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Updated: Aug 17, 2026

Mouse Oocyte Microinjection, Maturation and Ploidy Assessment
Published on: July 23, 2011
Testing for nondisjunction in the mouse
Abstract:
Tests for nondisjunction have been carried out in male and female mice. Ten-day fetal progeny of control and treated adults have been karyotyped to establish spontaneous and induced levels of aneuploidy. In males, the effects of 100 rad x-rays on type A spermatogonia and early primary spermatocytes, and the effects of Mitomycin C (2 mg/kg) on early primary spermatocytes, have been tested. The results show insensitivity of primary spermatocytes to both agents, but a 3.5-fold increase in nondisjunction following spermatogonial irradiation. In females, comparisons have been made between young controls, young x-rayed (5 rad), aged controls and aged x-rayed (5 rad) animals. The "ageing effect" on nondisjunction is observed, but too few fetuses have been analyzed to reach conclusions regarding enhancement of nondisjunction levels by low doses of x-rays.
Insights
Spermatogonial irradiation in male mice significantly increased nondisjunction, while primary spermatocytes showed insensitivity to radiation and Mitomycin C. Female mice exhibited an "ageing effect" on nondisjunction, requiring further study for low-dose x-ray effects.
Area of Science:
- Reproductive biology
- Genetics
- Toxicology
Background:
- Nondisjunction, the failure of chromosomes to separate properly during cell division, can lead to aneuploidy and developmental abnormalities.
- Understanding the factors that induce nondisjunction is crucial for assessing reproductive risks.
- Mice are a common model organism for studying genetic toxicology and reproductive effects.
Purpose of the Study:
- To investigate the induction of nondisjunction in male and female mice by specific agents.
- To determine the sensitivity of different germ cell stages to genotoxic agents.
- To evaluate the influence of age and low-dose radiation on nondisjunction in females.
Main Methods:
- Karyotyping of 10-day fetal progeny from control and treated adult mice.
- Exposure of male mice to 100 rad x-rays (affecting spermatogonia and primary spermatocytes) or Mitomycin C (affecting primary spermatocytes).
- Exposure of female mice of different ages to 5 rad x-rays.
Main Results:
- Spermatogonial irradiation in males resulted in a 3.5-fold increase in nondisjunction.
- Primary spermatocytes in males demonstrated insensitivity to both x-rays and Mitomycin C.
- An "ageing effect" on nondisjunction was observed in female mice, but low-dose x-ray effects were inconclusive due to small sample size.
Conclusions:
- Spermatogonia are a sensitive target for radiation-induced nondisjunction in male mice.
- Early primary spermatocytes are resistant to induced nondisjunction by the tested agents.
- Female reproductive aging influences nondisjunction rates, warranting further investigation into low-dose radiation effects.
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