Physical and functional interaction between the Bloom's syndrome gene product and the largest subunit of chromatin assembly factor 1

Molecular and Cellular Biology

Volumn 24, Issue 11, 2004, Pages 4710-4719

  Jiao, Renjie ^a   Bachrati, Csanád Z ^b   Pedrazzi, Graziella ^a   Kuster, Patrick ^a   Petkovic, Maja ^a   Li, Ji Liang ^b   Egli, Dieter ^a   Hickson, Ian D ^b   Stagljar, Igor ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

^b UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BLM PROTEIN; BS PROTEIN; CHROMATIN ASSEMBLY FACTOR 1 PROTEIN; GENE PRODUCT; HELICASE; HP 150 PROTEIN; HYDROXYUREA; PROTEIN; RECQ HELICASE; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BLOOM SYNDROME; BLOOM SYNDROME GENE; CANCER SUSCEPTIBILITY; CELL CYCLE S PHASE; CELL NUCLEUS; CELL SURVIVAL; CHROMATIN ASSEMBLY AND DISASSEMBLY; CHROMATIN CONDENSATION; CONTROLLED STUDY; DNA DAMAGE; DNA REPAIR; DNA REPLICATION; DNA SYNTHESIS; GENE MUTATION; HUMAN; HUMAN CELL; IN VITRO STUDY; IN VIVO STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN INTERACTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION;

ADENOSINE TRIPHOSPHATASES; CHROMOSOMAL PROTEINS, NON-HISTONE; DNA HELICASES; DNA REPAIR; DNA-BINDING PROTEINS; HELA CELLS; HUMANS; PROTEIN INTERACTION MAPPING;

ANIMALIA;

EID: 2442680431     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.24.11.4710-4719.2004     Document Type: Article

References (55)

1. Ababou, M., V. Dumaire, Y. Lecluse, and M. Amor-Gueret. 2002. Bloom's syndrome protein response to ultraviolet-C and hydroxyurea-mediated DNA synthesis inhibition. Oncogene 21:2079-2088.
2. Ababou, M., S. Dutertre, Y. Lecluse, R. Onclercq, B. Chatton, and M. Amor-Gueret. 2000. ATM-dependent phosphorylation and accumulation of endogenous BLM protein in response to ionizing radiation. Oncogene 19: 5595-5563.
3. Adachi, Y., and U. K. Laemmli. 1992. Identification of nuclear pre-replication centers poised for DNA synthesis in Xenopus egg extracts: immunolocalization study of replication protein A. J. Cell Biol. 119:1-15.
4. Bachrati, C. Z., and I. D. Hickson. 2003. RecQ helicases: suppressors of tumorigenesis and premature aging. Biochem. J. 374:577-606.
5. Beamish, H., P. Kedar, H. Kaneko, P. Chen, T. Fukao, C. Peng, S. Beresten, N. Gueven, D. Purdie, S. Lees-Miller, N. A. Ellis, N. Kondo and M. F. Lavin. 2002. Functional link between BLM defective in Bloom's syndrome and the ataxia-telangiectasia-mutated protein, ATM. J. Biol. Chem. 277:30515-30523.
6. Bischof, O., S.-H. Kim, J. Irying, S. Beresten, N. A. Ellis, and J. Campisi. 2001. Regulation and localization of the Bloom's syndrome protein in response to DNA damage. J. Cell Biol. 153:367-380.
7. Braybrooke, J. P., J.-L. Li, L. Wu, F. Caple, F. E. Benson and I. D. Hickson. 2003. Functional interaction between the Bloom's-syndrome helicase and the RAD51 paralog, RAD51L3 (RAD51D). J. Biol. Chem. 278:48357-48366.
8. Brosh, R. M., Jr. J. L. Li, M. K. Kenny, J. K. Karow, M. P. Cooper, R. P. Kureekattil, I. D. Hickson, and V. A. Bohr. 2000. Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity. J. Biol. Chem. 275:23500-23508.
9. Cardoso, M. C., H. Leonbardt, and B. Nadal-Ginard. 1993. Reversal of terminal differentiation and control of DNA replication: cyclin A and Cdk2 specifically localize at subnuclear sites of DNA replication. Cell 74:979-992.
10. Chakraverty, R. K., and I. D. Hickson. 1999. Defending genome integrity during DNA replication: a proposed role for RecQ family helicases. Bioessays 21:286-294.
11. Davalos, A. R., and J. Campisi. 2003. Bloom syndrome cells undergo p53-dependent apoptosis and delayed assembly of BRCA1 and NBS1 repair complexes at stalled replication forks. J. Cell Biol. 162:1197-1209.
12. Ellis, N. A., J. Groden, T. Z. Ye, J. Straughen, D. J. Lennon, S. Ciocci, M. Proytcheva and J. German. 1995. The Bloom's syndrome gene product is homologous to RecQ helicases. Cell 83:655-666.
13. Franchitto, A., and P. Pichierri. 2002. Bloom's syndrome protein is required for correct relocalization of RAD50/MRE11/NBS1 complex after replication fork arrest. J. Cell Biol. 157:19-30.
14. Friedberg, E. C., U. K. Ehmann and J. I. Williams. 1979. Human diseases associated with DNA repair. Adv. Radiat. Biol. 8:85-174.
15. Gaillard, P.-H., E. M. Martini, P. D. Kaufman, B. Stillman, E. Moustacchi and G. Almouzni. 1996. Chromatin assembly coupled to DNA repair: a new role for chromatin assembly factor I. Cell 86:887-896.
16. German, J., and N. A. Ellis. 1998. Bloom syndrome, p. 301-315. In B. Vogelstein and K. W. Kinzler (ed.), The genetic basis of human cancer. McGraw-Hill, New York, N.Y.
17. Green, C. M., and G. Almouzni. 2003. Local action of the chromatin assembly factor CAF-1 at sites of nucleotide excision repair in vivo. EMBO J. 22:5163-5174.
18. Hand, R., and J. German. 1975. A retarded rate of DNA chain growth in Bloom's syndrome. Proc. Natl. Acad. Sci. USA 72:758-762.
19. Hickson, I. D. 2003. RecQ helicases: caretakers of the genome. Nat. Rev. Cancer 3:169-178.
20. Hoek, M., and B. Stillman. 2003. Chromatin assembly factor 1 is essential and couples chromatin assembly to DNA replication in vivo. Proc. Natl. Acad. Sci. USA 100:12183-12188.
21. Ishov, A. M., A. G. Sotnikov, D. Negorev, O. V. Vladimirova, N. Neff, T. Kamitani, E. T. Yeh, J. F. Strauss, and G. G. Maul. 1999. PML is critical for ND10 formation and recruits the PML-interacting protein daxx to this nuclear structure when modified by SUMO-1. J. Cell Biol. 147:221-234.
22. Karow, J. K., R. K. Chakraverty, and I. D. Hickson. 1997. The Bloom's syndrome gene product is a 3′-5′ DNA helicase. J. Biol. Chem. 272:30611-30614.
23. Karow, J. K., A. Constantinou, J.-L. Li, S. C. West, and I. D. Hickson. 2000. The Bloom's syndrome gene product promotes branch migration of Holliday junctions. Proc. Natl. Acad. Sci. USA 97:6504-6508.
24. Kaufman, P. D., R. Kobayashi, N. Kessler, and B. Stillman. 1995. The p150 and p60 subunits of chromatin assembly factor I: a molecular link between newly synthesized histones and DNA replication. Cell 81:1105-1114.
25. Krude, T. 1995. Chromatin assembly factor 1 (CAF-1) colocalizes with replication foci in HeLa cell nuclei. Exp. Cell Res. 220:304-311.
26. Langland, G., J. Kordich, J. Creaney, K. H. Goss, K. Lillard-Wetherell, K. Bebenek, T. A. Kunkel, and J. Groden. 2001. The Bloom's syndrome protein (BLM) interacts with MLH1 but is not required for DNA mismatch repair. J. Biol. Chem. 276:30031-30035.
27. Liao, S., J. Graham, and H. Yan. 2000. The function of Xenopus Bloom's syndrome protein homolog (xBLM) in DNA replication. Genes Dev. 14: 2570-2575.
28. Lindenmuth, D. M., A. J. van Wijnen, S. Hiebert, J. L. Stein, J. B. Lian, and G. S. Stein. 1997. Subcellular partitioning of transcription factors during osteoblast differentiation: developmental association of the AML/CBFa/PEBP2a-related transcription factor-NMP-2 with the nuclear matrix. J. Cell. Biochem. 66:123-132.
29. Lonn, U., S. Lonn, U. Nylen, G. Winblad, and J. German. 1990. An abnormal profile of DNA replication intermediates in Bloom's syndrome. Cancer Res. 50:3141-3145.
30. Martini, E., D. M. J. Roche, K. Marheineke, A. Verreault, and G. Almouzni. 1998. Recruitment of phosphorylated chromatin assembly factor 1 to chromatin following UV irradiation of human cells. J. Cell Biol. 143:563-575.
31. Meetei, A. R., S. Sechi, M. Wallisch, D. Yang, M. K. Young, H. Joenje, M. E. Hoatlin, and W. Wang. 2003. A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome. Mol. Cell. Biol. 23:3417-3426.
32. Moens, P. B., R. Freire, M. Tarsounas, B. Spyropoulos, and S. P. Jackson. 2000. Expression and nuclear localization of BLM, a chromosome stability protein mutated in Bloom's syndrome, suggest a role in recombination during meiotic prophase. J. Cell Sci. 113:663-672.
33. Moggs, J. G., P. Grandi, J.-P. Quivy, Z. O. Jonsson, U. Hübscher, P. B. Becker, and G. Almouzni. 2000. A CAF-1-PCNA-mediated chromatin assembly pathway triggered by sensing DNA damage. Mol. Cell. Biol. 20:1206-1218.
34. Mohaghegh, P., and I. D. Hickson. 2001. DNA helicase deficiencies associated with cancer predisposition and premature ageing disorders. Hum. Mol. Genet. 10:741-746.
35. Neff, N. F., N. A. Ellis, T. Z. Ye, J. Noonan, K. Huang, M. Sanz, and M. Proytcheva. 1999. The DNA helicase activity of BLM is necessary for the correction of the genomic instability of Bloom syndrome cells. Mol. Biol. Cell 10:665-676.
36. Opresko, P. L., C. von Kobbe, J.-P. Laine, J. Harrigan, I. D. Hickson, and V. A. Bohr. 2002. Telemere-binding protein TRF2 binds to and stimulates the werner and bloom syndrome helicases. J. Biol. Chem. 277:4378-4386.
37. Pedrazzi, G., C. Z. Bachrati, N. Selak, I. Studer, M. Petkovic, I. D. Hickson, J. Jiricny, and I. Stagljar. 2003. The Bloom's syndrome helicase interacts directly with the human DNA mismatch repair protein hMSH6. Biol. Chem. 384:1155-1164.
38. Pedrazzi, G., C. Perrera, H. Blaser, P. Kuster, G. Marra, S. L. Davies, G.-H. Ryu, R. Freire, I. D. Hickson, J. Jiricny, and I. Stagljar. 2001. Direct association of Bloom's syndrome gene product with the human mismatch repair protein MLH1. Nucleic Acids Res. 29:4378-4386.
39. Quivy, J.-P., P. Grandi, and G. Almouzni. 2001. Dimerization of the largest subunit of chromatin assembly factor 1: importance in vitro and during Xenopus early development. EMBO J. 20:2015-2027.
40. Ray, J. H., and J. German. 1983. The cytogenetics of the chromosome-breakage syndromes, p. 135-167. In J. German (ed.), Chromosome mutation and neoplasia. Alan R. Liss, Inc., New York, N.Y.
41. Sengupta, S., S. P. Linke, R. Pedeux, Q. Yang, J. Farnsworth, S. H. Garfield, K. Valerie, J. W. Shay, N. A. Ellis, B. Wasylyk, and C. C. Harris. 2003. BLM helicase-dependent transport of p53 to sites of stalled DNA replication forks modulates homologous recombination. EMBO J. 22:1210-1222.
42. Smith, S., and B. Stillman. 1991. Immunological characterization of chromatin assembly factor I, a human cell factor required for chromatin assembly during DNA replication in vitro. J. Biol. Chem. 266:12041-12047.
43. Smith, S., and B. Stillman. 1989. Purification and characterization of CAF-I, a human cell factor required for chromatin assembly during DNA replication in vitro. Cell 58:15-25.
44. Stavropoulos, D. J., P. S. Bradshaw, X. Li, I. Pasic, K. Truong, M. Ikura, M. Ungrin, and M. S. Meyn. 2002. The bloom syndrome helicase BLM interacts with TRFs in ALT cells and promotes telomeric DNA synthesis. Hum. Mol. Genet. 11:3135-3144.
45. Taddei, A., R. D., J. B. Sibarita, B. M. Turner, and G. Almouzni. 1999, Duplication and maintenance of heterochromatin domains. J. Cell Biol. 147:1153-1166.
46. Venkitaraman, A. R. 2002. Cancer susceptibility and the functions of BRCA1 and BRCA2. Cell 108:171-182.
47. Verreault, A., P. D. Kaufman, R. Kobayashi, and B. Stillman. 1996. Nucleosome assembly by a complex of CAF-1 and acetylated histones H3/H4. Cell 87:95-104.
48. von Kobbe, C., P. Karmakar, L. Dawut, P. Opresko, X. Zeng, R. M. Brosh Jr., I. D. Hickson, and V. A. Bohr. 2002. Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins. J. Biol. Chem. 277:22035-22044.
49. Wang, X. W., A. Tseng, N. A. Ellis, E. A. Spillare, S. P. Linke, A. I. Robles, H. Seker, Q. Yang, P. Hu, S. Beresten, N. A. Bemmels, S. Garfield, and C. C. Harris. 2001. Functional interaction of p53 and BLM DNA helicase in apoptosis. J. Biol. Chem. 276:32948-32955.
50. Wang, Y., D. Cortez, P. Yazdi, N. Neff, S. J. Elledge, and J. Qin. 2000. BASC, a super complex of BRCA1-associated proteins involved in the recognition and repair of aberrant DNA structures. Genes Dev. 14:927-939.
51. Wu, L., S. L. Davies, and I. D. Hickson. 2000. Roles of RecQ family helicases in the maintenance of genome stability. Cold Spring Harbor Symp. Quant. Biol. 65:573-581.
52. Wu, L., S. L. Davies, N. C. Levitt, and I. D. Hickson. 2001. Potential role for the BLM helicase in recombinational repair via a conserved interaction with RAD51. J. Biol. Chem. 276:19375-19381,
53. Wu, L., S. L. Davies, P. S. North, H. Goulaouic, J. F. Riou, H. Turley, K. C. Gatter, and I. D. Hickson. 2000. The Bloom's syndrome gene product interacts with topoisomerase III. J. Biol. Chem. 275:9636-9644.
54. Wu, L., and I. D. Hickson. 2003. The Bloom's syndrome helicase suppresses crossing over during homologous recombination. Nature 426:870-874.
55. Yankiwski, V., R. A. Marciniak, L. Guarente, and N. F. Neff. 2000. Nuclear structure in normal and Bloom syndrome cells. Proc. Natl. Acad. Sci. USA 97:5214-5219.