Induced rates of mitotic crossing over and possible mitotic gene conversion per wing anlage cell in Drosophila melanogaster by X rays and fission neutrons

As a model for chromosome aberrations, radiation-induced mitotic recombination of mwh and flr genes in Drosophila melanogaster strain (mwh +/+ flr) was quantitatively studied. Fission neutrons were five to six times more effective than X rays per unit dose in producing either crossover-mwh/flr twins...

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Bibliographic Details
Published in:Genetics (Austin) Vol. 126; no. 1; pp. 157 - 166
Main Authors: Ayaki, T. (Nagasaki University School of Medicine, Nagasaki, Japan), Fujikawa, K, Ryo, H, Itoh, T, Kondo, S
Format: Journal Article
Language:English
Published: Bethesda, MD Genetics Soc America 01-09-1990
Genetics Society of America
Subjects:
ADN
RBE
DNA
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Summary:As a model for chromosome aberrations, radiation-induced mitotic recombination of mwh and flr genes in Drosophila melanogaster strain (mwh +/+ flr) was quantitatively studied. Fission neutrons were five to six times more effective than X rays per unit dose in producing either crossover-mwh/flr twins and mwh singles-or flr singles, indicating that common processes are involved in the production of crossover and flr singles. The X-ray-induced rate/wing anlage cell/Gy for flr singles was 1 x 10-5, whereas that of crossover was 2 x 1O-4; the former and the latter rate are of the same order of magnitude as those of gene conversion and crossover in yeast, respectively. Thus, we conclude that proximal-marker "flr" singles induced in the transheterozygote are gene convertants. Using the model based on yeast that recombination events result from repair of double-strand breaks or gaps, we propose that mitotic recombination in the fly is a secondary result of recombinational DNA repair. Evidence for recombinational misrepair in the fly is given. The relative ratio of radiation-induced mitotic crossover to spontaneous meiotic crossover is one order of magnitude higher in the fly than in yeast and humans
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ISSN:0016-6731
1943-2631
1943-2631
DOI:10.1093/genetics/126.1.157