCL1. | LitMetric

Reconstitution Assay of miRNA Biogenesis by Arabidopsis DCL1.

Bio Protoc

Department of Biochemistry and Biophysics, Institute of Plant Genomics and Biotechnology, Texas A&M University, College Station, TX, USA.

Published: April 2015


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Article Abstract

microRNAs (miRNAs) are small non-coding RNAs, regulating most if not all, biological processes in eukaryotic organisms. miRNAs are initially processed from primary transcripts (pri-miRNAs) to produce miRNA precursors (pre-miRNAs), that are further processed into miRNA and its complementary strands (miRNA/*). In Arabidopsis, and possibly other plants, the processing from pri-miRNAs to pre-miRNAs and from pre-miRNAs to miRNA/* are both implemented through Dicer-like 1 (DCL1) complexes. Recently, we demonstrated isolation of DCL1 complexes of unprecedented quality from We further successfully reconstituted DCL1 cleavage assays that were able to fully recapitulate miRNA biogenesis. Here we provide a detailed protocol of DCL1 reconstitution assays. The protocol comprises three major parts (Figure 1): 1) Preparation of pri- and pre-miRNA transcripts (Procedures A-C); 2) Purification of the recombinant Arabidopsis DCL1 machinery from () through immunoprecipitation (IP) (Procedures D and E); and 3) processing of radioisotope-labeled pri- or pre-miRNAs using the isolated DCL1 complexes (Procedure F). It is our desire that the protocol be a powerful tool for the RNAi community to study mechanistic issues or to develop RNA silencing technologies.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943580PMC
http://dx.doi.org/10.21769/bioprotoc.1454DOI Listing

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