RNA molecules stimulate prion protein conversion

Nature. 2003 Oct 16;425(6959):717-20. doi: 10.1038/nature01979.


Much evidence supports the hypothesis that the infectious agents of prion diseases are devoid of nucleic acid, and instead are composed of a specific infectious protein. This protein, PrP(Sc), seems to be generated by template-induced conformational change of a normally expressed glycoprotein, PrP(C) (ref. 2). Although numerous studies have established the conversion of PrP(C) to PrP(Sc) as the central pathogenic event of prion disease, it is unknown whether cellular factors other than PrP(C) might be required to stimulate efficient PrP(Sc) production. We investigated the biochemical amplification of protease-resistant PrP(Sc)-like protein (PrPres) using a modified version of the protein-misfolding cyclic amplification method. Here we report that stoichiometric transformation of PrP(C) to PrPres in vitro requires specific RNA molecules. Notably, whereas mammalian RNA preparations stimulate in vitro amplification of PrPres, RNA preparations from invertebrate species do not. Our findings suggest that host-encoded stimulatory RNA molecules may have a role in the pathogenesis of prion disease. They also provide a practical approach to improve the sensitivity of diagnostic techniques based on PrPres amplification.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Brain / metabolism
  • Caenorhabditis elegans / genetics
  • Cricetinae
  • Drosophila melanogaster / genetics
  • Endonucleases / metabolism
  • Escherichia coli / genetics
  • Female
  • Mesocricetus / genetics
  • Mice
  • Prion Diseases / genetics
  • Prion Diseases / metabolism*
  • Prions / chemistry*
  • Prions / metabolism*
  • Protein Conformation
  • Protein Folding*
  • RNA / genetics
  • RNA / isolation & purification
  • RNA / metabolism*
  • Saccharomyces cerevisiae / genetics
  • Scrapie / genetics
  • Scrapie / metabolism
  • Species Specificity


  • Prions
  • RNA
  • Endonucleases