Abstract
UNDERSTANDING the mechanisms by which ribozymes catalyse chemical reactions requires a detailed knowledge of their structure. The secondary structure of the group I introns has been confirmed by comparison of over 70 published sequences1–4, by chemical protection studies5, and by genetic experiments involving compensatory mutations2,6,7. Phylogenetic data can also be used to identify tertiary interactions in RNA molecules. This was first done by Levitt8, who predicted tertiary interactions in transfer RNA, which were subsequently confirmed by X-ray crystallography9. More recently, sequence comparison data have been used to predict tertiary interactions in ribosomal RNA10. We have searched a complete alignment of the core regions of group I introns1,2 for evolutionary covariations that could not be ascribed to classical Watson–Crick or wobble base pairings. Here we describe two examples of phylogenetic covariation that are most simply explained by postulating hydrogen-bonded base-triples similar to those found in tRNA. Genetic experiments with the Tetrahymena and sunY introns confirm the importance of these interactions for the structure of the ribozyme.
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References
Cech, T. R. Gene 73, 259–271 (1988).
Couture, S. et al. J. molec. Biol. in the press.
Michel, F., Jacquier, A. & Dujon, B. Biochimie 64, 867–881 (1982).
Davies, R. W., Waring, R. B., Ray, J. A., Brown, T. A. & Scazzocchio, C. Nature 300, 719–724 (1982).
Inoue, T. & Cech, T. R. Proc. natn. Acad. Sci. U.S.A. 82, 648–652 (1985).
Williamson, C. L., Tierney, W. M., Kerker, J. & Burke, J. M. J. biol. Chem. 262, 14672–14682 (1987).
Flor, P. J., Flanegan, J. B. & Cech, T. R. EMBO J. 8, 3391–3399 (1989).
Levitt, M. Nature 224, 759–763 (1969).
Klug, A., Ladner, J. & Robertus, J. D. J. molec. Biol. 89, 511–516 (1974).
Woese, C. R. & Gutell, R. R. Proc. natn. Acad. Sci. U.S.A. 87, 663–667 (1990).
Shub, D. A. et al. Proc. natn. Acad. Sci. U.S.A. 85, 1151–1155 (1988).
Doudna, J. A., Gerber, A. S., Cherry, J. M. & Szostak, J. W. in Cold Spring Harbor Symp. quant. Biol. 52, 173–180 (1987).
Burke, J. M. et al. Nucleic Acids Res. 15, 7217–7221 (1987).
Kunkel, T. A. Proc. natn. Acad. Sci. U.S.A. 82, 488–492 (1985).
Michel, F., Netter, P., Xu, M.-Q. & Shub, D. Genes Dev. 4, 777–788 (1990).
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Michel, F., Ellington, A., Couture, S. et al. Phylogenetic and genetic evidence for base-triples in the catalytic domain of group I introns. Nature 347, 578–580 (1990). https://doi.org/10.1038/347578a0
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DOI: https://doi.org/10.1038/347578a0
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