In vitro reconstitution of chaperone-mediated human RISC assembly

RNA. 2018 Jan;24(1):6-11. doi: 10.1261/rna.063891.117. Epub 2017 Oct 2.

Abstract

To silence target mRNAs, small RNAs and Argonaute (Ago) proteins need to be assembled into RNA-induced silencing complexes (RISCs). Although the assembly of Drosophila melanogaster RISC was recently reconstituted by Ago2, the Dicer-2/R2D2 heterodimer, and five chaperone proteins, the absence of a reconstitution system for mammalian RISC assembly has posed analytical challenges. Here we describe reconstitution of human RISC assembly using Ago2 and five recombinant chaperone proteins: Hsp90β, Hsc70, Hop, Dnaja2, and p23. Our data show that ATP hydrolysis by both Hsp90β and Hsc70 is required for RISC assembly of small RNA duplexes but not for that of single-stranded RNAs. The reconstitution system lays the groundwork for further studies of small RNA-mediated gene silencing in mammals.

Keywords: Argonaute; RISC; chaperone; microRNA; siRNA.

MeSH terms

  • Adenosine Triphosphate / chemistry
  • Argonaute Proteins / chemistry*
  • Base Pairing
  • HEK293 Cells
  • HSP70 Heat-Shock Proteins / chemistry
  • HSP90 Heat-Shock Proteins / chemistry
  • Humans
  • Hydrolysis
  • MicroRNAs / chemistry
  • Protein Multimerization
  • RNA-Induced Silencing Complex / chemistry*
  • Thermodynamics

Substances

  • AGO2 protein, human
  • Argonaute Proteins
  • HSP70 Heat-Shock Proteins
  • HSP90 Heat-Shock Proteins
  • HSP90AB1 protein, human
  • MicroRNAs
  • RNA-Induced Silencing Complex
  • mirnlet7 microRNA, human
  • Adenosine Triphosphate