Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

atonal is the proneural gene for Drosophila photoreceptors

Abstract

THE Drosophila peripheral nervous system comprises four major types of sensory element: external sense organs (such as mechano-sensory bristles), chordotonal organs (internal stretch receptors), multiple dendritic neurons, and photoreceptors. During development, the selection of neural precursors for external sense organs requires the proneural genes of the achaete–scute complex, which encode basic-helix–loop–helix transcription factors1–3. These genes do not, however, control precursor selection for chordotonal organs or photoreceptors4,5, raising the question of whether other proneural genes exist6 or a different mechanism of neurogenesis operates. Here we show that atonal (ato), originally isolated as a proneural gene for chordotonal organs7, is also the proneural gene for photo-receptors. Pattern formation in the Drosophila eye involves a succession of cell fate specifications. Of the eight photoreceptors within each ommatidium of the compound eye, the photoreceptor R8 is the first to appear in the eye imaginal disc, right behind the mor-phogenetic furrow8–10. The appearance of other photoreceptors (Rl–7) follows in a defined sequence that is thought to arise by induction from R8 (refs 8, 9, 11, 12). We find that photoreceptor formation requires the function of atonal at the morphogenetic furrow and that atonal is specifically required for R8 selection. Formation of other photoreceptors does not directly require atonal function, but does depend on R8 selection by atonal. Thus, photo-receptors are selected by two mechanisms: R8 by a proneural mechanism, and Rl–7 by local recruitment.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Similar content being viewed by others

References

  1. Ghysen, A. & Dambly-Chaudière, C. Trends Genet. 56, 251–255 (1989).

    Article  Google Scholar 

  2. Campuzano, S. & Modolell, J. Trends Genet. 8, 202–208 (1992).

    Article  CAS  Google Scholar 

  3. Ghysen, A., Dambly-Chaudière, C., Jan, L. Y. & Jan, Y. N. Genes Dev. 7, 723–733 (1993).

    Article  CAS  Google Scholar 

  4. Dambly-Chaudière, C. & Ghysen, A. Genes Dev. 1, 297–306 (1987).

    Article  Google Scholar 

  5. Jiménez, F. & Campos-Ortega, J. A. J. Neurogen. 4, 179 (1987).

    Google Scholar 

  6. Basler, K. & Hafen, E. BioEssays 13, 621–631 (1991).

    Article  CAS  Google Scholar 

  7. Jarman, A. P., Grau, Y., Jan, L. Y. & Jan, Y. N. Cell 73, 1307–1321 (1993).

    Article  CAS  Google Scholar 

  8. Tomlinson, A. & Ready, D. F. Devl Biol. 120, 366–376 (1987).

    Article  CAS  Google Scholar 

  9. Ready, D. F. Trends Neurosci. 12, 102–110 (1989).

    Article  CAS  Google Scholar 

  10. Baker, N. E., Mlodzik, M. & Rubin, G. M. Science 250, 1370–1377 (1990).

    Article  ADS  CAS  Google Scholar 

  11. Banerjee, U. & Zipursky, S. L. Neuron 4, 177–187 (1990).

    Article  CAS  Google Scholar 

  12. Rubin, G. R. Trends Genet. 7, 372–377 (1991).

    Article  CAS  Google Scholar 

  13. Baker, N. E. & Rubin, G. M. Nature 340, 150–153 (1989).

    Article  ADS  CAS  Google Scholar 

  14. Zipursky, S. L., Venkatesh, T. R., Teplow, D. B. & Benzer, S. Cell 36, 15–26 (1984).

    Article  CAS  Google Scholar 

  15. Mlodzic, M., Baker, N. E. & Rubin, G. M. Genes Dev. 4, 1848–1861 (1990).

    Article  Google Scholar 

  16. Heberlein, U., Wolff, T. & Rubin, G. M. Cell 75, 913–926 (1993).

    Article  CAS  Google Scholar 

  17. Ma, C., Zhou, Y., Beachy, P. A. & Moses, K. Cell 75, 927–938 (1993).

    Article  CAS  Google Scholar 

  18. Heberlein, U., Hariharan, I. K. & Rubin, G. M. Devl Biol. 160, 51–63 (1993).

    Article  CAS  Google Scholar 

  19. Cagan, R. L. & Ready, D. L. Genes Dev. 3, 1099–1112 (1989).

    Article  CAS  Google Scholar 

  20. Karpilow, J., Kolodkin, A., Bork, T. & Venkatesh, T. Genes Dev. 3, 1834–1844 (1989).

    Article  CAS  Google Scholar 

  21. Mclver, S. B. in Comprehensive Insect Physiology, Biochemistry and Pharmacology Vol. 6 (eds Gilbert, L. I. & Kerkut, D. A.) (Pergamon, New York, 1985).

    Google Scholar 

  22. Meyerowitz, E. M. & Kankel, D. R. Devl Biol. 62, 112–142 (1978).

    Article  CAS  Google Scholar 

  23. Fischbach, K. F. & Technau G. Devl Biol. 104, 219–239 (1984).

    Article  CAS  Google Scholar 

  24. Lindsley, D. L. & Zimm, G. G. in Tne Genome of Drosophila melangoaster (Academic, San Diego, 1992).

    Google Scholar 

  25. Brand, A. H. & Perrimon, N. Development 118, 401–415 (1993).

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Jarman, A., Grell, E., Ackerman, L. et al. atonal is the proneural gene for Drosophila photoreceptors. Nature 369, 398–400 (1994). https://doi.org/10.1038/369398a0

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/369398a0

This article is cited by

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing