Literature DB >> 3116423

Mechanistic and methodological aspects of chemically-induced somatic mutation and recombination in Drosophila melanogaster.

E W Vogel1, J A Zijlstra.   

Abstract

This study presents the analysis of chemically-induced somatic mutations and chromosomal damage in the eye imaginal discs of Drosophila larvae, assayed later as twin (TS) and single light (LS) mosaic spots in the adult eyes. Regarding the question as to what kind of DNA alterations contribute to somatic cell mutagenicity, the approach followed here has been to investigate the possible differences in response between male (hemizygous for an X) and female (homozygous) larvae, rod-X/rod-X versus ring-X/rod-X genotypes and inversion-heterozygotes versus genotypes not carrying an inversion. The systems chosen for this analysis were the white-coral/white (wco/w) and the white+/white (w+/w) eye mosaic system. The principle findings with 12 mutagens of different modes of action are as follows: (1) At least 98% of all TS and LS induced by cisplatin (DDP) in wco/w female larvae and about 95% of those by formaldehyde (FA) appear as the result of recombinogenic activity between the two homologous X-chromosomes. The corresponding estimates for MMS, EMS and ENU are 81%, 73% and 61%, respectively. (2) The long scS1L sc8R inversion, which also contains In(1)dl-49, suppresses induction of TS to 83-93%. There was also a sharp decline in the frequency of LS in inversion heterozygotes for DDP (91%), FA (86%), MMS (52%) and EMS (47%). (3) Ethylnitrosourea (ENU) was the mutagen for which introduction of the inverted chromosome reduced only slightly (23%) the frequency of LS, indicating that the majority of them were somatic mutations (and deletions) at the white locus. (4) In w/RX females heterozygous for a ring-X chromosome, the frequency of LS was only approximately one tenth of that of the control (w+/w) group, after exposure to MMS or DDP. The explanation is that exchange processes involving the ring frequently lead to genetic imbalance with subsequent cell killing.

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Year:  1987        PMID: 3116423     DOI: 10.1016/0165-1161(87)90010-0

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  6 in total

1.  Cisplatin increases meiotic crossing-over in mice.

Authors:  W H Hanneman; M E Legare; S Sweeney; J C Schimenti
Journal:  Proc Natl Acad Sci U S A       Date:  1997-08-05       Impact factor: 11.205

2.  Combining Drosophila melanogaster somatic-mutation-recombination and electron-spin-resonance-spectroscopy data to interpret epidemiologic observations on chromium carcinogenicity.

Authors:  A J Katz; A Chiu; J Beaubier; X Shi
Journal:  Mol Cell Biochem       Date:  2001-06       Impact factor: 3.396

3.  Overexpression of a Rrp1 transgene reduces the somatic mutation and recombination frequency induced by oxidative DNA damage in Drosophila melanogaster.

Authors:  A Szakmary; S M Huang; D T Chang; P A Beachy; M Sander
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-20       Impact factor: 11.205

4.  Positional cloning and characterization of Mei1, a vertebrate-specific gene required for normal meiotic chromosome synapsis in mice.

Authors:  Brian J Libby; Laura G Reinholdt; John C Schimenti
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-10       Impact factor: 11.205

Review 5.  Genetic and cellular mechanisms in chromium and nickel carcinogenesis considering epidemiologic findings.

Authors:  Arthur Chiu; A J Katz; Jefferson Beaubier; Nancy Chiu; Xianglin Shi
Journal:  Mol Cell Biochem       Date:  2004-01       Impact factor: 3.396

6.  In vivo evaluation of the toxic activity and genotoxicity of the Hymenaea courbaril L.'s resin in Drosophila melanogaster.

Authors:  Jorge Anaya-Gil; Patricia Ramos-Morales; Adriana Muñoz-Hernandez; Adriana Bermúdez; Harold Gomez-Estrada
Journal:  Saudi J Biol Sci       Date:  2021-09-13       Impact factor: 4.219

  6 in total

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