Hostname: page-component-848d4c4894-sjtt6 Total loading time: 0 Render date: 2024-06-25T00:05:22.681Z Has data issue: false hasContentIssue false

Genetic studies in Eudorina

Published online by Cambridge University Press:  14 April 2009

Nawin C. Mishra
Affiliation:
McMaster University, Hamilton, Ontario, Canada
S. F. H. Threlkeld
Affiliation:
McMaster University, Hamilton, Ontario, Canada

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

A formal genetic analysis of the heterothallic, colonial green alga Eudorina elegans has been described. Wild-type strains were found to be sensitive to different drugs when grown on minimal agar containing very low concentrations of these drugs. Mutant strains resistant to high concentrations of drugs have been isolated. These are msr-500 (resistant to 500 μg/ml of DL-methionine-DL-sulfoximine), ery-r-100 (resistant to 100 μg/ml of erythromycin) and sr-100 (resistant to 100 μg/ml of streptomycin). The wild-type phenotypes sensitive to these drugs have been designated as mss-500, ery-s-100 and ss-100 respectively. The sr-100 also showed cross-resistance to other antibiotics belonging to the streptomycin group.

On genetic analysis, the msr-500 and ery-s-100 were found to be inherited in a Mendelian way. These alleles are not linked to each other or to the mating type locus. The inheritance of mating type was found to be due to a single gene difference.

The inheritance of ss-100/sr-100 was found to be non-chromosomal and was characteristically uniparental, always transmitted through the female parent. The evidence for the non-chromosomal gene (NC genes) controlling sr-100/ss-100 phenotypes in this organism has been derived from the exceptional zygotes in which the male parent apparently transmits streptomycin resistance to the progeny. Although ultraviolet or gamma-radiation resulted in normal survival curves of the exposed cells, no mutant deficient in any nutritional requirement was isolated.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1968

References

REFERENCES

Ebersold, W. R. (1962). In Physiology and Biochemistry of Algae: Biochemical Genetics, p. 735. New York: Academic Press.Google Scholar
Goldstein, M. E. (1963). Speciation and mating behaviour in Eudorina. Ph.D. thesis, Indiana University, Bloomington, Indiana, U.S.A.Google Scholar
Goldstein, M. E. (1964). Speciation and mating behaviour in Eudorina. J. Protozoology 11, 317.CrossRefGoogle Scholar
Gowans, C. S. (1956). Genetic investigation on Chlamydomonas eugametos. Ph.D. thesis, Stanford University, U.S.A.Google Scholar
Lederberg, J. & Lederberg, E. M. (1952). Replica plating and indirect selection of bacterial mutants. J. Bact. 63, 399.CrossRefGoogle ScholarPubMed
Levine, R. P. & Ebersold, W. T. (1961). The genetics and cytology of Chlamydomonas. A. Rev. Microbiol. 14, 170.Google Scholar
Mishra, N. C. (1967). Genetic studies in Eudorina and Neurospora. Ph.D. thesis, McMaster University, Hamilton, Ontario, Canada.Google Scholar
Sager, R. & Ramanis, Z. (1963). The particulate nature of non-chromosomal genes in Chlamydomonas. Proc. natn. Acad. Sci., U.S.A. 50, 260.CrossRefGoogle Scholar
Starr, R. C. (1960). The culture collection of algae at Indiana University. Am. J. Bot. 47, 67.CrossRefGoogle Scholar
Wetherall, D. F. & Krauss, R. W. (1957). X-ray induced mutation in Chalmydomonas eugametos. Am. J. Bot. 44, 609.Google Scholar
Wilbois, A. D. (1958). Sexual isolation in Pandorina morum. Ph.D. thesis, Indiana University, Indiana, U.S.A.Google Scholar