Literature DB >> 199138

Dominant lethal mutations in male mice.

U H Ehling.   

Abstract

Dominant lethal mutations are due to chromosome aberrations as demonstrated by analysis of first cleavage. With a sample size of 40-45 mice per dose the induction of dominant lethal mutations by 10 mg/kg of methyl methanesulfonat (MMS) can be detected in spermatids in the mating interval 9-12 days posttreatment (6-11%). In the same mating interval a dose of 150 mg/kg of MMS induces 100% dominant lethal mutations. MMS and other chemical mutagens can be characterized by their different spermatogenic response. The germ cell stage specific induction of dominant lethal mutations by chemical agents is very likely due to their different pathways and therefore, to different effects on the structural and macromolecular changes during spermatogenesis. The feasibility of standardizing test protocol for the dominant lethal assay in mice, based on collaborative studies, is discussed. The reproducibility of results and the sensitivity of the induction of dominant lethal mutations in the collaborative studies demonstrate the usefullness of the method for mutagenicity screening.

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Year:  1977        PMID: 199138     DOI: 10.1007/bf00293658

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  19 in total

1.  A mammalian spot test: induction of genetic alterations in pigment cells of mouse embryos with x-rays and chemical mutagens.

Authors:  R Fahrig
Journal:  Mol Gen Genet       Date:  1975-07-10

2.  Micronuclei in mouse bone-marrow cells. A simple in vivo model for the evaluation of drug-induced chromosomal aberrations.

Authors:  B E Matter; J Grauwiler
Journal:  Mutat Res       Date:  1974-05       Impact factor: 2.433

3.  Recent findings concerning dose response relationship in mutagenicity testing of chemicals.

Authors:  H Frohberg; M S Schencking
Journal:  Arch Toxicol       Date:  1974-03-29       Impact factor: 5.153

4.  Differential spermatogenic response of mice to the induction of dominant-lethal mutations by n-propyl methanesulfonate and isopropyl methanesulfonate.

Authors:  U H Ehling; D G Doherty; H V Malling
Journal:  Mutat Res       Date:  1972-06       Impact factor: 2.433

5.  Chemical mutagens in the human environment.

Authors:  S S Epstein; H Shafner
Journal:  Nature       Date:  1968-07-27       Impact factor: 49.962

6.  Induction of dominant lethal mutations by alkylating agents in male mice.

Authors:  U H Ehling; R B Cumming; H V Malling
Journal:  Mutat Res       Date:  1968 May-Jun       Impact factor: 2.433

7.  Validation of the in vivo somatic mutation method in the mouse as a prescreen for germinal point mutations.

Authors:  L B Russell
Journal:  Arch Toxicol       Date:  1977-09-21       Impact factor: 5.153

8.  Mutagenicity testing and risk estimation with mammals.

Authors:  U H Ehling
Journal:  Mutat Res       Date:  1976-11-01       Impact factor: 2.433

9.  Heritable translocation test and dominant-lethal assay in mice with methyl methanesulfonate.

Authors:  R Lang; I D Adler
Journal:  Mutat Res       Date:  1977       Impact factor: 2.433

10.  The dominant-lethal test: potential limitations and statistical considerations for safety evaluation.

Authors:  S Green; J A Springer
Journal:  Environ Health Perspect       Date:  1973-12       Impact factor: 9.031

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  4 in total

1.  Differential response of mouse male germ-cell stages to radiation-induced specific-locus and dominant mutations.

Authors:  W L Russell; J W Bangham; L B Russell
Journal:  Genetics       Date:  1998-04       Impact factor: 4.562

2.  Statistical problems in mutagenicity tests.

Authors:  J Vollmar
Journal:  Arch Toxicol       Date:  1977-09-21       Impact factor: 5.153

3.  Induction of dominant lethal mutations in male mice by fosfestrol.

Authors:  U H Ehling
Journal:  Arch Toxicol       Date:  1979-07-11       Impact factor: 5.153

4.  Action of N-isopropyl-alpha-(2-methylhydrazino)-p-toluamide hydrochloride (procarbazine hydrochloride) in the germ tissue of mice: dominant lethal effects.

Authors:  G T Roberts; F M Johnson; H V Malling; R K Sharma
Journal:  Arch Toxicol       Date:  1979-02-23       Impact factor: 5.153

  4 in total

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