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Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster

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Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster. / Hoffmann, A. A.; Clancy, D. J.; Merton, E.
In: Genetics, Vol. 136, No. 3, 1994, p. 993-999.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Hoffmann, AA, Clancy, DJ & Merton, E 1994, 'Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster', Genetics, vol. 136, no. 3, pp. 993-999.

APA

Hoffmann, A. A., Clancy, D. J., & Merton, E. (1994). Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster. Genetics, 136(3), 993-999.

Vancouver

Author

Hoffmann, A. A. ; Clancy, D. J. ; Merton, E. / Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster. In: Genetics. 1994 ; Vol. 136, No. 3. pp. 993-999.

Bibtex

@article{7603e776dfb24d24bc30b4c52829a912,
title = "Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster",
abstract = "In Drosophila melanogaster, weak incompatibility in crosses between infected and uninfected strains is associated with a Wolbachia microorganism. Crosses between infected males and uninfected females show a reduction (15-30%) in egg hatch. Progeny tests indicated that the infection is widespread in Australian D. melanogaster populations and that populations are polymorphic for the presence of the infection. The infection status of 266 lines from 12 populations along the eastern coast of Australia was determined by 4',6-diamidino-2-phenylindole (DAPI) staining of embryos. All populations contained both infected and uninfected flies. Infection frequencies varied between populations but there was no discernible geographical pattern. Laboratory experiments indicated that the infection was not associated with a reduction in fecundity as in Drosophila simulans. Incompatibility levels could not be increased by laboratory selection on isofemale lines. Factors contributing to the persistence of the infection in D. melanogaster populations are discussed.",
author = "Hoffmann, {A. A.} and Clancy, {D. J.} and E. Merton",
note = "Mar Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster",
year = "1994",
language = "English",
volume = "136",
pages = "993--999",
journal = "Genetics",
issn = "1943-2631",
publisher = "Genetics Society of America",
number = "3",

}

RIS

TY - JOUR

T1 - Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster

AU - Hoffmann, A. A.

AU - Clancy, D. J.

AU - Merton, E.

N1 - Mar Cytoplasmic Incompatibility in Australian Populations of Drosophila-Melanogaster

PY - 1994

Y1 - 1994

N2 - In Drosophila melanogaster, weak incompatibility in crosses between infected and uninfected strains is associated with a Wolbachia microorganism. Crosses between infected males and uninfected females show a reduction (15-30%) in egg hatch. Progeny tests indicated that the infection is widespread in Australian D. melanogaster populations and that populations are polymorphic for the presence of the infection. The infection status of 266 lines from 12 populations along the eastern coast of Australia was determined by 4',6-diamidino-2-phenylindole (DAPI) staining of embryos. All populations contained both infected and uninfected flies. Infection frequencies varied between populations but there was no discernible geographical pattern. Laboratory experiments indicated that the infection was not associated with a reduction in fecundity as in Drosophila simulans. Incompatibility levels could not be increased by laboratory selection on isofemale lines. Factors contributing to the persistence of the infection in D. melanogaster populations are discussed.

AB - In Drosophila melanogaster, weak incompatibility in crosses between infected and uninfected strains is associated with a Wolbachia microorganism. Crosses between infected males and uninfected females show a reduction (15-30%) in egg hatch. Progeny tests indicated that the infection is widespread in Australian D. melanogaster populations and that populations are polymorphic for the presence of the infection. The infection status of 266 lines from 12 populations along the eastern coast of Australia was determined by 4',6-diamidino-2-phenylindole (DAPI) staining of embryos. All populations contained both infected and uninfected flies. Infection frequencies varied between populations but there was no discernible geographical pattern. Laboratory experiments indicated that the infection was not associated with a reduction in fecundity as in Drosophila simulans. Incompatibility levels could not be increased by laboratory selection on isofemale lines. Factors contributing to the persistence of the infection in D. melanogaster populations are discussed.

M3 - Journal article

VL - 136

SP - 993

EP - 999

JO - Genetics

JF - Genetics

SN - 1943-2631

IS - 3

ER -