Multiple Products from the shavenbaby-ovo Gene Region of Drosophila melanogaster: Relationship to Genetic Complexity

REFERENCES

• Altschul, S. F., W. Gish, W. Miller, E. W. Myers, and D. J. Lipman. 1990. Basic local alignment search tool. J. Mol. Biol. 215:403–410.
   PubMed Web of Science ®Google Scholar
• Amrein, Η., T. Maniatis, and R. Nöthiger. 1990. Alternatively spliced transcripts of the sex-determining gene tra-2 encode functional proteins of different size. EMBO J. 9:3619–3629.
   PubMed Web of Science ®Google Scholar
• Benton, W. D., and R. W. Davis. 1977. Screening λgt recombinant clones by hybridization to single plaques in situ. Science 196:180–182.
   PubMed Web of Science ®Google Scholar
• Bopp, D., L. R. Bell, T. W. Cline, and P. Schedl. 1991. Developmental distribution of female-specific Sex-lethal proteins in Drosophila melanogaster. Genes Dev. 5:403–415.
   PubMed Web of Science ®Google Scholar
• Brown, N. H., and F. C. Kafatos. 1988. Functional cDNA libraries from Drosophila embryos. J. Mol. Biol. 203:425–437.
   PubMed Web of Science ®Google Scholar
• Busson, D., M. Gans, K. Komitopoulou, and M. Masson. 1983. Genetic analysis of three dominant female sterile mutations located on the X-chromosome of Drosophila melanogaster. Genetics 105:309–325.
   PubMedGoogle Scholar
• Cavener, D. R., and S. C. Ray. 1991. Eukaryotic start and stop translation sites. Nucleic Acids Res. 19:3185–3192.
   PubMed Web of Science ®Google Scholar
• Cherbas, L., and P. Cherbas. 1993. The arthropod initiator: the capsite consensus plays an important role in transcription. Insect Biochem. Mol. Biol. 23:81–90.
   PubMedGoogle Scholar
• Cline, T. W. 1993. The Drosophila sex determination signal: how do flies count to two? Trends Genet. 9:385–390.
   PubMedGoogle Scholar
• Davis, R. W., D. Botstein, and J. R. Roth. 1980. Advanced bacterial genetics, a manual for genetic engineering. Cold Spring Harbor Press, Cold Spring Harbor, N.Y.
   Google Scholar
• Freund, R., and M. Meselson. 1984. Long terminal repeat nucleotide sequence and specific insertion of the gypsy transposon. Proc. Natl. Acad. Sci. USA 81:4462–4464.
   PubMedGoogle Scholar
• Frohman, M. A., M. K. Dush, and G. R. Martin. 1988. Rapid amplification of cDNA ends. Proc. Natl. Acad. Sci. USA 85:8998–9002.
   PubMed Web of Science ®Google Scholar
• Garfinkel, M. D., A. R. Lobe, and A. P. Mahowald. 1992. Molecular genetics of the Drosophila melanogaster ovo locus, a gene required for sex determination of germline cells. Genetics 130:791–803.
   PubMedGoogle Scholar
• Granadino, B., P. Santamaria, and L. Sánchez. 1993. Sex determination in the germ line of Drosophila melanogaster: activation of the gene Sex-lethal. Development 118:813–816.
   PubMedGoogle Scholar
• Harvey, R. J., and M. G. Darlison. 1991. Random-primed cDNA synthesis facilitates the isolation of multiple 5′-cDNA ends by RACE. Nucleic Acids. Res. 19:4002.
   PubMedGoogle Scholar
• Huynh, T. V., R. A. Young, and R. W. Davis. 1985. Constructing and screening cDNA libraries in λgt10 and λgt11, p. 49–78. In D. M. Glover (ed.), DNA cloning, a practical approach, vol. 1. IRL Press, Oxford.
   Google Scholar
• Jain, R., and R. H. Gomer. 1992. Increasing specificity from the PCR-RACE technique. BioTechniques 12:58–59.
   PubMedGoogle Scholar
• Mahowald, A. P., and M. P. Kambysellis. 1980. Oogenesis, p. 141–224. In M. Ashburner, and T. R. F. Wright (ed.), The genetics and biology of Drosophila, vol. 2d. Academic Press, London.
   Google Scholar
• Maniatis, T., E. F. Fritsch, and J. Sambrook. 1982. Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
   Google Scholar
• Mattox, W. W., M. J. Palmer, and B. S. Baker. 1990. Alternative splicing of the sex determination gene tra-2 is sex-specific in the germ line but not in the soma. Genes Dev. 4:789–805.
   PubMed Web of Science ®Google Scholar
• McKeown, M., J. M. Belote, and R. T. Boggs. 1988. Ectopic expression of the female transformer gene product leads to female differentiation of chromosomally male Drosophila. Cell 53:887–895.
   PubMed Web of Science ®Google Scholar
• Mevel-Ninio, M., M. C. Mariol, and M. Gans. 1989. Mobilization of the gypsy and copia retrotransposons in Drosophila melanogaster induces reversion of the ovoD dominant female-sterile mutations: molecular analysis of revertant alleles. EMBO J. 8:1549–1558.
   PubMedGoogle Scholar
• Mevel-Ninio, M., R. Terracol, and F. C. Kafatos. 1991. The ovo gene of Drosophila encodes a zinc finger protein required for female germ line development. EMBO J. 10:2259–2266.
   PubMedGoogle Scholar
• Mount, S. M., C. Burks, G. Hertz, G. D. Stormo, O. White, and C. Fields. 1992. Splicing signals in Drosophila: intron size, information content, and consensus sequences. Nucleic Acids Res. 20:4255–4262.
   PubMed Web of Science ®Google Scholar
• Oliver, B., Y.-J. Kim, and B. S. Baker. 1993. Sex-lethal, master and slave: a hierarchy of germline sex determination in Drosophila. Development 119:897–908.
   PubMedGoogle Scholar
• Oliver, B., D. Pauli, and A. P. Mahowald. 1990. Genetic evidence that the ovo locus is involved in Drosophila germ line sex determination. Genetics 125:535–550. (Corrigendum, 126:477.)
   PubMedGoogle Scholar
• Oliver, B., N. Perrimon, and A. P. Mahowald. 1987. The ovo locus is required for sex-specific germline maintenance in Drosophila. Genes Dev. 1:913–923.
   PubMed Web of Science ®Google Scholar
• Pauli, D., and A. P. Mahowald. 1990. Germ-line sex determination in Drosophila melanogaster. Trends Genet. 6:259–264.
   PubMed Web of Science ®Google Scholar
• Proudfoot, N., and G. G. Brownlee. 1976. 3′ non-coding region sequences in eukaryotic messenger RNA. Nature (London) 263:211–214.
   PubMed Web of Science ®Google Scholar
• Ptashne, M. 1988. How eukaryotic transcription activators work. Nature (London) 335:683–689.
   PubMed Web of Science ®Google Scholar
• Sambrook, J., E. F. Fritsch, and T. Maniatis. 1989. Molecular cloning: a laboratory manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.
   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
• Schuster, D. M., G. W. Buchman, and A. Rashtchian. 1992. A simple and efficient method for amplification of cDNA ends using 5′ RACE. Focus 14:46–52.
   Google Scholar
• Steinhauser, W. R., R. C. Walsh, and L. J. Kalfayan. 1989. Sequence and structure of the Drosophila melanogaster ovarian tumor gene and generation of an antibody specific for the ovarian tumor protein. Molec. Cell. Biol. 9:5726–5732.
   PubMedGoogle Scholar
• Steinmann-Zwicky, M. 1992. How do germ cells choose their sex: Drosophila as a paradigm. BioEssays 14:513–518.
   PubMed Web of Science ®Google Scholar
• Steinmann-Zwicky, M. 1993. Sex determination in Drosophila: sis-b, a major numerator element of the X:A ratio in the soma, does not contribute to the X:A ratio in the germ line. Development 117:763–767.
   PubMedGoogle Scholar
• Steinmann-Zwicky, M., H. Schmid, and R. Nöthiger. 1989. Cell-autonomous and inductive signals can determine the sex of the germ line of Drosophila by regulating the gene Sxl. Cell 57:157–166.
   PubMedGoogle Scholar
• Tautz, D., and C. Pfeifle. 1989. A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback. Chromosoma 98:81–85.
   PubMed Web of Science ®Google Scholar
• Wei, G., B. Oliver, and A. P. Mahowald. 1991. Gonadal dysgenesis reveals sexual dimorphism in the embryonic germline of Drosophila. Genetics 129:203–210.
   PubMedGoogle Scholar
• Wei, G., B. Oliver, D. Pauli, and A. P. Mahowald. 1994. Evidence for sex transformation of germline cells in ovarian tumor mutants of Drosophila. Dev. Biol. 161:318–320.
   PubMedGoogle Scholar
• Wharton, K. A., B. Yedvobnick, V. G. Finnerty, and S. Artavanis-Tsakonas. 1985. opa: a novel family of transcribed repeats shared by the Notch locus and other developmentale regulated loci in D. melanogaster. Cell 40:55–62.
   PubMedGoogle Scholar
• Wieschaus, E., C. Nüsslein-Volhard, and G. Jurgens. 1984. Mutations affecting the pattern of the larval cuticle in Drosophila melanogaster. III. Zygotic loci on the X-chromosome and the fourth chromosome. Wilhelm Roux's Arch. Dev. Biol. 193:296–307.
   PubMedGoogle Scholar