Abstract
Twelve strains of Fusarium moniliforme were examined for their ability to sector spontaneously on toxic chlorate medium. All strains sectored frequently; 91% of over 1200 colonies examined formed chlorate-resistant, mutant sectors. Most of these mutants had lesions in the nitrate reduction pathway and were unable to utilize nitrate (nit mutants). nit mutations occurred in seven loci: a structural gene for nitrate reductase (nit1), a regulatory gene specific for the nitrate reduction pathway (nit3), and five genes controlling the production of a molybdenum-containing cofactor that is necessary for nitrate reductase activity (nit2, nit4, nit5, nit6, nit7). No mutations affecting nitrite reductase or a major nitrogen regulatory locus were found among over 1000 nit mutants. Mutations of nit1 were recovered most frequently (39-66%, depending on the strain) followed by nit3 mutations (23-42%). The frequency of isolation of each mutant type could be altered, however, by changing the source of nitrogen in the chlorate medium. We concluded that genetic control of nitrate reduction in F. moniliforme is similar to that in Aspergillus and Neurospora, but that the overall regulation of nitrogen metabolism may be different.
Full Text
The Full Text of this article is available as a PDF (747.5 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Arst H. N., Jr, Cove D. J. Nitrogen metabolite repression in Aspergillus nidulans. Mol Gen Genet. 1973 Nov 2;126(2):111–141. doi: 10.1007/BF00330988. [DOI] [PubMed] [Google Scholar]
- Engels W. R. The P family of transposable elements in Drosophila. Annu Rev Genet. 1983;17:315–344. doi: 10.1146/annurev.ge.17.120183.001531. [DOI] [PubMed] [Google Scholar]
- Garrett R. H., Amy N. K. Nitrate assimilation in fungi. Adv Microb Physiol. 1978;18:1–65. doi: 10.1016/s0065-2911(08)60414-2. [DOI] [PubMed] [Google Scholar]
- Green M. M. Transposable elements in Drosophila and other Diptera. Annu Rev Genet. 1980;14:109–120. doi: 10.1146/annurev.ge.14.120180.000545. [DOI] [PubMed] [Google Scholar]
- Haefner K. A simple apparatus for producing agar layers of uniform thickness for microbiological micromanipulator work. Z Allg Mikrobiol. 1967;7(3):229–231. [PubMed] [Google Scholar]
- Kathariou S., Spieth P. T. Spore Killer Polymorphism in FUSARIUM MONILIFORME. Genetics. 1982 Sep;102(1):19–24. doi: 10.1093/genetics/102.1.19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marzluf G. A. Regulation of nitrogen metabolism and gene expression in fungi. Microbiol Rev. 1981 Sep;45(3):437–461. doi: 10.1128/mr.45.3.437-461.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McClintock B. The significance of responses of the genome to challenge. Science. 1984 Nov 16;226(4676):792–801. doi: 10.1126/science.15739260. [DOI] [PubMed] [Google Scholar]
- Paquin C. E., Williamson V. M. Temperature effects on the rate of ty transposition. Science. 1984 Oct 5;226(4670):53–55. doi: 10.1126/science.226.4670.53. [DOI] [PubMed] [Google Scholar]
- Perrine K. G., Marzluf G. A. Amber nonsense mutations in regulatory and structural genes of the nitrogen control circuit of Neurospora crassa. Curr Genet. 1986;10(9):677–684. doi: 10.1007/BF00410916. [DOI] [PubMed] [Google Scholar]
- Roeder G. S., Farabaugh P. J., Chaleff D. T., Fink G. R. The origins of gene instability in yeast. Science. 1980 Sep 19;209(4463):1375–1380. doi: 10.1126/science.6251544. [DOI] [PubMed] [Google Scholar]
- Tomsett A. B., Garrett R. H. The isolation and characterization of mutants defective in nitrate assimilation in Neurospora crassa. Genetics. 1980 Jul;95(3):649–660. doi: 10.1093/genetics/95.3.649. [DOI] [PMC free article] [PubMed] [Google Scholar]
