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The SV40 small t intron is accurately and efficiently spliced in tobacco cells

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Abstract

We have introduced the SV40 small t intron into tobacco cells as part of a cauliflower mosaic virus 35S promoter-chloramphenicol acetyltransferase-SV40 transcription unit. We find that the small t intron is efficiently and accurately spliced in transgenic tobacco cells that carry this transcription unit. Our results indicate that there is substantial conservation of RNA processing signals between plants and animals, more than has been previously assumed. They also suggest that pre-mRNA processing in plants requires multiple branch sites for efficient processing.

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References

  1. Barta A, Sommergruber K, Thompson D, Hartmuth K, Matzke MA, Matzke AJM: The expression of a nopaline synthase-human growth hormone chimaeric gene in transformed tobacco and sunflower tissue. Plant Mol Biol 6: 347–357 (1986).

    Google Scholar 

  2. Brown JWS, Feix G, Frendewey D: Accurate in vitro splicing of two pre-mRNA plant introns in a Hela cell nuclear extract. EMBO J 5: 2749–2758 (1986).

    PubMed  Google Scholar 

  3. Goodall GJ, Filipowicz W: The AU-rich sequences present in the introns of plant nuclear pre-mRNAs are required for splicing. Cell 58: 473–483 (1989).

    Article  PubMed  Google Scholar 

  4. Gorman CM, Moffat LF, Howard BH: Recombinant genomes which express choramphenicol acetyltrans-ferase in mammalian cells. Mol Cell Biol 2: 1144–1151 (1982).

    Google Scholar 

  5. Gubler U, Hoffmann BJ: A simple and very effective method for generating cDNA libraries. Gene 25: 263–269 (1983).

    Article  PubMed  Google Scholar 

  6. Hartmuth K, Barta A: In vitro processing of a plant pre-mRNA in a Hela cell nuclear extract. Nucleic Acids Res 14: 7513–7528 (1986).

    PubMed  Google Scholar 

  7. Hunt AG, Chu NM, Odell JT, Nagy F, Chua N-H: Plant cells do not properly recognize animal gene polyadenylation signals. Plant Mol Biol 7: 23–35 (1987).

    Google Scholar 

  8. Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning: A Laboratory Manual (Second Edition). Cold Spring Harbor Laboratory Press, Cold Spring Harbor Laboratory, NY (1989).

    Google Scholar 

  9. Sanger F, Niklen S, Coulson AR: DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74: 5463–5467 (1977).

    PubMed  Google Scholar 

  10. Schardl C, Byrd AD, Benzion G, Altschuler M, Hildebrand DF, Hunt AG: Design and construction of a versatile system for the expression of foreign genes in plants. Gene 61: 1–11 (1987).

    PubMed  Google Scholar 

  11. Tooze J: DNA Tumor Viruses, 2nd ed. Cold Spring Harbor Laboratory Cold Spring Harbor, NY (1981).

    Google Scholar 

  12. Van Santen VL, Spritz RA: Splicing of plant pre-mRNAs in animal systems and vice versa. Gene 56: 253–265 (1987).

    Article  PubMed  Google Scholar 

  13. Wiebauer K, Herrero J-J, Filipowicz W: Nuclear pre-mRNA processing in plants: Distinct modes of 3′-splicesite selection in plants and animals. Mol Cell Biol 8: 2042–2051 (1988).

    PubMed  Google Scholar 

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Hunt, A.G., Mogen, B.D., Chu, N.M. et al. The SV40 small t intron is accurately and efficiently spliced in tobacco cells. Plant Mol Biol 16, 375–379 (1991). https://doi.org/10.1007/BF00023989

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  • DOI: https://doi.org/10.1007/BF00023989

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