Literature DB >> 3857620

Lack of evidence for skeletal abnormalities in offspring of mice exposed to ethylnitrosourea.

D P Lovell, D B Willis, F M Johnson.   

Abstract

Using morphometrical methods, we investigated variation in the skeletons of more than 400 offspring of C57BL/6J and DBA/2J male mice that had received either a 250 mg/kg dose of the mutagen ethylnitrosourea or a solvent control. Sperm involved in the matings developed from cells in the spermatogonial stage at the time the animals were injected. Although variants were detected, differences in frequencies of gross abnormalities and minor variations in shape between treated and control groups were almost all nonsignificant. There were also no major differences in measures of variability within the groups of offspring from either the treated males or the control group. Additional examination of the skeleton for changes in the frequency of a series of nonmetrical variants also provided no evidence of differences between the treated and control groups that could be attributed to induced mutations. These results conflict with previous findings that ethylnitrosourea is a potent inducer of dominant skeletal mutations.

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Year:  1985        PMID: 3857620      PMCID: PMC397664          DOI: 10.1073/pnas.82.9.2852

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  17 in total

1.  EFFECTS OF LOW-LEVEL IRRADIATION ON FITNESS AND SKELETAL VARIATION IN AN INBRED MOUSE STRAIN.

Authors:  A G SEARLE
Journal:  Genetics       Date:  1964-11       Impact factor: 4.562

2.  Dominant mutations affecting the skeleton in offspring of x-irradiated male mice.

Authors:  U H Ehling
Journal:  Genetics       Date:  1966-12       Impact factor: 4.562

3.  Gamma-ray-induced dominant mutations that cause skeletal abnormalities in mice. I. Plan, summary of results and discussion.

Authors:  P B Selby; P R Selby
Journal:  Mutat Res       Date:  1977-06       Impact factor: 2.433

4.  Mutagenicity testing and risk estimation with mammals.

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

5.  Variants and mutants. A critical comment to P.B. Selby and S.L. Niemann, Non-breeding-test methods for dominant skeletal mutations shown by ethylnitrosourea to be easily applicable to offspring examined in specific-locus experiments.

Authors:  U H Ehling
Journal:  Mutat Res       Date:  1984-07       Impact factor: 2.433

6.  Variation in the shape of the mouse mandible. 1. Effect of age and sex on the results obtained from the discriminant functions used for genetic monitoring.

Authors:  D P Lovell; P Totman; F M Johnson
Journal:  Genet Res       Date:  1984-02       Impact factor: 1.588

7.  Non-breeding-test methods for dominant skeletal mutations shown by ethylnitrosourea to be easily applicable to offspring examined in specific-locus experiments.

Authors:  P B Selby; S L Niemann
Journal:  Mutat Res       Date:  1984-06       Impact factor: 2.433

8.  Morphometric studies in inbred and hybrid house mice. I. Patterns in the mean values.

Authors:  L Leamy
Journal:  J Hered       Date:  1982 May-Jun       Impact factor: 2.645

9.  Morphometric studies in inbred and hybrid house mice. II. Patterns in the variances.

Authors:  L Leamy
Journal:  J Hered       Date:  1982 Jul-Aug       Impact factor: 2.645

10.  Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse.

Authors:  W L Russell; E M Kelly; P R Hunsicker; J W Bangham; S C Maddux; E L Phipps
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

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  1 in total

1.  Detection of new MHC mutations in mice by skin grafting, tumor transplantation and monoclonal antibodies: a comparison.

Authors:  I K Egorov; O S Egorov
Journal:  Genetics       Date:  1988-02       Impact factor: 4.562

  1 in total

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