1934
DOI: 10.1073/pnas.20.1.36
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On the Occurrence of Translocations and Autosomal Non-Disjunction in Drosophila melanogaster

Abstract: Recent findings on different plants indicate that the presence of extra chromosomes in an organism facilitates the occurrence of exchanges of non-homologous chromosomal parts. It seemed desirable to test if such exchanges occur also in heteroploid Drosophila melanogaster both from the point of the validity of the generalization of the findings as well as for the possibility of finding a method to obtain non-homologous exchanges in non-radiated flies. Triploid Drosophilae were chosen for this investigation. Tra… Show more

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Cited by 7 publications
(3 citation statements)
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“…Screening recombinant progeny provided irrevocable evidence that recombination involved physical exchange of DNA. Comparable results were also observed in Drosophila by Stern (1934) . Many species of evening primrose carry multiple reciprocal translocations and form multi-chromosomal meiotic rings involving all 14 chromosomes ( Cleland, 1972 ).…”
Section: Discussionsupporting
confidence: 79%
“…Screening recombinant progeny provided irrevocable evidence that recombination involved physical exchange of DNA. Comparable results were also observed in Drosophila by Stern (1934) . Many species of evening primrose carry multiple reciprocal translocations and form multi-chromosomal meiotic rings involving all 14 chromosomes ( Cleland, 1972 ).…”
Section: Discussionsupporting
confidence: 79%
“…Such a compensating system can be provided by triploid females, in which the proper kind of aneuploid gametes occurs with a predictable frequency. This method has been successfully used for investigations of autosomal non-disjunction or loss in males (STERN, 1934;PONTECORVO, 1942;FROST, 1961 a ) . But considering the interchromosomal effect of inversions on crossing-over it is of more interest to study what happens in the females.…”
Section: Methodsmentioning
confidence: 99%
“…A candidate for mediating PCV formation is Crossveinless-C (Cv-C), whose viable mutant allele displays a PCV-less phenotype [18]. Recently, cv-c was identified as RhoGAP88C required for a variety of embryo morphogenesis [19].…”
Section: Introductionmentioning
confidence: 99%