Abstract
The latitudinal cline in P-M gonadal dysgenesis potential in eastern Australia has been shown to comprise three regions which are, from north to south respectively, P, Q, and M, with the P-to-Q and Q-to-M transitions occurring over relatively short distances. The P element complements of 30 lines from different regions of the cline were determined by molecular techniques. The total amount of P element-hybridizing DNA was high in all lines, and it did not correlate in any obvious way with the P-M phenotypes of individual lines. The number of potentially full-sized P elements per genome was high in lines from the P regions, but variable or low among lines from the Q and M regions, and thus declined overall from north to south. A particular P element deletion-derivative, the KP element, occurred in all the tested lines. The number of KP elements was low in lines from the P region, much higher in lines from the Q region, and highest among lines from the M region, thus forming a cline reciprocal to that of the full-sized P elements. Another transposable element, hobo, which has been described as causing dysgenic traits similar to those of P-M hybrid dysgenesis, was shown to be present in all lines and to vary among them in number, but not in any latitudinal pattern. The P-M cline in gonadal dysgenesis potential can be inferred to be based on underlying clinal patterns of genomic P element complements. P activity of a line was positively correlated with the number of full-sized P elements in the line, and negatively correlated with the number of KP elements. Among Q and M lines, regulatory ability was not correlated with numbers of KP elements.
Full Text
The Full Text of this article is available as a PDF (4.3 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Anxolabéhère D., Kidwell M. G., Periquet G. Molecular characteristics of diverse populations are consistent with the hypothesis of a recent invasion of Drosophila melanogaster by mobile P elements. Mol Biol Evol. 1988 May;5(3):252–269. doi: 10.1093/oxfordjournals.molbev.a040491. [DOI] [PubMed] [Google Scholar]
- Anxolabéhère D., Nouaud D., Périquet G., Tchen P. P-element distribution in Eurasian populations of Drosophila melanogaster: A genetic and molecular analysis. Proc Natl Acad Sci U S A. 1985 Aug;82(16):5418–5422. doi: 10.1073/pnas.82.16.5418. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bingham P. M., Kidwell M. G., Rubin G. M. The molecular basis of P-M hybrid dysgenesis: the role of the P element, a P-strain-specific transposon family. Cell. 1982 Jul;29(3):995–1004. doi: 10.1016/0092-8674(82)90463-9. [DOI] [PubMed] [Google Scholar]
- Black D. M., Jackson M. S., Kidwell M. G., Dover G. A. KP elements repress P-induced hybrid dysgenesis in Drosophila melanogaster. EMBO J. 1987 Dec 20;6(13):4125–4135. doi: 10.1002/j.1460-2075.1987.tb02758.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blackman R. K., Grimaila R., Koehler M. M., Gelbart W. M. Mobilization of hobo elements residing within the decapentaplegic gene complex: suggestion of a new hybrid dysgenesis system in Drosophila melanogaster. Cell. 1987 May 22;49(4):497–505. doi: 10.1016/0092-8674(87)90452-1. [DOI] [PubMed] [Google Scholar]
- Boussy I. A. A latitudinal cline in P-M gonadal dysgenesis potential in Australian Drosophila melanogaster populations. Genet Res. 1987 Feb;49(1):11–18. doi: 10.1017/s0016672300026677. [DOI] [PubMed] [Google Scholar]
- Boussy I. A., Kidwell M. G. The P-M hybrid dysgenesis cline in Eastern Australian Drosophila melanogaster: discrete P, Q and M regions are nearly contiguous. Genetics. 1987 Apr;115(4):737–745. doi: 10.1093/genetics/115.4.737. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Daniels S. B., Clark S. H., Kidwell M. G., Chovnick A. Genetic transformation of Drosophila melanogaster with an autonomous P element: phenotypic and molecular analyses of long-established transformed lines. Genetics. 1987 Apr;115(4):711–723. doi: 10.1093/genetics/115.4.711. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Daniels S. B., Strausbaugh L. D., Armstrong R. A. Molecular analysis of P element behavior in Drosophila simulans transformants. Mol Gen Genet. 1985;200(2):258–265. doi: 10.1007/BF00425433. [DOI] [PubMed] [Google Scholar]
- Daniels S. B., Strausbaugh L. D. The distribution of P-element sequences in Drosophila: the willistoni and saltans species groups. J Mol Evol. 1986;23(2):138–148. doi: 10.1007/BF02099908. [DOI] [PubMed] [Google Scholar]
- Engels W. R. A trans-acting product needed for P factor transposition in Drosophila. Science. 1984 Dec 7;226(4679):1194–1196. doi: 10.1126/science.6095450. [DOI] [PubMed] [Google Scholar]
- Engels W. R., Preston C. R. Components of hybrid dysgenesis in a wild population of Drosophila melanogaster. Genetics. 1980 May;95(1):111–128. doi: 10.1093/genetics/95.1.111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Engels W. R., Preston C. R. Hybrid dysgenesis in Drosophila melanogaster: the biology of female and male sterility. Genetics. 1979 May;92(1):161–174. doi: 10.1093/genetics/92.1.161. [DOI] [PMC free article] [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]
- Kaplan N., Darden T., Langley C. H. Evolution and extinction of transposable elements in Mendelian populations. Genetics. 1985 Feb;109(2):459–480. doi: 10.1093/genetics/109.2.459. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kidwell M. G., Kidwell J. F., Sved J. A. Hybrid Dysgenesis in DROSOPHILA MELANOGASTER: A Syndrome of Aberrant Traits Including Mutation, Sterility and Male Recombination. Genetics. 1977 Aug;86(4):813–833. doi: 10.1093/genetics/86.4.813. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Laski F. A., Rio D. C., Rubin G. M. Tissue specificity of Drosophila P element transposition is regulated at the level of mRNA splicing. Cell. 1986 Jan 17;44(1):7–19. doi: 10.1016/0092-8674(86)90480-0. [DOI] [PubMed] [Google Scholar]
- McGinnis W., Shermoen A. W., Beckendorf S. K. A transposable element inserted just 5' to a Drosophila glue protein gene alters gene expression and chromatin structure. Cell. 1983 Aug;34(1):75–84. doi: 10.1016/0092-8674(83)90137-x. [DOI] [PubMed] [Google Scholar]
- Nitasaka E., Mukai T., Yamazaki T. Repressor of P elements in Drosophila melanogaster: Cytotype determination by a defective P element carrying only open reading frames 0 through 2. Proc Natl Acad Sci U S A. 1987 Nov;84(21):7605–7608. doi: 10.1073/pnas.84.21.7605. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O'Hare K., Rubin G. M. Structures of P transposable elements and their sites of insertion and excision in the Drosophila melanogaster genome. Cell. 1983 Aug;34(1):25–35. doi: 10.1016/0092-8674(83)90133-2. [DOI] [PubMed] [Google Scholar]
- Rushlow C. A., Bender W., Chovnick A. Studies on the mechanism of heterochromatic position effect at the rosy locus of Drosophila melanogaster. Genetics. 1984 Nov;108(3):603–615. doi: 10.1093/genetics/108.3.603. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sakoyama Y., Todo T., Ishiwa-Chigusa S., Honjo T., Kondo S. Structures of defective P transposable elements prevalent in natural Q and Q-derived M strains of Drosophila melanogaster. Proc Natl Acad Sci U S A. 1985 Sep;82(18):6236–6239. doi: 10.1073/pnas.82.18.6236. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simmons G. M. Sterility-mutability correlation. On the correlation between sterility and mutability during P-M hybrid dysgenesis in Drosophila melanogaster. Genet Res. 1987 Aug;50(1):73–76. doi: 10.1017/s0016672300023363. [DOI] [PubMed] [Google Scholar]
- Simmons M. J., Bucholz L. M. Transposase titration in Drosophila melanogaster: a model of cytotype in the P-M system of hybrid dysgenesis. Proc Natl Acad Sci U S A. 1985 Dec;82(23):8119–8123. doi: 10.1073/pnas.82.23.8119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Streck R. D., Macgaffey J. E., Beckendorf S. K. The structure of hobo transposable elements and their insertion sites. EMBO J. 1986 Dec 20;5(13):3615–3623. doi: 10.1002/j.1460-2075.1986.tb04690.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yannopoulos G., Stamatis N., Monastirioti M., Hatzopoulos P., Louis C. hobo is responsible for the induction of hybrid dysgenesis by strains of Drosophila melanogaster bearing the male recombination factor 23.5MRF. Cell. 1987 May 22;49(4):487–495. doi: 10.1016/0092-8674(87)90451-x. [DOI] [PubMed] [Google Scholar]