Slicing-independent RISC activation requires the argonaute PAZ domain

Curr Biol. 2012 Aug 21;22(16):1536-42. doi: 10.1016/j.cub.2012.06.040. Epub 2012 Jul 12.


Small RNAs regulate genetic networks through a ribonucleoprotein complex called the RNA-induced silencing complex (RISC), which, in mammals, contains at its center one of four Argonaute proteins (Ago1-Ago4). A key regulatory event in the RNA interference (RNAi) and microRNA (miRNA) pathways is Ago loading, wherein double-stranded small-RNA duplexes are incorporated into RISC (pre-RISC) and then become single-stranded (mature RISC), a process that is not well understood. The Agos contain an evolutionarily conserved PAZ (Piwi/Argonaute/Zwille) domain whose primary function is to bind the 3' end of small RNAs. We created multiple PAZ-domain-disrupted mutant Ago proteins and studied their biochemical properties and biological functionality in cells. We found that the PAZ domain is dispensable for Ago loading of slicing-competent RISC. In contrast, in the absence of slicer activity or slicer-substrate duplex RNAs, PAZ-disrupted Agos bound duplex small interfering RNAs, but were unable to unwind or eject the passenger strand and form functional RISC complexes. We have discovered that the highly conserved PAZ domain plays an important role in RISC activation, providing new mechanistic insights into how miRNAs regulate genes, as well as new insights for future design of miRNA- and RNAi-based therapeutics.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Argonaute Proteins / metabolism*
  • HEK293 Cells
  • Humans
  • MicroRNAs / metabolism*
  • Point Mutation
  • Protein Structure, Tertiary
  • RNA-Induced Silencing Complex / metabolism*


  • Argonaute Proteins
  • MicroRNAs
  • RNA-Induced Silencing Complex

Associated data

  • GEO/GSE39146