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
. 1981 Jun;78(6):3619–3623. doi: 10.1073/pnas.78.6.3619

DNA double-strand breaks induced in normal human cells during the repair of ultraviolet light damage.

M O Bradley, V I Taylor
PMCID: PMC319622  PMID: 6267601

Abstract

DNA double-strand breaks (DSBs) are formed in normal human IMR-90 cells during repair incubation after 100 and 300 J.m-2 of ultraviolet light. By contrast, no DSBs are formed after exposure to ultraviolet light in human XPA cells (from a patient with xeroderma pigmentosum complementation group A), which are unable to excise pyrimidine dimers. The DSBs are not due to immediate cell death, because all the cells excluded trypan blue at the time of assay and because XPA cells, which are much more sensitive to ultraviolet light than are IMR-90 cells, did not form DSBs after exposure to ultraviolet light. The DSBs do not appear to be due to either DNA synthesis or cellular single-strand endonucleases. We suggest that repair-induced DSBs would be potent lesions that might lead to cytotoxicity, chromosome aberrations, deletion mutations, and perhaps cellular transformation.

Full text

PDF
3619

Selected References

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

  1. Bonura T., Smith K. C. Enzymatic production of deoxyribonucleic acid double-strand breaks after ultraviolet irradiation of Escherichia coli K-12. J Bacteriol. 1975 Feb;121(2):511–517. doi: 10.1128/jb.121.2.511-517.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bonura T., Smith K. C. Quantitative evidence for enzymatically-indeced DNA double-strand breaks as lethal lesions in UV irradiated pol+ and polA1 strains of E. coli K-12. Photochem Photobiol. 1975 Dec;22(6):243–248. doi: 10.1111/j.1751-1097.1975.tb06743.x. [DOI] [PubMed] [Google Scholar]
  3. Bradley M. O., Dice J. F., Hayflick L., Schimke R. T. Protein alterations in aging WI38 cells as determined by proteolytic susceptibility. Exp Cell Res. 1975 Nov;96(1):103–112. doi: 10.1016/s0014-4827(75)80042-5. [DOI] [PubMed] [Google Scholar]
  4. Cleaver J. E. Nucleosome structure controls rates of excision repair in DNA of human cells. Nature. 1977 Dec 1;270(5636):451–453. doi: 10.1038/270451a0. [DOI] [PubMed] [Google Scholar]
  5. Cooper H. K., Margison G. P., O'Connor P. J., Itzhaki R. F. Heterogeneous distribution of DNA alkylation products in rat liver chromatin after in vivo administration of N,N-di[14C]methylnitrosamine. Chem Biol Interact. 1975 Dec;11(6):483–492. doi: 10.1016/0009-2797(75)90024-1. [DOI] [PubMed] [Google Scholar]
  6. Edenberg H., Hanawalt P. Size of repair patches in the DNA of ultraviolet-irradiated HeLa cells. Biochim Biophys Acta. 1972 Jul 20;272(3):361–372. doi: 10.1016/0005-2787(72)90389-9. [DOI] [PubMed] [Google Scholar]
  7. Harm W. Effects of dose fractionation on ultraviolet survival of Escherichia coli. Photochem Photobiol. 1968 Jan;7(1):73–86. doi: 10.1111/j.1751-1097.1968.tb05831.x. [DOI] [PubMed] [Google Scholar]
  8. Kuo M. T., Hsu T. C. Bleomycin causes release of nucleosomes from chromatin and chromosomes. Nature. 1978 Jan 5;271(5640):83–84. doi: 10.1038/271083a0. [DOI] [PubMed] [Google Scholar]
  9. Lehmann A. R. Postreplication repair of DNA in ultraviolet-irradiated mammalian cells. J Mol Biol. 1972 May 28;66(3):319–337. doi: 10.1016/0022-2836(72)90418-4. [DOI] [PubMed] [Google Scholar]
  10. Mitelman F., Levan G. Clustering of aberrations to specific chromosomes in human neoplasms. III. Incidence and geographic distribution of chromosome aberrations in 856 cases. Hereditas. 1978;89(2):207–232. doi: 10.1111/j.1601-5223.1978.tb01277.x. [DOI] [PubMed] [Google Scholar]
  11. 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]
  12. Regan J. D., Setlow R. B., Ley R. D. Normal and defective repair of damaged DNA in human cells: a sensitive assay utilizing the photolysis of bromodeoxyuridine. Proc Natl Acad Sci U S A. 1971 Apr;68(4):708–712. doi: 10.1073/pnas.68.4.708. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Smerdon M. J., Tlsty T. D., Lieberman M. W. Distribution of ultraviolet-induced DNA repair synthesis in nuclease sensitive and resistant regions of human chromatin. Biochemistry. 1978 Jun 13;17(12):2377–2386. doi: 10.1021/bi00605a020. [DOI] [PubMed] [Google Scholar]
  14. Waters R., Regan J. D. Recombination of UV-induced pyrimidine dimers in human fibroblasts. Biochem Biophys Res Commun. 1976 Oct 4;72(3):803–807. doi: 10.1016/s0006-291x(76)80204-5. [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