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Title: Mechanisms of mutagenesis: Analysis through the use of alcohol dehydrogenase in Drosophila: Final report

Technical Report ·
OSTI ID:7187205

Our original objective was to understand the mechanism of mutagenesis of several important mutagens in higher organisms. Our approach was to try to deduce this mechanism by working backwards from its final effects. The strategy that we used in an effort to carry out our studies was to make mutations in the alcohol dehydrogenase gene of Drosophila melanogaster and sequence the modified genes. Most of our work was focused on an array of mutants that we had induced with formaldehyde, a potent mutagen in Drosophila, and with ethyl methane sulfonate. Over the course of the project period we cloned and sequenced the ADH gene from four formalde-induced mutants and from one EMS mutant. We showed that the four formaldehyde-induced mutants contained small deletions within the protein-coding region of their ADH genes ranging in size from between 6 and 34 bp. The one EMS-induced mutant was shown by DNA sequencing to bear an AT to GC sequence change at a tryptophan codon near the c-terminal coding portion of the gene. These results have significantly increased our understanding of the mechanism(s) of mutagenesis in higher organisms. 20 refs., 1 fig.

Research Organization:
Rutgers-the State Univ., Piscataway, NJ (USA). Waksman Inst. of Microbiology
DOE Contract Number:
AC02-81EV10566
OSTI ID:
7187205
Report Number(s):
DOE/EV/10566-7; ON: DE87003871
Country of Publication:
United States
Language:
English