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RESEARCH PRODUCT

Cholinergic Control of Synchronized Seminal Emissions in Drosophila

Yaël GrosjeanJean-françois FerveurClaude EveraertsAngel Acebes

subject

MaleSemen/*metabolismSexual Behavior Animal0302 clinical medicineHuman fertilizationDrosophila ProteinsMatingmedia_commonGenetics0303 health sciencesAgricultural and Biological Sciences(all)ReproductionNuclear ProteinsImmunohistochemistryCell biologyDrosophila melanogasterCholinergic FibersFemaleDrosophila melanogasterGeneral Agricultural and Biological SciencesDrosophila melanogaster/genetics/*metabolism/physiologymedia_common.quotation_subjectFeminization (biology)Sexual BehaviorInvertebrate/physiologyTranscription Factors/geneticsFertilityBiologyCrossesGeneral Biochemistry Genetics and Molecular Biology03 medical and health sciencesGeneticSemenCholinergic Fibers/*metabolism/physiologyAnimalsFeminizationCholinergic neuronReproduction/physiologyCrosses Genetic030304 developmental biologyBiochemistry Genetics and Molecular Biology(all)Animalbiology.organism_classificationSpermGanglia InvertebrateNuclear Proteins/geneticsCholinergicGangliaFeminization/*genetics030217 neurology & neurosurgeryTranscription Factors

description

0960-9822 (Print) Comparative Study Journal Article Research Support, Non-U.S. Gov't; In many animal species, copulation involves the coordinated release of both sperm and seminal fluid, including substances that change female fertility and postmating behavior. In Drosophila melanogaster, these substances increase female fertility and prevent mating with a second male. By using a PGal4 strain, we targeted together with other cells a dozen cholinergic neurons found only in the male abdominal ganglion (Abg-MAch). Genetic feminization apparently deleted these neurons in males and significantly increased their copulation duration, blocked their fertility in 60% of cases, and only weakly repressed remating in females. Genetic repression of Gal4 activity in all cholinergic neurons completely rescued copulation duration and fertility, and totally prevented remating, indicating that Abg-MAch neurons were functional. The conditional blocking of the synaptic activity of these neurons during copulation induced separate effects on the transfer of the seminal substances involved in fertilization and those involved in remating. These effects were dissociated only when Abg-MAch neurons were feminized, indicating that their presence is required to synchronize the emission of the male substance(s) that changes reproductive behaviors.

10.1016/j.cub.2004.04.003http://dx.doi.org/10.1016/j.cub.2004.04.003