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Convergent transcription induces transcriptional gene silencing in fission yeast and mammalian cells

Abstract

We show that convergent transcription induces transcriptional gene silencing (TGS) in trans for both fission yeast and mammalian cells. This method has advantages over existing strategies to induce gene silencing. Previous studies in fission yeast have characterized TGS as a cis-specific process involving RNA interference that maintains heterochromatic regions such as centromeres. In contrast, in mammalian cells, gene silencing is known to occur through a post-transcriptional mechanism that uses exogenous short interfering RNAs or endogenous microRNAs to inactivate mRNA. We now show that the introduction of convergent transcription plasmids into either Schizosaccharomyces pombe or mammalian cells allows the production of double-stranded RNA from inserted gene fragments, resulting in TGS of endogenous genes. We predict that using convergent transcription to induce gene silencing will be a generally useful strategy and allow for a fuller molecular understanding of the biology of TGS.

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Figure 1: S. pombe transformed convergent transcription plasmids are silenced by RNAi.
Figure 2: CTura4 plasmids induce TGS of endogenous ura4 in S. pombe.
Figure 3: Integrated convergent transcription constructs promote endogenous ura4 TGS in trans.
Figure 4: Transfection of mammalian CTura4 plasmid induces ACTG1 TGS.
Figure 5: In vitro and in vivo analysis of nuclear dicer activity.
Figure 6: Specificity of TGS induction by CTγACT1 transfection.
Figure 7: Spatial and temporal properties of plasmid-induced TGS.

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References

  1. Grewal, S.I. RNAi-dependent formation of heterochromatin and its diverse functions. Curr. Opin. Genet. Dev. 20, 134–141 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Baulcombe, D. RNA silencing in plants. Nature 431, 356–363 (2004).

    Article  CAS  PubMed  Google Scholar 

  3. Bartel, D.P. MicroRNAs: target recognition and regulatory functions. Cell 136, 215–233 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Verdel, A., Vavasseur, A., Le Gorrec, M. & Touat-Todeschini, L. Common themes in siRNA-mediated epigenetic silencing pathways. Int. J. Dev. Biol. 53, 245–257 (2009).

    Article  CAS  PubMed  Google Scholar 

  5. Carthew, R.W. & Sontheimer, E.J. Origins and mechanisms of miRNAs and siRNAs. Cell 136, 642–655 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Hutvagner, G. & Simard, M.J. Argonaute proteins: key players in RNA silencing. Nat. Rev. Mol. Cell Biol. 9, 22–32 (2008).

    Article  CAS  PubMed  Google Scholar 

  7. Bühler, M. & Moazed, D. Transcription and RNAi in heterochromatic gene silencing. Nat. Struct. Mol. Biol. 14, 1041–1048 (2007).

    Article  PubMed  Google Scholar 

  8. Gullerova, M. & Proudfoot, N.J. Cohesin complex promotes transcriptional termination between convergent genes in S. pombe. Cell 132, 983–995 (2008).

    Article  CAS  PubMed  Google Scholar 

  9. Gullerova, M., Moazed, D. & Proudfoot, N.J. Autoregulation of convergent RNAi genes in fission yeast. Genes Dev. 25, 556–568 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Gu, S.G. et al. Amplification of siRNA in Caenorhabditis elegans generates a transgenerational sequence-targeted histone H3 lysine 9 methylation footprint. Nat. Genet. 44, 157–164 (2012).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Kavi, H.H., Fernandez, H., Xie, W. & Birchler, J.A. Genetics and biochemistry of RNAi in Drosophila. Curr. Top. Microbiol. Immunol. 320, 37–75 (2008).

    CAS  PubMed  Google Scholar 

  12. Wang, Z., Morris, J.C., Drew, M.E. & Englund, P.T. Inhibition of Trypanosoma brucei gene expression by RNA interference using an integratable vector with opposing T7 promoters. J. Biol. Chem. 275, 40174–40179 (2000).

    Article  CAS  PubMed  Google Scholar 

  13. Alibu, V.P., Storm, L., Haile, S., Clayton, C. & Horn, D. A doubly inducible system for RNA interference and rapid RNAi plasmid construction in Trypanosoma brucei. Mol. Biochem. Parasitol. 139, 75–82 (2005).

    Article  CAS  PubMed  Google Scholar 

  14. Shi, H. et al. Genetic interference in Trypanosoma brucei by heritable and inducible double-stranded RNA. RNA 6, 1069–1076 (2000).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Giordano, E., Rendina, R., Peluso, I. & Furia, M. RNAi triggered by symmetrically transcribed transgenes in Drosophila melanogaster. Genetics 160, 637–648 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  16. Tran, N., Cairns, M.J., Dawes, I.W. & Arndt, G.M. Expressing functional siRNAs in mammalian cells using convergent transcription. BMC Biotechnol. 3, 21 (2003).

    Article  PubMed  PubMed Central  Google Scholar 

  17. Clemens, M.J. PKR—a protein kinase regulated by double-stranded RNA. Int. J. Biochem. Cell Biol. 29, 945–949 (1997).

    Article  CAS  PubMed  Google Scholar 

  18. Jin, J., Cid, M., Poole, C.B. & McReynolds, L.A. Protein mediated miRNA detection and siRNA enrichment using p19. Biotechniques 48, xvii–xxiii (2010).

    Article  CAS  PubMed  Google Scholar 

  19. Simmer, F. et al. Hairpin RNA induces secondary small interfering RNA synthesis and silencing in trans in fission yeast. EMBO Rep. 11, 112–118 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Urosevic, N. Is flavivirus resistance interferon type I-independent? Immunol. Cell Biol. 81, 224–229 (2003).

    Article  CAS  PubMed  Google Scholar 

  21. Bridge, A.J., Pebernard, S., Ducraux, A., Nicoulaz, A.L. & Iggo, R. Induction of an interferon response by RNAi vectors in mammalian cells. Nat. Genet. 34, 263–264 (2003).

    Article  CAS  PubMed  Google Scholar 

  22. Haussecker, D. & Proudfoot, N.J. Dicer-dependent turnover of intergenic transcripts from the human β-globin gene cluster. Mol. Cell Biol. 25, 9724–9733 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  23. Sinkkonen, L., Hugenschmidt, T., Filipowicz, W. & Svoboda, P. Dicer is associated with ribosomal DNA chromatin in mammalian cells. PLoS ONE 5, e12175 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  24. Cobb, B.S. et al. T cell lineage choice and differentiation in the absence of the RNase III enzyme Dicer. J. Exp. Med. 201, 1367–1373 (2005).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Premsrirut, P.K. et al. A rapid and scalable system for studying gene function in mice using conditional RNA interference. Cell 145, 145–158 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Schönborn, J. et al. Monoclonal antibodies to double-stranded RNA as probes of RNA structure in crude nucleic acid extracts. Nucleic Acids Res. 19, 2993–3000 (1991).

    Article  PubMed  PubMed Central  Google Scholar 

  27. Schmitter, D. et al. Effects of Dicer and Argonaute down-regulation on mRNA levels in human HEK293 cells. Nucleic Acids Res. 34, 4801–4815 (2006).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Maida, Y. & Masutomi, K. RNA-dependent RNA polymerases in RNA silencing. Biol. Chem. 392, 299–304 (2011).

    Article  CAS  PubMed  Google Scholar 

  29. Bühler, M., Verdel, A. & Moazed, D. Tethering RITS to a nascent transcript initiates RNAi- and heterochromatin-dependent gene silencing. Cell 125, 873–886 (2006).

    Article  PubMed  Google Scholar 

  30. Iida, T., Nakayama, J. & Moazed, D. siRNA-mediated heterochromatin establishment requires HP1 and is associated with antisense transcription. Mol. Cell 31, 178–189 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Shinagawa, T. & Ishii, S. Generation of Ski-knockdown mice by expressing a long double-strand RNA from an RNA polymerase II promoter. Genes Dev. 17, 1340–1345 (2003).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Nejepinska, J. et al. dsRNA expression in the mouse elicits RNAi in oocytes and low adenosine deamination in somatic cells. Nucleic Acids Res. 40, 399–413 (2012).

    Article  CAS  PubMed  Google Scholar 

  33. Morris, K.V., Chan, S.W., Jacobsen, S.E. & Looney, D.J. Small interfering RNA-induced transcriptional gene silencing in human cells. Science 305, 1289–1292 (2004).

    Article  CAS  PubMed  Google Scholar 

  34. Seila, A.C. et al. Divergent transcription from active promoters. Science 322, 1849–1851 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Core, L.J. & Lis, J.T. Transcription regulation through promoter-proximal pausing of RNA polymerase II. Science 319, 1791–1792 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Preker, P. et al. RNA exosome depletion reveals transcription upstream of active human promoters. Science 322, 1851–1854 (2008).

    Article  CAS  PubMed  Google Scholar 

  37. Janowski, B.A. & Corey, D.R. Inhibiting transcription of chromosomal DNA using antigene RNAs. Nucleic Acids Symp. Ser. (Oxf) 49, 367–368 (2005).

    Article  Google Scholar 

  38. Janowski, B.A. et al. Activating gene expression in mammalian cells with promoter-targeted duplex RNAs. Nat. Chem. Biol. 3, 166–173 (2007).

    Article  CAS  PubMed  Google Scholar 

  39. Yue, X. et al. Transcriptional regulation by small RNAs at sequences downstream from 3′ gene termini. Nat. Chem. Biol. 6, 621–629 (2010).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  40. Alló, M. et al. Control of alternative splicing through siRNA-mediated transcriptional gene silencing. Nat. Struct. Mol. Biol. 16, 717–724 (2009).

    Article  PubMed  Google Scholar 

  41. Tufarelli, C. et al. Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease. Nat. Genet. 34, 157–165 (2003).

    Article  CAS  PubMed  Google Scholar 

  42. Carlile, M. et al. Strand selective generation of endo-siRNAs from the Na/phosphate transporter gene Slc34a1 in murine tissues. Nucleic Acids Res. 37, 2274–2282 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  43. Fukagawa, T. et al. Dicer is essential for formation of the heterochromatin structure in vertebrate cells. Nat. Cell Biol. 6, 784–791 (2004).

    Article  CAS  PubMed  Google Scholar 

  44. Clemens, M.J. & Elia, A. The double-stranded RNA-dependent protein kinase PKR: structure and function. J. Interferon Cytokine Res. 17, 503–524 (1997).

    Article  CAS  PubMed  Google Scholar 

  45. Ashe, H.L., Monks, J., Wijgerde, M., Fraser, P. & Proudfoot, N.J. Intergenic transcription and transinduction of the human β-globin locus. Genes Dev. 11, 2494–2509 (1997).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Mattick, J.S. The genetic signatures of noncoding RNAs. PLoS Genet. 5, e1000459 (2009).

    Article  PubMed  PubMed Central  Google Scholar 

  47. Tam, O.H. et al. Pseudogene-derived small interfering RNAs regulate gene expression in mouse oocytes. Nature 453, 534–538 (2008).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  48. Werner, A. & Sayer, J.A. Naturally occurring antisense RNA: function and mechanisms of action. Curr. Opin. Nephrol. Hypertens. 18, 343–349 (2009).

    Article  CAS  PubMed  Google Scholar 

  49. Faghihi, M.A. & Wahlestedt, C. Regulatory roles of natural antisense transcripts. Nat. Rev. Mol. Cell Biol. 10, 637–643 (2009).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Kaneko, H. et al. DICER1 deficit induces Alu RNA toxicity in age-related macular degeneration. Nature 471, 325–330 (2011).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  51. Giles, K.E., Ghirlando, R. & Felsenfeld, G. Maintenance of a constitutive heterochromatin domain in vertebrates by a Dicer-dependent mechanism. Nat. Cell Biol. 12, 94–99 (2010).

    Article  CAS  PubMed  Google Scholar 

  52. Turner, A.M. & Morris, K.V. Controlling transcription with noncoding RNAs in mammalian cells. Biotechniques 48, ix–xvi (2010).

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We thank T. Gligoris for advice and encouragement, E. White for help with HeLa cell culture and J. Monks for cloning. This work was supported by grants from Cancer Research UK and the Wellcome Trust to N.J.P. and by L'Oreal/UNESCO woman in science UK and Ireland award to M.G.

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M.G. performed all the experimental analyses. M.G. and N.J.P. designed the experiments and wrote the manuscript.

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Correspondence to Monika Gullerova or Nick J Proudfoot.

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Competing interests

Convergent transcription–mediated TGS as described in these studies is the subject of worldwide patent WO/2012/114111 held by ISIS Innovation of Oxford University.

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Gullerova, M., Proudfoot, N. Convergent transcription induces transcriptional gene silencing in fission yeast and mammalian cells. Nat Struct Mol Biol 19, 1193–1201 (2012). https://doi.org/10.1038/nsmb.2392

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