Abstract
The Drosophila fruitless (fru) gene product Fru has been postulated to be a neural sex determination factor that directs development of the central nervous system (CNS), thereby producing male-typical courtship behaviour and inducing male-specific muscle1,2,3,4,5,6. Male-specific Fru protein is expressed in small groups of neurons scattered throughout the CNS of male, but not female, Drosophila4,7. Collectively, these observations suggest that Fru ‘masculinizes’ certain neurons, thereby establishing neural substrates for male-typical behaviour. However, specific differences between neurons resulting from the presence or absence of Fru are unknown. Previous studies have suggested that Fru might result in sexual differences in the CNS at the functional level, as no overt sexual dimorphism in CNS structure was discernible8,9,10. Here we identify a subset of fru-expressing interneurons in the brain that show marked sexual dimorphism in their number and projection pattern. We also demonstrate that Fru supports the development of neurons with male-specific dendritic fields, which are programmed to die during female development as a result of the absence of Fru. Thus, Fru expression can produce a male-specific neural circuit, probably used during heterosexual courtship, by preventing cell death in identifiable neurons.
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Acknowledgements
We thank E. Nilsson for critical reading of the manuscript, J. Maeyama and E. Matsuda for their participation in the early stages of this work, and M. Haga for technical assistance. We also thank K. Ito for the NP21 strain, A. Gould for the Df(3L)H99 FRT A2 strain, K. White for the Df(3L)XR38 strain, H. Steller for the hidA206 strain, A. Hofbauer for the monoclonal nc82 antibody, T. Awasaki, the Bloomington and Kyoto Stock Centers for Drosophila strains, and H. Aonuma for allowing us access to a confocal microscope. This work was supported in part by Special Cooperation Funds for Promoting Science and Technology from MEXT (Ministry of Education, Culture, Sports, Science and Technology in Japan) to K.-I.K. and D.Y.
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Supplementary information
Supplementary Figure S1
This figure shows different patterns of projections observed in the male mAL neurons. Eight types are distinguishable. (DOC 338 kb)
Supplementary Figure S2
This figure shows the involvement of fru in the formation of mAL sexual dimorphism. Phenotipic analysis shows that NP21 is an allele of fruitless. (DOC 415 kb)
Supplementary Figure S3
This figure shows that the mAL neurons which escaped from cell death in females do not express Fru. (DOC 139 kb)
Supplementary Figure S4
This figure shows that male-specific neurons in optic lobe are transmedullary (Tm) neurons connecting the distal medulla with lobula regions. The Tm neurons are present just as in males when cell death was blocked in females and they are not present in the fru mutant male. (DOC 164 kb)
Supplementary Table S1
This table shows courtship behaviour of flies. The NP21 homozygous males displayed dramatically reduced level of courtship behaviour toward males as well as females. The tra1 mutant females vigorously courted partner females, whereas the females in which rpr+ was deleted did not display any male-typical courtship behaviour. (DOC 22 kb)
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Kimura, KI., Ote, M., Tazawa, T. et al. Fruitless specifies sexually dimorphic neural circuitry in the Drosophila brain. Nature 438, 229–233 (2005). https://doi.org/10.1038/nature04229
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DOI: https://doi.org/10.1038/nature04229
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