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Hybrid dysgenesis in natural populations of Drosophila melanogaster in Japan. II. Strains which cannot induce P-M dysgenesis may completely suppress functional P element activity

Published online by Cambridge University Press:  14 April 2009

Nobuko Hagiwara ,
Etsuko Nakamura ,
Etsuko T. Matsuura  and
Sadao I. Chigusa
Nobuko Hagiwara
Affiliation:
Department of Biology, Ochanomizu University, Bunkyo-ku, Tokyo 112, Japan
Etsuko Nakamura
Affiliation:
Department of Biology, Ochanomizu University, Bunkyo-ku, Tokyo 112, Japan
Etsuko T. Matsuura
Affiliation:
Department of Biology, Ochanomizu University, Bunkyo-ku, Tokyo 112, Japan
Sadao I. Chigusa*
Affiliation:
Department of Biology, Ochanomizu University, Bunkyo-ku, Tokyo 112, Japan
*
2To whom correspondence should be addressed.
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Many inbred and isofemale lines derived from wild populations of Drosophila melanogaster were tested for gonadal dysgenic sterility, male recombination and snw secondary mutation. Among them, we have found strains whose dysgenic offspring show negligible sterility, and undetectable male recombination and snw mutation. They can be considered to be neutral strains in the strict sense. Such neutral strains appear to carry only defective P elements in their genomes. Taking the observations of Karess & Rubin (1984) into account, it is suggested that some defective P elements retain the function necessary for P cytotype. Cytotype determination mechanisms are discussed.

Type
Research Article
Information
Genetics Research , Volume 50 , Issue 2 , October 1987 , pp. 105 - 111
Copyright
Copyright © Cambridge University Press 1987

References

Bregliano, J. C. & Kidwell, M. G. (1983). Hybrid dysgenesis determinants in mobile genetic elements. Mobile Genetic Element (ed. Shapiro, J. A.) pp. 363–410. New York: Academic Press.Google Scholar
Engels, W. R. (1979 a). Extrachromosomal control of mutability in Drosophila melanogaster. Proceedings of the National Academy of Sciences of the U.S.A. 76, 4011–4015.CrossRefGoogle ScholarPubMed
Engels, W. R. (1979 b). Hybrid dysgenesis in Drosophila melanogaster: rules of inheritance of female sterility. Genetical Research 33, 219–236.CrossRefGoogle Scholar
Engels, W. R. (1980). Hybrid dysgenesis in Drosophila and stochastic loss hypothesis. Cold Spring Harbor Symposia on Quantitative Biology 45, 561–565.CrossRefGoogle Scholar
Engels, W. R. (1983). The P family of transposable element in Drosophila. Annual Review of Genetics 17, 315–344.Google Scholar
Engels, W. R. (1984). A trans-acting product needed for P factor transposition in Drosophila. Science 226, 1194–1196.CrossRefGoogle ScholarPubMed
Engels, W. R. & Preston, C. R. (1980). Components of hybrid dysgenesis in a wild population of Drosophila melangoaster. Genetics 95, 111–128.CrossRefGoogle Scholar
Engels, W. R. & Preston, C. R. (1981). Characteristics of a ‘neutral’ strain in the P-M system of hybrid dysgenesis. Drosophila Information Service 56, 35–37.Google Scholar
Grindley, N. D. F. (1983). Transposition of Tn3 and related transposons. Cell 32, 3–5.CrossRefGoogle ScholarPubMed
Isberg, R. R., Lazaar, A. L. & Syvanen, M. (1982). Regulation of Tn5 by the right-repeat proteins; control of the transcription reaction? Cell 30, 883–892.CrossRefGoogle Scholar
Johnson, R. C., Yin, J. C. P. & Reznikoff, W. S. (1982). Control of Tn5 transcription in Escherichia coli is mediated by protein from the right repeat. Cell 30, 873–882.CrossRefGoogle ScholarPubMed
Karess, R. E. & Rubin, G. M. (1984). Analysis of P transposable element functions in Drosophila. Cell 38, 135–146.CrossRefGoogle ScholarPubMed
Kato, H. K., Matsuura, E. T. & Chigusa, S. I. (1984). An experimental study on P element spread in natural population of Drosophila melangoaster. Japanese Journal of Genetics 59, 672.Google Scholar
Kidwell, M. G. (1979). Hybrid dysgenesis in Drosophila melanogaster: the relationship between the P-M and I-R interaction systems. Genetical Research 33, 205–217.CrossRefGoogle Scholar
Kidwell, M. G. (1981). Hybrid dysgenesis in Drosophila melanogaster: the genetics of cytotype determination in a neutral strain. Genetics 98, 275–290.CrossRefGoogle Scholar
Kidwell, M. G. (1983). Evolution of hybrid dysgenesis determinants in Drosophila melanogaster. Proceedings of the National Academy of Sciences of the U.S.A. 80, 1655–1659.CrossRefGoogle ScholarPubMed
Kidwell, M. G. (1985). Hybrid dysgenesis in Drosphila melanogaster: nature and inheritance of P element regulation. Genetics 111, 337–350.CrossRefGoogle Scholar
Kocur, G. J., Dricer, E. A. & Simmons, M. J. (1986). Sterility and hypermutability in the P-M system of hybrid dysgenesis in Drosophila melangoaster. Genetics 114, 1147–1163.CrossRefGoogle Scholar
Laski, F. A., Rio, D. C. & Rubin, G. M. (1986). Tissue specificity of Drosophila P-element transposition is regulated at the level of mRNA splicing. Cell 44, 7–19.CrossRefGoogle ScholarPubMed
Lindsley, D. & Grell, E. (1968). Genetic variation of Drosophila melanogaster. Carnegie Institution of Washington, Publication No. 627.Google Scholar
O'Hare, K. & Rubin, G. M. (1983). Structure of transposable elements and their sites of insertion and excision in the Drosophila melanogaster genome. Cell 34, 25–35.CrossRefGoogle ScholarPubMed
Ohishi, K., Takanashi, E. & Chigusa, S. I. (1982). Hybrid dysgenesis in natural population of Drosophila melano-gaster in Japan. I. Complete absence of the P factor in an island population. Japanese Journal of Genetics 57, 423–428.Google Scholar
Raymond, J. D. & Simmons, M. J. (1981). An increase in the X-linked lethal mutation rate associated with an unstable locus in Drosophila melanogaster. Genetics 98, 291–302.CrossRefGoogle ScholarPubMed
Rio, D. C., Laski, F. A. & Rubin, G. M. (1986). Identification and immunochemical analysis of biologically active Drosophila P element transposase. Cell 44, 21–32.CrossRefGoogle ScholarPubMed
Rubin, G. M. & Spradling, A. C. (1982). Genetic transformation of Drosophila with transposable element vectors. Science 218, 348–353.CrossRefGoogle ScholarPubMed
Rubin, G. M., Kidwell, M. G. & Bingham, P. M. (1982). The molecular basis of P-M hybrid dysgenesis: the nature of induced mutations. Cell 29, 987–994.CrossRefGoogle ScholarPubMed
Satta, Y., Gojobori, T., Maruyama, T. & Chigusa, S. I. (1985 a). Tn3 resolvase-like sequence in P-transposable element of Drosophila melanogaster. Japanese Journal of Genetics 60, 261–266.Google Scholar
Satta, Y., Gojobori, T., Maruyama, T., Saigo, K. & Chigusa, S. I. (1985 b). Homology between P-transposable element of Drosophila melanogaster and bacterial transposase gene of Tn3. Japanese Journal of Genetics 60, 499–503.Google Scholar
Simmons, M. J., Johnson, N. A., Fahey, T. M., Nellett, S. M. & Raymond, J. D. (1980). High mutability in male hybrids of Drosophila melanogaster. Genetics 96, 479–490.CrossRefGoogle ScholarPubMed
Simmons, M. J., Raymond, J. D., Johnson, N. A. & Fahey, T. M. (1984 a). A comparison of mutation rates for specific loci and chromosome regions in dysgenic hybrid males of Drosophila melanogaster. Genetics 106, 85–94.CrossRefGoogle ScholarPubMed
Simmons, M. J., Raymond, J. D., Culbert, T. P. & Laverty, T. R. (1984 b). Analysis of dysgenesis-induced lethal mutations on the X chromosome of a Q strain of Drosophila melanogaster. Genetics 107, 49–63.CrossRefGoogle Scholar
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 of the U.S.A. 82, 8119–8123.CrossRefGoogle Scholar
Simmons, M. J., Raymond, J. D., Laverty, T. R., Doll, R. F., Raymond, N. C., Kocur, G. J. & Drier, E. A. (1985). Chromosomal effects on mutability in the P-M system of hybrid dysgenesis in Drosophila melanogaster. Genetics 111, 869–884.CrossRefGoogle Scholar
Spradling, A. C. & Rubin, G. M. (1982). Transposition of cloned P elements into Drosophila germ line chromosomes. Science 218, 341–347.CrossRefGoogle ScholarPubMed
Takada, S., Murai, M., Takanashi, E., Ohishi, K., Fukami, K., Hagiwara, N., Satta, Y. & Ishiwa, S. (1983). On the P-M system in natural population of D. melanogaster in and around Japan. Japanese Journal of Genetics 58, 686.Google Scholar