Complementary Transcripts from Two Genes Necessary for Normal Meiosis in the Yeast Saccharomyces cerevisiae

Literature Cited

• Adelman, J. P., C. T. Bond, J. Douglass, and E. Herbert. 1987. Two mammalian genes transcribed from opposite strands of the same DNA locus. Science 235:1514–1517.
   PubMed Web of Science ®Google Scholar
• Atcheson, C. L., B. DiDomenico, S. Frackman, R. E. Esposito, and R. T. Elder. 1987. Isolation, DNA sequence, and regulation of a meiosis-specific eukaryotic recombination gene. Proc. Natl. Acad. Sci. USA 84:8035–8039.
   PubMedGoogle Scholar
• Bass, B. L., and H. Weintraub. 1988. An unwinding activity that covalently modifies its double-stranded RNA substrate. Cell 55:1089–1098.
   PubMed Web of Science ®Google Scholar
• Cummins, C. M., M. R. Culbertson, and G. Knapp. 1985. Frameshift suppressor mutations outside the anticodon in yeast proline tRNAs containing an intervening sequence. Mol. Cell. Biol. 5:1760–1771.
   PubMedGoogle Scholar
• Cummins, C. M., R. F. Gaber, M. R. Culbertson, R. Mann, and G. R. Fink. 1980. Frameshift suppression in Saccharomyces cerevisiae. III. Isolation and genetic properties of group III suppressors. Genetics 95:855–879.
   PubMedGoogle Scholar
• Dawes, I. W. 1983. Genetic control and gene expression during meiosis and sporulation in Saccharomyces cerevisiae, p. 29–64. In J. F. T. Spencer, D. M. Spencer, and A. W. R. Smith (ed.), Yeast genetics: fundamental and applied aspects. Springer-Verlag, New York.
   Google Scholar
• Earnshaw, W. C. 1987. Anionic regions in nuclear proteins. J. Cell Biol. 105:1479–1482.
   PubMedGoogle Scholar
• Esposito, R. E., and S. Klapholz. 1981. Meiosis and ascospore development, p. 211–287. In J. N. Strathem, E. W. Jones, and J. R. Broach (ed.), The molecular biology of the yeast Saccharomyces: life cycle and inheritance. Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
   Google Scholar
• Garber, A. T., and J. Segall. 1986. The SPS4 gene of Saccharomyces cerevisiae encodes a major sporulation-specific mRNA. Mol. Cell. Biol. 6:4478–4485.
   PubMedGoogle Scholar
• Goebel, M. G., and T. D. Petes. 1986. Most of the yeast genomic sequences are not essential for cell growth and division. Cell 46:983–992.
   PubMedGoogle Scholar
• Gottlin-Ninfa, E., and D. B. Kaback. 1986. Isolation and functional analysis of sporulation-induced transcribed sequences from Saccharomyces cerevisiae. Mol. Cell. Biol. 6:2185–2197.
   PubMedGoogle Scholar
• Green, P. J., O. Pines, and M. Inouye. 1986. The role of antisense RNA in gene regulation. Annu. Rev. Biochem. 55:569–597.
   PubMed Web of Science ®Google Scholar
• Henikoff, S., and M. K. Eghtedarzadeh. 1987. Conserved arrangement of nested genes at the Drosophila gart locus. Genetics 17:711–725.
   Google Scholar
• Henikoff, S., M. A. Keene, K. Fechtel, and J. W. Fristrom. 1986. Gene within a gene: nested Drosophila genes encode unrelated proteins on opposite DNA strands. Cell 44:33–42.
   PubMed Web of Science ®Google Scholar
• Hinnen, A., J. B. Hicks, and G. R. Fink. 1977. Transformation of yeast. Proc. Natl. Acad. Sci. USA 75:1929–1933.
   Google Scholar
• Inouye, M., and N. Delihas. 1988. Small RNAs in the prokaryotes: a growing list of diverse roles. Cell 53:5–7.
   PubMedGoogle Scholar
• Jentsch, S., J. P. McGrath, and A. Varshavsky. 1987. The yeast DNA repair gene RAD6 encodes a ubiquitin-conjugating enzyme. Nature (London) 329:131–134.
   PubMed Web of Science ®Google Scholar
• Kaback, D. B., and L. R. Feldberg. 1985. Saccharomyces cerevisiae exhibits a sporulation-specific temporal pattern of transcript accumulation. Mol. Cell. Biol. 5:751–761.
   PubMed Web of Science ®Google Scholar
• Kimelman, D., and M. W. Kirschner. 1989. An antisense mRNA directs the covalent modification of the transcript encoding fibroblast growth factor in Xenopus oocytes. Cell 59:687–696.
   PubMed Web of Science ®Google Scholar
• Klapholz, S., and R. E. Esposito. 1980. Isolation of spol2-1 and spol3-1 from a natural variant of yeast that undergoes a single meiotic division. Genetics 96:567–588.
   PubMedGoogle Scholar
• Klapholz, S., and R. E. Esposito. 1980. Recombination and chromosome segregation during the single division meiosis in spo12-1 and spo13-1 diploids. Genetics 96:589–611.
   PubMedGoogle Scholar
• Klapholz, S., and R. E. Esposito. 1982. A new mapping method employing a meiotic Rec− mutant of yeast. Genetics 100:387–412.
   PubMed Web of Science ®Google Scholar
• Klapholz, S., C. S. Waddell, and R. E. Esposito. 1985. The role of the SPO11 gene in meiotic recombination in yeast. Genetics 110:187–216.
   PubMed Web of Science ®Google Scholar
• Kunes, S. J., H. Ma, K. Overbye, M. S. Fox, and D. Botstein. 1987. Fine structure recombination analysis of cloned genes using yeast transformation. Genetics 115:73–81.
   PubMedGoogle Scholar
• Law, D. T. S., and J. Segal1. 1988. The SPS100 gene of Saccharomyces cerevisiae is activated late in the sporulation process and contributes to spore wall maturation. Mol. Cell. Biol. 8:912–922.
   PubMed Web of Science ®Google Scholar
• Magee, P. T. 1987. Transcription during meiosis, p. 355–382. In P. Moens (ed.), Meiosis. Academic Press, Inc., New York.
   Google Scholar
• Malone, R. E., and R. E. Esposito. 1981. Recombinationless meiosis in Saccharomyces cerevisiae. Mol. Cell. Biol. 1:891–901.
   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
• McLaughlin, C. S., J. R. Warner, M. Edmonds, H. Hakazato, and M. H. Vaughan. 1973. Polyadenylic acid sequences in yeast messenger ribonucleic acid. J. Biol. Chem. 248:1466–1471.
   PubMedGoogle Scholar
• McNeil, J. G., and M. Smith. 1986. Transcription initiation of the Saccharomyces cerevisiae iso-1-cytochrome c gene: multiple, independent T-A-T-A sequences. J. Mol. Biol. 187:363–378.
   PubMedGoogle Scholar
• Melton, D. A., P. A. Krieg, M. R. Rebagliati, T. Maniatis, K. Zinn, and M. R. Green. 1984. Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 12:7035–7056.
   PubMed Web of Science ®Google Scholar
• Messing, J. 1983. New M13 vectors for cloning. Methods Enzymol. 101:20–78.
   PubMed Web of Science ®Google Scholar
• Miyajima, N., R. Horiuchi, Y. Shibuya, S. Fukushige, K. Matsubara, K. Toyoshima, and T. Yamamoto. 1989. Two erbA homologs encoding proteins with different T3 binding capacities are transcribed from opposite DNA strands of the same genetic locus. Cell 57:31–39.
   PubMed Web of Science ®Google Scholar
• Morrison, A., E. J. Miller, and L. Prakash. 1988. Domain structure and function analysis of the carboxy-terminal polyacidic sequence of the RAD6 protein of Saccharomyces cerevisiae. Mol. Cell. Biol. 8:1179–1185.
   PubMedGoogle Scholar
• Orr-Weaver, T. L., J. W. Szostak, and R. J. Rothstein. 1983. Genetic applications of yeast transformation with linear and gapped plasmids. Methods Enzymol. 101:228–245.
   PubMed Web of Science ®Google Scholar
• Percival-Smith, A., and J. Segall. 1986. Characterization and mutational analysis of a cluster of three genes expressed preferentially during sporulation of Saccharomyces cerevisiae. Mol. Cell. Biol. 6:2443–2451.
   PubMedGoogle Scholar
• Polisky, B. 1988. ColE1 replication control circuitry: sense from antisense. Cell 55:929–932.
   PubMedGoogle Scholar
• Rose, M., and D. Botstein. 1983. Structure and function of the yeast URA3 gene: differentially regulated expression of hybrid β-galactosidase from overlapping coding sequences in yeast. J. Mol. Biol. 170:883–904.
   PubMedGoogle Scholar
• Rothstein, R. 1983. One-step gene disruption in yeast. Methods Enzymol. 101:670–676.
   Google 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
• Spencer, C. A., R. D. Gietz, and R. B. Hodgetts. 1986. Overlapping transcription units in the dopa decarboxylase region of Drosophila. Nature (London) 322:279–281.
   PubMed Web of Science ®Google Scholar
• Stinchcomb, D. T., C. Mann, and R. W. Davis. 1982. Centromeric DNA from Saccharomyces cerevisiae. J. Mol. Biol. 158:157–179.
   PubMed Web of Science ®Google Scholar
• Struhl, K., D. T. Stinchcomb, S. Scherer, and R. W. Davis. 1979. High-frequency transformation of yeast: autonomous replication of hybrid DNA molecules. Proc. Natl. Acad. Sci. USA 76:1035–1039.
   PubMed Web of Science ®Google Scholar
• Sung, P., S. Prakash, and L. Prakash. 1988. The RAD6 protein of Saccharomyces cerevisiae polyubiquitinates histones, and its acidic domain mediates this activity. Genes Dev. 2:1476–1485.
   PubMedGoogle Scholar
• Tollervey, D., J. A. Wise, and C. Guthrie. 1983. A U4-like small nuclear RNA is dispensable in yeast. Cell 35:753–762.
   PubMed Web of Science ®Google Scholar
• Tsuboi, M. 1983. The isolation and genetic analysis of sporulation-deficient mutants in Saccharomyces cerevisiae. Mol. Gen. Genet. 191:17–21.
   PubMedGoogle Scholar
• Wagstaff, J. E., S. Klapholz, and R. E. Esposito. 1982. Meiosis in haploid yeast. Proc. Natl. Acad. Sci. USA 79:2986–2990.
   PubMedGoogle Scholar
• Wang, H.-T., S. Frackman, J. Kowalisyn, R. E. Esposito, and R. Elder. 1987. Developmental regulation of SPO13, a gene required for separation of homologous chromosomes at meiosis I. Mol. Cell. Biol. 7:1425–1435.
   PubMedGoogle Scholar
• Williams, T., and M. Fried. 1986. A mouse locus at which transcription from both DNA strands produces mRNAs complementary at their 3′ ends. Nature (London) 322:275–279.
   PubMed Web of Science ®Google Scholar
• Winston, F., F. Chumley, and G. R. Fink. 1983. Eviction and transplacement of mutant genes in yeast. Methods Enzymol. 101:211–228.
   PubMedGoogle Scholar
• Yamashita, I., and S. Fukui. 1985. Transcriptional control of the sporulation-specific glucoamylase gene in the yeast Saccharomyces cerevisiae. Mol. Cell. Biol. 5:3069–3073.
   PubMed Web of Science ®Google Scholar
• Yarger, J. G., G. Armilei, and M. C. Gorman. 1986. Transcription terminator-like element within a Saccharomyces cerevisiae promoter region. Mol. Cell. Biol. 6:1095–1101.
   PubMedGoogle Scholar
• Yeh, E., J. Carbon, and K. Bloom. 1986. Tightly centromere- linked gene (SPO15) essential for meiosis in the yeast Saccharomyces cerevisiae. Mol. Cell. Biol. 6:158–167.
   PubMedGoogle Scholar