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. 1977 Aug;4(8):2619–2628. doi: 10.1093/nar/4.8.2619

Nonuniform distribution of DNA repair in chromatin after treatment with methyl methanesulfonate.

W J Bodell
PMCID: PMC342596  PMID: 198747

Abstract

The distribution of methyl methanesulfonate induced DNA repair was measured in mouse mammary cell chromatin by digestion of "repair labeled" nuclei with micrococcal nuclease. The results indicate that there is a nonuniform distribution of DNA repair in chromatin. The chromatin fraction digested during the first 5 minutes of incubation with micrococcal nuclease appears to be a primary site of DNA repair after methyl methanesulfoante treatment. The observed nonuniform distribution of DNA repair in chromatin may be due to 1)a nonrandom alkylation of DNA in chromatin by methyl methanesulfonate or 2)areas in chromatin of increased accessibility for the repair enzymes to the DNA lesions.

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Selected References

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

  1. Axel R. Cleavage of DNA in nuclei and chromatin with staphylococcal nuclease. Biochemistry. 1975 Jul;14(13):2921–2925. doi: 10.1021/bi00684a020. [DOI] [PubMed] [Google Scholar]
  2. Axel R., Melchior W., Jr, Sollner-Webb B., Felsenfeld G. Specific sites of interaction between histones and DNA in chromatin. Proc Natl Acad Sci U S A. 1974 Oct;71(10):4101–4105. doi: 10.1073/pnas.71.10.4101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Berliner J., Himes S. W., Aoki C. T., Norman A. The sites of unscheduled DNA synthesis within irradiated human lymphocytes. Radiat Res. 1975 Sep;63(3):544–552. [PubMed] [Google Scholar]
  4. Bodell W. J., Banerjee M. R. Reduced DNA repair in mouse satellite DNA after treatment with methylmethanesulfonate, and N-methyl-N-nitrosourea. Nucleic Acids Res. 1976 Jul;3(7):1689–1701. doi: 10.1093/nar/3.7.1689. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Buhl S. N., Setlow R. B., Regan J. D. DNA repair in Potorous tridactylus. Biophys J. 1974 Oct;14(10):791–803. doi: 10.1016/S0006-3495(74)85949-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Camerini-Otero R. D., Sollner-Webb B., Felsenfeld G. The organization of histones and DNA in chromatin: evidence for an arginine-rich histone kernel. Cell. 1976 Jul;8(3):333–347. doi: 10.1016/0092-8674(76)90145-8. [DOI] [PubMed] [Google Scholar]
  7. Caspersson T., Haglund U., Lindell B., Zech L. Radiation-induced non-random chromosome breakage. Exp Cell Res. 1972 Dec;75(2):541–543. doi: 10.1016/0014-4827(72)90469-7. [DOI] [PubMed] [Google Scholar]
  8. Curtis H. J., Leith J., Tilley J. Chromosome aberrations in liver cells of dogs of different ages. J Gerontol. 1966 Apr;21(2):268–270. doi: 10.1093/geronj/21.2.268. [DOI] [PubMed] [Google Scholar]
  9. Curtis H. J., Miller K. Chromosome aberrations in liver cells of guinea pigs. J Gerontol. 1971 Jul;26(3):292–293. doi: 10.1093/geronj/26.3.292. [DOI] [PubMed] [Google Scholar]
  10. Finch J. T., Noll M., Kornberg R. D. Electron microscopy of defined lengths of chromatin. Proc Natl Acad Sci U S A. 1975 Sep;72(9):3320–3322. doi: 10.1073/pnas.72.9.3320. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Frei J. V., Lawley P. D. Methylation of DNA in various organs of C57B1 mice by a carcinogenic dose of N-methyl-N-nitrosourea and stabiltty of some methylation products up to 18 hours. Chem Biol Interact. 1975 Jun;10(6):413–427. doi: 10.1016/0009-2797(75)90072-1. [DOI] [PubMed] [Google Scholar]
  12. Harris C. C., Connor R. J., Jackson F. E., Lieberman M. W. Intranuclear distribution of DNA repair synthesis induced by chemical carcinogens or ultraviolet light in human diploid fibroblasts. Cancer Res. 1974 Dec;34(12):3461–3468. [PubMed] [Google Scholar]
  13. Holmberg M., Jonasson J. Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes. Hereditas. 1973;74(1):57–67. doi: 10.1111/j.1601-5223.1973.tb01104.x. [DOI] [PubMed] [Google Scholar]
  14. Irving C. C., Veazey R. A. Persistent binding of 2-acetylaminofluorene to rat liver DNA in vivo and consideration of the mechanism of binding of N-hydroxy-2-acetylaminofluorene to rat liver nucleic acids. Cancer Res. 1969 Oct;29(10):1799–1804. [PubMed] [Google Scholar]
  15. Kakunaga T. Requirement for cell replication in the fixation and expression of the transformed state in mouse cells treated with 4-nitroquinoline-1-oxide. Int J Cancer. 1974 Dec 15;14(6):736–742. doi: 10.1002/ijc.2910140607. [DOI] [PubMed] [Google Scholar]
  16. Kakunaga T. The role of cell division in the malignant transformation of mouse cells treated with 3-methylcholanthrene. Cancer Res. 1975 Jul;35(7):1637–1642. [PubMed] [Google Scholar]
  17. Kornberg R. D., Thomas J. O. Chromatin structure; oligomers of the histones. Science. 1974 May 24;184(4139):865–868. doi: 10.1126/science.184.4139.865. [DOI] [PubMed] [Google Scholar]
  18. Kriek E. Persistent binding of a new reaction product of the carcinogen N-hydroxy-N-2-acetylaminofluorene with guanine in rat liver DNA in vivo. Cancer Res. 1972 Oct;32(10):2042–2048. [PubMed] [Google Scholar]
  19. Lieberman M. W., Dipple A. Removal of bound carcinogen during DNA repair in nondividing human lymphocytes. Cancer Res. 1972 Sep;32(9):1855–1860. [PubMed] [Google Scholar]
  20. Massie H. R., Baird M. B., Nicolosi R. J., Samis H. V. Changes in the structure of rat liver DNA in relation to age. Arch Biochem Biophys. 1972 Dec;153(2):736–741. doi: 10.1016/0003-9861(72)90392-x. [DOI] [PubMed] [Google Scholar]
  21. Modak S. P., Price G. B. Exogenous DNA polymerase-catalysed incorporation of deoxyribonucleotide monophosphates in nuclei of fixed mouse-brain cells. Exp Cell Res. 1971 Apr;65(2):289–296. doi: 10.1016/0014-4827(71)90004-8. [DOI] [PubMed] [Google Scholar]
  22. Moses H. L., Webster R. A., Martin G. D., Spelsberg T. C. Binding of polycyclic aromatic hydrocarbons to transcriptionally active nuclear subfractions of AKR mouse embryo cells. Cancer Res. 1976 Aug;36(8):2905–2910. [PubMed] [Google Scholar]
  23. Natarajan A. T., Ahnström G. Heterochromatin and chromosome aberrations. Chromosoma. 1969;28(1):48–61. doi: 10.1007/BF00325989. [DOI] [PubMed] [Google Scholar]
  24. Natarajan A. T., Ahnström G. The localisation of radiation induced chromosome aberrations in relation to the distribution of heterochromatin in Secale cereale. Chromosoma. 1970;30(2):250–257. doi: 10.1007/BF00282004. [DOI] [PubMed] [Google Scholar]
  25. Natarajan A. T., Schmid W. Differential response of constitutive and facultative heterochromatin in the manifestation of mitomycin induced chromosome aberrations in Chinese hamster cells in vitro. Chromosoma. 1971;33(1):48–62. doi: 10.1007/BF00326383. [DOI] [PubMed] [Google Scholar]
  26. Noll M. Subunit structure of chromatin. Nature. 1974 Sep 20;251(5472):249–251. doi: 10.1038/251249a0. [DOI] [PubMed] [Google Scholar]
  27. Olins A. L., Olins D. E. Spheroid chromatin units (v bodies). Science. 1974 Jan 25;183(4122):330–332. doi: 10.1126/science.183.4122.330. [DOI] [PubMed] [Google Scholar]
  28. Oudet P., Gross-Bellard M., Chambon P. Electron microscopic and biochemical evidence that chromatin structure is a repeating unit. Cell. 1975 Apr;4(4):281–300. doi: 10.1016/0092-8674(75)90149-x. [DOI] [PubMed] [Google Scholar]
  29. Paterson M. C., Lohman P. H., Sluyter M. L. Use of UV endonuclease from Micrococcus luteus to monitor the progress of DNA repair in UV-irradiated human cells. Mutat Res. 1973 Aug;19(2):245–256. doi: 10.1016/0027-5107(73)90083-3. [DOI] [PubMed] [Google Scholar]
  30. Price G. B., Modak S. P., Makinodan T. Age-associated changes in the DNA of mouse tissue. Science. 1971 Mar 5;171(3974):917–920. doi: 10.1126/science.171.3974.917. [DOI] [PubMed] [Google Scholar]
  31. Ramanathan R., Rajalakshmi S., Sarma D. S., Farber E. Nonrandom nature of in vivo methylation of dimethylnitrosamine and the subsequent removal of methylated products from rat liver chromatin DNA. Cancer Res. 1976 Jun;36(6):2073–2079. [PubMed] [Google Scholar]
  32. Ramanathan R., Rajalakshmi S., Sarma D. S. Non-random nature of in vivo interaction of 3H-N-hydroxy-2-acetylaminofluorene and its subsequent removal from rat liver chromatin-DNA. Chem Biol Interact. 1976 Aug;14(3-4):375–377. doi: 10.1016/0009-2797(76)90116-2. [DOI] [PubMed] [Google Scholar]
  33. Reeves B. R., Margoles C. Preferential location of chlorambucil-induced breakage in the chromosomes of normal human lymphocytes. Mutat Res. 1974 Jun;26(3):205–208. doi: 10.1016/s0027-5107(74)80076-x. [DOI] [PubMed] [Google Scholar]
  34. Regan J. D., Trosko J. E., Carrier W. L. Evidence for excision of ultraviolet-induced pyrimidine dimers from the DNA of human cells in vitro. Biophys J. 1968 Mar;8(3):319–325. doi: 10.1016/S0006-3495(68)86490-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. STEVENSON K. G., CURTIS H. J. Chromosomal aberrations in irradiated and nitrogen mustard-treated mice. Radiat Res. 1961 Dec;15:774–784. [PubMed] [Google Scholar]
  36. Scudiero D., Strauss B. Increased repair in DNA growing point regions after treatment of human lymphoma cells with N-methyl-N'-nitro-N-nitrosoguanidine. Mutat Res. 1976 Jun;35(2):311–324. doi: 10.1016/0027-5107(76)90194-9. [DOI] [PubMed] [Google Scholar]
  37. Simpson R. T., Whitlock J. P., Jr Chemical evidence that chromatin DNA exists as 160 base pair beads interspersed with 40 base pair bridges. Nucleic Acids Res. 1976 Jan;3(1):117–127. doi: 10.1093/nar/3.1.117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Sirover M. A., Loeb L. A. Erroneous base-pairing induced by a chemical carcinogen during DNA synthesis. Nature. 1974 Nov 29;252(5482):414–416. doi: 10.1038/252414a0. [DOI] [PubMed] [Google Scholar]
  39. Sirover M. A., Loeb L. A. Restriction of carcinogen-induced error incorporation during in vitro DNA synthesis. Cancer Res. 1976 Feb;36(2 Pt 1):516–523. [PubMed] [Google Scholar]
  40. Takebe H., Nii S., Ishii M. I., Utsumi H. Comparative studies of host-cell reactivation, colony forming ability and excision repair after UV irradiation of xeroderma pigmentosum, normal human and some other mammalian cells. Mutat Res. 1974 Dec;25(3):383–390. doi: 10.1016/0027-5107(74)90067-0. [DOI] [PubMed] [Google Scholar]
  41. Wheeler K. T., Lett J. T. On the possibility that DNA repair is related to age in non-dividing cells. Proc Natl Acad Sci U S A. 1974 May;71(5):1862–1865. doi: 10.1073/pnas.71.5.1862. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Wilkins R. J., Hart R. W. Preferential DNA repair in human cells. Nature. 1974 Jan 4;247(5435):35–36. doi: 10.1038/247035a0. [DOI] [PubMed] [Google Scholar]

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