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A discontinuous hammerhead ribozyme embedded in a mammalian messenger RNA

Abstract

Structured RNAs embedded in the untranslated regions (UTRs) of messenger RNAs can regulate gene expression. In bacteria, control of a metabolite gene is mediated by the self-cleaving activity of a ribozyme embedded in its 5′ UTR1. This discovery has raised the question of whether gene-regulating ribozymes also exist in eukaryotic mRNAs. Here we show that highly active hammerhead ribozymes2,3 are present in the 3′ UTRs of rodent C-type lectin type II (Clec2) genes4,5,6,7. Using a hammerhead RNA motif search with relaxed delimitation of the non-conserved regions, we detected ribozyme sequences in which the invariant regions, in contrast to the previously identified continuous hammerheads8,9,10, occur as two fragments separated by hundreds of nucleotides. Notably, a fragment pair can assemble to form an active hammerhead ribozyme structure between the translation termination and the polyadenylation signals within the 3′ UTR. We demonstrate that this hammerhead structure can self-cleave both in vitro and in vivo, and is able to reduce protein expression in mouse cells. These results indicate that an unrecognized mechanism of post-transcriptional gene regulation involving association of discontinuous ribozyme sequences within an mRNA may be modulating the expression of several CLEC2 proteins that function in bone remodelling and the immune response of several mammals.

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Figure 1: Sequence arrangement and secondary structure model of the rodent Clec2d hammerhead ribozymes.
Figure 2: The discontinuous hammerhead ribozyme-containing 3′ UTRs (hcu) self-cleave in vitro.
Figure 3: The discontinuous mouse Clec2 hammerhead ribozymes embedded in the 3′ UTRs downregulate protein expression in vivo.
Figure 4: RT–PCR analysis of the in vivo expression products.

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References

  1. Winkler, W. C. et al. Control of gene expression by a natural metabolite-responsive ribozyme. Nature 428, 281–286 (2004)

    Article  ADS  CAS  Google Scholar 

  2. Khvorova, A., Lescoute, A., Westhof, E. & Jayasena, S. D. Sequence elements outside the hammerhead ribozyme catalytic core enable intracellular activity. Nature Struct. Biol. 10, 708–712 (2003)

    Article  CAS  Google Scholar 

  3. Martick, M. & Scott, W. G. Tertiary contacts distant from the active site prime a ribozyme for catalysis. Cell 126, 309–320 (2006)

    Article  CAS  Google Scholar 

  4. Zhou, H. et al. Osteoclast inhibitory lectin, a family of new osteoclast inhibitors. J. Biol. Chem. 277, 48808–48815 (2002)

    Article  CAS  Google Scholar 

  5. Plougastel, B., Dubbelde, C. & Yokoyama, W. M. Cloning of Clr, a new family of lectin-like genes localized between mouse Nkrp1a and Cd69 . Immunogenetics 53, 209–214 (2001)

    Article  CAS  Google Scholar 

  6. Carlyle, J. R. et al. Missing self-recognition of Ocil/Clr-b by inhibitory NKR-P1 natural killer cell receptors. Proc. Natl Acad. Sci. USA 101, 3527–3532 (2004)

    Article  ADS  CAS  Google Scholar 

  7. Hao, L., Klein, J. & Nei, M. Heterogeneous but conserved natural killer receptor gene complexes in four major orders of mammals. Proc. Natl Acad. Sci. USA 103, 3192–3197 (2006)

    Article  ADS  CAS  Google Scholar 

  8. Przybilski, R. et al. Functional hammerhead ribozymes naturally encoded in the genome of Arabidopsis thaliana . Plant Cell 17, 1877–1885 (2005)

    Article  CAS  Google Scholar 

  9. Rojas, A. A. et al. Hammerhead-mediated processing of satellite pDo500 family transcripts from Dolichopoda cave crickets. Nucleic Acids Res. 28, 4037–4043 (2000)

    Article  CAS  Google Scholar 

  10. Flores, R. et al. Hammerhead ribozyme structure and function in plant RNA replication. Methods Enzymol. 341, 540–552 (2001)

    Article  CAS  Google Scholar 

  11. Gautheret, D., Major, F. & Cedergren, R. Pattern searching/alignment with RNA primary and secondary structures: an effective descriptor for tRNA. Comput. Appl. Biosci. 6, 325–331 (1990)

    CAS  PubMed  Google Scholar 

  12. Eddy, S. R. RNABOB: a program to search for RNA secondary structure motifs in sequence databases. 〈http://selab.janelia.org/software.html〉 (2008)

  13. Zhou, H. et al. A novel osteoblast-derived C-type lectin that inhibits osteoclast formation. J. Biol. Chem. 276, 14916–14923 (2001)

    Article  CAS  Google Scholar 

  14. Carlyle, J. R. et al. Molecular and genetic basis for strain-dependent NK1.1 alloreactivity of mouse NK cells. J. Immunol. 176, 7511–7524 (2006)

    Article  CAS  Google Scholar 

  15. Kent, W. J. et al. The human genome browser at UCSC. Genome Res. 12, 996–1006 (2002)

    Article  CAS  Google Scholar 

  16. Salehi-Ashtiani, K., Luptak, A., Litovchick, A. & Szostak, J. W. A genomewide search for ribozymes reveals an HDV-like sequence in the human CPEB3 gene. Science 313, 1788–1792 (2006)

    Article  ADS  CAS  Google Scholar 

  17. Teixeira, A. et al. Autocatalytic RNA cleavage in the human β-globin pre-mRNA promotes transcription termination. Nature 432, 526–530 (2004)

    Article  ADS  CAS  Google Scholar 

  18. Ferbeyre, G., Smith, J. M. & Cedergren, R. Schistosome satellite DNA encodes active hammerhead ribozymes. Mol. Cell. Biol. 18, 3880–3888 (1998)

    Article  CAS  Google Scholar 

  19. Serganov, A. & Patel, D. J. Ribozymes, riboswitches and beyond: regulation of gene expression without proteins. Nature Rev. Genet. 8, 776–790 (2007)

    Article  CAS  Google Scholar 

  20. Canny, M. D. et al. Fast cleavage kinetics of a natural hammerhead ribozyme. J. Am. Chem. Soc. 126, 10848–10849 (2004)

    Article  CAS  Google Scholar 

  21. Osborne, E. M., Schaak, J. E. & Derose, V. J. Characterization of a native hammerhead ribozyme derived from schistosomes. RNA 11, 187–196 (2005)

    Article  CAS  Google Scholar 

  22. Martick, M. Structural Study of how the Hammerhead Ribozyme Solves the Problem of Catalysis. PhD thesis, Univ. California, 〈http://www.proquest.com/〉 (2007)

    Google Scholar 

  23. Yen, L. et al. Exogenous control of mammalian gene expression through modulation of RNA self-cleavage. Nature 431, 471–476 (2004)

    Article  ADS  CAS  Google Scholar 

  24. Meaux, S. & Van Hoof, A. Yeast transcripts cleaved by an internal ribozyme provide new insight into the role of the cap and poly(A) tail in translation and mRNA decay. RNA 12, 1323–1337 (2006)

    Article  CAS  Google Scholar 

  25. Lockyer, A. E. et al. The phylogeny of the Schistosomatidae based on three genes with emphasis on the interrelationships of Schistosoma Weinland, 1858. Parasitology 126, 203–224 (2003)

    Article  CAS  Google Scholar 

  26. Garneau, N. L., Wilusz, J. & Wilusz, C. J. The highways and byways of mRNA decay. Nature Rev. Mol. Cell Biol. 8, 113–126 (2007)

    Article  CAS  Google Scholar 

  27. Kent, W. J. BLAT–the BLAST-like alignment tool. Genome Res. 12, 656–664 (2002)

    Article  CAS  Google Scholar 

  28. Stern, S., Moazed, D. & Noller, H. F. Structural analysis of RNA using chemical and enzymatic probing monitored by primer extension. Methods Enzymol. 164, 481–489 (1988)

    Article  CAS  Google Scholar 

  29. Larkin, M. A. et al. Clustal W and Clustal X version 2.0. Bioinformatics 23, 2947–2948 (2007)

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We thank M. Hall and K. Chakrabarti for assistance with cell culture, members of Haussler and Ares laboratories for sharing tissue culture space, M. Robertson for the transcriptase and A. Zahler for discussion. This work was supported by the National Institutes of Health grant R01043393.

Author Contributions L.H.H. and M.M. did the sequence searches, designed the study, performed the experiments, analysed the data and wrote the manuscript.

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Correspondence to Monika Martick.

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Martick, M., Horan, L., Noller, H. et al. A discontinuous hammerhead ribozyme embedded in a mammalian messenger RNA. Nature 454, 899–902 (2008). https://doi.org/10.1038/nature07117

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