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A Drosophila mutant defective in extracellular calcium-dependent photoreceptor deactivation and rapid desensitization

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Abstract

CALCIUM is involved in the adaptation of vertebrate photoreceptors to light1,2 and may have a similar role in invertebrate phototransduction3,4. But the molecular mechanisms mediating this stimulus-dependent regulation are not well understood in any G protein-coupled transduction system. We have developed a preparation of isolated Drosophila photoreceptors that has allowed us to carry out an electrophysiological characterization of the light-activated response in these sensory neurons using patch-clamp techniques. We report here that extracellular calcium entering through the light-activated conductance is a key regulator of both the activation and deactivation phases of the phototransduction cascade, and that inaC mutant photoreceptors5 are specifically defective in the calcium-dependent deactivation mechanism. These data suggest that the light-dependent calcium influx inactivates this cascade through a biochemical pathway that requires the inaC gene product, and that this mechanism represents a molecular basis for stimulus-dependent regulation of visual transduction in Drosophila photoreceptors.

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References

  1. Fain, G. L. & Matthews, H. R. Trends Neurosci. 13, 378–384 (1990).

    Article  CAS  Google Scholar 

  2. Pugh, E. N. & Lamb, T. D. Vision Res. 30, 1923–1948 (1990).

    Article  CAS  Google Scholar 

  3. Payne, R. Photobiochem. Photobiophys. 13, 373–397 (1986).

    CAS  Google Scholar 

  4. Fein, A. & Payne, R. in Facets of Vision (eds Stavenga, D. & Hardie, R.) 173–185 (Springer, Berlin, 1989).

    Book  Google Scholar 

  5. Pak, W. L. in Neurogenetics, Genetic Approaches to the Nervous System (ed. Breakfield, X. O.) 67–99 (Elsevier, New York, 1979).

    Google Scholar 

  6. Tomlinson, A. Development 104, 183–193 (1988).

    CAS  Google Scholar 

  7. Hardie, R. C. in Progress in Sensory Physiology (ed. Ottoson, D.) 1–79 (Springer, New York, 1983).

    Google Scholar 

  8. O'Tousa, J. E. et al. Cell 40, 839–850 (1985).

    Article  CAS  Google Scholar 

  9. Zuker, C. S., Cowman, A. F. & Rubin, G. M. Cell 40, 851–858 (1985).

    Article  CAS  Google Scholar 

  10. Bainbridge, S. P. & Bownes, M. J. Embryol. exp. Morph. 66, 57–80 (1981).

    CAS  PubMed  Google Scholar 

  11. Hardie, R. C., Voss, D., Pongs, O. & Laughlin, S. B. Neuron 6, 477–486 (1991).

    Article  CAS  Google Scholar 

  12. Matthews, H. R., Murphy, R. L. W., Fain, G. L. & Lamb, T. D. Nature 334, 67–69 (1988).

    Article  ADS  CAS  Google Scholar 

  13. Nakatani, K. & Yau, K.-W. Nature 334, 69–71 (1988).

    Article  ADS  CAS  Google Scholar 

  14. Koch, K. & Stryer, L. Nature 334, 64–66 (1988).

    Article  ADS  CAS  Google Scholar 

  15. Rubin, L. J. & Brown, J. E. Biophys. J. 47, 38 (1985).

    Google Scholar 

  16. Payne, R., Corson, D. W., Fein, A. & Berridge, M. J. J. gen. Physiol. 88, 127–142 (1986).

    Article  CAS  Google Scholar 

  17. Brown, J. E. & Blinks, J. R. J. gen. Physiol. 64, 643–665 (1974).

    Article  CAS  Google Scholar 

  18. Fein, A. & Lisman, J. E. Science 187, 1094–1096 (1975).

    Article  ADS  CAS  Google Scholar 

  19. Lisman, J. E. & Brown, J. E. J. gen. Physiol. 59, 701–719 (1972).

    Article  CAS  Google Scholar 

  20. Horn, R. & Marty, A. J. gen. Physiol. 92, 145–159 (1988).

    Article  CAS  Google Scholar 

  21. Tsien, R. Y. Biochemistry 19, 2396–2404 (1980).

    Article  CAS  Google Scholar 

  22. Koenig, J. & Merriam, J. Drosoph. Inf. Serv. 52, 50–51 (1977).

    Google Scholar 

  23. Hengstenberg, R. & Gotz, K. G. Kybernetik 3, 276 (1967).

    Article  CAS  Google Scholar 

  24. Pak, W. L. in Handbook of Genetics (ed. King, R. C.) 703–733 (Plenum, New York, London, 1975).

    Google Scholar 

  25. Dizhoor, A. M. et al. Science 251, 915–918 (1991).

    Article  ADS  CAS  Google Scholar 

  26. Lambrecht, H. G. & Koch, K. W. EMBO J. 10, 793 (1991).

    Article  CAS  Google Scholar 

  27. Kawamura, S. & Murakami, M. Nature 349, 420–423 (1991).

    Article  ADS  CAS  Google Scholar 

  28. Hamill, O. P., Marty, A., Neher, E., Sakmann, B. & Sigworth, F. Pflügers Arch. 391, 85–100 (1981).

    Article  CAS  Google Scholar 

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Ranganathan, R., Harris, G., Stevens, C. et al. A Drosophila mutant defective in extracellular calcium-dependent photoreceptor deactivation and rapid desensitization. Nature 354, 230–232 (1991). https://doi.org/10.1038/354230a0

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  • DOI: https://doi.org/10.1038/354230a0

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