Identification and Characterization of Inebriated, a Gene Affecting Neuronal Excitability in Drosophila

References

• Atkinson N., Robertson G., Ganetzky B. A component of Calcium-activated potassium channels encoded by the Drosophila slo locus. Science 1991; 254: 551–555
   PubMedGoogle Scholar
• Baumann A., Krah-Jentgens I., Muller F., Muller-Holtkamp F., Seidel R., Kecskemethy N., Casal J., Ferrus A., Pongs O. Molecular organization of the maternal effect region of the Shaker complex of Drosophila: characterization of an IA channel transcript with homology to vertebrate Na+ channel. EMBO J. 1987; 6: 3419–3429
   PubMed Web of Science ®Google Scholar
• Belardetti F., Kandel E. R., Siegelbaum S. A. Neuronal inhibition by the peptide FMRFamide involves opening S-K+ channels. Nature 1987; 325: 153–156
   PubMedGoogle Scholar
• Benoit P. R., Mambrini J. Modification of transmitter release by ions which prolong the presynaptic action potential. J. Physiol. 1970; 213: 21–30
   Google Scholar
• Budnik V., Zhong Y., Wu C.-F. Morphological plasticity of motor axons in Drosophila mutants with altered excitability. J. Neurosci. 1990; 10: 3754–3768
   PubMed Web of Science ®Google Scholar
• Butler A., Wei A., Baker K., Salkoff L. A family of putative potassium channel genes in. Drosophila Science 1989; 243: 943–947
   PubMedGoogle Scholar
• Coombs J., Scheuer T., Rossie S., Catterall W. A. Evidence that cAMP-dependent phos-phorylation promotes sodium channel inactivation in embryonic rat brain cells in primary cultures. Biophys. J 1988; 53: 542a
   Google Scholar
• Datyner N. B., Gage P. W. Phasic secretion of acetylcholine at a mammalian neuromuscular junction. J Physiol. 1980; 303: 299–314
   PubMedGoogle Scholar
• Elkins T., Ganetzky B. The roles of potassium currents in Drosophila flight muscles. J Neurosci 1988; 8: 428–434
   PubMed Web of Science ®Google Scholar
• Elkins T., Zinn K., McAllister L., Hoffmann F. M., Goodman C. S. Genetic analysis of a Drosophila neural cell adhesion molecule: interaction of Fasciclin I and Abelson tyrosine kinase mutations. Cell 1990; 60: 565–575
   PubMed Web of Science ®Google Scholar
• Ganetzky B. Genetics of membrane excitability in Drosophila: lethal interactions between two temperature-sensitive paralytic mutations. Genetics 1984; 108: 897–911
   PubMedGoogle Scholar
• Ganetzky B., Wu C.-F. Indirect suppression involving behavioral mutants with altered nerve excitability in Drosophila. Genetics 1982a; 100: 597–614
   PubMed Web of Science ®Google Scholar
• Ganetzky B., Wu C.-F. Drosophila mutants with opposing effects on nerve excitability: Genetic and spatial interactions in repetitive firing. J Neurophys 1982b; 47: 501–514
   PubMed Web of Science ®Google Scholar
• Ganetzky B., Wu C.-F. Neurogenetic analysis of potassium currents in Drosophila: Synergistic effects on neuromuscular transmission in double mutants. J. Neurogenet 1983; 1: 17–28
   PubMed Web of Science ®Google Scholar
• Garber S. S., Hoshi T., Aldrich R. W. Interaction of forskolin with voltage-gated K+ channels in PC12 cells. J. Neurosci. 1990; 10: 3361–3368
   PubMedGoogle Scholar
• Gertler F. B., Bennett R. L., Clark M. J., Hoffmann F. M. Drosophila abl tryrosine kinase in embryonic CNS axons: a role in axonogenesis is revealed through dosage sensitive interactions with. disabled. Cell 1989; 58: 103–113
   PubMedGoogle Scholar
• Harris W. R. Forskolin reduces a transient potassium current in lobster neurons by a cAMP-independent mechanism. Brain Res 1989; 489: 59–66
   PubMedGoogle Scholar
• Hoshi T., Garber S. S., Aldrich R. W. Effect of forskolin on voltage-gated K+ channel is independent of adenylae cyclase activation. Science 1988; 240: 1652–1655
   PubMed Web of Science ®Google Scholar
• Jan L. Y., Jan Y. N. Properties of the larval neuromuscular junction in. Drosophila melanogaster. J. Physiol. 1976; 262: 189–214
   Google Scholar
• Jan Y. N., Jan L. Y., Dennis M. J. Two mutations of synaptic transmission in. Drosophila Proc. R. Soc. Lond. Ser. B 1977; 198: 87–108
   PubMed Web of Science ®Google Scholar
• Jan Y. N., Jan L. Y. Genetic dissection of short-term and long-term facilitation at the Drosophila neuromuscular junction. Proc. Natl. Acad. Sci. USA 1978; 75: 515–519
   PubMedGoogle Scholar
• Jan Y. N., Jan L. Y. Genetic dissection of synaptic transmission in Drosophila melanogaster. Insect Neurobiology and Pesticide Actions, F. E. Rickett. Society of Chemical Industry, London 1979; 161–168
   Google Scholar
• Kamb A., Iverson L. E., Tanouye M. A. Molecular characterization of Shaker, a Drosophila gene that encodes a potassium channel. Cell 1987; 50: 405–413
   PubMed Web of Science ®Google Scholar
• Kaplan W. D., Trout I W.E, II. The behavior of four neurological mutants of Drosophila. Genetics 1969; 61: 399–409
   PubMed Web of Science ®Google Scholar
• Katz B., Miledi R. The release of acetylcholine from nerve endings by graded electrical pulses. Proc. R. Soc. B. 1967a; 167: 23–38
   PubMedGoogle Scholar
• Katz B., Miledi R. A study of synaptic transmission in the absence of nerve impulses. J. Physiol 1967b; 192: 407–436
   PubMed Web of Science ®Google Scholar
• Krause D., Lee S. C., Deutsch C. Forskolin effects on the voltage-gated K+ conductance of human T cells. Pflugers Arch. 1988; 412: 133–140
   PubMedGoogle Scholar
• Latorre R., Oberhauser A., Labarca P., Alvarez O. Varieties of calcium-activated potassium channels. Annu. Rev. Physiol. 1989; 51: 358–399
   Google Scholar
• Loughney K., Kreber R., Ganetzky B. Cloning and sequence analysis of the para locus, a sodium channel gene in Drosophila. Cell 1989; 58: 1143–1154
   PubMed Web of Science ®Google Scholar
• Mallart A., Angautpetit D., Bourretpoulain C., Ferrus A. Nerve Terminal Excitability and Neuromuscular Transmission in T(X; Y)V7 and Shaker Mutants of. Drosophila-elanogaster. J Neurogenet. 1991; 7: 75–84
   PubMed Web of Science ®Google Scholar
• Miller R. J. Receptor-mediated regulation of calcium channels and neurotransmitter release. FASEB J. 1990; 4: 3291–3299
   PubMed Web of Science ®Google Scholar
• Papazian D. M., Schwarz T. L., Tempel B. L., Jan Y. N., Jan L. Y. Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene from. Drosophila. Science 1987; 237: 749–753
   PubMed Web of Science ®Google Scholar
• Rudy B. Diversity and ubiquity of K channels. Neuroscience 1988; 25: 729–749
   PubMed Web of Science ®Google Scholar
• Salkoff L., Wyman R. Genetic modification of potassium channels in Drosophila Shaker mutants. Nature 1981; 293: 228–230
   PubMed Web of Science ®Google Scholar
• Saito M., Wu C.-F. The slo mutation alters membrance excitability and Ca-activated K currents in cultures of Drosophila “giant” neurons. Soc. Neurosci. Abstr. 1990; 16: 670
   Google Scholar
• Siegelbaum S. A., Camardo J., Kandel E. R. Serotonin and cyclic AMP close single K channels in Aplysia sensory neurones. Nature 1982; 299: 413–417
   PubMed Web of Science ®Google Scholar
• Singh S., Wu C.-F. Complete separation of four potassium currents in Drosophila. Neuron 1989; 2: 1325–1329
   PubMed Web of Science ®Google Scholar
• Standen N., Quayle J., Davies N., Brayden J., Huang Y., Nelson M. Hyperpolarizing vasodilators activate ATP-sensitive K channels in arterial smooth muscle. Science 1989; 245: 177–180
   PubMed Web of Science ®Google Scholar
• Stern M., Ganetzky B. Altered synaptic transmission in Drosophila Hyperkinetic mutants. J Neurogenet. 1989; 5: 215–228
   PubMed Web of Science ®Google Scholar
• Stern M., Kreber R., Ganetzky B. Dosage effects of a Drosophila sodium channel gene on behavior and axonal excitability. Genetics 1990; 124: 133–143
   Google Scholar
• Tempel B. L., Papazian D. M., Schwarz T. L., Jan Y. N., Jan L. Y. Sequence of a probable potassium channel component encoded at the Shaker locus of. Drosophila. Science 1987; 237: 770–775
   PubMed Web of Science ®Google Scholar
• Timpe L. C., Jan L. Y. Gene dosage and complementation analysis of the Shaker locus in Drososphila. J Neurosci 1987; 7: 1307–1317
   PubMed Web of Science ®Google Scholar
• Warmke J., Drysdale R., Ganetzky B. A distinct potassium channel polypeptide encoded by the Drosophila eag locus. Science 1991; 252: 1560–1562
   PubMed Web of Science ®Google Scholar
• White M. M. Forskolin alters acetylcholine receptor gating by a mechanism independent of adenylate cyclase activation. Molec. Pharmacol. 1988; 34: 427–430
   PubMedGoogle Scholar
• Wu C.-F., Ganetzky B., Jan L. Y., Jan Y. N., Benzer S. A Drosophila mutant with a temperature-sensitive block in nerve conduction. Proc. Natl. Acad. Sci. U.S.A. 1978; 75: 4047–4051
   PubMed Web of Science ®Google Scholar
• Wu C.-F., Ganetzky B., Haugland F., Liu A.-X. Potassium currents in Drosophila: Different components affected by mutations in two genes. Science 1983; 220: 1076–1078
   PubMed Web of Science ®Google Scholar
• Wu C.-F., Haugland F. N. Voltage clamp analysis membrane currents in larval muscle fibers of Drosophila: alterations of potassium currents in Sh mutants. J. Neurosci. 1985; 5: 2626–2640
   PubMed Web of Science ®Google Scholar
• Wu C.-F., Tsai M.-C., Chen M.-L., Zhong Y., Singh S., Lee C. Y. Actions of dendrotoxin on K+ channels and neuromuscular transmission in Drosophila melanogaster, and its effects in synergy with K+ channel-specific drugs and mutations. J. Exp. Biol 1989; 147: 21–41
   PubMedGoogle Scholar
• Yatani A., Codina J., Brown A. M., Birnbaumer L. Direct activation of mammalian atrial muscarinic potassium channels by GTP regulatory protein GK-. Science 1987; 235: 207–211
   PubMed Web of Science ®Google Scholar
• Zhong Y., Wu C.-F. Alteration of four identified K1 currents in Drosophila muscle by mutations in. eag. Science 1991; 252: 1562–1564
   PubMed Web of Science ®Google Scholar