Reciprocal Behaviour Associated with Altered Homeostasis and Photosensitivity of Drosophila Clock Mutants

References

• Aschoff J. Frequenzanderung der Aktivitatsperiodik bei Mausen im Dauerlicht und Dauerdunkel. Pflugers Arch. 1952; 255: 197–203
   PubMed Web of Science ®Google Scholar
• Aschoff J. Tierische Periodik unter dem Einfluss von Zeitgebern. Z. Tierpsychol. 1958; 15: 1–30
   Google Scholar
• Aschoff J. Periodik licht- und dunkelaktiver Tiere unter konstanten Umgebungsbedingungen. Pflugers Arch. 1959; 270: 9
   PubMed Web of Science ®Google Scholar
• Aschoff J. Orcadian rhythms: influences of internal and external factors on the period measured in constant conditions. Z. Tierpsychol. 1979; 49: 225–249
   PubMedGoogle Scholar
• Aschoff J., Gerecke U., Kureck A., Pohl H., Rieger P., Saint Paul U. V., Wever R. Interdependent parameters of circadian activity rhythms in birds and man. Biochronometry, M. Menaker. National Academy of Sciences, Washington 1971; 3–27
   Google Scholar
• Baylies M. K., Bargiello T. A., Jackson F. R., Young M. W. Changes in abundance or structure of the per gene product can alter periodicity of the Drosophila clock. Nature 1987; 326: 390–392
   PubMed Web of Science ®Google Scholar
• Brody S., Martins S. A. Circadian rhythms in Neurospora crassa: effects of unsaturated fatty acids. J. Bacterial. 1979; 137: 912–915
   PubMedGoogle Scholar
• Bruce V. G. Mutants of the biological clock in Chlamydomonas reinhardi. Genetics 1972; 70: 537–548
   PubMed Web of Science ®Google Scholar
• Dowse H. B., Hall J. C., Ringo J. M. Circadian and ultradian rhythms in period mutants of Drosophila melanogaster. Behav. Genet. 1987; 17: 19–35
   PubMed Web of Science ®Google Scholar
• Dowse H. B., Ringo J. M. Further evidence that the circadian clock in Drosophila is a population of coupled ultradian oscillators. J. Biol. Rhythms 1987; 2: 65–76
   PubMedGoogle Scholar
• Dushay M., Rosbash M., Hall J. C. The disconnected visual system mutations in Drosophila melanogaster drastically disrupt circadian rhythms. J. Biol. Rhythms 1989; 4: 1–27
   PubMed Web of Science ®Google Scholar
• Feldman J. F. Lengthening the period of a biological clock in Euglena by cycloheximide, an inhibitor of protein synthesis. Proc. Natl. Acad. Sci. USA 1967; 57: 1080–1087
   PubMed Web of Science ®Google Scholar
• Feldman J. F., Dunlap J. C. Neurospora crassa: a unique system for studying circadian rhythms. Photochem. Photobiol. Rev. 1983; 7: 319–368
   Google Scholar
• Feldman J. F., Hoyle M. N. Isolation of circadian clock mutants of Neurospora crassa. Genetics 1973; 75: 605–613
   PubMed Web of Science ®Google Scholar
• Hall J. C., Rosbash M. Genetic and molecular analysis of biological rhythms. J. Biol. Rhythms 1987; 2: 153–178
   PubMedGoogle Scholar
• Helfrich C. Role of the optic lobes in the regulation of the locomotor activity rhythm of Drosophila melanogaster: behavioural analysis of neural mutants. J. Neurogenet. 1986; 3: 321–343
   PubMed Web of Science ®Google Scholar
• Helfrich C., Engelmann W. Circadian rhythm of the locomotor activity in Drosophila melanogaster and its mutants ‘sine oculis’ and ‘small optic lobes’. Physiol. Enlomol. 1983; 8: 257–272
   Web of Science ®Google Scholar
• Konopka R. J. Circadian clock mutants of Drosophila melanogaster. Ph.D. Dissertation, California Institute of Technology. 1972
   Google Scholar
• Konopka R. J. Effects of Drosophila photoreceptor mutations on the circadian activity rhythm. Soc. Neurosci. Abstr. 1980; 6: 706
   Google Scholar
• Konopka R. J. Genetics of biological rhythms in Drosophila. Ann. Rev. Genet. 1987a; 21: 227–236
   PubMedGoogle Scholar
• Konopka R. J. Neurogenetics of Drosophila circadian rhythms. Evolutionary Genetics of Invertebrate Behaviour, M. Huettel. Plenum Press, New York 1987b; 215–222
   Google Scholar
• Konopka R. J., Benzer S. Clock mutants of Drosophila melanogaster. Proc. Natl. Acad. Sci. USA 1971; 65: 2112–2116
   Google Scholar
• Kramm K. R. Circadian activity of the red squirrel Tamiasciurus hudsonicus in continuous darkness and continuous illumination. Int. J. Biometeorol. 1975; 19: 232–245
   PubMed Web of Science ®Google Scholar
• Kyriacou C. P., Hall J. Circadian rhythm mutations in Drosophila melanogaster affect short term fluctuations in the male's courtship song. Proc. Natl. Acad. Sci. USA 1980; 77: 6729–6733
   PubMed Web of Science ®Google Scholar
• Kyriacou C. P., Hall J. C. Interspecific genetic control of courtship song production and reception in Drosophila. Science 1986; 232: 494–497
   PubMed Web of Science ®Google Scholar
• Liu X., Lorenz L., Yu Q., Hall J. C., Rosbash M. Spatial and temporal expression of the period gene in Drosophila melanogaster. Genes Dev. 1988; 2: 228–238
   PubMed Web of Science ®Google Scholar
• Loros J. J., Feldman J. F. Loss of temperature compensation of circadian period length in the frq-9 mutant of Neurospora crassa. J. Biol. Rhythms 1986; 1: 187–198
   PubMedGoogle Scholar
• Pittendrigh C. S. On temperature independence in the clock system controlling emergence time in Drosophila. Proc. Natl. Acad. Sci. USA 1954; 40: 1018–1029
   PubMed Web of Science ®Google Scholar
• Pittendrigh C. S. Circadian oscillations in cells and the circadian organization of multicellular systems. The Neurosciences: Third Study Program, F. O. Schmitt, F. G. Worden. MIT Press, Cambridge 1974; 437–458
   Google Scholar
• Pittendrigh C. S., Caldarola P. C. General homeostasis of the frequency of circadian oscillators. Proc. Natl. Acad. Sci. USA 1973; 70: 2697–2701
   PubMed Web of Science ®Google Scholar
• Pittendrigh C. S., Daan S. A functional analysis of circadian pacemakers in nocturnal rodents. I. The stability and lability of spontaneous frequency. J. Comp. Physiol. 1976a; 106: 223–252
   Web of Science ®Google Scholar
• Pittendrigh C. S., Daan S. A functional analysis of circadian pacemakers in nocturnal rodents. IV. Entrainment: pacemaker as clock. J. Comp. Physiol. 1976b; 106: 291–331
   Web of Science ®Google Scholar
• Pittendrigh C. S., Daan S. A functional analysis of circadian pacemakers in nocturnal rodents. V. Pacemaker structure: a clock for all seasons. J. Comp. Physiol. 1976c; 106: 333–355
   Web of Science ®Google Scholar
• Saez L., Young M. W. In situ localization of the per clock protein during development of Drosophila melanogaster. Molec. Cell. Biol. 1988; 8: 5378–5385
   PubMed Web of Science ®Google Scholar
• Siwicki K. K., Eastman C., Petersen G., Rosbash M., Hall J. C. Antibodies to the period gene product of Drosophila reveal diverse tissue distribution and rhythmic changes in the visual system. Neuron 1988; 1: 141–150
   PubMed Web of Science ®Google Scholar
• Smith R. F., Konopka R. J. Circadian clock phenotypes of chromosome aberrations with a breakpoint at the per locus. Molec. Gen. Genet. 1981; 183: 243–251
   PubMedGoogle Scholar
• Yu Q., Jacquier A. C., Citri Y., Hamblen M., Hall J. C., Rosbash M. Molecular mapping of point mutations in the period gene that stop or speed up biological clocks in Drosophila melanogaster. Proc. Natl. Acad. Set USA 1987; 84: 784–788
   PubMed Web of Science ®Google Scholar