- THIS ARTICLE
- Full Text (PDF)
- Alert me when this article is cited
- Alert me if a correction is posted
- SERVICES
- Email this article to a friend
- Similar articles in this journal
- Similar articles in PubMed
- Alert me to new issues of the journal
- Download to citation manager
- Reprints & Permissions
- CITING ARTICLES
- Citing Articles via HighWire
- Citing Articles via Google Scholar
- GOOGLE SCHOLAR
- Articles by Ryo, H.
- Articles by Kondo, S.
- Search for Related Content
- PUBMED
- PubMed Citation
- Articles by Ryo, H.
- Articles by Kondo, S.
COMPARISON OF SOMATIC REVERSIONS BETWEEN THE IVORY ALLELE AND TRANSPOSON-CAUSED MUTANT ALLELES AT THE WHITE LOCUS OF DROSOPHILA MELANOGASTER AFTER LARVAL TREATMENT WITH X RAYS AND ETHYL METHANESULFONATE
Haruko Ryo 1, Mi Ae Yoo 1, Kazuo Fujikawa 2, and Sohei Kondo 1
1 Department of Fundamental Radiology, Faculty of Medicine,
Osaka University, Kita-ku, Osaka 530
2 Drug Safety Evaluation Laboratories, Central Research Division,
Takeda Chemical Industries Ltd., Yodogawa-ku, Osaka 532, Japan
Somatic reversion of strains with the ivory (wi) allele, a mutation associated with a tandem duplication of a DNA sequence at the white locus, increased with the age of larvae at the time of X-irradiation as expected from the increase in the number of target cells. In contrast, two independently isolated strains with unstable w+ loci associated with insertion of transposable elements showed higher reversion frequencies after treatment with X rays or ethyl methanesulfonate (EMS) at early larval stages than at late stages. Nevertheless, both the w i strain and the two unstable w+ strains reverted at nearly equal rates after treatment with X rays or EMS at early larval stages. Possible similarity in "hot spot" structure for the high reversibility of the two types of mutations is discussed in relation to production of presumed "mutator-type" cofactors specific to the transposon-caused mutations at early larval stages.
Submitted on October 29, 1984Accepted on February 14, 1985
This article has been cited by other articles:
![]() |
V. Sideraki, W. Huang, T. Palzkill, and H. F. Gilbert A secondary drug resistance mutation of TEM-1 beta -lactamase that suppresses misfolding and aggregation PNAS, December 8, 2000; (2000) 11454198. [Abstract] [Full Text] |
||||
![]() |
S. Suarez, O. Cabre, A. Velazquez, R. Marcos, and N. Xamena Sequence analysis of the boundaries of the tandem duplication from the white-ivory mutant of Drosophila melanogaster and two chemically induced revertants Mutagenesis, July 1, 2000; 15(4): 357 - 359. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Sideraki, W. Huang, T. Palzkill, and H. F. Gilbert A secondary drug resistance mutation of TEM-1 beta -lactamase that suppresses misfolding and aggregation PNAS, January 2, 2001; 98(1): 283 - 288. [Abstract] [Full Text] [PDF] |
||||

