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Mating rhythms of Drosophila: rescue of tim(01 )mutants by D. ananassae timeless

BACKGROUND: It is reported that the circadian rhythms of female mating activity differ among Drosophila species and are controlled by an endogenous circadian clock. Here, we found that the mating rhythm of D. ananassae differed from that of D. melanogaster. Moreover, to evaluate the effect of clock...

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Detalles Bibliográficos
Autores principales: Nishinokubi, Izumi, Shimoda, Masami, Ishida, Norio
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1450320/
https://www.ncbi.nlm.nih.gov/pubmed/16522214
http://dx.doi.org/10.1186/1740-3391-4-4
Descripción
Sumario:BACKGROUND: It is reported that the circadian rhythms of female mating activity differ among Drosophila species and are controlled by an endogenous circadian clock. Here, we found that the mating rhythm of D. ananassae differed from that of D. melanogaster. Moreover, to evaluate the effect of clock gene products on mating activities, we examined the mating activity of D. melanogaster timeless (tim(01)) transgenic fly harboring heat-shock promotor driven-D. ananassae timeless (tim) gene (hs-AT tim(01)). METHODS: Flies were maintained under light/dark (LD) cycles for several days and then they were transferred to constant dark (DD) conditions at 25°C. Transformant flies were heat-shocked for 30 min (PZT 10.5–11.0 or PZT 22.5–23.0; PZT means Projected Zeitgeber Time) at 37°C every day. Daily expressions of D. ananassae TIMELESS (TIM) protein in transgenic flies were measured by western blotting. To examine whether the timing of D. ananassae TIM protein induction by heat shock can change the patterns of the behavior activities of D. melanogaster tim(01 )flies, we measured locomotor and mating activity rhythms under DD at 25°C ± 0.5°C except when heat shock was applied. RESULTS: Heat shock applied at PZT 10.5–11.0 and at PZT 22.5–23.0 induced high TIM levels during subjective night and day, respectively, in hs-AT tim(01 )flies. The locomotor rhythm of these flies was changed from diurnal to nocturnal by the timing of D. ananassae TIM induction. However, the mating rhythm of these flies could not be entrained by the timing of D. ananassae TIM induction. CONCLUSION: The pattern of mating activity rhythms of D. ananassae and of D. melanogaster differed. The mating activity rhythms of D. melanogaster tim(01 )flies harboring hs-AT tim appeared after heat-shock but the pattern and phase differed from those of wild-type D. ananassae and D. melanogaster. Moreover, the mating rhythm of these flies could not be entrained by the timing of D. ananassae TIM induction although the locomotor rhythm of hs-AT tim(01 )was changed from diurnal to nocturnal according to the timing of D. ananassae TIM induction. These data suggest that species-specific mating activities require output pathways different from those responsible for locomotor rhythms.