Genetic Analysis of chaste, a New Mutation of Drosophila melanogaster Characterized by Extremely Low Female Sexual Receptivity

References

• Artero R., Prokop A., Paricio N., Begemann G., Pueyo I., Mlodzik M., et al. The muscleblind gene participates in the organization of Z-bands and epidermal attachments of Drosophila muscles and is regulated by dmef2. Devel Biol 1998; 195: 131–143
   PubMed Web of Science ®Google Scholar
• Ashburner M., Golic K. G., Hawley R. S. Pairing-dependent phenomena. Drosophila: A Laboratory Handbook2nd edn. CSHL Press, New York 2005; 1051–1073
   Google Scholar
• Baba K., Takeshita A., Majima K., Ueda R., Kondo S., Juni N., et al. The Drosophila Bruton's tyrosine kinase (Btk) homolog is required for adult survival and male genital formation. Mol Cell Biol 1999; 19: 4405–4413
   PubMed Web of Science ®Google Scholar
• Begemann G., Paricio N., Artero R., Kiss I., Pérez-Alonso M., Mlodzik M. muscleblind, a gene required for photoreceptor differentiation in Drosophila, encodes novel nuclar Cys3His-type zinc-finger-containing proteins. Development 1997; 124: 4321–4331
   PubMed Web of Science ®Google Scholar
• Carson H. L. Sexual selection: a driver of genetic change in Hawaiian Drosophila. J Hered 1997; 88: 343–352
   PubMed Web of Science ®Google Scholar
• Conte C., Dastugue B., Vaury C. Promoter competition as a mechanism of transcriptional interference mediated by retrotransposons. EMBO J 2002; 21: 3908–3916
   PubMed Web of Science ®Google Scholar
• Cooley L., Kelly R., Spradling A. Insertional mutagenesis of the Drosophila genome with single P-elements. Science 1988; 239: 1121–1128
   PubMed Web of Science ®Google Scholar
• Cullen B. R., Lomedico P. T., Ju G. Transcriptional interference in avian retroviruses - implications for the promoter insertion model of leukaemogenesis. Nature 1984; 307: 241–245
   PubMed Web of Science ®Google Scholar
• Datta S. R., Vasconcelos M. L., Ruta V., Luo S., Wong A., Demir E., et al. The Drosophila pheromone cVA activates a sexually dimorphic neural circuit. Nature 2008; 452: 473–477
   PubMed Web of Science ®Google Scholar
• Finley K. D., Edeen P. T., Foss M., Gross E., Ghbeish N., Palmer R. H., et al. dissatisfaction encodes a Tailless-like nuclear receptor expressed in a subset of CNS neurons controlling Drosophila sexual behavior. Neuron 1998; 21: 1363–1374
   PubMed Web of Science ®Google Scholar
• Finley K. D., Taylor B. J., Milstein M., McJeiwn M. dissatisfaction, a gene involved in sex-specific behavior and neural development of Drosophila melanogaster. Proc Natl Acad Sci USA 1997; 94: 913–918
   PubMed Web of Science ®Google Scholar
• Fuyama Y. Genetic evidence that ovulation reduces sexual receptivity in Drosophila melanogaster females. Behav Genet 1995; 25: 581–587
   PubMed Web of Science ®Google Scholar
• Geyer P. K., Green M. M., Corces V. G. Tissue-specific transcriptional enhancers may act in trans on the gene located in the homologous chromosome: the molecular basis of transvection in Drosophila. EMBO J 1990; 9: 2247–2256
   PubMed Web of Science ®Google Scholar
• Gould J. L., Gould C. G. Sexual Selection. Scientific American Library, a division of HPHLP, New York 1989
   Google Scholar
• Hall J. C. The mating of a fly. Science 1994; 264: 1702–1714
   PubMed Web of Science ®Google Scholar
• Ho T.H., Charlet-B N., Poulos M.G., Singh G., Swanson I.C., Cooper T.A. Muscleblind proteins regulate alternative splicing. Embo J 2004; 23: 3103–3112
   PubMed Web of Science ®Google Scholar
• Jowett T. Preparation of nucleic acids. Drosophila: A Practical Aapproach. IRL Press, OxfordUK 1986
   Google Scholar
• Kaneshiro K. Speciation in the Hawaiian Drosophila. BioScience 1988; 38: 258–263
   Web of Science ®Google Scholar
• Kania A., Salzberg A., Bhat M., D'Evelyn D., He Y., Kiss I., et al. P-element mutations affecting embryonic peripheral nervous system development in Drosophila melanogaster. Genetics 1995; 139: 1663–1678
   PubMed Web of Science ®Google Scholar
• Kerr C., Ringo J., Dowse H., Johnson E. icebox, a recessive X-linked mutation in Drosophila causing low sexual receptiveness. J Neurogenet 1997; 11: 213–229
   PubMed Web of Science ®Google Scholar
• Kimura K-I., Hachiya T., Koganezawa M., Tazawa T., Yamamoto D. fruitless and doublesex coordinate to generate male-specific neurons that can initiate courtship. Neuron 2008; 59: 759–769
   PubMed Web of Science ®Google Scholar
• Kimura K.I., Ote M., Tazawa T., Yamamoto D. Fruitless specifies sexually dimorphic neural circuitry in the Drosophila brain. Nature 2005; 438: 229–233
   PubMed Web of Science ®Google Scholar
• Kubli E. Sexual behaviour: a receptor for sex control in Drosophila females. Curr Biol 2008; 18: R210–R212
   PubMed Web of Science ®Google Scholar
• Li L. B., Yu Z., Teng X., Bonini N. M. RNA toxicity is a component of ataxin-3 degeneration in Drosophila. Nature 2008; 453: 1107–1111
   PubMed Web of Science ®Google Scholar
• Lindsey D. L., Zimm G. G. The Genome of Drosophila melanogaster. Academic Press, San Diego 1992
   Google Scholar
• Lukacsovich T., Asztalos Z., Awano W., Baba K., Kondo S., Niwa S., et al. Dual-tagging gene-trap of novel genes in Drosophila melanogaster. Genetics 2001; 157: 727–742
   PubMed Web of Science ®Google Scholar
• Morris J. R., Chen J., Filandrinos S. T., Dunn R. C., Fisk R., Geyer P. K., et al. An analysis of transvection at the yellow locus of Drosophila melanogaster. Genetics 1999; 151: 633–651
   PubMed Web of Science ®Google Scholar
• Nakano Y., Fujitani K., Kurihara J., Ragan J., Usui-Aoki K., Shimoda L., et al. Mutations in the novel membrane protein Spinster interfere with programmed cell death and cause neural degeneration in Drosophila melanogaster. Mol Cell Biol 2001; 21: 3775–3778
   PubMed Web of Science ®Google Scholar
• Neckameyer W. Dopamine modulates female sexual receptiveness in Drosophila melanogaster. J Neurogenet 1998; 12: 101–114
   PubMed Web of Science ®Google Scholar
• O'Dell K. M. C. The effect of the inactive mutation on longevity, sex, rhythm, and resistance to p-cresol in Drosophila melanogaster. Heredity 1993; 70: 393–399
   PubMed Web of Science ®Google Scholar
• O'Dell K., Coulon J. F., David J. C., Papin C., Fuzeau-Braesch S., Jallon J.-M. The inactive mutation reduces the level of octopamine in the Drosophila brain. C R Seanc Acad Sci Paris 1987; 305: 199–202
   Google Scholar
• Pirrotta V. Vectors for P-mediated transformation in Drosophila. Vectors: A Survey of Molecular Cloning Vectors and Their Uses, R. L. Rodriguez, D. T. Denhardt. Butterworths, Boston 1988; 437–456
   Google Scholar
• Ringo J. Sexual receptiveness in insects. Ann Rev Entmol 1996; 41: 473–494
   PubMed Web of Science ®Google Scholar
• Ringo J. M., Werczberger R., Altaratz M., Segal D. Female sexual receptiveness is defective in juvenile hormone-deficient mutants of the apterous gene of Drosophila melanogaster. Behav Genet 1991; 21: 453–469
   PubMed Web of Science ®Google Scholar
• Rubin G. M., Spradling A. C. Genetic transformation of Drosophila with transposable element vectors. Science 1982; 218: 348–353
   PubMed Web of Science ®Google Scholar
• Sanders L. E., Arbeitman M. N. doublesex establishes sexual dimorphism in the Drosophila central nervous system in an isoform-dependent manner by directing cell number. Devel Biol 2008; 320: 378–390
   PubMed Web of Science ®Google Scholar
• Shearwin K. E., Callen B. P., Egan J. B. Transcriptional interference—a crash course. Trends Genet 2005; 21: 339–345
   PubMed Web of Science ®Google Scholar
• Suzuki K., Juni N., Yamamoto D. Enhanced mate refusal in female Drosophila induced by a mutation in the spinster locus. Appl Entomol Zool 1997; 32: 235–243
   Web of Science ®Google Scholar
• Thummel C. S., Pirrotta V. New pCaSpeR P element vectors. Dros Inf Serv 1992; 71: 150
   Google Scholar
• Tompkins L., Hall J. C. Identification of brain sites controlling female receptiveness in mosaics of Drosophila melanogaster. Genetics 1983; 103: 179–196
   PubMed Web of Science ®Google Scholar
• Usui-Aoki K., Ito H., Ui-Tei K., Takahashi K., Lukacsovich T., Awano W., et al. Formation of the male-specific muscle in female Drosophila by ectopic fruitless expression. Nat Cell Biol 2000; 2: 500–506
   PubMed Web of Science ®Google Scholar
• Vincente-Crespo M., Pascual M., Fernandez-Costa J.M., Garcia-Lopez A., Monferrer L., et al. Drosophila Muscleblind is involved in troponin T alternative splicing and apoptosis. PLoS ONE 2008; 3: e1613
   PubMed Web of Science ®Google Scholar
• Vincente M., Monferrer L., Poulos M.G., Houselev J., Mockton D.G., O'Dell K.M., et al. Muscleblind isoforms are functionally distinct and regulate (alpha)-actinin splicing. Differentiation 2007; 75: 427–440
   PubMed Web of Science ®Google Scholar
• Yamamoto D., Nakano Y. Sexual behavior mutants revisited: molecular and cellular basis of Drosophila mating. Cell Mol Life Sci 1999; 56: 634–646
   PubMed Web of Science ®Google Scholar
• Yamamoto D., Nakano Y. Genes for sexual behavior. Biochem Biophys Res Commun 1998; 246: 1–6
   PubMed Web of Science ®Google Scholar
• Yamamoto D., Jallon J.-M., Komatsu A. Genetic dissection of mating behavior in Drosophila melanogaster. Ann Rev Entomol 1997; 42: 551–585
   PubMed Web of Science ®Google Scholar
• Yokokura T., Ueda R., Yamamoto D. Phenotypic and molecular characterization of croaker, a new mating behavior mutant of Drosophila melanogaster. Jpn J Genet 1995; 70: 103–117
   PubMedGoogle Scholar