Skip to main content
Environmental Health Perspectives logoLink to Environmental Health Perspectives
. 1979 Aug;31:151–159. doi: 10.1289/ehp.7931151

Microtus oeconomus (Rodentia), a useful mammal for studying the induction of sex-chromosome nondisjunction and diploid gametes in male germ cells.

A D Tates
PMCID: PMC1637652  PMID: 387396

Abstract

Preliminary data indicate that chemicals can also increase the frequency of sex-chromosome nondisjunction. Positive results--which certainly need further confirmation--have been obtained for MMS, p-fluorophenylalanine, vincristine, procarbazine, carbendazim, and bleomycin. Nocodazole, benomyl, colcemic, 6-mercaptopurine, and halothane were all negative at the concentrations tested. For the induction of diploid spermatids positive results were only obtained for MMS and parafluorophenylalanine. In view of the results obtained, the Microtus system is considered a very useful tool for analyzing factors contributing to the high frequency of aneuploidy and triploidy among abortuses and of aneuploidy in liveborn infants of men. A method is described for the detection of sex-chromosome nondisjunction and diploid spermatids in male germ cells of the field vole Microtus oeconomus. The method is based on the unique distribution pattern of heterochromatin in Microtus cells, which makes it possible to identify X and Y chromosomes in early spermatids with a simple C-banding procedure. Slide preparation is easy. Scoring of early spermatids for extra sex-chromosomes is simple and 2000-4000 cells per hour can be examined. With the Microtus system it has now been demonstrated that radiation of spermatocyte stages with doses of 50, 100 and 200 R results in a higher frequency of sex chromosome nondisjunction and of diploid gametes. Both types of aberrant gametes can be produced during the first and second meiotic division.

Full text

PDF
151

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bignami M., Aulicino F., Velcich A., Carere A., Morpurgo G. Mutagenic and recombinogenic action of pesticides in Aspergillus nidulans. Mutat Res. 1977 Dec;46(6):395–402. doi: 10.1016/0165-1161(77)90017-6. [DOI] [PubMed] [Google Scholar]
  2. Cox D. M. A quantitative analysis of colcemid-induced chromosomal nondisjunction in Chinese hamster cells in vitro. Cytogenet Cell Genet. 1973;12(3):165–174. doi: 10.1159/000130452. [DOI] [PubMed] [Google Scholar]
  3. De Brabander M., Geuens G., Van De Veire R., Thoneé F., Aerts F., Desplenter L., De Cree J., Borgers M. The effects of R U7934 (NSC 238159), a new antimicrotubular substance, on the ultrastructure of neoplastic cells in vivo. Eur J Cancer. 1977 Jun;13(6):511–528. doi: 10.1016/0014-2964(77)90113-x. [DOI] [PubMed] [Google Scholar]
  4. Generoso W. M., Preston R. J., Brewen J. G. 6-mercaptopurine, an inducer of cytogenetic and dominant-lethal effects in premeiotic and early meiotic germ cells of male mice. Mutat Res. 1975 Jun;28(3):437–447. doi: 10.1016/0027-5107(75)90237-7. [DOI] [PubMed] [Google Scholar]
  5. Grant C. J., Powell J. N., Radford S. G. The induction of chromosomal abnormalities by inhalational anaesthetics. Mutat Res. 1977 Jun;46(3):177–184. doi: 10.1016/0165-1161(77)90024-3. [DOI] [PubMed] [Google Scholar]
  6. Hittelman W. N., Rao P. N. Bleomycin-induced damage in prematurely condensed chromosomes and its relationship to cell cycle progression in CHO cells. Cancer Res. 1974 Dec;34(12):3433–3439. [PubMed] [Google Scholar]
  7. Holden H. E., Ray V. A., Wahrenburg M. G., Zelenski J. D. Mutagenicity studies with 6-mercaptopurine. I. Cytogenetic activity in vivo. Mutat Res. 1973 Nov;20(2):257–263. doi: 10.1016/0027-5107(73)90195-4. [DOI] [PubMed] [Google Scholar]
  8. Kappas A. On the mechanisms of induced somatic recombination by certain fungicides in Aspergillus nidulans. Mutat Res. 1978 Aug;51(2):189–197. doi: 10.1016/s0027-5107(78)80018-9. [DOI] [PubMed] [Google Scholar]
  9. Kato H., Yosida T. H. Nondisjunction of chromosomes in a synchronized cell population initiated by reversal of Colcemid inhibition. Exp Cell Res. 1970 Jun;60(3):459–464. doi: 10.1016/0014-4827(70)90544-6. [DOI] [PubMed] [Google Scholar]
  10. Knill-Jones R. P., Newman B. J., Spence A. A. Anesthetic practice and pregnancy. Controlled survey of male anaesthetists in the United Kingdom. Lancet. 1975 Oct 25;2(7939):807–809. [PubMed] [Google Scholar]
  11. Maier P., Schmid W. Ten model mutagens evaluated by the micronucleus test. Mutat Res. 1976 Nov;40(4):325–337. doi: 10.1016/0165-1218(76)90031-8. [DOI] [PubMed] [Google Scholar]
  12. Promchainant C. Cytogenetic effect of bleomycin on human leukocytes in vitro. Mutat Res. 1975 Apr;28(1):107–112. doi: 10.1016/0027-5107(75)90320-6. [DOI] [PubMed] [Google Scholar]
  13. Shanfield B., Käfer E. Chemical induction of mitotic recombination in Aspergillus nidulans. Genetics. 1971 Feb;67(2):209–219. doi: 10.1093/genetics/67.2.209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Stavrovskaya A. A., Kopnin B. P. Colcemid-induced polyploidy and aneuploidy in normal and tumour cells in vitro. Int J Cancer. 1975 Nov 15;16(5):730–737. doi: 10.1002/ijc.2910160505. [DOI] [PubMed] [Google Scholar]
  15. Tates A. D., Pearson P. L., Geraedts J. P. Identification of X and Y spermatozoa in the northern vole, Microtus oeconomus. J Reprod Fertil. 1975 Jan;42(1):195–198. doi: 10.1530/jrf.0.0420195. [DOI] [PubMed] [Google Scholar]
  16. Tates A. D., Pearson P. L., van der Ploeg M., de Vogel N. The induction of sex-chromosomal nondisjunction and diploid spermatids following x-irradiation of pre-spermatid stages in the northern vole Microtus oeconomus. Mutat Res. 1979 Jun;61(1):87–101. doi: 10.1016/0027-5107(79)90010-1. [DOI] [PubMed] [Google Scholar]
  17. Tidd D. M., Paterson A. R. A biochemical mechanism for the delayed cytotoxic reaction of 6-mercaptopurine. Cancer Res. 1974 Apr;34(4):738–746. [PubMed] [Google Scholar]

Articles from Environmental Health Perspectives are provided here courtesy of National Institute of Environmental Health Sciences

RESOURCES