Hostname: page-component-586b7cd67f-2plfb Total loading time: 0 Render date: 2024-11-26T12:59:56.988Z Has data issue: false hasContentIssue false

Comparison of the regulation of P elements in M and M′ strains of Drosophila melanogaster

Published online by Cambridge University Press:  14 April 2009

Stéphane Ronsseray*
Affiliation:
Laboratoire de Génétique des Populations, Universités Paris6 et 7, Tour 42, 2 place jussieu, F75005 Paris, France
Monique Lehmann
Affiliation:
Laboratoire de Génétique des Populations, Universités Paris6 et 7, Tour 42, 2 place jussieu, F75005 Paris, France
Georges Periquet
Affiliation:
Laboratoire de Biocénotique Expérimentale des Agrosystèmes, Faculté des Sciences, Parc Grandmont, 37200 Tours, France
*
* Corresponding author.
Rights & Permissions [Opens in a new window]

Summary

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.

M and M′ strains of Drosophila melanogaster in the P-M system of hybrid dysgenesis were compared in two series of tests, with the following results. (1) The singed-weak hypermutability regulation test showed that M′ strains had lower P excision rates than M strains, suggesting that P-elements repression must occur in M′ strains although it is not detectable by gonadal dysgenesis assays. (2) The evolution of mixed P + M and mixed P + M′ populations was compared, using a strong P strain. The P + M cultures invariably evolved in a few generations into strong P cultures, while the P + M′ cultures evolved into P-type cultures with reduced P-factor potentials. However, after 30 generations of culture, both these types of mixed cultures had similar P copy numbers, suggesting that regulation of copy number had occurred in them.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1989

References

Anxolabéhère, D., Kai, H., Periquet, G. & Ronsseray, S. (1984). The geographical distribution of the P-M hybrid dysgenesis system in Drosophila melanogaster, Génétique, Selection et Evolution 16, 1526.CrossRefGoogle Scholar
Anxolabéhère, D., Kidwell, M. G. & Periquet, G. (1988). Molecular characteristics of diverse populations are consistent with the hypothesis of a recent invasion of Drosophila melanogaster by mobile P elements. Molecular Biology and Evolution 5 (3), 252269.Google ScholarPubMed
Anxolabéhère, D., Nouaud, D., Periquet, G. & Ronsseray, S. (1986). Evolution des potentialités dysgénésiques du système P–M dans des populations expérimentales mixtes P, Q, M et M′ de Drosophila melanogaster. Genetica 69, 8195.CrossRefGoogle Scholar
Anxolabéhère, D., Nouaud, D., Periquet, G. & Tchen, P. (1985). P element distribution in Eurasian populations of Drosophila melanogaster: a genetic and molecular analysis. Proceedings of the National Academy of Sciences USA 82, 54185422.CrossRefGoogle ScholarPubMed
Black, D. M., Jackson, M. S., Kidwell, M. G. & Dover, G. A. (1987). KP elements repress P-induced hybrid dysgenesis in Drosophila melanogaster. EMBO Journal 6, 41134123.CrossRefGoogle ScholarPubMed
Boussy, I. A., Healy, M. J., Oakeshott, G. J. & Kidwell, M. G. (1988). Molecular analysis of the P-M gonadal dysgenesis cline in eastern Australian Drosophila melanogaster. Genetics 119, 875888.CrossRefGoogle Scholar
Engels, W. R. (1979 a). Hybrid dysgenesis in Drosophila melanogaster: rules of inheritance of female sterility. Genetical Research 33, 219236.CrossRefGoogle Scholar
Engels, W. R. (1979 b). Extrachromosomal control of mutability in Drosophila melanogaster. Proceedings of the National Academy of Sciences USA 76, 40114015.CrossRefGoogle ScholarPubMed
Engels, W. R. (1981 a). Germline hypermutability in Drosophila and its relation to hybrid dysgenesis and cytotype. Genetics 98, 565587.CrossRefGoogle ScholarPubMed
Engels, W. R. (1981 b). Hybrid dysgenesis in Drosophila and the recent loss hypothesis. Cold Spring Harbor Symposia on Quantitative Biology 45, 561565.CrossRefGoogle Scholar
Engels, W. R. (1984). A trans-acting product needed for P factor transposition in Drosophila. Science 226, 11941196.CrossRefGoogle ScholarPubMed
Engels, W. R. (1988). P elements in Drosophila. In Mobile DNA (ed. Berg, D. and Howe, M.). ASM Publications: (in the press).Google Scholar
Jongeward, G., Simmons, M. J. & Health, E. (1987). The instability of a P element insertion mutation is affected by chromosomes derived paternally from a pseudo-M strain of Drosophila melanogaster. Drosophila Information Service 66, 7780.Google Scholar
Kidwell, M. G. (1983 a). Hybrid dysgenesis in Drosophila melanogaster: factors affecting -chromosomal contaminations in the P–M system. Genetics 104, 317341.CrossRefGoogle ScholarPubMed
Kidwell, M. G. (1983 b). Evolution of hybrid dysgenesis determinants in Drosophila melanogaster. Proceedings of the National Academy of Sciences USA 80, 16551659.CrossRefGoogle ScholarPubMed
Kidwell, M. G., Kidwell, J. F. & Sved, J. A. (1977). Hybrid dysgenesis in Drosophila melanogaster: a syndrome of aberrant traits including mutation, sterility and male recombination. Genetics 86, 813833.CrossRefGoogle ScholarPubMed
Kidwell, M. G., Kimura, K. & Black, D. M. (1988). Evolution of hybrid dysgenesis potential following P element contamination in Drosophila melanogaster. Genetics 119, 815828.CrossRefGoogle ScholarPubMed
Kidwell, M. G., Novy, J. B. & Feeley, S. M. (1981). Rapid unidirectionnal change of hybrid dysgenesis potential in Drosophila. Journal of Heredity 72, 3238.CrossRefGoogle Scholar
Nitasaka, E., Mukai, T. & Yamazaki, T. (1987). Repressor of P elements in Drosophila melanogaster: cytotype determination by a defective P element carrying only open reading frames 0 to 2. Proceedings of the National Academy of Sciences USA 84, 76057608.CrossRefGoogle Scholar
O'Hare, K. & Rubin, G. M. (1983). Structure of P transposable elements and their sites of insertion and excision in the Drosophila melanogaster genome. Cell 34, 2535.CrossRefGoogle ScholarPubMed
Roiha, H., Rubin, G. M. & O'Hare, K. (1988). P element insertion and rearrangements at the singed locus in Drosophila melanogaster. Genetics 119, 7583.CrossRefGoogle ScholarPubMed
Schaeffer, R. E., Kidwell, M. G. & Fausto-Sterling, A. (1979). Hybrid dysgenesis in Drosophila melanogaster: morphological and cytological studies of ovarian dysgenesis. Genetics 92, 11411152.CrossRefGoogle Scholar
Simmons, G. (1987). Sterility-mutability correlation. Genetical Research 50, 7376.CrossRefGoogle ScholarPubMed
Simmons, M. J. & Bucholz, L. M. (1985). Transposase titration in Drosophila melanogaster: a model of cytotype in the P–M system of hybrid dysgenesis. Proceedings of the National Academy of Sciences USA 82, 81198123.CrossRefGoogle Scholar
Simmons, M. J., Raymond, J. D., Boeidigheimer, M. J. & Zunt, J. R. (1987). The influence of non-autonomous P elements on hybrid dysgenesis in Drosophila melanogaster. Genetics 117, 671685.CrossRefGoogle Scholar
Tchen, P., Anxolabéhère, D., Nouaud, D. & Periquet, G. (1985). Hybridization on squashed flies: a method to detect gene sequences in individual Drosophila. Analytical Biochemistry 150, 415420.CrossRefGoogle Scholar