scholarly journals AN INFLUENCE OF MATERNAL NUTRITION UPON THE GROSS CHROMOSOMAL MUTATION FREQUENCY RECOVERED FROM X-RAYED SPERM OF DROSOPHILA MELANOGASTER

Genetics ◽  
1963 ◽  
Vol 48 (5) ◽  
pp. 703-710
Author(s):  
Irwin H Herskowitz
Genetics ◽  
1979 ◽  
Vol 92 (1) ◽  
pp. 151-160
Author(s):  
H Traut

ABSTRACT When females of Drosophila melanogaster are treated with chemical or physical mutagens, not only in one but also in both of the two homologous X chromosomes of a given oocyte, a recessive sex-linked lethal mutation may be induced. A method is described that discriminates between such "single" and "double mutations." A theory is developed to show how a comparison between the expected and the observed frequency of double mutations yields an indication of the intercellular distribution (random or nonrandom) of recessive lethal mutations induced by mutagenic agents in oocytes and, consequently, of the distribution (homogeneous or nonhomogeneous) of those agents.—Three agents were tested: FUdR (12.5, 50.0 and 81.0,μg/ml), mitomycin C (130.0 μg/ml) and X rays (2000 R, 150 kV). After FUdR feeding, no increase in the mutation frequency usually observed in D. melanogaster without mutagenic treatment was obtained (u=0.13%, namely three single mutations among 2332 chromosomes tested). After mitomycin C feeding, 104. single and three double mutations were obtained. All of the 50 mutations observed after X irradiation were single mutations. The results obtained in the mitomycin C and radiation experiments favor the assumption of a random intercellular distribution of recessive lethal mutations induced by these two agents in oocytes of D. melanogaster. Reasons are discussed why for other types of mutagenic agents nonrandom distributions may be observed with our technique.


2007 ◽  
Vol 81 (9) ◽  
pp. 4900-4903
Author(s):  
Christophe Terzian ◽  
Michel Henry ◽  
Andreas Meyerhans ◽  
Simon Wain-Hobson ◽  
Jean-Pierre Vartanian

ABSTRACT The retroviral mutation rate is susceptible to a number of variables, including the balance between intracellular deoxynucleoside triphosphate (dNTP) pools. While this follows from tissue culture studies, the issue has never been addressed directly in vivo. To explore this question in a tractable experimental system, we analyzed the impact of thymidine treatment on the synthesis of gypsy retroelement cDNA from Drosophila melanogaster during development through to hatching. The mutation frequency was enhanced approximately 16-fold over the levels seen in the experimental background. Due to the lack of proofreading, these gypsy elements represent hypervariable loci within the Drosophila genome, suggesting that dNTP pool imbalances in vivo are mutagenic.


2009 ◽  
Vol 171 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Keiji Ogura ◽  
Junji Magae ◽  
Yasushi Kawakami ◽  
Takao Koana

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