Abstract
Although the fungus Neurospora crassa is a relatively simple lower eukaryote, its circadian system may be more complex than previously thought. In this paper we review evidence suggesting that there may be several output pathways coupled in complex ways to a single oscillator, or that there may be more than one oscillator driving independent output pathways. We have described two new rhythms in Neurospora that are not tightly coupled to the rhythm of conidiation bands that is the standard assay for the state of the Neurospora circadian clock. The first is a rhythm in the timing of differentiation, i.e. the production of aerial hyphae and spores. Large regions of the mycelium differentiate synchronously, as if responding to a spatially widespread signal. This rhythm may be distinct from the timer that sets the determination switch controlling the spatial pattern of conidiation bands. The second new rhythm is an oscillation in the levels of the neutral lipid diacylglycerol (DAG). This rhythm is found in all regions of a colony and is not always in phase with the rhythm of conidiation bands. The DAG rhythm shares some characteristics with the differentiation rhythm and has the potential to act as the signal that induces rhythmic differentiation.
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Selected References
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- Aronson B. D., Johnson K. A., Dunlap J. C. Circadian clock locus frequency: protein encoded by a single open reading frame defines period length and temperature compensation. Proc Natl Acad Sci U S A. 1994 Aug 2;91(16):7683–7687. doi: 10.1073/pnas.91.16.7683. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bell-Pedersen D., Crosthwaite S. K., Lakin-Thomas P. L., Merrow M., Økland M. The Neurospora circadian clock: simple or complex? Philos Trans R Soc Lond B Biol Sci. 2001 Nov 29;356(1415):1697–1709. doi: 10.1098/rstb.2001.0968. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chopra A., Khuller G. K. Lipid metabolism in fungi. Crit Rev Microbiol. 1984;11(3):209–271. doi: 10.3109/10408418409105904. [DOI] [PubMed] [Google Scholar]
- Dharmananda S., Feldman J. F. Spatial Distribution of Circadian Clock Phase in Aging Cultures of Neurospora crassa. Plant Physiol. 1979 Jun;63(6):1049–1054. doi: 10.1104/pp.63.6.1049. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dunlap J. C. Molecular bases for circadian clocks. Cell. 1999 Jan 22;96(2):271–290. doi: 10.1016/s0092-8674(00)80566-8. [DOI] [PubMed] [Google Scholar]
- Hodgkin M. N., Pettitt T. R., Martin A., Michell R. H., Pemberton A. J., Wakelam M. J. Diacylglycerols and phosphatidates: which molecular species are intracellular messengers? Trends Biochem Sci. 1998 Jun;23(6):200–204. doi: 10.1016/s0968-0004(98)01200-6. [DOI] [PubMed] [Google Scholar]
- Hubbard S. C., Brody S. Glycerophospholipid variation in choline and inositol auxotrophs of Neurospora crassa. Internal compensation among zwitterionic and anionic species. J Biol Chem. 1975 Sep 25;250(18):7173–7181. [PubMed] [Google Scholar]
- Iwasaki H., Dunlap J. C. Microbial circadian oscillatory systems in Neurospora and Synechococcus: models for cellular clocks. Curr Opin Microbiol. 2000 Apr;3(2):189–196. doi: 10.1016/s1369-5274(00)00074-6. [DOI] [PubMed] [Google Scholar]
- Juretić D. The effect of phosphatidylcholine depletion on biochemical and physical properties of a Neurospora crassa membrane mutant. Biochim Biophys Acta. 1977 Sep 5;469(2):137–150. doi: 10.1016/0005-2736(77)90176-6. [DOI] [PubMed] [Google Scholar]
- Lakin-Thomas P. L., Brody S. Circadian rhythms in Neurospora crassa: lipid deficiencies restore robust rhythmicity to null frequency and white-collar mutants. Proc Natl Acad Sci U S A. 2000 Jan 4;97(1):256–261. doi: 10.1073/pnas.97.1.256. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lakin-Thomas P. L. Choline depletion, frq mutations, and temperature compensation of the circadian rhythm in Neurospora crassa. J Biol Rhythms. 1998 Aug;13(4):268–277. doi: 10.1177/074873098129000101. [DOI] [PubMed] [Google Scholar]
- Lakin-Thomas P. L. Circadian rhythms: new functions for old clock genes. Trends Genet. 2000 Mar;16(3):135–142. doi: 10.1016/s0168-9525(99)01945-9. [DOI] [PubMed] [Google Scholar]
- Lakin-Thomas P. L., Coté G. G., Brody S. Circadian rhythms in Neurospora crassa: biochemistry and genetics. Crit Rev Microbiol. 1990;17(5):365–416. doi: 10.3109/10408419009114762. [DOI] [PubMed] [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 Fall;1(3):187–198. doi: 10.1177/074873048600100302. [DOI] [PubMed] [Google Scholar]
- Merrow M., Brunner M., Roenneberg T. Assignment of circadian function for the Neurospora clock gene frequency. Nature. 1999 Jun 10;399(6736):584–586. doi: 10.1038/21190. [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]
- Ramsdale M., Lakin-Thomas P. L. sn-1,2-diacylglycerol levels in the fungus Neurospora crassa display circadian rhythmicity. J Biol Chem. 2000 Sep 8;275(36):27541–27550. doi: 10.1074/jbc.M002911200. [DOI] [PubMed] [Google Scholar]
- Springer M. L., Yanofsky C. A morphological and genetic analysis of conidiophore development in Neurospora crassa. Genes Dev. 1989 Apr;3(4):559–571. doi: 10.1101/gad.3.4.559. [DOI] [PubMed] [Google Scholar]
