Abstract
A scheme has been devised for efficient isolation of recessive meiotic mutants of Neurospora crassa. These mutants were detected by their reduced fertility or by the abortion of ascospores. Their isolation involved the selection and screening of strains arising from ascospores disomic (n + 1) for linkage group I (LG I), which bears the mating-type locus. These strains are self-fertile heterokaryons that contain two types of haploid nuclei of opposite mating type (A + a). Selfings of these strains are homozygous for genes on all linkage groups except LGI and therefore allow the expression of recessive mutants with an altered sexual cycle. Using this selection procedure, three classes of mutants were detected. In one class, mutants had an early block in perithecial development (class I), and in another mutants had altered perithecia, but apparently unaltered fertility (class III). No recessive mutants were observed and all mutants tested (eight of class I and two of class III) were expressed only when used as the maternal parent. A third mutant class displayed normal production of perithecia, but defective formation of asci (class IIA), or black ascospores (class IIB). Four of 13 class IIA mutants were analyzed, and two of them [asc(DL131) and asc(DL400)] were definitely recessive. Analysis of 10 of 13 class IIB mutants disclosed six recessive, mutually complementing mutants: asc(DL95), asc(DL243), asc(DL711), asc(DL879), asc(DL917m) and asc(DL961). Mutants asc(DL95), asc(DL243) and the previously studied mei-1 mutant (Smith 1975) complemented one another in crosses, but did not recombine. These may be alleles of the same gene, or they may comprise a gene cluster.
Full Text
The Full Text of this article is available as a PDF (850.5 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Boyd J. B., Golino M. D., Nguyen T. D., Green M. M. Isolation and characterization of X-linked mutants of Drosophila melanogaster which are sensitive to mutagens. Genetics. 1976 Nov;84(3):485–506. doi: 10.1093/genetics/84.3.485. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bresch C., Müller G., Egel R. Genes involved in meiosis and sporulation of a yeast. Mol Gen Genet. 1968;102(4):301–306. doi: 10.1007/BF00433721. [DOI] [PubMed] [Google Scholar]
- DeLange A. M., Griffiths A. J. Meiosis in Neurospora crassa. II. Genetic and cytological characterization of three meiotic mutants. Genetics. 1980 Oct;96(2):379–398. doi: 10.1093/genetics/96.2.379. [DOI] [PMC free article] [PubMed] [Google Scholar]
- ESSER K., STRAUB J. Genetische Untersuchungen an Sordaria macrospora Auersw., Kompensation und Induktion bei genbedingten Entwicklungsdefekten. Z Vererbungsl. 1958;89(5):729–746. [PubMed] [Google Scholar]
- Esposito M. S., Bolotin-Fukuhara M., Esposito R. E. Antimutator activity during mitosis by a meiotic mutant of yeast. Mol Gen Genet. 1975 Aug 5;139(1):9–18. doi: 10.1007/BF00267991. [DOI] [PubMed] [Google Scholar]
- Esposito M. S., Esposito R. E. The genetic control of sporulation in Saccharomyces. I. The isolation of temperature-sensitive sporulation-deficient mutants. Genetics. 1969 Jan;61(1):79–89. doi: 10.1093/genetics/61.1.79. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Garnjobst L., Wilson J. F. HETEROCARYOSIS AND PROTOPLASMIC INCOMPATIBILITY IN NEUROSPORA CRASSA. Proc Natl Acad Sci U S A. 1956 Sep;42(9):613–618. doi: 10.1073/pnas.42.9.613. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Griffiths A. J., Delange A. M. Mutations of the a Mating-Type Gene in NEUROSPORA CRASSA. Genetics. 1978 Feb;88(2):239–254. doi: 10.1093/genetics/88.2.239. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hodgkin J., Horvitz H. R., Brenner S. Nondisjunction Mutants of the Nematode CAENORHABDITIS ELEGANS. Genetics. 1979 Jan;91(1):67–94. doi: 10.1093/genetics/91.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Howe H. B., Jr Phenotypic diversity among alleles at the per-1 locus of Neurospora crassa. Genetics. 1976 Apr;82(4):595–603. doi: 10.1093/genetics/82.4.595. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Iyengar G. A., Deka P. C., Kundu S. C., Sen S. K. DNA syntheses in course of meiotic development in Neurospora crassa. Genet Res. 1977 Feb;29(1):1–8. doi: 10.1017/s0016672300017067. [DOI] [PubMed] [Google Scholar]
- Johnson T. E. Isolation and characterization of perithecial development mutants in neurospora. Genetics. 1978 Jan;88(1):27–47. doi: 10.1093/genetics/88.1.27. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Malling H. V., De Serres F. J. Genetic effects of N-methyl-N'-nitro-N-nitrosoguanidine in Neurospora crassa. Mol Gen Genet. 1970;106(3):195–207. doi: 10.1007/BF00340379. [DOI] [PubMed] [Google Scholar]
- Miklos G. L., Smith-White S. An analysis of the instability of segregation-distorter in Drosophila melanogaster. Genetics. 1971 Feb;67(2):305–317. doi: 10.1093/genetics/67.2.305. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mylyk O. M., Threlkeld S. F. A genetic study of female sterility in Neurospora crassa. Genet Res. 1974 Aug;24(1):91–102. doi: 10.1017/s001667230001510x. [DOI] [PubMed] [Google Scholar]
- Newmeyer D. A suppressor of the heterokaryon-incompatibility associated with mating type in Neurospora crassa. Can J Genet Cytol. 1970 Dec;12(4):914–926. doi: 10.1139/g70-115. [DOI] [PubMed] [Google Scholar]
- Newmeyer D., Galeazzi D. R. A meiotic uv-sensitive mutant that causes deletion of duplications in neurospora. Genetics. 1978 Jun;89(2):245–269. doi: 10.1093/genetics/89.2.245. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Newmeyer D., Schroeder A. L., Galeazzi D. R. An apparent connection between histidine, recombination, and repair in Neurospora. Genetics. 1978 Jun;89(2):271–279. doi: 10.1093/genetics/89.2.271. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perkins D. D., Barry E. G. The cytogenetics of Neurospora. Adv Genet. 1977;19:133–285. doi: 10.1016/s0065-2660(08)60246-1. [DOI] [PubMed] [Google Scholar]
- Pittenger T H. The General Incidence of Pseudo-Wild Types in Neurospora Crassa. Genetics. 1954 May;39(3):326–342. doi: 10.1093/genetics/39.3.326. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Prakash L., Prakash S. Isolation and characterization of MMS-sensitive mutants of Saccharomyces cerevisiae. Genetics. 1977 May;86(1):33–55. doi: 10.1093/genetics/86.1.33. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodarte-Ramón U. S., Mortimer R. K. Radiation-induced recombination in Saccharomyces: isolation and genetic study of recombination-deficient mutants. Radiat Res. 1972 Jan;49(1):133–147. [PubMed] [Google Scholar]
- Rodarte-Ramón U. S. Radiation-induced recombination in Saccharomyces: the genetic control of recombination in mitosis and meiosis. Radiat Res. 1972 Jan;49(1):148–154. [PubMed] [Google Scholar]