Physical and Functional Interaction between DNA Ligase IIIα and Poly(ADP-Ribose) Polymerase 1 in DNA Single-Strand Break Repair

REFERENCES

• Ausubel, F. M., R. Brent, R. Kingston, D. Morre, J. Seidman, A. Smith, and K. Struhl. 1994. Current protocols in molecular biology. John Wiley and Sons, Inc., New York, N.Y.
   Google Scholar
• Caldecott, K. W., S. Aoufouchi, P. Johnson, and S. Shall. 1996. XRCC1 polypeptide interacts with DNA polymerase β and possibly poly (ADP-ribose) polymerase, and DNA ligase III is a novel molecular nick-sensor in vitro. Nucleic Acids Res. 24: 4387–4394.
   PubMed Web of Science ®Google Scholar
• Caldecott, K. W., C. K. McKeown, J. D. Tucker, S. Ljunquist, and L. H. Thompson. 1994. An interaction between the mammalian DNA repair protein XRCC1 and DNA ligase III. Mol. Cell. Biol. 14: 68–76.
   PubMed Web of Science ®Google Scholar
• Caldecott, K. W., C. K. McKeown, J. D. Tucker, L. Stanker, and L. H. Thompson. 1996. Characterization of the Xrcc1-DNA ligase III complex in vitro and its absence from mutant hamster cells. Nucleic Acids Res. 23: 4836–4843.
   Google Scholar
• Callebaut, I., and J. P. Mornon. 1997. From BRCA1 to RAP1: a widespread BRCT module closely associated with DNA repair. FEBS Lett. 400: 25–30.
   PubMed Web of Science ®Google Scholar
• Chen, J., A. E. Tomkinson, W. Ramos, Z. B. Mackey, S. Danehower, C. A. Walter, R. A. Schultz, J. M. Besterman, and I. Husain. 1995. Mammalian DNA ligase III: molecular cloning, chromosomal localization, and expression in spermatocytes undergoing meiotic recombination. Mol. Cell. Biol. 15: 5412–5422.
   PubMedGoogle Scholar
• de Murcia, G., and J. Menissier-de Murcia. 1994. Poly(ADP) ribose polymerase: a molecular nick sensor. Trends Biochem. Sci. 19: 172–176.
   PubMed Web of Science ®Google Scholar
• Frosina, G., P. Fortini, O. Rossi, F. Carrozzino, G. Raspaglio, L. S. Cox, D. P. Dane, A. Abbondandolo, and E. Dogliotti. 1996. Two pathways of base excision repair in mammalian cells. J. Biol. Chem. 271: 9573–9578.
   PubMed Web of Science ®Google Scholar
• Giner, H., F. Simonin, G. de Murcia, and J. Menissier-de Murcia. 1992. Overproduction and large scale purification of human poly (ADP-ribose) polymerase using a baculovirus expression system. Gene 11: 279–283.
   Google Scholar
• Husain, I., A. E. Tomkinson, W. A. Burkhart, M. B. Moyer, W. Ramos, Z. B. Mackey, J. M. Besterman, and J. Chen. 1995. Purification and characterization of DNA ligase III from bovine testes. J. Biol. Chem. 270: 9683–9690.
   PubMedGoogle Scholar
• Koonin, E. V., S. F. Alschul, and P. Bork. 1996. Functional motifs. Nat. Genet. 13: 266–267.
   PubMed Web of Science ®Google Scholar
• Kubota, Y., R. A. Nash, A. Klungland, P. Schar, D. E. Barnes, and T. Lindahl. 1996. Reconstitution of DNA base excision-repair with purified human proteins: interaction between DNA polymerase β and the XRCC1 protein. EMBO J. 15: 6662–6670.
   PubMed Web of Science ®Google Scholar
• Laemmli, U. K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680–685.
   PubMed Web of Science ®Google Scholar
• Lakshmipathy, U., and C. Campbell. 1999. The human DNA ligase III gene encodes nuclear and mitochondrial proteins. Mol. Cell. Biol. 19: 3869–3876.
   PubMed Web of Science ®Google Scholar
• Lakshmipathy, U., and C. Campbell. 2000. Mitochondrial DNA ligase III function is independent of Xrcc1. Nucleic Acids Res. 28: 3880–3886.
   PubMed Web of Science ®Google Scholar
• Mackey, Z. B., C. Niedergang, J. M. Murcia, J. Leppard, K. Au, J. Chen, G. de Murcia, and A. E. Tomkinson. 1999. DNA ligase III is recruited to DNA strand breaks by a zinc finger motif homologous to that of poly(ADP-ribose) polymerase. Identification of two functionally distinct DNA binding regions within DNA ligase III. J. Biol. Chem. 274: 21679–21687.
   PubMedGoogle Scholar
• Mackey, Z. B., W. Ramos, D. S. Levin, C. A. Walter, J. R. McCarrey, and A. E. Tomkinson. 1996. An alternative splicing event, which occurs in mouse pachytene spermatocytes, generates a form of DNA ligase III with distinct biochemical properties that may function in meiotic recombination. Mol. Cell. Biol. 17: 989–998.
   Google Scholar
• Marintchev, A., M. Mullen, M. W. Maciejewski, B. Pan, M. R. Gryk, and G. P. Mullen. 1999. Solution structure of the single-strand break repair protein XRCC1 N-terminal domain. Nat. Struct. Biol. 6: 884–893.
   PubMedGoogle Scholar
• Masson, M., C. Niedergang, V. Schreiebr, S. Muller, J. Menissier de Murcia, and G. de Murcia. 1998. XRCC1 is specifically associated with poly(ADP-ribose) polymerase and negatively regulates its activity following DNA damage. Mol. Cell. Biol. 18: 3563–3571.
   PubMed Web of Science ®Google Scholar
• Moore, D. J., R. M. Taylor, P. Clements, and K. W. Caldecott. 2000. Mutation of a BRCT domain selectively disrupts DNA single-strand break repair in noncycling Chinese hamster ovary cells. Proc. Natl. Acad. Sci. USA 97: 13649–13654.
   PubMedGoogle Scholar
• Nash, R. A., K. Caldecott, D. E. Barnes, and T. Lindahl. 1997. XRCC1 protein interacts with one of two distinct forms of DNA ligase III. Biochemistry 36: 5207–5211.
   PubMed Web of Science ®Google Scholar
• Perez-Jannotti, R. M., S. M. Klein, and D. F. Bogenhagen. 2001. Two forms of mitochondrial DNA ligase III are produced in Xenopus laevis oocytes. J. Biol. Chem. 276: 48978–48987.
   PubMedGoogle Scholar
• Pleschke, J. M., H. E. Kleczkowska, M. Strohm, and F. R. Althaus. 2000. Poly(ADP-ribose) binds to specific domains in checkpoint proteins. J. Biol. Chem. 275: 40974–40980.
   PubMed Web of Science ®Google Scholar
• Ron, D., and H. Dressler. 1992. pGSTag—a versatile bacterial expression plasmid for enzymatic labeling of recombinant proteins. BioTechniques 13: 866–868.
   PubMedGoogle Scholar
• Satoh, M., and T. Lindahl. 1992. Role of poly(ADP-ribose) formation in DNA repair. Nature 356: 356–358.
   PubMed Web of Science ®Google Scholar
• Schreiber, V., J. C. Ame, P. Dolle, I. Schultz, B. Rinaldi, V. Fraulob, J. Menissier-de Murcia, and G. de Murcia. 2002. Poly(ADP-ribose) polymerase-2 (PARP-2) is required for efficient base excision repair in association with PARP-1 and XRCC1. J. Biol. Chem. 277: 23028–23036.
   PubMed Web of Science ®Google Scholar
• Taylor, R. M., D. J. Moore, J. Whitehouse, P. Johnson, and K. W. Caldecott. 2000. A cell cycle-specific requirement for the XRCC1 BRCT II domain during mammalian DNA strand break repair. Mol. Cell. Biol. 20: 735–740.
   PubMedGoogle Scholar
• Thompson, L. H., K. W. Brookman, L. E. Dillehay, A. V. Carrano, J. A. Mazrimas, C. L. Mooney, and J. L. Minkler. 1982. A CHO-cell strain having hypersensitivity to mutagens, a defect in strand break repair, and an extraordinary baseline frequency of sister chromatid exchange. Mutat. Res. 95: 247–254.
   Google Scholar
• Thompson, L. H., K. W. Brookman, N. J. Jones, S. A. Allen, and A. V. Carrano. 1990. Molecular cloning of the human XRCC1 gene, which corrects defective DNA strand break repair and sister chromatid exchange. Mol. Cell. Biol. 10: 6160–6171.
   PubMed Web of Science ®Google Scholar
• Tomkinson, A. E., and Z. B. Mackey. 1998. Structure and function of mammalian DNA ligases. Mutat. Res. 407: 1–9.
   PubMedGoogle Scholar
• Vidal, A. E., S. Boiteux, I. D. Hickson, and J. P. Radicella. 2001. XRCC1 coordinates the initial and late stages of DNA abasic site repair though protein-protein interactions. EMBO J. 20: 6530–6539.
   PubMed Web of Science ®Google Scholar
• Wei, Y.-F., P. Robins, K. Carter, K. Caldecott, D. J. C. Pappin, G.-L. Yu, R.-P. Wang, B. K. Shell, R. A. Nash, P. Schar, D. E. Barnes, W. A. Haseltine, and T. Lindahl. 1995. Molecular cloning and expression of human cDNAs encoding a novel DNA ligase IV and DNA ligase III, an enzyme active in DNA repair and genetic recombination. Mol. Cell. Biol. 15: 3206–3216.
   PubMedGoogle Scholar
• Whitehouse, C. J., R. M. Taylor, A. Thistlethwaite, H. Zhang, F. Karimi-Busheri, D. D. Lasko, M. Weinfeld, and K. W. Caldecott. 2001. XRCC1 stimulates human polynucleotide kinase at damaged DNA termini and accelerates DNA single-strand break repair. Cell 104: 107–117.
   PubMed Web of Science ®Google Scholar
• Wu, Y., R. Hickey, K. Lawlor, P. Wills, F. Yu, H. Ozer, R. Starr, J. Y. Quan, M. Lee, and M. Malkas. 1994. A 17S multiprotein form of murine DNA polymerase mediates polyoma virus DNA synthesis. J. Cell. Biochem. 54: 32–46.
   PubMedGoogle Scholar
• Zahradka, P., and K. Ebisuzaki. 1982. A shuttle mechanism for DNA-protein interactions. The regulation of poly(ADP-ribose) polymerase. Eur. J. Biochem. 127: 579–585.
   PubMedGoogle Scholar
• Zdzienicka, M. Z., G. P. Vanderschans, A. T. Natarajan, L. H. Thompson, I. Neuteboom, and J. W. I. M. Simmons. 1992. A Chinese hamster ovary cell mutant (EMC-11) with sensitivity to simple alkylating agents and a very high level of sister chromatid exchanges. Mutagenesis 7: 265–269.
   PubMedGoogle Scholar