Skip to main content
Genetics logoLink to Genetics
. 2000 Mar;154(3):1291–1300. doi: 10.1093/genetics/154.3.1291

Mutation frequency and specificity with age in liver, bladder and brain of lacI transgenic mice.

G R Stuart 1, Y Oda 1, J G de Boer 1, B W Glickman 1
PMCID: PMC1460990  PMID: 10757770

Abstract

Mutation frequency and specificity were determined as a function of age in nuclear DNA from liver, bladder, and brain of Big Blue lacI transgenic mice aged 1.5-25 months. Mutations accumulated with age in liver and accumulated more rapidly in bladder. In the brain a small initial increase in mutation frequency was observed in young animals; however, no further increase was observed in adult mice. To investigate the origin of mutations, the mutational spectra for each tissue and age were determined. DNA sequence analysis of mutant lacI transgenes revealed no significant changes in mutational specificity in any tissue at any age. The spectra of mutations found in aging animals were identical to those in younger animals, suggesting that they originated from a common set of DNA lesions manifested during DNA replication. The data also indicated that there were no significant age-related mutational changes due to oxidative damage, or errors resulting from either changes in the fidelity of DNA polymerase or the efficiency of DNA repair. Hence, no evidence was found to support hypotheses that predict that oxidative damage or accumulation of errors in nuclear DNA contributes significantly to the aging process, at least in these three somatic tissues.

Full Text

The Full Text of this article is available as a PDF (129.7 KB).

Selected References

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

  1. Adams W. T., Skopek T. R. Statistical test for the comparison of samples from mutational spectra. J Mol Biol. 1987 Apr 5;194(3):391–396. doi: 10.1016/0022-2836(87)90669-3. [DOI] [PubMed] [Google Scholar]
  2. Adelman R., Saul R. L., Ames B. N. Oxidative damage to DNA: relation to species metabolic rate and life span. Proc Natl Acad Sci U S A. 1988 Apr;85(8):2706–2708. doi: 10.1073/pnas.85.8.2706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Alexander P. The role of DNA lesions in the processes leading to aging in mice. Symp Soc Exp Biol. 1967;21:29–50. [PubMed] [Google Scholar]
  4. Ames B. N., Shigenaga M. K., Gold L. S. DNA lesions, inducible DNA repair, and cell division: three key factors in mutagenesis and carcinogenesis. Environ Health Perspect. 1993 Dec;101 (Suppl 5):35–44. doi: 10.1289/ehp.93101s535. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Ames B. N., Shigenaga M. K. Oxidants are a major contributor to aging. Ann N Y Acad Sci. 1992 Nov 21;663:85–96. doi: 10.1111/j.1749-6632.1992.tb38652.x. [DOI] [PubMed] [Google Scholar]
  6. Andrew S. E., Reitmair A. H., Fox J., Hsiao L., Francis A., McKinnon M., Mak T. W., Jirik F. R. Base transitions dominate the mutational spectrum of a transgenic reporter gene in MSH2 deficient mice. Oncogene. 1997 Jul 10;15(2):123–129. doi: 10.1038/sj.onc.1201180. [DOI] [PubMed] [Google Scholar]
  7. Anson R. M., Sentürker S., Dizdaroglu M., Bohr V. A. Measurement of oxidatively induced base lesions in liver from Wistar rats of different ages. Free Radic Biol Med. 1999 Aug;27(3-4):456–462. doi: 10.1016/s0891-5849(99)00091-x. [DOI] [PubMed] [Google Scholar]
  8. Brackley M. E., De Boer J. G., Glickman B. W. Use of log-linear analysis to construct explanatory models for TDBP- and AFB1-induced mutation spectra in lacI transgenic animals. Mutat Res. 1999 Mar 10;425(1):55–69. doi: 10.1016/s0027-5107(98)00249-8. [DOI] [PubMed] [Google Scholar]
  9. Brodsky W. Y., Uryvaeva I. V. Cell polyploidy: its relation to tissue growth and function. Int Rev Cytol. 1977;50:275–332. doi: 10.1016/s0074-7696(08)60100-x. [DOI] [PubMed] [Google Scholar]
  10. Buettner V. L., Hill K. A., Halangoda A., Sommer S. S. Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age. Environ Mol Mutagen. 1999;33(4):320–324. doi: 10.1002/(sici)1098-2280(1999)33:4<320::aid-em9>3.0.co;2-s. [DOI] [PubMed] [Google Scholar]
  11. Buettner V. L., Nishino H., Sommer S. S. Large deletion detected with the Big Blue transgenic mouse mutagenesis assay. Mutat Res. 1996 Dec 12;361(2-3):187–189. doi: 10.1016/s0165-1161(96)00032-5. [DOI] [PubMed] [Google Scholar]
  12. Cameron I. L. Cell renewal in the organs and tissues of the nongrowing adult mouse. Tex Rep Biol Med. 1970 Fall;28(3):203–248. [PubMed] [Google Scholar]
  13. Cariello N. F., Piegorsch W. W., Adams W. T., Skopek T. R. Computer program for the analysis of mutational spectra: application to p53 mutations. Carcinogenesis. 1994 Oct;15(10):2281–2285. doi: 10.1093/carcin/15.10.2281. [DOI] [PubMed] [Google Scholar]
  14. Cheng K. C., Cahill D. S., Kasai H., Nishimura S., Loeb L. A. 8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G----T and A----C substitutions. J Biol Chem. 1992 Jan 5;267(1):166–172. [PubMed] [Google Scholar]
  15. Chung F. L., Nath R. G., Nagao M., Nishikawa A., Zhou G. D., Randerath K. Endogenous formation and significance of 1,N2-propanodeoxyguanosine adducts. Mutat Res. 1999 Mar 8;424(1-2):71–81. doi: 10.1016/s0027-5107(99)00009-3. [DOI] [PubMed] [Google Scholar]
  16. Clayson D. B., Pringle J. A. The influence of a foreign body on the induction of tumours in the bladder epithelium of the mouse. Br J Cancer. 1966 Sep;20(3):564–568. doi: 10.1038/bjc.1966.70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Cohen S. M., Ellwein L. B. Cell proliferation and bladder tumor promotion. Prog Clin Biol Res. 1991;369:347–355. [PubMed] [Google Scholar]
  18. Curry J., Karnaoukhova L., Guenette G. C., Glickman B. W. Influence of sex, smoking and age on human hprt mutation frequencies and spectra. Genetics. 1999 Jul;152(3):1065–1077. doi: 10.1093/genetics/152.3.1065. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Curtis H. J. Genetic factors in aging. Adv Genet. 1971;16:305–324. [PubMed] [Google Scholar]
  20. Dollé M. E., Giese H., Hopkins C. L., Martus H. J., Hausdorff J. M., Vijg J. Rapid accumulation of genome rearrangements in liver but not in brain of old mice. Nat Genet. 1997 Dec;17(4):431–434. doi: 10.1038/ng1297-431. [DOI] [PubMed] [Google Scholar]
  21. Dycaico M. J., Provost G. S., Kretz P. L., Ransom S. L., Moores J. C., Short J. M. The use of shuttle vectors for mutation analysis in transgenic mice and rats. Mutat Res. 1994 Jun 1;307(2):461–478. doi: 10.1016/0027-5107(94)90257-7. [DOI] [PubMed] [Google Scholar]
  22. Enesco H. E., Samborsky J. Liver polyploidy: influence of age and of dietary restriction. Exp Gerontol. 1983;18(1):79–87. doi: 10.1016/0531-5565(83)90054-2. [DOI] [PubMed] [Google Scholar]
  23. Erfle H. L., Walsh D. F., Holcroft J., Hague N., de Boer J. G., Glickman B. W. An efficient laboratory protocol for the sequencing of large numbers of lacI mutants recovered from Big Blue transgenic animals. Environ Mol Mutagen. 1996;28(4):393–396. doi: 10.1002/(SICI)1098-2280(1996)28:4<393::AID-EM13>3.0.CO;2-A. [DOI] [PubMed] [Google Scholar]
  24. Farsund T. Cell kinetics of mouse urinary bladder epithelium. I. Circadian and age variations in cell proliferation and nuclear DNA content. Virchows Arch B Cell Pathol. 1975;18(1):35–49. doi: 10.1007/BF02889232. [DOI] [PubMed] [Google Scholar]
  25. Gensler H. L., Bernstein H. DNA damage as the primary cause of aging. Q Rev Biol. 1981 Sep;56(3):279–303. doi: 10.1086/412317. [DOI] [PubMed] [Google Scholar]
  26. Gossen J. A., Martus H. J., Wei J. Y., Vijg J. Spontaneous and X-ray-induced deletion mutations in a LacZ plasmid-based transgenic mouse model. Mutat Res. 1995 Sep;331(1):89–97. doi: 10.1016/0027-5107(95)00055-n. [DOI] [PubMed] [Google Scholar]
  27. Hampsey D. M., Ernst J. F., Stewart J. W., Sherman F. Multiple base-pair mutations in yeast. J Mol Biol. 1988 Jun 5;201(3):471–486. doi: 10.1016/0022-2836(88)90629-8. [DOI] [PubMed] [Google Scholar]
  28. Helbock H. J., Beckman K. B., Shigenaga M. K., Walter P. B., Woodall A. A., Yeo H. C., Ames B. N. DNA oxidation matters: the HPLC-electrochemical detection assay of 8-oxo-deoxyguanosine and 8-oxo-guanine. Proc Natl Acad Sci U S A. 1998 Jan 6;95(1):288–293. doi: 10.1073/pnas.95.1.288. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Hirano T., Yamaguchi R., Asami S., Iwamoto N., Kasai H. 8-hydroxyguanine levels in nuclear DNA and its repair activity in rat organs associated with age. J Gerontol A Biol Sci Med Sci. 1996 Sep;51(5):B303–B307. doi: 10.1093/gerona/51a.5.b303. [DOI] [PubMed] [Google Scholar]
  30. Jost S. P. Cell cycle of normal bladder urothelium in developing and adult mice. Virchows Arch B Cell Pathol Incl Mol Pathol. 1989;57(1):27–36. doi: 10.1007/BF02899062. [DOI] [PubMed] [Google Scholar]
  31. Jost S. P., Potten C. S. Urothelial proliferation in growing mice. Cell Tissue Kinet. 1986 Mar;19(2):155–160. doi: 10.1111/j.1365-2184.1986.tb00725.x. [DOI] [PubMed] [Google Scholar]
  32. Kawanishi M., Matsuda T., Sasaki G., Yagi T., Matsui S., Takebe H. A spectrum of mutations induced by crotonaldehyde in shuttle vector plasmids propagated in human cells. Carcinogenesis. 1998 Jan;19(1):69–72. doi: 10.1093/carcin/19.1.69. [DOI] [PubMed] [Google Scholar]
  33. Ketterling R. P., Vielhaber E. L., Lind T. J., Thorland E. C., Sommer S. S. The rates and patterns of deletions in the human factor IX gene. Am J Hum Genet. 1994 Feb;54(2):201–213. [PMC free article] [PubMed] [Google Scholar]
  34. 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]
  35. 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]
  36. Korr H. Proliferation of different cell types in the brain. Adv Anat Embryol Cell Biol. 1980;61:1–72. doi: 10.1007/978-3-642-67577-5. [DOI] [PubMed] [Google Scholar]
  37. Korr H., Schilling W. D., Schultze B., Maurer W. Autoradiographic studies of glial proliferation in different areas of the brain of the 14-day-old rat. Cell Tissue Kinet. 1983 Jul;16(4):393–413. [PubMed] [Google Scholar]
  38. Kowald A., Kirkwood T. B. A network theory of ageing: the interactions of defective mitochondria, aberrant proteins, free radicals and scavengers in the ageing process. Mutat Res. 1996 May;316(5-6):209–236. doi: 10.1016/s0921-8734(96)90005-3. [DOI] [PubMed] [Google Scholar]
  39. Matsuda T., Kawanishi M., Yagi T., Matsui S., Takebe H. Specific tandem GG to TT base substitutions induced by acetaldehyde are due to intra-strand crosslinks between adjacent guanine bases. Nucleic Acids Res. 1998 Apr 1;26(7):1769–1774. doi: 10.1093/nar/26.7.1769. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Morley A. A. The somatic mutation theory of ageing. Mutat Res. 1995 Oct;338(1-6):19–23. doi: 10.1016/0921-8734(95)00007-s. [DOI] [PubMed] [Google Scholar]
  41. Narayanan L., Fritzell J. A., Baker S. M., Liskay R. M., Glazer P. M. Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2. Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3122–3127. doi: 10.1073/pnas.94.7.3122. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Nath R. G., Ocando J. E., Chung F. L. Detection of 1, N2-propanodeoxyguanosine adducts as potential endogenous DNA lesions in rodent and human tissues. Cancer Res. 1996 Feb 1;56(3):452–456. [PubMed] [Google Scholar]
  43. Ono T., Miyamura Y., Ikehata H., Yamanaka H., Kurishita A., Yamamoto K., Suzuki T., Nohmi T., Hayashi M., Sofuni T. Spontaneous mutant frequency of lacZ gene in spleen of transgenic mouse increases with age. Mutat Res. 1995 Oct;338(1-6):183–188. doi: 10.1016/0921-8734(95)00023-y. [DOI] [PubMed] [Google Scholar]
  44. Ostrovsky YuM Endogenous ethanol--its metabolic, behavioral and biomedical significance. Alcohol. 1986 Jul-Aug;3(4):239–247. doi: 10.1016/0741-8329(86)90032-7. [DOI] [PubMed] [Google Scholar]
  45. Piegorsch W. W., Bailer A. J. Statistical approaches for analyzing mutational spectra: some recommendations for categorical data. Genetics. 1994 Jan;136(1):403–416. doi: 10.1093/genetics/136.1.403. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Provost G. S., Kretz P. L., Hamner R. T., Matthews C. D., Rogers B. J., Lundberg K. S., Dycaico M. J., Short J. M. Transgenic systems for in vivo mutation analysis. Mutat Res. 1993 Jul;288(1):133–149. doi: 10.1016/0027-5107(93)90215-2. [DOI] [PubMed] [Google Scholar]
  47. Provost G. S., Short J. M. Characterization of mutations induced by ethylnitrosourea in seminiferous tubule germ cells of transgenic B6C3F1 mice. Proc Natl Acad Sci U S A. 1994 Jul 5;91(14):6564–6568. doi: 10.1073/pnas.91.14.6564. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Rogers B. J., Provost G. S., Young R. R., Putman D. L., Short J. M. Intralaboratory optimization and standardization of mutant screening conditions used for a lambda/lacI transgenic mouse mutagenesis assay (I). Mutat Res. 1995 Mar;327(1-2):57–66. doi: 10.1016/0027-5107(94)00081-f. [DOI] [PubMed] [Google Scholar]
  49. Shane B. S., deBoer J. G., Glickman B. W., Cunningham M. L. Oxazepam is mutagenic in vivo in Big Blue transgenic mice. Carcinogenesis. 1999 Jul;20(7):1315–1321. doi: 10.1093/carcin/20.7.1315. [DOI] [PubMed] [Google Scholar]
  50. Shigenaga M. K., Ames B. N. Oxidants and mitogenesis as causes of mutation and cancer: the influence of diet. Basic Life Sci. 1993;61:419–436. doi: 10.1007/978-1-4615-2984-2_37. [DOI] [PubMed] [Google Scholar]
  51. Skopek T. R., Kort K. L., Marino D. R. Relative sensitivity of the endogenous hprt gene and lacI transgene in ENU-treated Big Blue B6C3F1 mice. Environ Mol Mutagen. 1995;26(1):9–15. doi: 10.1002/em.2850260103. [DOI] [PubMed] [Google Scholar]
  52. Suri A., deBoer J., Kusser W., Glickman B. W. A 3 milliTesla 60 Hz magnetic field is neither mutagenic nor co-mutagenic in the presence of menadione and MNU in a transgenic rat cell line. Mutat Res. 1996 Nov 11;372(1):23–31. doi: 10.1016/S0027-5107(96)00105-4. [DOI] [PubMed] [Google Scholar]
  53. Szilard L. ON THE NATURE OF THE AGING PROCESS. Proc Natl Acad Sci U S A. 1959 Jan;45(1):30–45. doi: 10.1073/pnas.45.1.30. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Taguchi T., Ohashi M. Changes in fidelity levels of DNA polymerases alpha-1, alpha-2, and beta during ageing in rats. Mech Ageing Dev. 1997 Dec 1;99(1):33–47. doi: 10.1016/s0047-6374(97)00092-4. [DOI] [PubMed] [Google Scholar]
  55. Winegar R. A., Lutze L. H., Hamer J. D., O'Loughlin K. G., Mirsalis J. C. Radiation-induced point mutations, deletions and micronuclei in lacI transgenic mice. Mutat Res. 1994 Jun 1;307(2):479–487. doi: 10.1016/0027-5107(94)90258-5. [DOI] [PubMed] [Google Scholar]
  56. You Y. H., Halangoda A., Buettner V., Hill K., Sommer S., Pfeifer G. Methylation of CpG dinucleotides in the lacI gene of the Big Blue transgenic mouse. Mutat Res. 1998 Dec 3;420(1-3):55–65. doi: 10.1016/s1383-5718(98)00147-8. [DOI] [PubMed] [Google Scholar]
  57. Young R. R., Rogers B. J., Provost G. S., Short J. M., Putman D. L. Interlaboratory comparison: liver spontaneous mutant frequency from lambda/lacI transgenic mice (Big Blue) (II). Mutat Res. 1995 Mar;327(1-2):67–73. doi: 10.1016/0027-5107(94)00080-o. [DOI] [PubMed] [Google Scholar]
  58. Zhang X. B., Urlando C., Tao K. S., Heddle J. A. Factors affecting somatic mutation frequencies in vivo. Mutat Res. 1995 Oct;338(1-6):189–201. doi: 10.1016/0921-8734(95)00024-z. [DOI] [PubMed] [Google Scholar]
  59. de Boer J. G., Erfle H., Holcroft J., Walsh D., Dycaico M., Provost S., Short J., Glickman B. W. Spontaneous mutants recovered from liver and germ cell tissue of low copy number lacI transgenic rats. Mutat Res. 1996 Jun 10;352(1-2):73–78. doi: 10.1016/0027-5107(95)00254-5. [DOI] [PubMed] [Google Scholar]
  60. de Boer J. G., Erfle H., Walsh D., Holcroft J., Provost J. S., Rogers B., Tindall K. R., Glickman B. W. Spectrum of spontaneous mutations in liver tissue of lacI transgenic mice. Environ Mol Mutagen. 1997;30(3):273–286. [PubMed] [Google Scholar]
  61. de Boer J. G., Mirsalis J. C., Provost G. S., Tindall K. R., Glickman B. W. Spectrum of mutations in kidney, stomach, and liver from lacI transgenic mice recovered after treatment with tris(2,3-dibromopropyl)phosphate. Environ Mol Mutagen. 1996;28(4):418–423. doi: 10.1002/(SICI)1098-2280(1996)28:4<418::AID-EM17>3.0.CO;2-I. [DOI] [PubMed] [Google Scholar]
  62. de Boer J. G., Provost S., Gorelick N., Tindall K., Glickman B. W. Spontaneous mutation in lacI transgenic mice: a comparison of tissues. Mutagenesis. 1998 Mar;13(2):109–114. doi: 10.1093/mutage/13.2.109. [DOI] [PubMed] [Google Scholar]

Articles from Genetics are provided here courtesy of Oxford University Press

RESOURCES