Skip to main content
Log in

Role for a bidentate ribonuclease in the initiation step of RNA interference

  • Letter
  • Published:

From Nature

View current issue Submit your manuscript

Abstract

RNA interference (RNAi) is the mechanism through which double-stranded RNAs silence cognate genes1,2,3,4,5. In plants, this can occur at both the transcriptional and the post-transcriptional levels1,2,5; however, in animals, only post-transcriptional RNAi has been reported to date. In both plants and animals, RNAi is characterized by the presence of RNAs of about 22 nucleotides in length that are homologous to the gene that is being suppressed6,7,8. These 22-nucleotide sequences serve as guide sequences that instruct a multicomponent nuclease, RISC, to destroy specific messenger RNAs6. Here we identify an enzyme, Dicer, which can produce putative guide RNAs. Dicer is a member of the RNase III family of nucleases that specifically cleave double-stranded RNAs, and is evolutionarily conserved in worms, flies, plants, fungi and mammals. The enzyme has a distinctive structure, which includes a helicase domain and dual RNase III motifs. Dicer also contains a region of homology to the RDE1/QDE2/ARGONAUTE family that has been genetically linked to RNAi9,10.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 1: Generation of 22-nucleotide sequences and degradation of mRNA by distinct enzymatic complexes.
Figure 2: Production of 22-nucleotide sequences by CG4792/Dicer.
Figure 3: Dicer participates in RNAi.

Similar content being viewed by others

References

  1. Baulcombe, D. C. RNA as a target and an initiator of post-transcriptional gene silencing in transgenic plants. Plant Mol. Biol. 32, 79–88 (1996).

    Article  CAS  PubMed  Google Scholar 

  2. Wassenegger, M. & Pelissier, T. A model for RNA-mediated gene silencing in higher plants. Plant Mol. Biol. 37, 349–62 ( 1998).

    Article  CAS  PubMed  Google Scholar 

  3. Montgomery, M. K. & Fire, A. Double-stranded RNA as a mediator in sequence-specific genetic silencing and co-suppression. Trends Genet. 14, 255–258 (1998).

    Article  CAS  PubMed  Google Scholar 

  4. Sharp, P. A. RNAi and double-strand RNA. Genes Dev. 13, 139–141 (1999).

    Article  CAS  PubMed  Google Scholar 

  5. Sijen, T. & Kooter, J. M. Post-transcriptional gene-silencing: RNAs on the attack or on the defense? BioEssays 22, 520–531 (2000).

    Article  CAS  PubMed  Google Scholar 

  6. Hammond, S. M., Bernstein, E., Beach, D. & Hannon, G. J. An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells. Nature 404, 293– 296 (2000).

    Article  ADS  CAS  PubMed  Google Scholar 

  7. Hamilton, A. J. & Baulcombe, D. C. A species of small antisense RNA in posttranscriptional gene silencing in plants. Science 286, 950–952 ( 1999).

    Article  CAS  PubMed  Google Scholar 

  8. Zamore, P. D., Tuschl, T., Sharp, P. A. & Bartel, D. P. RNAi: double-stranded RNA directs the ATP-dependent cleavage of mRNA at 21 to 23 nucleotide intervals. Cell 101, 25–33 (2000).

    Article  CAS  PubMed  Google Scholar 

  9. Tabara, H. et al. The rde-1 gene, RNA interference, and transposon silencing in C. elegans. Cell 99, 123– 132 (1999).

    Article  CAS  PubMed  Google Scholar 

  10. Catalanotto, C., Azzalin, G., Macino, G. & Cogoni, C. Gene silencing in worms and fungi. Nature 404, 245 (2000).

    Article  ADS  CAS  PubMed  Google Scholar 

  11. Tuschl, T., Zamore, P. D., Lehmann, R., Bartel, D. P. & Sharp, P. A. Targeted mRNA degradation by double-stranded RNA in vitro. Genes Dev. 13, 3191 –3197 (1999).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Nicholson, A. W. Function, mechanism and regulation of bacterial ribonucleases. FEMS Microbiol. Rev. 23, 371–390 (1999).

    Article  CAS  PubMed  Google Scholar 

  13. Filippov, V., Solovyev, V., Filippova, M. & Gill, S. S. A novel type of RNase III family proteins in eukaryotes. Gene 245, 213–221 (2000).

    Article  CAS  PubMed  Google Scholar 

  14. Bass, B. L. Double-stranded RNA as a template for gene silencing. Cell 101, 235–238 (2000).

    Article  CAS  PubMed  Google Scholar 

  15. Gillespie, D. E. & Berg, C. A. Homeless is required for RNA localization in Drosophila oogenesis and encodes a new member of the DE-H family of RNA-dependent ATPases. Genes Dev. 9, 2495–2508 (1995).

    Article  CAS  PubMed  Google Scholar 

  16. Jacobsen, S. E., Running, M. P. & Meyerowitz, E. M. Disruption of an RNA helicase/RNAse III gene in Arabidopsis causes unregulated cell division in floral meristems. Development 126, 5231–5243 (1999).

    CAS  PubMed  Google Scholar 

  17. Matsuda, S. et al. Molecular cloning and characterization of a novel human gene (HERNA) which encodes a putative RNA-helicase. Biochim. Biophys. Acta 1490, 163–169 ( 2000).

    Article  CAS  PubMed  Google Scholar 

  18. Wianny, F. & Zernicka-Goetz, M. Specific interference with gene function by double-stranded RNA in early mouse development. Nature Cell Biol. 2, 70–75 (2000).

    Article  CAS  PubMed  Google Scholar 

  19. Sonnhammer, E. L., Eddy, S. R. & Durbin, R. Pfam: a comprehensive database of protein domain families based on seed alignments. Proteins Struct. Funct. Genet. 28, 405–420 (1997).

    Article  CAS  PubMed  Google Scholar 

  20. Cerutti, L., Mian, N. & Bateman, A. Domains in gene silencing and cell differentiation proteins: the novel PAZ domain and redefinition of the Piwi domain. Trends Biochem. Sci. 25, 481–482 (2000).

    Article  CAS  PubMed  Google Scholar 

  21. Bohmert, K. et al. AGO1 defines a novel locus of Arabidopsis controlling leaf development. EMBO J. 17, 170– 180 (1998).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Yang, D., Lu, H. & Erickson, J. W. Evidence that processed small dsRNAs may mediate sequence-specific mRNA degradation during RNAi in Drosophila embryos. Curr. Biol. 10, 1191–1200 ( 2000).

    Article  CAS  PubMed  Google Scholar 

  23. Fagard, M., Bouter, S., Morel, J. B., Bellini, C. & Vaucheret, H. AGO1, QDE-2, and RDE-1 are related proteins required for post-transcriptional gene silencing in plants, quelling in fungi, and RNA interference in animals. Proc. Natl Acad. Sci. USA 97, 11650–11654 (2000).

    Article  ADS  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank A. Nicholson for his gift of purified RNase III, and P. Fisher, M. McConnel and M. Pang for providing aid and materials for large-scale fly embryo culture. The Homeless clone was a gift from D. E. Gillespie and C. A. Berg. We also thank R. Kobayashi and R. Martiennsen for discussion and critical reading of the manuscript, and K. Velinzon for FACS. A.A.C. is an Anderson Fellow of the Watson School of Biological Sciences and a Predoctoral Fellow of the Howard Hughes Medical Institute. S.M.H. is a visiting scientist from Genetica, (Cambridge, MA). G.J.H. is a Pew Scholar in the biomedical sciences. This work was supported in part by grants from the NIH (G.J.H.).

Author information

Authors and Affiliations

Authors

Supplementary information

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bernstein, E., Caudy, A., Hammond, S. et al. Role for a bidentate ribonuclease in the initiation step of RNA interference . Nature 409, 363–366 (2001). https://doi.org/10.1038/35053110

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/35053110

  • Springer Nature Limited

This article is cited by

Navigation