Abstract
Phase shifts of the circadian conidiation rhythm in Neurospora crassa were induced by 3-hour treatments of mycelia in liquid medium with diethylstilbestrol (DES), dienestrol (DIE), hexestrol (HEX), diethylstilbestroldipropionate (DESP), and dienestroldiacetate (DIEA). Over a 24-hour period beginning 24 hours after the transition from light to constant dark, maximum phase shifts occurred about 36 hours. DES was the most effective of the drugs tested, giving 10-hour phase advances at 20 micromolar. DIE and HEX caused similar phase shifts as DES at 40 micromolar. The two derivatives of the last, DESP and DIEA, were much less effective in shifting phase; only a few hours of phase advance result from treatments at 80 micromolar concentrations.
The activity of isolated plasma membrane ATPase was inhibited by DES and partially by HEX, but not by DIE, DESP, or DIEA. O2 consumption of the mycelia was inhibited equally by DES, DIE, and HEX, while DIEA and DESP had little effect. Phase-shifts by DES cannot be interpreted as evidence that plasma membrane ATPase is a component of the circadian clock.
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Selected References
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- Bowman B. J., Mainzer S. E., Allen K. E., Slayman C. W. Effects of inhibitors on the plasma membrane and mitochondrial adenosine triphosphatases of Neurospora crassa. Biochim Biophys Acta. 1978 Sep 11;512(1):13–28. doi: 10.1016/0005-2736(78)90214-6. [DOI] [PubMed] [Google Scholar]
- Bowman B. J., Slayman C. W. The effects of vanadate on the plasma membrane ATPase of Neurospora crassa. J Biol Chem. 1979 Apr 25;254(8):2928–2934. [PubMed] [Google Scholar]
- Bowman E. J., Bowman B. J., Slayman C. W. Isolation and characterization of plasma membranes from wild type Neurospora crassa. J Biol Chem. 1981 Dec 10;256(23):12336–12342. [PubMed] [Google Scholar]
- Burgoyne R. D. A model for the molecular basis of circadian rhythm involving monovalent ion-mediated translational control. FEBS Lett. 1978 Oct 1;94(1):17–19. doi: 10.1016/0014-5793(78)80896-5. [DOI] [PubMed] [Google Scholar]
- Byington K. H., Smoly J. M., Morey A. V., Green D. E. On the fragmentation of mitochondria by diethylstilbesterol. I. Conditions for maximizing fragmentation. Arch Biochem Biophys. 1968 Dec;128(3):762–773. doi: 10.1016/0003-9861(68)90085-4. [DOI] [PubMed] [Google Scholar]
- Bünning E., Moser I. Influence of valinomycin on circadian leaf movements of Phaseolus. Proc Natl Acad Sci U S A. 1972 Sep;69(9):2732–2733. doi: 10.1073/pnas.69.9.2732. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bünning E., Moser I. Light-induced phase shifts of circadian leaf movements of phaseolus: comparison with the effects of potassium and of ethyl alcohol. Proc Natl Acad Sci U S A. 1973 Dec;70(12 Pt 1-2):3387–3389. doi: 10.1073/pnas.70.12.3387. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Diekmann C., Brody S. Circadian rhythms in Neurospora crassa: oligomycin-resistant mutations affect periodicity. Science. 1980 Feb 22;207(4433):896–898. doi: 10.1126/science.6444467. [DOI] [PubMed] [Google Scholar]
- Keifer D. W., Spanswick R. M. Activity of the Electrogenic Pump in Chara corallina as Inferred from Measurements of the Membrane Potential, Conductance, and Potassium Permeability. Plant Physiol. 1978 Oct;62(4):653–661. doi: 10.1104/pp.62.4.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kiessig R. S., Herz J. M., Sweeney B. M. Shifting the phase of the circadian rhythm in bioluminescence in gonyaulax with vanillic Acid. Plant Physiol. 1979 Feb;63(2):324–327. doi: 10.1104/pp.63.2.324. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nakashima H. Effects of Membrane ATPase Inhibitors on Light-Induced Phase Shifting of the Circadian Clock in Neurospora crassa. Plant Physiol. 1982 Mar;69(3):619–623. doi: 10.1104/pp.69.3.619. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Njus D., Sulzman F. M., Hastings J. W. Membrane model for the circadian clock. Nature. 1974 Mar 8;248(5444):116–120. doi: 10.1038/248116a0. [DOI] [PubMed] [Google Scholar]
- Perlman J., Nakashima H., Feldman J. F. Assay and Characteristics of Circadian Rhythmicity in Liquid Cultures of Neurospora crassa. Plant Physiol. 1981 Mar;67(3):404–407. doi: 10.1104/pp.67.3.404. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sargent M. L., Kaltenborn S. H. Effects of medium composition and carbon dioxide on circadian conidiation in neurospora. Plant Physiol. 1972 Jul;50(1):171–175. doi: 10.1104/pp.50.1.171. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Slayman C. L., Slayman C. W. Depolarization of the plasma membrane of Neurospora during active transport of glucose: evidence for a proton-dependent cotransport system. Proc Natl Acad Sci U S A. 1974 May;71(5):1935–1939. doi: 10.1073/pnas.71.5.1935. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stroobant P., Scarborough G. A. Active transport of calcium in Neurospora plasma membrane vesicles. Proc Natl Acad Sci U S A. 1979 Jul;76(7):3102–3106. doi: 10.1073/pnas.76.7.3102. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sweeney B. M. The Potassium Content of Gonyaulax polyedra and Phase Changes in the Circadian Rhythm of Stimulated Bioluminescence by Short Exposures to Ethanol and Valinomycin. Plant Physiol. 1974 Mar;53(3):337–342. doi: 10.1104/pp.53.3.337. [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Otamendi M. E., Stoppani A. O. Action of diethylstilbestrol on the NADH-dehydrogenase region of the respiratory chain. Arch Biochem Biophys. 1974 Nov;165(1):21–33. doi: 10.1016/0003-9861(74)90137-4. [DOI] [PubMed] [Google Scholar]