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The Neurospora clock gene frequency shares a sequence element with the Drosophila clock gene period

Abstract

THE isolation and characterization of single gene mutations affecting the circadian biological clocks of several organisms (reviewed in ref. 1) has left little doubt that circadian rhythms can be subjected to classical genetical analysis. Many of these mutations occur at the same few genetic loci (frequency (frq) in the fungus Neurospora2, and period (per) in fruit fly Drosophila3); these loci represent the best studied clock-affecting genes known. Mutant strains are usually affected in more than one basic clock property1,4, suggesting an inter-relatedness at the molecular level among these basic properties that would not have been predicted a priori. The extensive background information available concerning the frq locus4 provides a basis for the molecular dissection of the Neurospora circadian clock—the most minimal circadian system thus far described. We report here the cloning and analysis of the frq locus and show it to be larger and more complex than would have been predicted from the available genetic data. Complete rescue of all of the pleiotropic mutant phenotypes5,6 of the recessive frq9 allele requires transformation with a 7.7-kilobase (kb) region of DNA encoding at least two transcripts. Sequence analysis of this region has allowed the identification of a common element between frq and per which, given the background similarities in their classical genetic characteristics, suggests the possibility of a common element in the clock mechanisms of these two organisms.

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References

  1. Hall, J. C. & Rosbash, M. A. Rev. Neurosci. 11, 373–393 (1988).

    Article  CAS  Google Scholar 

  2. Gardner, G. F. & Feldman, J. F. Genetics 96, 877–886 (1980).

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Konopka, R. J. Fed. Proc. 38, 2602–2605 (1979).

    CAS  PubMed  Google Scholar 

  4. Feldman, J. F. & Dunlap, J. C. Photochem. Photobiol. Rev. 7, 319–368 (1983).

    CAS  Google Scholar 

  5. Loros, J. J. & Feldman, J. F. J. biol. Rhythms 1, 187–198 (1986).

    Article  CAS  PubMed  Google Scholar 

  6. Loros, J. J., Richman, A. R. & Feldman, J. F. Genetics 14, 1095–1110 (1986).

    Google Scholar 

  7. Viebrock, A., Perz, A. & Siebald, W. A. EMBO J. 1, 565–571 (1982).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Perkins, D. D., Radford, A., Newmeyer, D. & Bjorkman, M. Microbiol. Rev. 46, 426–570 (1982).

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Vollmer, S. J. & Yanofsky, C. Proc. natn. Acad. Sci. U.S.A. 83, 1–5 (1986).

    Article  Google Scholar 

  10. Metzenberg, R. L., Stevens, J. N., Selker, E. U. & Morzycka-Wroblewska, E. Proc. natn. Acad. Sci. U.S.A. 82, 2067–2071 (1985).

    Article  ADS  CAS  Google Scholar 

  11. Tinoco, I. et al. Nature New Biol. 246, 40–41 (1973).

    Article  CAS  PubMed  Google Scholar 

  12. Kozak, M. Molec. cell. Biol. 8, 2737–2744 (1988).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Orbach, M. J., Porro, E. A. & Yanofsky, C. Molec. cell. Biol. 6, 2452–2461 (1986).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  14. Pearson, W. R. & Lipman, D. J. Proc. natn. Acad. Sci. U.S.A. 85, 2444–2448 (1988).

    Article  ADS  CAS  Google Scholar 

  15. Lipman, W. J. & Pearson, W. R. Science 227, 1435–1441 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  16. Doolittle, R. F. Of URFs and ORFS (University Science Books, Mill Valley, 1986).

    Google Scholar 

  17. Jackson, F. R., Bargiello, T. A., Yun, S. H. & Young, M. W. Nature 320, 185–188 (1986).

    Article  ADS  CAS  PubMed  Google Scholar 

  18. Citri, Y. et al. Nature 326, 42–47 (1987).

    Article  ADS  CAS  PubMed  Google Scholar 

  19. Reddy, P., Jacquier, A. C., Abovich, N., Petersen, G. & Rosbach, M. Cell 46, 53–61 (1986).

    Article  CAS  PubMed  Google Scholar 

  20. Gonzalez, G. A. et al. Nature 337, 749–752 (1989).

    Article  ADS  CAS  PubMed  Google Scholar 

  21. Dayhoff, M. O. in Atlas of Protein Sequence and Structure Vol. 5, suppl. 3. (ed. Dayhoff, M. O.) 1–8 (Natn. biomed. Res. Found., Silver Spring, 1978).

    Google Scholar 

  22. Shin, H. S., Bargiello, T. A., Clark, B. T., Jackson, F. R. & Young, M. W. Nature 317, 445–448 (1985).

    Article  ADS  CAS  PubMed  Google Scholar 

  23. Weber, M. L., deGroot, E. J. & Schweiger, H. G. Molec. gen. Genet. 209, 1–7 (1987).

    Article  Google Scholar 

  24. McClung, R. M., Phillips, J. D., Orbach, M. J. & Dunlap, J. C. Expl. Mycol. (in the press).

  25. Davis, R. L. & deSerres Meth. Enzym. 71A, 79–143 (1970).

    Article  Google Scholar 

  26. Dunlap, J. C. & Feldman, J. F. Proc. Natn. Acad. Sci. U.S.A. 85, 1096–1100 (1988).

    Article  ADS  CAS  Google Scholar 

  27. Loros, J. J., Denome, S. & Dunlap, J. C. Science 243, 385–388 (1989).

    Article  ADS  CAS  PubMed  Google Scholar 

  28. Hu, N. & Messing, J. Gene 17, 271–277 (1982).

    Article  CAS  PubMed  Google Scholar 

  29. Feng, D. F., Johnson, M. S. & Doolittle, R. F. J. molec. Evol. 21, 1112–125 (1985).

    Article  Google Scholar 

  30. Schwartz, R. M. & Dayhoff, M. O. in Atlas of Protein Sequence and Structure Vol. 5, Suppl. 3 (ed. Dayhoff, M. O.) 353–358 (Natn. biomed. Res. Found, Silver Spring, 1978).

    Google Scholar 

  31. Henikoff, S. Gene 28, 351–359 (1984).

    Article  CAS  PubMed  Google Scholar 

  32. Sanger, F., Nicklen, S. & Coulson, A. R. Proc. natn. Acad. Sci. U.S.A. 74, 5463–5467 (1977).

    Article  ADS  CAS  Google Scholar 

  33. Myers, E. & Miller, W. CABIOS 4, 11–17 (1988).

    CAS  PubMed  Google Scholar 

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McClung, C., Fox, B. & Dunlap, J. The Neurospora clock gene frequency shares a sequence element with the Drosophila clock gene period. Nature 339, 558–562 (1989). https://doi.org/10.1038/339558a0

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