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Circadian clock in Xenopus eye controlling retinal serotonin N-acetyltransferase

Abstract

Circadian rhythms are controlled by endogenous oscillators or clocks. These clocks exhibit a persistent period of approximately 24 h in constant conditions, a specific phase relationship to a periodic cue (zeitgeber) in the external environment, and plasticity in that the phase of the clock may be altered in response to a phase change in the zeitgeber1. Although many processes exhibit circadian rhythmicity, the nature and location of endogenous clocks remain poorly defined. Recent evidence in vertebrates suggests that the mammalian suprachiasmatic nucleus and the avian pineal gland contain clocks that affect the rhythmicity of indoleamine metabolism2. The vertebrate retina also exhibits a circadian rhythm of serotonin N-acetytransferase activity (NAT, EC 2.1.1.4)3–5, a key enzyme controlling melatonin synthesis, and of photoreceptor disk shedding6,7. The latter process may be regulated by melatonin8, and the immediate cellular events seem to be controlled locally within the eye9–11. Although sustained oscillation and entrainment were not demonstrated, data suggesting that an ocular circadian clock influences disk shedding have been reported9. We sought evidence for an ocular clock by studying retinal NAT activity in Xenopus eye cups maintained in culture and report here both sustained oscillation and entrainment of the in vitro system. The data indicate that in addition to the suprachiasmatic nucleus and pineal gland, the eye itself must be regarded as the locus of a circadian clock in vertebrates.

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References

  1. Aschoff, J. in Handbook of Behavioral Neurobiology Vol. 4 (ed. Aschoff, J.) 81–93 (Plenum, New York, 1981).

    Google Scholar 

  2. Takahashi, J. S. & Zatz, M. Science 217, 1104–1111 (1982).

    Article  ADS  CAS  Google Scholar 

  3. Binkley, S., Reilly, K. B. & Hryschyshyn, M. J. comp. Physiol. 139, 103–108 (1980).

    Article  CAS  Google Scholar 

  4. Hamm, H. E. & Menaker, M. Proc. natn. Acad. Sci. U.S.A. 77, 4998–5002 (1980).

    Article  ADS  CAS  Google Scholar 

  5. Iuvone, P. M. & Besharse, J. C. Brain Res. (in the press).

  6. La Vail, M. M. Science 194, 1071–1074 (1976).

    Article  ADS  CAS  Google Scholar 

  7. Besharse, J. C., Hollyfield, J. G. & Rayborn, M. E. J. Cell Biol. 75, 507–527 (1977).

    Article  CAS  Google Scholar 

  8. Besharse, J. C. & Dunis, D. A. Science 219, 1341–1343 (1983).

    Article  ADS  CAS  Google Scholar 

  9. Tierstein, P. S., Goldman, A. I. & O'Brien, P. J. Invest. Ophthal. vis. Sci. 19, 1268–1273 (1980).

    Google Scholar 

  10. Hollyfield, J. G. & Basinger, S. F. Nature 274, 794–796 (1978).

    Article  ADS  CAS  Google Scholar 

  11. Besharse, J. C., Terrill, R. O. & Dunis, D. A. Invest. Ophthal. vis. Sci. 19, 1512–1517 (1980).

    CAS  PubMed  Google Scholar 

  12. Kasal, C. A. & Perez-Polo, J. R. J. Neurosci. Res. 5, 579–585 (1980).

    Article  CAS  Google Scholar 

  13. Klein, D. C. & Weller, J. L. Science 169, 1093–1095 (1970).

    Article  ADS  CAS  Google Scholar 

  14. Menaker, M. & Binkley, S. in Handbook of Behavioral Neurobiology Vol. 4 (ed. Aschoff, J.) 243–255 (Plenum, New York, 1981).

    Google Scholar 

  15. Redman, J., Armstrong, S. & Ng, K. T. Science 219, 1089–1091 (1983).

    Article  ADS  CAS  Google Scholar 

  16. Reiter, R. J. Am. J. Anat. 162, 287–313 (1981).

    Article  CAS  Google Scholar 

  17. Levinson, G. & Burnside, B. Invest. Opthal. vis. Sci. 20, 294–303 (1981).

    CAS  Google Scholar 

  18. Brandenburg, J., Bobbert, A. C. & Eggelmeyer, F. Behav. Brain Res. 7, 113–123 (1983).

    Article  CAS  Google Scholar 

  19. Besharse, J. C. Prog. Retinal Res. 1, 81–124 (1982).

    Article  CAS  Google Scholar 

  20. Flannery, J. G. thesis, Univ. California, Santa Barbara (1982).

  21. Inouye, S. T. & Kuwamura, H. Proc. natn. Acad. Sci. U.S.A. 76, 5962–5966 (1979).

    Article  ADS  CAS  Google Scholar 

  22. Binkley, S. A., Reibman, J. B. & Reilly, K. B. Science 202, 1198–1201 (1978).

    Article  ADS  CAS  Google Scholar 

  23. Kasal, C. A., Menaker, M. & Perez-Polo, J. R. Science 203, 656–658 (1979).

    Article  ADS  CAS  Google Scholar 

  24. Deguchi, T. Science 203, 1245–1247 (1979).

    Article  ADS  CAS  Google Scholar 

  25. Jacklet, J. W. Science 164, 562–563 (1969).

    Article  ADS  CAS  Google Scholar 

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Besharse, J., Iuvone, P. Circadian clock in Xenopus eye controlling retinal serotonin N-acetyltransferase. Nature 305, 133–135 (1983). https://doi.org/10.1038/305133a0

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