Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1992 Sep 1;89(17):7866–7870. doi: 10.1073/pnas.89.17.7866

Mutational spectrum at the Hprt locus in splenic T cells of B6C3F1 mice exposed to N-ethyl-N-nitrosourea.

T R Skopek 1, V E Walker 1, J E Cochrane 1, T R Craft 1, N F Cariello 1
PMCID: PMC49815  PMID: 1518807

Abstract

We have determined the mutational spectrum of N-ethyl-N-nitrosourea (ENU) in exon 3 of the hypoxanthine (guanine) phosphoribosyltransferase gene (Hprt) in splenic T cells following in vivo exposure of male B6C3F1 mice (5-7 weeks old) to ENU. Hprt- mutants were isolated by culturing splenic T cells in microtiter dishes containing medium supplemented with interleukin 2, concanavalin A, and 6-thioguanine. DNA was extracted from 6-thioguanine-resistant colonies and amplified by the polymerase chain reaction (PCR) using primers flanking Hprt exon 3. Identification of mutant sequences and purification of mutant DNA from contaminating wild-type Hprt DNA was accomplished by denaturing-gradient gel electrophoresis. Purified mutant DNA was then sequenced. Treatment of mice with ENU at 40 mg/kg of body weight produced a Hprt- mutant frequency of 7.3 x 10(-5) in splenic T cells, approximately 35-fold above background levels. Sixty-nine of the 521 Hprt- mutants analyzed contained mutations in exon 3 (13%). Transversions and transitions at A.T base pairs dominated the spectrum; 62 of the 69 exon 3 mutations were at A.T base pairs (14 different sites). Thirteen of 14 thymine bases undergoing mutation (61 of 62 mutations at A.T bases) were located on the nontranscribed strand of exon 3. The majority of the remaining mutations (6 of 69) were transitions at a single G.C base pair. These results suggest the importance of thymidine alkylation in ENU-induced mutagenesis in vivo. The mouse Hprt- T-cell cloning/sequencing assay described here may represent a useful system for studying the molecular mechanism of chemically induced mutation occurring in vivo in an endogenous gene.

Full text

PDF
7866

Selected References

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

  1. Aidoo A., Lyn-Cook L. E., Mittelstaedt R. A., Heflich R. H., Casciano D. A. Induction of 6-thioguanine-resistant lymphocytes in Fischer 344 rats following in vivo exposure to N-ethyl-N-nitrosourea and cyclophosphamide. Environ Mol Mutagen. 1991;17(3):141–151. doi: 10.1002/em.2850170302. [DOI] [PubMed] [Google Scholar]
  2. Albertini R. J., Castle K. L., Borcherding W. R. T-cell cloning to detect the mutant 6-thioguanine-resistant lymphocytes present in human peripheral blood. Proc Natl Acad Sci U S A. 1982 Nov;79(21):6617–6621. doi: 10.1073/pnas.79.21.6617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Beranek D. T. Distribution of methyl and ethyl adducts following alkylation with monofunctional alkylating agents. Mutat Res. 1990 Jul;231(1):11–30. doi: 10.1016/0027-5107(90)90173-2. [DOI] [PubMed] [Google Scholar]
  4. Bhanot O. S., Grevatt P. C., Donahue J. M., Gabrielides C. N., Solomon J. J. In vitro DNA replication implicates O2-ethyldeoxythymidine in transversion mutagenesis by ethylating agents. Nucleic Acids Res. 1992 Feb 11;20(3):587–594. doi: 10.1093/nar/20.3.587. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Bronstein S. M., Cochrane J. E., Craft T. R., Swenberg J. A., Skopek T. R. Toxicity, mutagenicity, and mutational spectra of N-ethyl-N-nitrosourea in human cell lines with different DNA repair phenotypes. Cancer Res. 1991 Oct 1;51(19):5188–5197. [PubMed] [Google Scholar]
  6. Bronstein S. M., Skopek T. R., Swenberg J. A. Efficient repair of O6-ethylguanine, but not O4-ethylthymine or O2-ethylthymine, is dependent upon O6-alkylguanine-DNA alkyltransferase and nucleotide excision repair activities in human cells. Cancer Res. 1992 Apr 1;52(7):2008–2011. [PubMed] [Google Scholar]
  7. Burns P. A., Gordon A. J., Kunsmann K., Glickman B. W. Influence of neighboring base sequence on the distribution and repair of N-ethyl-N-nitrosourea-induced lesions in Escherichia coli. Cancer Res. 1988 Aug 15;48(16):4455–4458. [PubMed] [Google Scholar]
  8. Cariello N. F., Keohavong P., Kat A. G., Thilly W. G. Molecular analysis of complex human cell populations: mutational spectra of MNNG and ICR-191. Mutat Res. 1990 Aug;231(2):165–176. doi: 10.1016/0027-5107(90)90023-w. [DOI] [PubMed] [Google Scholar]
  9. Chen R. H., Maher V. M., McCormick J. J. Effect of excision repair by diploid human fibroblasts on the kinds and locations of mutations induced by (+/-)-7 beta,8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10- tetrahydrobenzo[a]pyrene in the coding region of the HPRT gene. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8680–8684. doi: 10.1073/pnas.87.21.8680. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dempsey J. L., Morley A. A. Measurement of in vivo mutant frequency in lymphocytes in the mouse. Environ Mutagen. 1986;8(3):385–391. doi: 10.1002/em.2860080307. [DOI] [PubMed] [Google Scholar]
  11. Eckert K. A., Ingle C. A., Drinkwater N. R. N-ethyl-N-nitrosourea induces A:T to C:G transversion mutations as well as transition mutations in SOS-induced Escherichia coli. Carcinogenesis. 1989 Dec;10(12):2261–2267. doi: 10.1093/carcin/10.12.2261. [DOI] [PubMed] [Google Scholar]
  12. Ellison K. S., Dogliotti E., Connors T. D., Basu A. K., Essigmann J. M. Site-specific mutagenesis by O6-alkylguanines located in the chromosomes of mammalian cells: influence of the mammalian O6-alkylguanine-DNA alkyltransferase. Proc Natl Acad Sci U S A. 1989 Nov;86(22):8620–8624. doi: 10.1073/pnas.86.22.8620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Felley-Bosco E., Pourzand C., Zijlstra J., Amstad P., Cerutti P. A genotypic mutation system measuring mutations in restriction recognition sequences. Nucleic Acids Res. 1991 Jun 11;19(11):2913–2919. doi: 10.1093/nar/19.11.2913. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Fischer S. G., Lerman L. S. DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory. Proc Natl Acad Sci U S A. 1983 Mar;80(6):1579–1583. doi: 10.1073/pnas.80.6.1579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Jones I. M., Burkhart-Schultz K., Crippen T. L. Cloned mouse lymphocytes permit analysis of somatic mutations that occur in vivo. Somat Cell Mol Genet. 1987 Jul;13(4):325–333. doi: 10.1007/BF01534926. [DOI] [PubMed] [Google Scholar]
  16. Jones I. M., Burkhart-Schultz K., Strout C. L., Crippen T. L. Factors that affect the frequency of thioguanine-resistant lymphocytes in mice following exposure to ethylnitrosourea. Environ Mutagen. 1987;9(3):317–329. doi: 10.1002/em.2860090311. [DOI] [PubMed] [Google Scholar]
  17. Klein J. C., Bleeker M. J., Lutgerink J. T., van Dijk W. J., Brugghe H. F., van den Elst H., van der Marel G. A., van Boom J. H., Westra J. G., Berns A. J. Use of shuttle vectors to study the molecular processing of defined carcinogen-induced DNA damage: mutagenicity of single O4-ethylthymine adducts in HeLa cells. Nucleic Acids Res. 1990 Jul 25;18(14):4131–4137. doi: 10.1093/nar/18.14.4131. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Kohler S. W., Provost G. S., Fieck A., Kretz P. L., Bullock W. O., Sorge J. A., Putman D. L., Short J. M. Spectra of spontaneous and mutagen-induced mutations in the lacI gene in transgenic mice. Proc Natl Acad Sci U S A. 1991 Sep 15;88(18):7958–7962. doi: 10.1073/pnas.88.18.7958. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Kohler S. W., Provost G. S., Kretz P. L., Dycaico M. J., Sorge J. A., Short J. M. Development of a short-term, in vivo mutagenesis assay: the effects of methylation on the recovery of a lambda phage shuttle vector from transgenic mice. Nucleic Acids Res. 1990 May 25;18(10):3007–3013. doi: 10.1093/nar/18.10.3007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Kumar R., Sukumar S., Barbacid M. Activation of ras oncogenes preceding the onset of neoplasia. Science. 1990 Jun 1;248(4959):1101–1104. doi: 10.1126/science.2188364. [DOI] [PubMed] [Google Scholar]
  21. Lerman L. S., Silverstein K. Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis. Methods Enzymol. 1987;155:482–501. doi: 10.1016/0076-6879(87)55032-7. [DOI] [PubMed] [Google Scholar]
  22. Lewis S. E., Johnson F. M., Skow L. C., Popp D., Barnett L. B., Popp R. A. A mutation in the beta-globin gene detected in the progeny of a female mouse treated with ethylnitrosourea. Proc Natl Acad Sci U S A. 1985 Sep;82(17):5829–5831. doi: 10.1073/pnas.82.17.5829. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Melton D. W., Konecki D. S., Brennand J., Caskey C. T. Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene. Proc Natl Acad Sci U S A. 1984 Apr;81(7):2147–2151. doi: 10.1073/pnas.81.7.2147. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Morley A. A., Trainor K. J., Seshadri R., Ryall R. G. Measurement of in vivo mutations in human lymphocytes. Nature. 1983 Mar 10;302(5904):155–156. doi: 10.1038/302155a0. [DOI] [PubMed] [Google Scholar]
  25. Myers R. M., Fischer S. G., Maniatis T., Lerman L. S. Modification of the melting properties of duplex DNA by attachment of a GC-rich DNA sequence as determined by denaturing gradient gel electrophoresis. Nucleic Acids Res. 1985 May 10;13(9):3111–3129. doi: 10.1093/nar/13.9.3111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Nicklas J. A., O'Neill J. P., Sullivan L. M., Hunter T. C., Allegretta M., Chastenay B. F., Libbus B. L., Albertini R. J. Molecular analyses of in vivo hypoxanthine-guanine phosphoribosyltransferase mutations in human T-lymphocytes: II. Demonstration of a clonal amplification of hprt mutant T-lymphocytes in vivo. Environ Mol Mutagen. 1988;12(3):271–284. doi: 10.1002/em.2860120302. [DOI] [PubMed] [Google Scholar]
  27. O'Neill J. P., Sullivan L. M., Albertini R. J. In vitro induction, expression and selection of thioguanine-resistant mutants with human T-lymphocytes. Mutat Res. 1990 Feb;240(2):135–142. doi: 10.1016/0165-1218(90)90017-v. [DOI] [PubMed] [Google Scholar]
  28. Perantoni A. O., Rice J. M., Reed C. D., Watatani M., Wenk M. L. Activated neu oncogene sequences in primary tumors of the peripheral nervous system induced in rats by transplacental exposure to ethylnitrosourea. Proc Natl Acad Sci U S A. 1987 Sep;84(17):6317–6321. doi: 10.1073/pnas.84.17.6317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Recio L., Cochrane J., Simpson D., Skopek T. R., O'Neill J. P., Nicklas J. A., Albertini R. J. DNA sequence analysis of in vivo hprt mutation in human T lymphocytes. Mutagenesis. 1990 Sep;5(5):505–510. doi: 10.1093/mutage/5.5.505. [DOI] [PubMed] [Google Scholar]
  30. Richardson F. C., Dyroff M. C., Boucheron J. A., Swenberg J. A. Differential repair of O4-alkylthymidine following exposure to methylating and ethylating hepatocarcinogens. Carcinogenesis. 1985 Apr;6(4):625–629. doi: 10.1093/carcin/6.4.625. [DOI] [PubMed] [Google Scholar]
  31. Richardson K. K., Richardson F. C., Crosby R. M., Swenberg J. A., Skopek T. R. DNA base changes and alkylation following in vivo exposure of Escherichia coli to N-methyl-N-nitrosourea or N-ethyl-N-nitrosourea. Proc Natl Acad Sci U S A. 1987 Jan;84(2):344–348. doi: 10.1073/pnas.84.2.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Singer B. All oxygens in nucleic acids react with carcinogenic ethylating agents. Nature. 1976 Nov 25;264(5584):333–339. doi: 10.1038/264333a0. [DOI] [PubMed] [Google Scholar]
  33. Singer B. O-alkyl pyrimidines in mutagenesis and carcinogenesis: occurrence and significance. Cancer Res. 1986 Oct;46(10):4879–4885. [PubMed] [Google Scholar]
  34. Swenberg J. A., Dyroff M. C., Bedell M. A., Popp J. A., Huh N., Kirstein U., Rajewsky M. F. O4-ethyldeoxythymidine, but not O6-ethyldeoxyguanosine, accumulates in hepatocyte DNA of rats exposed continuously to diethylnitrosamine. Proc Natl Acad Sci U S A. 1984 Mar;81(6):1692–1695. doi: 10.1073/pnas.81.6.1692. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Vrieling H., Van Rooijen M. L., Groen N. A., Zdzienicka M. Z., Simons J. W., Lohman P. H., van Zeeland A. A. DNA strand specificity for UV-induced mutations in mammalian cells. Mol Cell Biol. 1989 Mar;9(3):1277–1283. doi: 10.1128/mcb.9.3.1277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Zimmer D. M., Aaron C. S., O'Neill J. P., Albertini R. J. Enumeration of 6-thioguanine-resistant T-lymphocytes in the peripheral blood of nonhuman primates (cynomolgus monkeys). Environ Mol Mutagen. 1991;18(3):161–167. doi: 10.1002/em.2850180304. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES