Suc1⁺ Encodes a Predicted 13-Kilodalton Protein that is Essential for Cell Viability and is Directly Involved in the Division Cycle of Schizosaccharomyces pombe

LITERATURE CITED

• Beach, D., B. Durkacz, and P. Nurse. 1982. Functionally homologous cell cycle control genes in budding and fission yeast. Nature (London) 300:706–709.
   PubMed Web of Science ®Google Scholar
• Beach, D., and P. Nurse. 1981. High-frequency transformation of the fission yeast Schizosaccharomyces pombe. Nature (London) 290:140–142.
   PubMed Web of Science ®Google Scholar
• Beach, D., M. Piper, and P. Nurse. 1982. Construction of a Schizosaccharomyces pombe gene bank in a yeast bacterial shuttle vector and its use to isolate genes by complementation. Mol. Gen. Genet. 187:326–329.
   PubMedGoogle Scholar
• Beach, D. H., L. Rodgers, and J. Gould. 1985. ranl+ controls the transition from mitotic division to meiosis in fission yeast. Curr. Genet. 10:297–311.
   PubMedGoogle Scholar
• Beggs, J. D. 1978. Transformation of yeast by a replicating hybrid plasmid. Nature (London) 275:104–108.
   PubMed Web of Science ®Google Scholar
• Berk, A. J., and P. A. Sharp. 1977. Sizing and mapping of early adenovirus mRNAs by gel electrophoresis of S1 endonucleasedigested hybrids. Cell 12:721–732.
   PubMed Web of Science ®Google Scholar
• Booher, R., and D. H. Beach. 1986. Site-specific mutagenesis of cdc2+, a cell cycle control gene of fission yeast Schizosaccharomyces pombe. Mol. Cell. Biol. 6:3523–3530.
   PubMedGoogle Scholar
• Breathnach, R., C. Benoise, K. O'Hare, F. Gannon, and P. Chambon. 1978. Ovalbumin gene. Evidence for a leader sequence in mRNA and DNA sequences at the exon-intron boundaries. Proc. Natl. Acad. Sci. USA 75:4853–4857.
   PubMed Web of Science ®Google Scholar
• Breathnach, R., and P. Chambon. 1981. Eukaryotic split genes. Annu. Rev. Biochem. 50:349–384.
   PubMed Web of Science ®Google Scholar
• Burke, J. F. 1984. High-sensitivity S1 mapping with singlestranded [32P]DNA probes synthesized from bacteriophage M13mp templates. Gene 30:63–68.
   PubMedGoogle Scholar
• Durkacz, B., A. Carr, and P. Nurse. 1986. Transcription of the cdc2 cell cycle control gene of the fission yeast Schizosaccharomyces pombe. EMBO J. 5:369–373.
   PubMed Web of Science ®Google Scholar
• Fukui, Y., and Y. Kaziro. 1985. Molecular cloning and sequence analysis of a ras gene from Schizosaccharomyces pombe. EMBO J. 4:687–691.
   PubMed Web of Science ®Google Scholar
• Gutz, H., H. Heslot, U. Leupold, and N. Loprieno. 1974. Schizosaccharomyces pombe, p. 395–446. In R. C. King (ed.) Handbook of genetics, vol. 1. Plenum Publishing Corp., New York.
   Google Scholar
• Hayles, J., D. H. Beach, B. Durkacz, and P. M. Nurse. 1986. The fission yeast cell cycle control gene cdc2 ; isolation of a sequence Sucl that suppresses cdc2 mutant function. Mol. Gen. Genet. 202:291–293.
   PubMedGoogle Scholar
• Hindley, J., and G. A. Phear. 1984. Sequence of the cell division gene cdc2 from Schizosaccharomyces pombe; patterns of splicing and homology to protein kinases. Gene 31:129–134.
   PubMed Web of Science ®Google Scholar
• Hiraoka, Y., T. Toda, and M. Yanagida. 1984. The NDA3 gene of fission yeast encodes β-tubulin: a cold sensitive nda3 mutation reversibly blocks spindle formation and chromosome movement in mitosis. Cell 39:349–358.
   PubMedGoogle Scholar
• Langford, C. J., F. J. Klinz, C. Donath, and D. Gallwitz. 1984. Point mutations identify conserved, intron-contained TACTAAC box as an essential splicing signal sequence in yeast. Cell 36:645–653.
   PubMed Web of Science ®Google Scholar
• Lörincz, A. T., and S. I. Reed. 1984. Primary structure homology between the product of yeast cell division control gene CDC28 and vertebrate oncogenes. Nature (London) 307:183–185.
   PubMed Web of Science ®Google Scholar
• Losson, R., and F. Lacroute. 1983. Plasmids carrying the yeast OMP decarboxylase structural and regulatory genes: transcription regulation in a foreign environment. Cell 32:371–377.
   PubMedGoogle Scholar
• Maniatis, T., E. F. Fritsch, and J. Sambrook. 1982. Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
   Google Scholar
• Maxam, A. B., and W. Gilbert. 1980. Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol. 65:499–560.
   PubMedGoogle Scholar
• Mitchison, J. M. 1970. Physiological and cytological methods of Schizosaccharomyces pombe, p. 131–165. In D. M. Prescott (ed.), Methods in cell physiology, vol. 4. Academic Press, Inc., New York.
   Google Scholar
• Norrander, J., T. Kempe, and J. Messing. 1983. Construction of improved M13 vectors using oligonucleotide-directed mutagenesis. Gene 26:101–106.
   PubMed Web of Science ®Google Scholar
• Nurse, P., and Y. Bissett. 1981. Gene required in G1 for commitment to cell cycle and in G2 for control of mitosis in fission yeast. Nature (London) 292:558–560.
   PubMed Web of Science ®Google Scholar
• Nurse, P., and P. Thuriaux. 1980. Regulatory genes controlling mitosis in the fission yeast Schizosaccharomyces pombe. Genetics 96:627–637.
   PubMed Web of Science ®Google Scholar
• Reed, S. I., J. A. Hadwiger, and A. T. Lörincz. 1985. Protein kinase activity associated with the product of the yeast cell gene CDC28. Proc. Natl. Acad. Sci. USA 82:4055–4059.
   PubMed Web of Science ®Google Scholar
• Roberts, T., S. Swanberg, A. Poteete, G. Riedel, and L. Backman. 1980. A plasmid cloning vehicle allowing a positive selection for inserted fragments. Gene 12:123–127.
   PubMedGoogle Scholar
• Rothstein, R. 1983. One-step gene disruption in yeast. Methods Enzymol. 101:202–211.
   PubMed Web of Science ®Google Scholar
• Sanger, F., A. R. Coulson, B. G. Barrel, A. J. H Smith, and B. A. Roe. 1980. Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing. J. Mol. Biol. 143:161–178.
   PubMed Web of Science ®Google Scholar
• Simanis, V., and P. Nurse. 1986. The cell cycle control gene cdc2+ of fission yeast encodes a protein kinase potentially regulated by phosphorylation. Cell 45:261–268.
   PubMed Web of Science ®Google Scholar
• Thomas, P. S. 1980. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc. Natl. Acad. Sci. USA 77:5201–5205.
   PubMed Web of Science ®Google Scholar
• Toda, T., Y. Adachi, Y. Hiraoka, and M. Yanagida. 1984. Identification of the pleiotropic cell division cycle gene NDA2 as one of two different α-tubulin genes in Schizosaccharomyces pombe. Cell 36:233–242.
   Google Scholar