Skip to main content
RNA logoLink to RNA
. 2002 Jun;8(6):842–850. doi: 10.1017/s1355838202024032

Gene silencing using micro-RNA designed hairpins.

Michael T McManus 1, Christian P Petersen 1, Brian B Haines 1, Jianzhu Chen 1, Phillip A Sharp 1
PMCID: PMC1370301  PMID: 12088155

Abstract

During RNA interference (RNAi), long dsRNA is processed to approximately 21 nt duplexes, short interfering RNAs (siRNAs), which silence genes through a mRNA degradation pathway. Small temporal RNAs (stRNAs) and micro-RNAs (miRNAs) are approximately 21 nt RNAs that are processed from endogenously encoded hairpin-structured precursors, and function to silence genes via translational repression. Here we report that synthetic hairpin RNAs that mimic siRNAs and miRNA precursor molecules can target a gene for silencing, and the mechanism of silencing appears to be through mRNA degradation and not translational repression. The sequence and structural configuration of these RNAs are important, and even slight modification in structure can affect the silencing activity of the hairpins. Furthermore, these RNAs are active when expressed by DNA vectors containing polymerase III promoters, opening the possibility for new approaches in stable RNAi-based loss of function studies.

Full Text

The Full Text of this article is available as a PDF (3.3 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Ambros V. Development. Dicing up RNAs. Science. 2001 Aug 3;293(5531):811–813. doi: 10.1126/science.1064400. [DOI] [PubMed] [Google Scholar]
  2. Banerjee Diya, Slack Frank. Control of developmental timing by small temporal RNAs: a paradigm for RNA-mediated regulation of gene expression. Bioessays. 2002 Feb;24(2):119–129. doi: 10.1002/bies.10046. [DOI] [PubMed] [Google Scholar]
  3. Bernstein E., Caudy A. A., Hammond S. M., Hannon G. J. Role for a bidentate ribonuclease in the initiation step of RNA interference. Nature. 2001 Jan 18;409(6818):363–366. doi: 10.1038/35053110. [DOI] [PubMed] [Google Scholar]
  4. Bernstein E., Denli A. M., Hannon G. J. The rest is silence. RNA. 2001 Nov;7(11):1509–1521. [PMC free article] [PubMed] [Google Scholar]
  5. Caplen N. J., Parrish S., Imani F., Fire A., Morgan R. A. Specific inhibition of gene expression by small double-stranded RNAs in invertebrate and vertebrate systems. Proc Natl Acad Sci U S A. 2001 Jul 31;98(17):9742–9747. doi: 10.1073/pnas.171251798. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Chanfreau G., Buckle M., Jacquier A. Recognition of a conserved class of RNA tetraloops by Saccharomyces cerevisiae RNase III. Proc Natl Acad Sci U S A. 2000 Mar 28;97(7):3142–3147. doi: 10.1073/pnas.070043997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Chuang C. F., Meyerowitz E. M. Specific and heritable genetic interference by double-stranded RNA in Arabidopsis thaliana. Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4985–4990. doi: 10.1073/pnas.060034297. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Elbashir S. M., Harborth J., Lendeckel W., Yalcin A., Weber K., Tuschl T. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature. 2001 May 24;411(6836):494–498. doi: 10.1038/35078107. [DOI] [PubMed] [Google Scholar]
  9. Elbashir S. M., Lendeckel W., Tuschl T. RNA interference is mediated by 21- and 22-nucleotide RNAs. Genes Dev. 2001 Jan 15;15(2):188–200. doi: 10.1101/gad.862301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Elbashir S. M., Martinez J., Patkaniowska A., Lendeckel W., Tuschl T. Functional anatomy of siRNAs for mediating efficient RNAi in Drosophila melanogaster embryo lysate. EMBO J. 2001 Dec 3;20(23):6877–6888. doi: 10.1093/emboj/20.23.6877. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Grishok A., Pasquinelli A. E., Conte D., Li N., Parrish S., Ha I., Baillie D. L., Fire A., Ruvkun G., Mello C. C. Genes and mechanisms related to RNA interference regulate expression of the small temporal RNAs that control C. elegans developmental timing. Cell. 2001 Jul 13;106(1):23–34. doi: 10.1016/s0092-8674(01)00431-7. [DOI] [PubMed] [Google Scholar]
  12. Grosshans Helge, Slack Frank J. Micro-RNAs: small is plentiful. J Cell Biol. 2002 Jan 7;156(1):17–21. doi: 10.1083/jcb.200111033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Hutvágner G., McLachlan J., Pasquinelli A. E., Bálint E., Tuschl T., Zamore P. D. A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA. Science. 2001 Jul 12;293(5531):834–838. doi: 10.1126/science.1062961. [DOI] [PubMed] [Google Scholar]
  14. Kennerdell J. R., Carthew R. W. Heritable gene silencing in Drosophila using double-stranded RNA. Nat Biotechnol. 2000 Aug;18(8):896–898. doi: 10.1038/78531. [DOI] [PubMed] [Google Scholar]
  15. Lagos-Quintana M., Rauhut R., Lendeckel W., Tuschl T. Identification of novel genes coding for small expressed RNAs. Science. 2001 Oct 26;294(5543):853–858. doi: 10.1126/science.1064921. [DOI] [PubMed] [Google Scholar]
  16. Lau N. C., Lim L. P., Weinstein E. G., Bartel D. P. An abundant class of tiny RNAs with probable regulatory roles in Caenorhabditis elegans. Science. 2001 Oct 26;294(5543):858–862. doi: 10.1126/science.1065062. [DOI] [PubMed] [Google Scholar]
  17. Lee Nan Sook, Dohjima Taikoh, Bauer Gerhard, Li Haitang, Li Ming-Jie, Ehsani Ali, Salvaterra Paul, Rossi John. Expression of small interfering RNAs targeted against HIV-1 rev transcripts in human cells. Nat Biotechnol. 2002 May;20(5):500–505. doi: 10.1038/nbt0502-500. [DOI] [PubMed] [Google Scholar]
  18. Lee R. C., Ambros V. An extensive class of small RNAs in Caenorhabditis elegans. Science. 2001 Oct 26;294(5543):862–864. doi: 10.1126/science.1065329. [DOI] [PubMed] [Google Scholar]
  19. Lee R. C., Feinbaum R. L., Ambros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell. 1993 Dec 3;75(5):843–854. doi: 10.1016/0092-8674(93)90529-y. [DOI] [PubMed] [Google Scholar]
  20. Mombaerts P., Terhorst C., Jacks T., Tonegawa S., Sancho J. Characterization of immature thymocyte lines derived from T-cell receptor or recombination activating gene 1 and p53 double mutant mice. Proc Natl Acad Sci U S A. 1995 Aug 1;92(16):7420–7424. doi: 10.1073/pnas.92.16.7420. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Myslinski E., Amé J. C., Krol A., Carbon P. An unusually compact external promoter for RNA polymerase III transcription of the human H1RNA gene. Nucleic Acids Res. 2001 Jun 15;29(12):2502–2509. doi: 10.1093/nar/29.12.2502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Paddison Patrick J., Caudy Amy A., Bernstein Emily, Hannon Gregory J., Conklin Douglas S. Short hairpin RNAs (shRNAs) induce sequence-specific silencing in mammalian cells. Genes Dev. 2002 Apr 15;16(8):948–958. doi: 10.1101/gad.981002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Paddison Patrick J., Caudy Amy A., Hannon Gregory J. Stable suppression of gene expression by RNAi in mammalian cells. Proc Natl Acad Sci U S A. 2002 Jan 29;99(3):1443–1448. doi: 10.1073/pnas.032652399. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Paul Cynthia P., Good Paul D., Winer Ira, Engelke David R. Effective expression of small interfering RNA in human cells. Nat Biotechnol. 2002 May;20(5):505–508. doi: 10.1038/nbt0502-505. [DOI] [PubMed] [Google Scholar]
  25. Reinhart B. J., Slack F. J., Basson M., Pasquinelli A. E., Bettinger J. C., Rougvie A. E., Horvitz H. R., Ruvkun G. The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegans. Nature. 2000 Feb 24;403(6772):901–906. doi: 10.1038/35002607. [DOI] [PubMed] [Google Scholar]
  26. Smith N. A., Singh S. P., Wang M. B., Stoutjesdijk P. A., Green A. G., Waterhouse P. M. Total silencing by intron-spliced hairpin RNAs. Nature. 2000 Sep 21;407(6802):319–320. doi: 10.1038/35030305. [DOI] [PubMed] [Google Scholar]
  27. Sui Guangchao, Soohoo Christina, Affar El Bachir, Gay Frédérique, Shi Yujiang, Forrester William C., Shi Yang. A DNA vector-based RNAi technology to suppress gene expression in mammalian cells. Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5515–5520. doi: 10.1073/pnas.082117599. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Svoboda P., Stein P., Hayashi H., Schultz R. M. Selective reduction of dormant maternal mRNAs in mouse oocytes by RNA interference. Development. 2000 Oct;127(19):4147–4156. doi: 10.1242/dev.127.19.4147. [DOI] [PubMed] [Google Scholar]
  29. Svoboda P., Stein P., Schultz R. M. RNAi in mouse oocytes and preimplantation embryos: effectiveness of hairpin dsRNA. Biochem Biophys Res Commun. 2001 Oct 12;287(5):1099–1104. doi: 10.1006/bbrc.2001.5707. [DOI] [PubMed] [Google Scholar]
  30. Tavernarakis N., Wang S. L., Dorovkov M., Ryazanov A., Driscoll M. Heritable and inducible genetic interference by double-stranded RNA encoded by transgenes. Nat Genet. 2000 Feb;24(2):180–183. doi: 10.1038/72850. [DOI] [PubMed] [Google Scholar]
  31. Vaucheret H., Béclin C., Fagard M. Post-transcriptional gene silencing in plants. J Cell Sci. 2001 Sep;114(Pt 17):3083–3091. doi: 10.1242/jcs.114.17.3083. [DOI] [PubMed] [Google Scholar]
  32. Wianny F., Zernicka-Goetz M. Specific interference with gene function by double-stranded RNA in early mouse development. Nat Cell Biol. 2000 Feb;2(2):70–75. doi: 10.1038/35000016. [DOI] [PubMed] [Google Scholar]
  33. Wightman B., Ha I., Ruvkun G. Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans. Cell. 1993 Dec 3;75(5):855–862. doi: 10.1016/0092-8674(93)90530-4. [DOI] [PubMed] [Google Scholar]
  34. Wu H., Yang P. K., Butcher S. E., Kang S., Chanfreau G., Feigon J. A novel family of RNA tetraloop structure forms the recognition site for Saccharomyces cerevisiae RNase III. EMBO J. 2001 Dec 17;20(24):7240–7249. doi: 10.1093/emboj/20.24.7240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Zamore P. D. RNA interference: listening to the sound of silence. Nat Struct Biol. 2001 Sep;8(9):746–750. doi: 10.1038/nsb0901-746. [DOI] [PubMed] [Google Scholar]
  36. Zhang K., Nicholson A. W. Regulation of ribonuclease III processing by double-helical sequence antideterminants. Proc Natl Acad Sci U S A. 1997 Dec 9;94(25):13437–13441. doi: 10.1073/pnas.94.25.13437. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from RNA are provided here courtesy of The RNA Society

RESOURCES