In Xenopus laevis, the Product of a Developmentally Regulated mRNA is Structurally and Functionaly Homologous to a Saccharomyces cerevisiae Protein Involved in Translation Fidelity

REFERENCES

• Akhmaloka and M. F. Tuite. Personal communication.
   Google Scholar
• Bravo, R., and J. Knowland. 1979. Classes of proteins synthe- tized in oocytes, eggs, embryos and differentiated tissues of Xenopus laevis. Differentiation 13:101–108.
   PubMedGoogle Scholar
• Breining, P., and W. Piepersberg. 1986. Yeast omnipotent suppressor SUP1 (SUP45): nucleotide sequence of the wild type and a mutant gene. Nucleic Acids Res. 14:5098–5107.
   Google Scholar
• Camonis, J. H., M. Cassan, and J.-P. Rousset. 1990. Of mice and yeast: versatile vectors which permit gene expression in both budding yeast and higher eukaryotic cells. Gene 86:263–268.
   PubMedGoogle Scholar
• Crouzet, M., F. Izgu, C. M. Grant, and M. F. Tuite. 1988. The allosuppressor gene SAL4 encodes a protein important for maintaining translational fidelity in Saccharomyces cerevisiae. Curr. Genet. 14:537–543.
   PubMed Web of Science ®Google Scholar
• Crouzet, M., and M. F. Tuite. 1987. Genetic control of translational fidelity in yeasts: molecular cloning and analysis of the allosuppressor gene SAL3. Mol. Gen. Genet. 210:581–583.
   PubMedGoogle Scholar
• DeMarini, D. J., M. Winey, D. Ursic, F. Webb, and M. R. Culbertson. 1992. SEN1, a positive effector of tRNA-splicing endonuclease in Saccharomyces cerevisiae. Mol. Cell. Biol. 12:2154–2164.
   PubMed Web of Science ®Google Scholar
• Dessen, P., C. Fondrat, C. Valencien, and C. Mugnier. 1990. BISANCE—a French service for access to biomolecular sequence databases. CABIOS 6:355–356.
   PubMedGoogle Scholar
• Firoozan, M., J. Duarte, C. Grant, and M. F. Tuite. 1991. Quantitation of read through of termination codons in yeast using a novel gene fusion assay. Yeast 7:173–183.
   PubMed Web of Science ®Google Scholar
• Gerlach, W. L. 1975. Mutational properties of some amberochre super-suppressors in Saccharomyces cerevisiae. Mol. Gen. Genet. 138:53–63.
   PubMedGoogle Scholar
• Grenett, H. E., P. Bounelis, and G. M. Fuller. 1992. Identification of a human cDNA with high homology to yeast omnipotent suppressor 45. Gene 110:239–243.
   PubMedGoogle Scholar
• Guarente, L. 1983. Yeast promoters and LacZ constructions designed to study expression of cloned genes in yeast. Methods Enzymol. 101C:181–191.
   Google Scholar
• Gurdon, J. B., and M. P. Wickens. 1983. Use of Xenopus oocytes for the expression of cloned genes. Methods Enzymol. 101:370–386.
   PubMed Web of Science ®Google Scholar
• Harlow, E., and D. Lane. 1988. Antibodies: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
   Google Scholar
• Hawthorne, D. C., and U. Leopold. 1974. Suppressors in yeast. Curr. Top. Microbiol. Immunol. 64:1–47.
   PubMedGoogle Scholar
• Hill, J. E., A. M. Myers, T. J. Koerner, and A. Tzagoloff. 1986. Yeast/E. coli shuttle vectors with multiple unique restriction sites. Yeast 2:163–167.
   PubMed Web of Science ®Google Scholar
• Inge-Vechtomov, S. G., and V. M. Andrianova. 1970. Accessive super-suppressors in yeast. Genetika 6:103–115.
   Google Scholar
• Kress, M. Personal communication.
   Google Scholar
• Leeds, P., S. W. Peltz, A. Jacobson, and M. R. Culbertson. 1991. The product of the yeast UPF1 gene is required for rapid turnover of mRNA containing a premature translational termination codon. Genes Dev. 5:2303–2314.
   PubMed Web of Science ®Google Scholar
• Leeds, P., J. M. Wood, B. S. Lee, and M. R. Culbertson. 1992. Gene products that promote mRNA turnover in Saccharomyces cerevisiae. Mol. Cell. Biol. 12:2165–2177.
   PubMed Web of Science ®Google Scholar
• Le Guellec, R., J. Paris, A. Couturier, C. Roghi, and M. Philippe. 1991. Cloning by differential screening of a Xenopus cDNA that encodes a kinesin-related protein. Mol. Cell. Biol. 11:3395–3398.
   PubMed Web of Science ®Google Scholar
• Lim, S. K., J. J. Mullins, C. M. Chen, K. Gross, and L. E. Maquat. 1989. Nonsense ∞dons in human β-globin result in the production of mRNA degradation products. EMBO J. 8:2613–2619.
   PubMedGoogle Scholar
• Mailer, J. L. 1985. Regulation of amphibian oocyte maturation. Cell Differ. 16:211–221.
   PubMedGoogle Scholar
• Meuler, D. C., and G. M. Malacinski. 1984. Molecular aspects of early development, p. 267–287. Plenum Press, New York.
   Google Scholar
• Miller, J. H. 1972. Experiments in molecular genetics. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
   Google Scholar
• Newport, J., and M. Kirschner. 1982. A major developmental transition in early Xenopus embryos. I. Characterization and timing of cellular changes at the midblastula transition. Cell 30:675–686.
   Google Scholar
• Palmer, E., J. Wilhem, and F. Sherman. 1979. Phenotypic suppression of nonsense mutants in yeast by aminoglycoside antibiotics. Nature (London) 277:148–150.
   PubMedGoogle Scholar
• Paris, J., R. Le Guellec, A. Couturier, K. Le Guellec, F. Omilli, J. Camonis, S. Macneill, and M. Philippe. 1991. Cloning by differential screening of a Xenopus cDNA coding for a protein highly homologous to cdc2. Proc. Natl. Acad. Sci. USA 88:1039–1043.
   PubMedGoogle Scholar
• Paris, J., and M. Philippe. 1990. Poly(A) metabolism and polysomal recruitment of maternal mRNAs during early Xenopus development. Dev. Biol. 140:221–224.
   PubMed Web of Science ®Google Scholar
• Paris, J., H. B. Osborne, A. Couturier, R. Le Guellec, and M. Philippe. 1988. Changes in the polyadenylation of specific stable RNAs during the early development of Xenopus laevis. Gene 72:169–176.
   PubMedGoogle Scholar
• Sanger, F., S. Nicklen, and A. R. Coulson. 1977. DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA 74:5463–5467.
   PubMed Web of Science ®Google Scholar
• Sawin, D. E., K. Le Guellec, M. Philippe, and T. J. Mitchison. 1992. Mitotic spindle organization by a plus-end directed microtubule motor. Nature (London) 359:540–543.
   PubMed Web of Science ®Google Scholar
• Sherman, F., G. R. Fink, and J. B. Hicks. 1986. Laboratory course manual for methods in yeast genetics. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
   Google Scholar
• Sing, A., D. Usric, and J. Davies. 1979. Phenotypic suppression and misreading in Saccharomyces cerevisiae. Nature (London) 277:146–148.
   PubMedGoogle Scholar
• Smith, R. C. 1986. Protein synthesis and messenger RNA levels along the animal—vegetal axis during early Xenopus development. J. Embryol. Exp. Morphol. 95:15–35.
   PubMedGoogle Scholar
• Solomon, M., M. Glotzer, T. H. Lee, M. Philippe, and M. Kirschner. 1990. Cyclin activation of p34cdc2. Cell 63:1013–1024.
   PubMed Web of Science ®Google Scholar
• Studier, F. W., and B. A. Moffat. 1986. Use of bacteriophage T7 RNA polymerase to direct selective high-level of cloned genes. J. Mol. Biol. 189:113–130.
   PubMed Web of Science ®Google Scholar
• Surguchov, A. P. 1988. Omnipotent nonsense suppressors: new clues to an old puzzle. Trends Biol. Sci. 13:120–123.
   PubMedGoogle Scholar
• Tabor, S., and C. C. Richardson. 1985. A bacteriophage T7 RNA polymerase/promoter system for controlled exclusive ex-pression of specific genes. Proc. Natl. Acad. Sci. USA 82:1074–1078.
   PubMed Web of Science ®Google Scholar
• Ter-Avanesgan, M. D., J. Zimmerman, S. G. Inge-Vechtomov, A. B. Sudarikov, V. N. Smirnov, and A. P. Surguchov. 1982. Ribosomal recessive suppressors cause a respiratory deficiency in yeast Saccharomyces cerevisiae. Mol. Gen. Genet. 185:319–323.
   PubMedGoogle Scholar