Effects of ageing on nuclear DNA integrity and metabolism in mussel cells (Mytilus edulis L.)

International Journal of Biochemistry and Cell Biology

Volumn 31, Issue 3-4, 1999, Pages 443-450

  Accomando, R ^a   Viarengo, A ^b   Moore, M N ^c   Marchi, B ^a  

^a UNIVERSITY OF GENOA   (Italy)

^b UNIVERSITY OF TURIN   (Italy)

^c PLYMOUTH MARINE LABORATORY   (United Kingdom)

Author keywords

Ageing; DNA damage; DNA repair; Mussel; Oxidative damage

Indexed keywords

CELL NUCLEUS DNA; DNA POLYMERASE; MALONALDEHYDE;

AGING; ANIMAL CELL; ARTICLE; DNA DAMAGE; DNA DENATURATION; DNA METABOLISM; DNA REPAIR; DNA REPLICATION; MUSSEL; NONHUMAN; OXIDATIVE STRESS;

MYTILUS EDULIS;

EID: 0032993684     PISSN: 13572725     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1357-2725(98)00154-X     Document Type: Article

References (60)

1. Hayflick L. Theories of biological aging. Exp. Geront. 20:1985;145-159.
2. R.R. Tice, R.B. Setlow, DNA repair and replication in aging organisms and cells, in: C.E. Finch, E.L. Schneider (Eds.), Handbook of the Biology of Aging, Van Nostrand Reinhold, New York, 1985, pp. 173-224.
3. Tollefsbol T.O., Cohen H.J. Expression of intracellular biochemical defects of lymphocytes in aging: proposal of a general aging mechanism which is not cell-specific. Exp. Geront. 21:1986;129-148.
4. Bohr V.A., Anson R.M. DNA damage, mutation and fine structure DNA repair in aging. Mutation Res. 338:1995;25-34.
5. Singh N.P., Danner D.B., Tice R.R., Pearson J.D., Brant L.J., Morris C.H., Schneider E.L. Basal DNA damage in individual human lynphocytes with age. Mutation Res. 256:1991;1-6.
6. Wei Q., Matanoski G.M., Farmer E.R., Hedayati M., Grossman L. DNA repair and aging in basal cell carcinoma: a molecular epidemiology study. Proc. Natl. Acad. Sci. USA. 90:1993;1614-1618.
7. King C.M., Gillespie E.S., McKenna P.G., Barnett Y.A. An investigation of mutation as a function of age in humans. Mutation Res. 316:1994;79-90.
8. Barnett Y.A., King C.M. An investigation of antioxidant status, DNA repair capacity and mutation as a function of age in humans. Mutation Res. 338:1995;115-128.
9. Targovnik H.S., Locher S.E., Hariharan P.V. Age associated alteration in DNA damage and repair capacity in Turbatrix aceti exposed to ionizing radiation. Int. J. Radiat. Biol. Relat. Stud. Phys. Chem. Med. 47:1985;255-260.
10. Gaubatz J.W., Tan B.H. Age-related studies on the removal of 7-methylguanine from DNA of mouse kidney tissue following N-methyl-N-nitrosourea treatment. Mutation Res. 295:1993;81-91.
11. Rao K.S., Vinay Kumar D., Bhaskar M.S., Sripad G. On the 'active' molecules of DNA-polymerase β in aging rat brain. Biochem. Mol. Biol. Int. 34:1994;287-294.
12. Srivastava V.K., Busbee D.L. Decreased fidelity of DNA polymerases and decreased DNA excision repair in aging mice: effects of caloric restriction. Biochem. Biophys. Res. Commun. 182:1992;712-721.
13. Holmes G.E., Bernstein C., Bernstein H. Oxidative and other DNA damages as the basis of aging: a review. Mutation Res. 275:1992;305-315.
14. Dice J.F. Cellular and molecular mechanisms of aging. Physiol. Rew. 73:1993;149-159.
15. Chetsanga C.J., Tuttle J., Jacoboni A., Johnson C. Age-associated structural alterations in senescent mouse brain DNA. Biochim. Biophys. Acta. 474:1977;180-187.
16. Dean R.G., Cutler R.G. Absence of significant age-dependent increase of single-stranded DNA extracted from mouse liver nuclei. Exp. Gerontol. 13:1978;287-292.
17. Finch C.E. Susceptibility of mouse liver DNA to digestion by S1 nuclease: absence of age-related change. Age. 2:1979;45-46.
18. Nakanishi K., Shima A., Fukuda M., Fujita S. Age-associated increase of single-strended regions in the DNA of mouse brain and liver cells. Mech. Ageing Dev. 10:1979;273-281.
19. Turner D.R., Morley R.S., Seshadri R.S., Sorell J.R. Age-related variations in human lymphocytes DNA. Mech. Ageing Dev. 17:1981;305-309.
20. Mori N., Goto S. Estimation of the single-stranded regions in the nuclear DNA of mouse tissues during aging with special reference to the brain. Arch. Gerontol. Geriatr. 1:1982;143-150.
21. Lawson T., Stohs S. Changes in endogenous DNA damage in aging mice in response to butylated hydroxyanisole and oltipratz. Mech. Aging Dev. 30:1985;179-185.
22. Zahn R.K., Reinmuller J., Beyer R., Pondeljak V. Age-correlated DNA damage in human muscle tissue. Mech. Ageing Dev. 41:1987;73-114.
23. Mullaart E., Boerrigter M.E.T.I., Brouwer A., Vijg J. Age-dependent accumulation of alkali-labile sites in DNA of postmitotic but not in that of mitotic rat liver cells. Mech. Ageing Dev. 45:1988;41-49.
24. Mullaart E., Boerrigter M.E.T.I., Boer G.J., Vijg J. Spontaneus DNA breaks in the rat brain during development and aging. Mutation Res. 237:1990;9-15.
25. Shugart L., Theodorakis C. Environmental genotoxicity:probing the underlying mechanisms. Environ. Health Perspect. 102:1994;13-17.
26. Ames B.N., Shigenaga M.K., Hagen T.M. Oxidants, antioxidants, and the degenerative diseases of aging. Proc. Natl. Acad. Sci. USA. 90:1993;7915-7922.
27. Agarwal S., Sohal R.S. DNA oxidative damage and life expectancy in houseflies. Proc. Natl. Acad. Sci. USA. 91:1994;12332-12335.
28. Higami Y., Shimokawa I., Okimoto T., Ikeda T. An age-related increase in the basal level of DNA damage and DNA vulnerability to oxygen radicals in the individual hepatocytes of male F344 rats. Mutation Res. 316:1994;59-67.
29. Higami Y., Shimokawa I., Okimoto T., Ikeda T. Vulnerability to oxygen radicals is more important than impaired repair in hepatocytic deoxyrribonucleic acid damage in aging. Lab. Invest. 71:1994;650-656.
30. Chicca M.C., Nesti C., Muzzoli M., Pasetti P., Pinamonti S. Correlation between age and DNA damage detected by FADU in human peripheral blood lymphocytes. Mutation Res. 316:1996;201-208.
31. Viarengo A., Pertica M., Canesi L., Accomando R., Mancinelli G., Orunesu M. Lipid peroxidation and level of antioxidant compounds (GSH, vitamin E) in the digestive glands of mussels of three different age groups exposed to anaerobic and aerobic conditions. Mar. Environ. Res. 28:1989;291-295.
32. Pacifici R.E., Davies K.J.A. Protein, lipid and DNA repair systems in oxidative stress: the free radical theory of aging revisited. Gerontology. 37:1991;166-180.
33. Viarengo A., Canesi L., Pertica M., Livingstone D.R., Orunesu M. Age-related lipid peroxidation in the digestive gland of mussels: The role of the antioxidant defense systems. Experientia. 47:1991;454-457.
34. J. Remacle, C. Michiels, M. Raes, The importance of antioxidant enzymes in cellular aging and degeneration, in: I. Ement, B. Chance (Eds.), Free radicals and aging, 1992, pp. 99-107.
35. Summerfield F.W., Tappel A.L. Detection and measurement by high-performance liquid chromatography of malondialdehyde crosslinks in DNA. Anal. Biochem. 143:1984;265-271.
36. Fraga C.G., Tappel Al L. Damage to DNA concurrent with lipid peroxidation in rat liver slices. Biochem. J. 252:1988;893-896.
37. Vaca C.E., Harms-Ringdahl M. Interaction of lipid peroxidation products with nuclear macromolecules. Biochim. Biophys. Acta. 1001:1989;35-43.
38. Ranjbar S., Hannigan B.M. DNA damage in human T-lymphoblastoid cell line Molt-3 induced by reactive oxygen species. Mutation Res. 285:1993;225-228.
39. Breen A.P., Murphy J.A. Reactions of oxyl radicals with DNA. Free Radic. Biol. Med. 18:1995;1033-1077.
40. Sarker A.H., Watanabe S., Seki S., Akiyama T., Okada S. Oxygen radical-induced single-strand DNA breaks and repair of the damage in a cell-free system. Mutation Res. 337:1995;85-95.
41. Gaubatz J.W., Tan B.H. Aging affects the levels of DNA damage in postmitotic cells. Ann. NY Acad. Sci. 719:1994;97-107.
42. D.P. Jones, The role of oxygen concentration in oxidative stress: hypoxic and hyperoxic models, in: H. Sies (Ed.), Oxidative stress, Academic Press, New York, 1985, pp. 152-189.
43. B.L. Bayne, R.J. Thompson, J. Widdows, Physiology: I, in: L.B. Bayne (Ed.), Marine mussels: their ecology and physiology, Cambridge University Press, Cambridge, London, New York, Melbourne, 1976, pp. 121-159.
44. Accomando R., Viarengo A., Zoncheddu A., Orunesu M. Biochemical characterization of the DNA polymerase activity present in isolated nuclei from mussel tissues: a possible system for the evaluation of the rate of DNA repair. Comp. Biochem. Physiol. 93B:1989;747-751.
45. Burton K. A study of the conditions and mechanisms of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acids. Biochem. J. 62:1956;315-321.
46. Accomando R., Viarengo A., Orunesu M. In vivo and in vitro effects of heavy metals on DNA polymerase activities in the digestive gland of Mytilus galloprovincialis Lam. Comp. Biochem. Physiol. 95C:1990;271-274.
47. Harthree E.F. Determination of protein: a modification of the Lowry method that gives a linear photometric response. Analyt. Biochem. 48:1972;422-427.
48. Accomando A., Viarengo A., Bordone R., Taningher M., Canesi L., Orunesu M. A rapid method for detecting DNA strand breaks in Mytilus galloprovincialis Lam. induced by genotoxic xenobiotic chemical. Int. J. Biochem. 23:1991;227-229.
49. Viarengo A., Canesi L., Pertica M., Poli G., Moore M.N., Orunesu M. Heavy metal effects on lipid peroxidation in the tissues of Mytilus galloprovincialis Lam. Comp. Biochem Physiol. 97C:1990;37-42.
50. Birnboim H.C., Jevcak J.J. Fluorimetric method for rapid detection of DNA strand breaks in human white blood cells produced by low doses of radiation. Cancer Res. 41:1981;1889-1892.
51. Kaufmann W.K., Kaufman D.G., Stenstrom M., Grisham J.W. Requirements for adenosine triphosphate in DNA repair in isolated hepatic nuclei. Biochem. Biophys. Res. Commun. 108:1982;1040-1047.
52. Zoncheddu A., Accomando R. Characteristics of the DNA polymerase β-directed unscheduled DNA synthesis in isolated nuclei from adult rat liver. Int. J. Biochem. 16:1984;39-395.
53. Hammond R.A., McClung J.K., Miller M.R. Effect of DNA polymerase inhibitors on DNA repair in intact and permeable human fibroblasts: evidence that DNA polymerases delta and beta are involved in DNA repair synthesis induced by N-methyl-N′-nitro-N-nitrosoguanidine. Biochemistry. 29:1990;191-286.
54. Park I.S., Park J.K., Koh H.Y., Park S.D. DNA single stranded gaps formed during DNA repair synthesis induced by methyl methanesulfonate are filled by sequential action of aphidicolin- and dideoxythymidine sensitive DNA polymerases in HeLa cells. Cell Biol. Toxicol. 7:1991;49-58.
55. Popanda O., Thielmann H.W. The function of DNA polymerases in DNA repair synthesis of ultraviolet-irradiated human fibroblasts. Biochim. Biophys. Acta. 1129:1992;155-160.
56. Grossman L. Enzymes involved in the repair of damaged DNA. Arch. Biochem. Biophys. 211:1981;511-522.
57. Wiebauer K., Jiricny J. Mismatch-specific thymine DNA glycosylase and DNA polymerase β mediate the correction of G·T mispairs in nuclear extracts from human cells. Proc. Natl. Acad. Sci. USA. 87:1990;5842-5845.
58. Sobol R.W., Horton J.K., Kunn R., Gu H., Singhal R., Prasad R., Rajewsky K., Wilson S.H. Requirement of mammalian DNA polymerase-β in base-excision repair. Nature. 379:1996;183-186.
59. Wood R.D., Shivji M.K.K. Which DNA polymerases are used for DNA-repair in eukaryotes? Carcinogenesis. 18:1997;605-610.
60. Canesi L., Viarengo A. Age-related differences in glutathione metabolism in mussel tissues (Mytilus edulis L.). Comp. Biochem Physiol. 116B:1997;217-221.