메뉴 건너뛰기




Volumn 596, Issue 1-2 SPEC. ISS., 2006, Pages 64-75

Loss of Ubr2, an E3 ubiquitin ligase, leads to chromosome fragility and impaired homologous recombinational repair

Author keywords

Fragile sites; Genome instability; Homologous recombination repair; Mitomycin C sensitivity; N end rule proteolytic pathway; Ubr2 ubiquitin ligase

Indexed keywords

DOUBLE STRANDED DNA; MITOMYCIN C; UBIQUITIN LIGASE UBR2; UBIQUITIN PROTEIN LIGASE E3; UNCLASSIFIED DRUG;

EID: 33646007680     PISSN: 00275107     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mrfmmm.2005.12.016     Document Type: Article
Times cited : (23)

References (106)
  • 2
    • 0035166684 scopus 로고    scopus 로고
    • Construction and analysis of mouse strains lacking the ubiquitin ligase UBR1 (E3alpha) of the N-end rule pathway
    • Kwon Y.T., Xia Z., Davydov I.V., Lecker S.H., and Varshavsky A. Construction and analysis of mouse strains lacking the ubiquitin ligase UBR1 (E3alpha) of the N-end rule pathway. Mol. Cell Biol. 21 (2001) 8007-8021
    • (2001) Mol. Cell Biol. , vol.21 , pp. 8007-8021
    • Kwon, Y.T.1    Xia, Z.2    Davydov, I.V.3    Lecker, S.H.4    Varshavsky, A.5
  • 3
    • 0242664014 scopus 로고    scopus 로고
    • Female lethality and apoptosis of spermatocytes in mice lacking the UBR2 ubiquitin ligase of the N-end rule pathway
    • Kwon Y.T., Xia Z., An J.Y., Tasaki T., Davydov I.V., Seo J.W., Sheng J., Xie Y., and Varshavsky A. Female lethality and apoptosis of spermatocytes in mice lacking the UBR2 ubiquitin ligase of the N-end rule pathway. Mol. Cell Biol. 23 (2003) 8255-8271
    • (2003) Mol. Cell Biol. , vol.23 , pp. 8255-8271
    • Kwon, Y.T.1    Xia, Z.2    An, J.Y.3    Tasaki, T.4    Davydov, I.V.5    Seo, J.W.6    Sheng, J.7    Xie, Y.8    Varshavsky, A.9
  • 4
    • 0026663539 scopus 로고
    • The ubiquitin system for protein degradation
    • Hershko A., and Ciechanover A. The ubiquitin system for protein degradation. Annu. Rev. Biochem. 61 (1992) 761-807
    • (1992) Annu. Rev. Biochem. , vol.61 , pp. 761-807
    • Hershko, A.1    Ciechanover, A.2
  • 5
    • 9744227183 scopus 로고    scopus 로고
    • Ubiquitin: structures, functions, mechanisms
    • Pickart C.M., and Eddins M.J. Ubiquitin: structures, functions, mechanisms. Biochim. Biophys. Acta 1695 (2004) 55-72
    • (2004) Biochim. Biophys. Acta , vol.1695 , pp. 55-72
    • Pickart, C.M.1    Eddins, M.J.2
  • 6
    • 20444404618 scopus 로고    scopus 로고
    • Regulated protein degradation
    • Varshavsky A. Regulated protein degradation. Trends Biochem. Sci. 30 (2005) 283-286
    • (2005) Trends Biochem. Sci. , vol.30 , pp. 283-286
    • Varshavsky, A.1
  • 7
    • 0029861143 scopus 로고    scopus 로고
    • The N-end rule: functions, mysteries, uses
    • Varshavsky A. The N-end rule: functions, mysteries, uses. Proc. Natl. Acad. Sci. U.S.A. 93 (1996) 12142-12149
    • (1996) Proc. Natl. Acad. Sci. U.S.A. , vol.93 , pp. 12142-12149
    • Varshavsky, A.1
  • 8
  • 9
    • 0025345753 scopus 로고
    • cis-trans recognition and subunit-specific degradation of short-lived proteins
    • Johnson E.S., Gonda D.K., and Varshavsky A. cis-trans recognition and subunit-specific degradation of short-lived proteins. Nature 346 (1990) 287-291
    • (1990) Nature , vol.346 , pp. 287-291
    • Johnson, E.S.1    Gonda, D.K.2    Varshavsky, A.3
  • 10
    • 27144557281 scopus 로고    scopus 로고
    • The N-end rule pathway as a nitric oxide sensor controlling the levels of multiple regulators
    • Hu R.G., Sheng J., Qi X., Xu Z., Takahashi T.T., and Varshavsky A. The N-end rule pathway as a nitric oxide sensor controlling the levels of multiple regulators. Nature 437 (2005) 981-986
    • (2005) Nature , vol.437 , pp. 981-986
    • Hu, R.G.1    Sheng, J.2    Qi, X.3    Xu, Z.4    Takahashi, T.T.5    Varshavsky, A.6
  • 12
    • 3242880404 scopus 로고    scopus 로고
    • The role of the DNA double-strand break response network in meiosis
    • Richardson C., Horikoshi N., and Pandita T.K. The role of the DNA double-strand break response network in meiosis. DNA Repair (Amst.) 3 (2004) 1149-1164
    • (2004) DNA Repair (Amst.) , vol.3 , pp. 1149-1164
    • Richardson, C.1    Horikoshi, N.2    Pandita, T.K.3
  • 14
    • 1642373913 scopus 로고    scopus 로고
    • Ataxia telangiectasia mutated expression and activation in the testis
    • Hamer G., Kal H.B., Westphal C.H., Ashley T., and de Rooij D.G. Ataxia telangiectasia mutated expression and activation in the testis. Biol. Reprod. 70 (2004) 1206-1212
    • (2004) Biol. Reprod. , vol.70 , pp. 1206-1212
    • Hamer, G.1    Kal, H.B.2    Westphal, C.H.3    Ashley, T.4    de Rooij, D.G.5
  • 15
    • 0029844048 scopus 로고    scopus 로고
    • Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma
    • Xu Y., Ashley T., Brainerd E.E., Bronson R.T., Meyn M.S., and Baltimore D. Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma. Genes Dev. 10 (1996) 2411-2422
    • (1996) Genes Dev. , vol.10 , pp. 2411-2422
    • Xu, Y.1    Ashley, T.2    Brainerd, E.E.3    Bronson, R.T.4    Meyn, M.S.5    Baltimore, D.6
  • 19
    • 22344439942 scopus 로고    scopus 로고
    • Dynamic molecular linkers of the genome: the first decade of SMC proteins
    • Losada A., and Hirano T. Dynamic molecular linkers of the genome: the first decade of SMC proteins. Genes Dev. 19 (2005) 1269-1287
    • (2005) Genes Dev. , vol.19 , pp. 1269-1287
    • Losada, A.1    Hirano, T.2
  • 20
    • 0141757494 scopus 로고    scopus 로고
    • Regulation and mechanisms of mammalian double-strand break repair
    • Valerie K., and Povirk L.F. Regulation and mechanisms of mammalian double-strand break repair. Oncogene 22 (2003) 5792-5812
    • (2003) Oncogene , vol.22 , pp. 5792-5812
    • Valerie, K.1    Povirk, L.F.2
  • 22
    • 0037268338 scopus 로고    scopus 로고
    • The Fanconi anaemia/BRCA pathway
    • D'Andrea A.D., and Grompe M. The Fanconi anaemia/BRCA pathway. Nat. Rev. Cancer 3 (2003) 23-34
    • (2003) Nat. Rev. Cancer , vol.3 , pp. 23-34
    • D'Andrea, A.D.1    Grompe, M.2
  • 24
    • 1842576658 scopus 로고    scopus 로고
    • The DNA crosslink-induced S-phase checkpoint depends on ATR-CHK1 and ATR-NBS1-FANCD2 pathways
    • Pichierri P., and Rosselli F. The DNA crosslink-induced S-phase checkpoint depends on ATR-CHK1 and ATR-NBS1-FANCD2 pathways. EMBO J. 23 (2004) 1178-1187
    • (2004) EMBO J. , vol.23 , pp. 1178-1187
    • Pichierri, P.1    Rosselli, F.2
  • 30
    • 0034707053 scopus 로고    scopus 로고
    • In search of the tumour-suppressor functions of BRCA1 and BRCA2
    • Scully R., and Livingston D.M. In search of the tumour-suppressor functions of BRCA1 and BRCA2. Nature 408 (2000) 429-432
    • (2000) Nature , vol.408 , pp. 429-432
    • Scully, R.1    Livingston, D.M.2
  • 31
    • 0022623269 scopus 로고
    • Recombinant retroviruses encoding simian virus 40 large T antigen and polyomavirus large and middle T antigens
    • Jat P.S., Cepko C.L., Mulligan R.C., and Sharp P.A. Recombinant retroviruses encoding simian virus 40 large T antigen and polyomavirus large and middle T antigens. Mol. Cell Biol. 6 (1986) 1204-1217
    • (1986) Mol. Cell Biol. , vol.6 , pp. 1204-1217
    • Jat, P.S.1    Cepko, C.L.2    Mulligan, R.C.3    Sharp, P.A.4
  • 32
    • 31544481848 scopus 로고    scopus 로고
    • The element(s) at the non-transcribed Xist locus of the active X chromosome controls chromosomal replication timing in the mouse
    • Diaz-Perez S., Ouyang Y., Perez V., Cisneros R., Regelson M., and Marahrens Y. The element(s) at the non-transcribed Xist locus of the active X chromosome controls chromosomal replication timing in the mouse. Genetics 171 2 (2005) 663-672
    • (2005) Genetics , vol.171 , Issue.2 , pp. 663-672
    • Diaz-Perez, S.1    Ouyang, Y.2    Perez, V.3    Cisneros, R.4    Regelson, M.5    Marahrens, Y.6
  • 33
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays
    • Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65 (1983) 55-63
    • (1983) J. Immunol. Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 34
    • 0035099044 scopus 로고    scopus 로고
    • BRCA2 is required for homology-directed repair of chromosomal breaks
    • Moynahan M.E., Pierce A.J., and Jasin M. BRCA2 is required for homology-directed repair of chromosomal breaks. Mol. Cell 7 (2001) 263-272
    • (2001) Mol. Cell , vol.7 , pp. 263-272
    • Moynahan, M.E.1    Pierce, A.J.2    Jasin, M.3
  • 35
    • 0033569684 scopus 로고    scopus 로고
    • XRCC3 promotes homology-directed repair of DNA damage in mammalian cells
    • Pierce A.J., Johnson R.D., Thompson L.H., and Jasin M. XRCC3 promotes homology-directed repair of DNA damage in mammalian cells. Genes Dev. 13 (1999) 2633-2638
    • (1999) Genes Dev. , vol.13 , pp. 2633-2638
    • Pierce, A.J.1    Johnson, R.D.2    Thompson, L.H.3    Jasin, M.4
  • 36
    • 0030305457 scopus 로고    scopus 로고
    • R: a language for data analysis and graphics
    • Ihaka R., and Gentleman R. R: a language for data analysis and graphics. J. Comput. Graphical Stat. 5 (1996) 299-314
    • (1996) J. Comput. Graphical Stat. , vol.5 , pp. 299-314
    • Ihaka, R.1    Gentleman, R.2
  • 37
    • 0041654220 scopus 로고
    • Multidimensional scaling by optimizing goodness of fit to a nonmetric hypothesis
    • Kruskal J.B. Multidimensional scaling by optimizing goodness of fit to a nonmetric hypothesis. Psychometrika 29 (1964) 1-27
    • (1964) Psychometrika , vol.29 , pp. 1-27
    • Kruskal, J.B.1
  • 38
    • 3943107573 scopus 로고    scopus 로고
    • Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints
    • Sancar A., Lindsey-Boltz L.A., Unsal-Kacmaz K., and Linn S. Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints. Annu. Rev. Biochem. 73 (2004) 39-85
    • (2004) Annu. Rev. Biochem. , vol.73 , pp. 39-85
    • Sancar, A.1    Lindsey-Boltz, L.A.2    Unsal-Kacmaz, K.3    Linn, S.4
  • 41
    • 0035140477 scopus 로고    scopus 로고
    • Genomic instability in Down syndrome and Fanconi anemia assessed by micronucleus analysis and single-cell gel electrophoresis
    • Maluf S.W., and Erdtmann B. Genomic instability in Down syndrome and Fanconi anemia assessed by micronucleus analysis and single-cell gel electrophoresis. Cancer Genet. Cytogenet. 124 (2001) 71-75
    • (2001) Cancer Genet. Cytogenet. , vol.124 , pp. 71-75
    • Maluf, S.W.1    Erdtmann, B.2
  • 42
    • 0035283417 scopus 로고    scopus 로고
    • Chromosomal instability in BRCA1- or BRCA2-defective human cancer cells detected by spontaneous micronucleus assay
    • Ban S., Shinohara T., Hirai Y., Moritaku Y., Cologne J.B., and MacPhee D.G. Chromosomal instability in BRCA1- or BRCA2-defective human cancer cells detected by spontaneous micronucleus assay. Mutat. Res. 474 (2001) 15-23
    • (2001) Mutat. Res. , vol.474 , pp. 15-23
    • Ban, S.1    Shinohara, T.2    Hirai, Y.3    Moritaku, Y.4    Cologne, J.B.5    MacPhee, D.G.6
  • 43
    • 11044234004 scopus 로고    scopus 로고
    • Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway
    • Alderton G.K., Joenje H., Varon R., Borglum A.D., Jeggo P.A., and O'Driscoll M. Seckel syndrome exhibits cellular features demonstrating defects in the ATR-signalling pathway. Hum. Mol. Genet. 13 (2004) 3127-3138
    • (2004) Hum. Mol. Genet. , vol.13 , pp. 3127-3138
    • Alderton, G.K.1    Joenje, H.2    Varon, R.3    Borglum, A.D.4    Jeggo, P.A.5    O'Driscoll, M.6
  • 44
    • 0037419723 scopus 로고    scopus 로고
    • Use of the cytokinesis-block micronucleus assay to measure radiation-induced chromosome damage in lymphoblastoid cell lines
    • Gutierrez-Enriquez S., and Hall J. Use of the cytokinesis-block micronucleus assay to measure radiation-induced chromosome damage in lymphoblastoid cell lines. Mutat. Res. 535 (2003) 1-13
    • (2003) Mutat. Res. , vol.535 , pp. 1-13
    • Gutierrez-Enriquez, S.1    Hall, J.2
  • 45
    • 0024461719 scopus 로고
    • Tissue specificity of chromosomal rearrangements in ataxia-telangiectasia
    • Kojis T.L., Schreck R.R., Gatti R.A., and Sparkes R.S. Tissue specificity of chromosomal rearrangements in ataxia-telangiectasia. Hum. Genet. 83 (1989) 347-352
    • (1989) Hum. Genet. , vol.83 , pp. 347-352
    • Kojis, T.L.1    Schreck, R.R.2    Gatti, R.A.3    Sparkes, R.S.4
  • 47
    • 0037173452 scopus 로고    scopus 로고
    • Micronuclei, nucleoplasmic bridges and nuclear buds induced in folic acid deficient human lymphocytes-evidence for breakage-fusion-bridge cycles in the cytokinesis-block micronucleus assay
    • Fenech M., and Crott J.W. Micronuclei, nucleoplasmic bridges and nuclear buds induced in folic acid deficient human lymphocytes-evidence for breakage-fusion-bridge cycles in the cytokinesis-block micronucleus assay. Mutat. Res. 504 (2002) 131-136
    • (2002) Mutat. Res. , vol.504 , pp. 131-136
    • Fenech, M.1    Crott, J.W.2
  • 48
    • 0037340936 scopus 로고    scopus 로고
    • Nucleoplasmic bridges are a sensitive measure of chromosome rearrangement in the cytokinesis-block micronucleus assay
    • Thomas P., Umegaki K., and Fenech M. Nucleoplasmic bridges are a sensitive measure of chromosome rearrangement in the cytokinesis-block micronucleus assay. Mutagenesis 18 (2003) 187-194
    • (2003) Mutagenesis , vol.18 , pp. 187-194
    • Thomas, P.1    Umegaki, K.2    Fenech, M.3
  • 49
    • 0027176828 scopus 로고
    • Association of fragile X syndrome with delayed replication of the FMR1 gene
    • Hansen R.S., Canfield T.K., Lamb M.M., Gartler S.M., and Laird C.D. Association of fragile X syndrome with delayed replication of the FMR1 gene. Cell 73 (1993) 1403-1409
    • (1993) Cell , vol.73 , pp. 1403-1409
    • Hansen, R.S.1    Canfield, T.K.2    Lamb, M.M.3    Gartler, S.M.4    Laird, C.D.5
  • 50
    • 0033051760 scopus 로고    scopus 로고
    • Allele-specific late replication and fragility of the most active common fragile site, FRA3B
    • Wang L., Darling J., Zhang J.S., Huang H., Liu W., and Smith D. Allele-specific late replication and fragility of the most active common fragile site, FRA3B. Hum. Mol. Genet. 8 (1999) 431-437
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 431-437
    • Wang, L.1    Darling, J.2    Zhang, J.S.3    Huang, H.4    Liu, W.5    Smith, D.6
  • 51
    • 0034117095 scopus 로고    scopus 로고
    • Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability
    • Hellman A., Rahat A., Scherer S.W., Darvasi A., Tsui L.C., and Kerem B. Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability. Mol. Cell Biol. 20 (2000) 4420-4427
    • (2000) Mol. Cell Biol. , vol.20 , pp. 4420-4427
    • Hellman, A.1    Rahat, A.2    Scherer, S.W.3    Darvasi, A.4    Tsui, L.C.5    Kerem, B.6
  • 54
    • 0033956004 scopus 로고    scopus 로고
    • Sensitivity to DNA cross-linking chemotherapeutic agents in mismatch repair-defective cells in vitro and in xenografts
    • Fiumicino S., Martinelli S., Colussi C., Aquilina G., Leonetti C., Crescenzi M., and Bignami M. Sensitivity to DNA cross-linking chemotherapeutic agents in mismatch repair-defective cells in vitro and in xenografts. Int. J. Cancer 85 (2000) 590-596
    • (2000) Int. J. Cancer , vol.85 , pp. 590-596
    • Fiumicino, S.1    Martinelli, S.2    Colussi, C.3    Aquilina, G.4    Leonetti, C.5    Crescenzi, M.6    Bignami, M.7
  • 55
    • 0025734557 scopus 로고
    • Cross-sensitivity of gamma-ray-sensitive hamster mutants to cross-linking agents
    • Caldecott K., and Jeggo P. Cross-sensitivity of gamma-ray-sensitive hamster mutants to cross-linking agents. Mutat. Res. 255 (1991) 111-121
    • (1991) Mutat. Res. , vol.255 , pp. 111-121
    • Caldecott, K.1    Jeggo, P.2
  • 56
    • 0345734278 scopus 로고    scopus 로고
    • Homologous recombination deficiency leads to profound genetic instability in cells derived from Xrcc2-knockout mice
    • Deans B., Griffin C.S., O'Regan P., Jasin M., and Thacker J. Homologous recombination deficiency leads to profound genetic instability in cells derived from Xrcc2-knockout mice. Cancer Res. 63 (2003) 8181-8187
    • (2003) Cancer Res. , vol.63 , pp. 8181-8187
    • Deans, B.1    Griffin, C.S.2    O'Regan, P.3    Jasin, M.4    Thacker, J.5
  • 57
    • 0023905947 scopus 로고
    • A Chinese hamster ovary cell line hypersensitive to ionizing radiation and deficient in repair replication
    • Fuller L.F., and Painter R.B. A Chinese hamster ovary cell line hypersensitive to ionizing radiation and deficient in repair replication. Mutat. Res. 193 (1988) 109-121
    • (1988) Mutat. Res. , vol.193 , pp. 109-121
    • Fuller, L.F.1    Painter, R.B.2
  • 58
    • 0033598437 scopus 로고    scopus 로고
    • Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination
    • Johnson R.D., Liu N., and Jasin M. Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination. Nature 401 (1999) 397-399
    • (1999) Nature , vol.401 , pp. 397-399
    • Johnson, R.D.1    Liu, N.2    Jasin, M.3
  • 59
    • 45949121186 scopus 로고
    • Isolation and cross-sensitivity of X-ray-sensitive mutants of V79-4 hamster cells
    • Jones N.J., Cox R., and Thacker J. Isolation and cross-sensitivity of X-ray-sensitive mutants of V79-4 hamster cells. Mutat. Res. 183 (1987) 279-286
    • (1987) Mutat. Res. , vol.183 , pp. 279-286
    • Jones, N.J.1    Cox, R.2    Thacker, J.3
  • 61
    • 2642516304 scopus 로고    scopus 로고
    • Recombination repair pathway in the maintenance of chromosomal integrity against DNA interstrand crosslinks
    • Sasaki M.S., Takata M., Sonoda E., Tachibana A., and Takeda S. Recombination repair pathway in the maintenance of chromosomal integrity against DNA interstrand crosslinks. Cytogenet. Genome Res. 104 (2004) 28-34
    • (2004) Cytogenet. Genome Res. , vol.104 , pp. 28-34
    • Sasaki, M.S.1    Takata, M.2    Sonoda, E.3    Tachibana, A.4    Takeda, S.5
  • 62
    • 16844383231 scopus 로고    scopus 로고
    • Extensive chromosomal instability in Rad51d-deficient mouse cells
    • Smiraldo P.G., Gruver A.M., Osborn J.C., and Pittman D.L. Extensive chromosomal instability in Rad51d-deficient mouse cells. Cancer Res. 65 (2005) 2089-2096
    • (2005) Cancer Res. , vol.65 , pp. 2089-2096
    • Smiraldo, P.G.1    Gruver, A.M.2    Osborn, J.C.3    Pittman, D.L.4
  • 65
    • 14644391577 scopus 로고    scopus 로고
    • The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability
    • Howlett N.G., Taniguchi T., Durkin S.G., D'Andrea A.D., and Glover T.W. The Fanconi anemia pathway is required for the DNA replication stress response and for the regulation of common fragile site stability. Hum. Mol. Genet. 14 (2005) 693-701
    • (2005) Hum. Mol. Genet. , vol.14 , pp. 693-701
    • Howlett, N.G.1    Taniguchi, T.2    Durkin, S.G.3    D'Andrea, A.D.4    Glover, T.W.5
  • 66
    • 0035688468 scopus 로고    scopus 로고
    • The Chinese hamster FANCG/XRCC9 mutant NM3 fails to express the monoubiquitinated form of the FANCD2 protein, is hypersensitive to a range of DNA damaging agents and exhibits a normal level of spontaneous sister chromatid exchange
    • Wilson J.B., Johnson M.A., Stuckert A.P., Trueman K.L., May S., Bryant P.E., Meyn R.E., D'Andrea A.D., and Jones N.J. The Chinese hamster FANCG/XRCC9 mutant NM3 fails to express the monoubiquitinated form of the FANCD2 protein, is hypersensitive to a range of DNA damaging agents and exhibits a normal level of spontaneous sister chromatid exchange. Carcinogenesis 22 (2001) 1939-1946
    • (2001) Carcinogenesis , vol.22 , pp. 1939-1946
    • Wilson, J.B.1    Johnson, M.A.2    Stuckert, A.P.3    Trueman, K.L.4    May, S.5    Bryant, P.E.6    Meyn, R.E.7    D'Andrea, A.D.8    Jones, N.J.9
  • 67
    • 0032907596 scopus 로고    scopus 로고
    • Involvement of the DNA mismatch repair system in antineoplastic drug resistance
    • Lage H., and Dietel M. Involvement of the DNA mismatch repair system in antineoplastic drug resistance. J. Cancer Res. Clin. Oncol. 125 (1999) 156-165
    • (1999) J. Cancer Res. Clin. Oncol. , vol.125 , pp. 156-165
    • Lage, H.1    Dietel, M.2
  • 72
    • 4344597147 scopus 로고    scopus 로고
    • The Fanconi anaemia gene FANCC promotes homologous recombination and error-prone DNA repair
    • Niedzwiedz W., Mosedale G., Johnson M., Ong C.Y., Pace P., and Patel K.J. The Fanconi anaemia gene FANCC promotes homologous recombination and error-prone DNA repair. Mol. Cell 15 (2004) 607-620
    • (2004) Mol. Cell , vol.15 , pp. 607-620
    • Niedzwiedz, W.1    Mosedale, G.2    Johnson, M.3    Ong, C.Y.4    Pace, P.5    Patel, K.J.6
  • 73
    • 0035161816 scopus 로고    scopus 로고
    • Functional interactions and signaling properties of mammalian DNA mismatch repair proteins
    • Bellacosa A. Functional interactions and signaling properties of mammalian DNA mismatch repair proteins. Cell Death Differ. 8 (2001) 1076-1092
    • (2001) Cell Death Differ. , vol.8 , pp. 1076-1092
    • Bellacosa, A.1
  • 74
    • 0034672057 scopus 로고    scopus 로고
    • Xrcc2 is required for genetic stability, embryonic neurogenesis and viability in mice
    • Deans B., Griffin C.S., Maconochie M., and Thacker J. Xrcc2 is required for genetic stability, embryonic neurogenesis and viability in mice. EMBO J. 19 (2000) 6675-6685
    • (2000) EMBO J. , vol.19 , pp. 6675-6685
    • Deans, B.1    Griffin, C.S.2    Maconochie, M.3    Thacker, J.4
  • 75
    • 0033501050 scopus 로고    scopus 로고
    • Disruption of muREC2/RAD51L1 in mice results in early embryonic lethality which can Be partially rescued in a p53(-/-) background
    • Shu Z., Smith S., Wang L., Rice M.C., and Kmiec E.B. Disruption of muREC2/RAD51L1 in mice results in early embryonic lethality which can Be partially rescued in a p53(-/-) background. Mol. Cell Biol. 19 (1999) 8686-8693
    • (1999) Mol. Cell Biol. , vol.19 , pp. 8686-8693
    • Shu, Z.1    Smith, S.2    Wang, L.3    Rice, M.C.4    Kmiec, E.B.5
  • 76
    • 0034074273 scopus 로고    scopus 로고
    • Midgestation lethality in mice deficient for the RecA-related gene, Rad51d/Rad51l3
    • Pittman D.L., and Schimenti J.C. Midgestation lethality in mice deficient for the RecA-related gene, Rad51d/Rad51l3. Genesis 26 (2000) 167-173
    • (2000) Genesis , vol.26 , pp. 167-173
    • Pittman, D.L.1    Schimenti, J.C.2
  • 77
    • 14044251525 scopus 로고    scopus 로고
    • The BRCA2-interacting protein BCCIP functions in RAD51 and BRCA2 focus formation and homologous recombinational repair
    • Lu H., Guo X., Meng X., Liu J., Allen C., Wray J., Nickoloff J.A., and Shen Z. The BRCA2-interacting protein BCCIP functions in RAD51 and BRCA2 focus formation and homologous recombinational repair. Mol. Cell Biol. 25 (2005) 1949-1957
    • (2005) Mol. Cell Biol. , vol.25 , pp. 1949-1957
    • Lu, H.1    Guo, X.2    Meng, X.3    Liu, J.4    Allen, C.5    Wray, J.6    Nickoloff, J.A.7    Shen, Z.8
  • 79
    • 21244464297 scopus 로고    scopus 로고
    • Hypersensitivity of Brca1-deficient MEF to the DNA interstrand crosslinking agent mitomycin C is associated with defect in homologous recombination repair and aberrant S-phase arrest
    • Yun J., Zhong Q., Kwak J.Y., and Lee W.H. Hypersensitivity of Brca1-deficient MEF to the DNA interstrand crosslinking agent mitomycin C is associated with defect in homologous recombination repair and aberrant S-phase arrest. Oncogene 24 (2005) 4009-4016
    • (2005) Oncogene , vol.24 , pp. 4009-4016
    • Yun, J.1    Zhong, Q.2    Kwak, J.Y.3    Lee, W.H.4
  • 80
    • 4944257913 scopus 로고    scopus 로고
    • ATR affecting cell radiosensitivity is dependent on homologous recombination repair but independent of nonhomologous end joining
    • Wang H., Wang H., Powell S.N., Iliakis G., and Wang Y. ATR affecting cell radiosensitivity is dependent on homologous recombination repair but independent of nonhomologous end joining. Cancer Res. 64 (2004) 7139-7143
    • (2004) Cancer Res. , vol.64 , pp. 7139-7143
    • Wang, H.1    Wang, H.2    Powell, S.N.3    Iliakis, G.4    Wang, Y.5
  • 81
    • 0037074013 scopus 로고    scopus 로고
    • ATR regulates fragile site stability
    • Casper A.M., Nghiem P., Arlt M.F., and Glover T.W. ATR regulates fragile site stability. Cell 111 (2002) 779-789
    • (2002) Cell , vol.111 , pp. 779-789
    • Casper, A.M.1    Nghiem, P.2    Arlt, M.F.3    Glover, T.W.4
  • 82
    • 3242712112 scopus 로고    scopus 로고
    • BRCA1 is required for common-fragile-site stability via its G2/M checkpoint function
    • Arlt M.F., Xu B., Durkin S.G., Casper A.M., Kastan M.B., and Glover T.W. BRCA1 is required for common-fragile-site stability via its G2/M checkpoint function. Mol. Cell Biol. 24 (2004) 6701-6709
    • (2004) Mol. Cell Biol. , vol.24 , pp. 6701-6709
    • Arlt, M.F.1    Xu, B.2    Durkin, S.G.3    Casper, A.M.4    Kastan, M.B.5    Glover, T.W.6
  • 83
    • 2642540828 scopus 로고    scopus 로고
    • Chromosomal mutagen sensitivity associated with mutations in BRCA genes
    • Speit G., and Trenz K. Chromosomal mutagen sensitivity associated with mutations in BRCA genes. Cytogenet. Genome Res. 104 (2004) 325-332
    • (2004) Cytogenet. Genome Res. , vol.104 , pp. 325-332
    • Speit, G.1    Trenz, K.2
  • 84
    • 0031924605 scopus 로고    scopus 로고
    • Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction
    • Le Beau M.M., Rassool F.V., Neilly M.E., Espinosa III R., Glover T.W., Smith D.I., and McKeithan T.W. Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction. Hum. Mol. Genet. 7 (1998) 755-761
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 755-761
    • Le Beau, M.M.1    Rassool, F.V.2    Neilly, M.E.3    Espinosa III, R.4    Glover, T.W.5    Smith, D.I.6    McKeithan, T.W.7
  • 85
    • 0000237085 scopus 로고
    • Fragile sites in human chromosomes as regions of late-replicating DNA
    • Laird C., Jaffe E., Karpen G., Lamb M., and Nelson R. Fragile sites in human chromosomes as regions of late-replicating DNA. Trends Genet. 3 (1987) 274-281
    • (1987) Trends Genet. , vol.3 , pp. 274-281
    • Laird, C.1    Jaffe, E.2    Karpen, G.3    Lamb, M.4    Nelson, R.5
  • 86
    • 3242887806 scopus 로고    scopus 로고
    • The interplay of Fanconi anemia proteins in the DNA damage response
    • Wang X., and D'Andrea A.D. The interplay of Fanconi anemia proteins in the DNA damage response. DNA Repair (Amst.) 3 (2004) 1063-1069
    • (2004) DNA Repair (Amst.) , vol.3 , pp. 1063-1069
    • Wang, X.1    D'Andrea, A.D.2
  • 87
    • 25144492769 scopus 로고    scopus 로고
    • Unraveling the Fanconi anemia-DNA repair connection
    • Thompson L.H. Unraveling the Fanconi anemia-DNA repair connection. Nat. Genet. 37 (2005) 921-922
    • (2005) Nat. Genet. , vol.37 , pp. 921-922
    • Thompson, L.H.1
  • 89
    • 0037076672 scopus 로고    scopus 로고
    • Autoubiquitination of the BRCA1*BARD1 RING ubiquitin ligase
    • Chen A., Kleiman F.E., Manley J.L., Ouchi T., and Pan Z.Q. Autoubiquitination of the BRCA1*BARD1 RING ubiquitin ligase. J. Biol. Chem. 277 (2002) 22085-22092
    • (2002) J. Biol. Chem. , vol.277 , pp. 22085-22092
    • Chen, A.1    Kleiman, F.E.2    Manley, J.L.3    Ouchi, T.4    Pan, Z.Q.5
  • 90
    • 0345276495 scopus 로고    scopus 로고
    • Regulation of BRCC, a holoenzyme complex containing BRCA1 and BRCA2, by a signalosome-like subunit and its role in DNA repair
    • Dong Y., Hakimi M.A., Chen X., Kumaraswamy E., Cooch N.S., Godwin A.K., and Shiekhattar R. Regulation of BRCC, a holoenzyme complex containing BRCA1 and BRCA2, by a signalosome-like subunit and its role in DNA repair. Mol. Cell 12 (2003) 1087-1099
    • (2003) Mol. Cell , vol.12 , pp. 1087-1099
    • Dong, Y.1    Hakimi, M.A.2    Chen, X.3    Kumaraswamy, E.4    Cooch, N.S.5    Godwin, A.K.6    Shiekhattar, R.7
  • 93
    • 25444455576 scopus 로고    scopus 로고
    • Centrosomal microtubule nucleation activity is inhibited by BRCA1-dependent ubiquitination
    • Sankaran S., Starita L.M., Groen A.C., Ko M.J., and Parvin J.D. Centrosomal microtubule nucleation activity is inhibited by BRCA1-dependent ubiquitination. Mol. Cell Biol. 25 (2005) 8656-8668
    • (2005) Mol. Cell Biol. , vol.25 , pp. 8656-8668
    • Sankaran, S.1    Starita, L.M.2    Groen, A.C.3    Ko, M.J.4    Parvin, J.D.5
  • 95
    • 27944459176 scopus 로고    scopus 로고
    • Cellular localization of human Rad51C and regulation of ubiquitin-mediated proteolysis of Rad51
    • Bennett B.T., and Knight K.L. Cellular localization of human Rad51C and regulation of ubiquitin-mediated proteolysis of Rad51. J. Cell Biochem. 96 (2005) 1095-1109
    • (2005) J. Cell Biochem. , vol.96 , pp. 1095-1109
    • Bennett, B.T.1    Knight, K.L.2
  • 96
    • 0034159893 scopus 로고    scopus 로고
    • Regulation of double-strand break-induced mammalian homologous recombination by UBL1, a RAD51-interacting protein
    • Li W., Hesabi B., Babbo A., Pacione C., Liu J., Chen D.J., Nickoloff J.A., and Shen Z. Regulation of double-strand break-induced mammalian homologous recombination by UBL1, a RAD51-interacting protein. Nucleic Acids Res. 28 (2000) 1145-1153
    • (2000) Nucleic Acids Res. , vol.28 , pp. 1145-1153
    • Li, W.1    Hesabi, B.2    Babbo, A.3    Pacione, C.4    Liu, J.5    Chen, D.J.6    Nickoloff, J.A.7    Shen, Z.8
  • 97
    • 0037068455 scopus 로고    scopus 로고
    • RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO
    • Hoege C., Pfander B., Moldovan G.L., Pyrowolakis G., and Jentsch S. RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO. Nature 419 (2002) 135-141
    • (2002) Nature , vol.419 , pp. 135-141
    • Hoege, C.1    Pfander, B.2    Moldovan, G.L.3    Pyrowolakis, G.4    Jentsch, S.5
  • 98
    • 22944474665 scopus 로고    scopus 로고
    • SUMO-modified PCNA recruits Srs2 to prevent recombination during S phase
    • Pfander B., Moldovan G.L., Sacher M., Hoege C., and Jentsch S. SUMO-modified PCNA recruits Srs2 to prevent recombination during S phase. Nature 436 (2005) 428-433
    • (2005) Nature , vol.436 , pp. 428-433
    • Pfander, B.1    Moldovan, G.L.2    Sacher, M.3    Hoege, C.4    Jentsch, S.5
  • 99
    • 19544366597 scopus 로고    scopus 로고
    • RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway
    • Yin J., Kwon Y.T., Varshavsky A., and Wang W. RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway. Hum. Mol. Genet. 13 (2004) 2421-2430
    • (2004) Hum. Mol. Genet. , vol.13 , pp. 2421-2430
    • Yin, J.1    Kwon, Y.T.2    Varshavsky, A.3    Wang, W.4
  • 101
    • 0034737004 scopus 로고    scopus 로고
    • Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome
    • Lindor N.M., Furuichi Y., Kitao S., Shimamoto A., Arndt C., and Jalal S. Rothmund-Thomson syndrome due to RECQ4 helicase mutations: report and clinical and molecular comparisons with Bloom syndrome and Werner syndrome. Am. J. Med. Genet. 90 (2000) 223-228
    • (2000) Am. J. Med. Genet. , vol.90 , pp. 223-228
    • Lindor, N.M.1    Furuichi, Y.2    Kitao, S.3    Shimamoto, A.4    Arndt, C.5    Jalal, S.6
  • 103
    • 0141567744 scopus 로고    scopus 로고
    • RecQ helicases: suppressors of tumorigenesis and premature aging
    • Bachrati C.Z., and Hickson I.D. RecQ helicases: suppressors of tumorigenesis and premature aging. Biochem. J. 374 (2003) 577-606
    • (2003) Biochem. J. , vol.374 , pp. 577-606
    • Bachrati, C.Z.1    Hickson, I.D.2
  • 104
    • 0033820714 scopus 로고    scopus 로고
    • Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome
    • Grant S.G., Wenger S.L., Latimer J.J., Thull D., and Burke L.W. Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome. Clin. Genet. 58 (2000) 209-215
    • (2000) Clin. Genet. , vol.58 , pp. 209-215
    • Grant, S.G.1    Wenger, S.L.2    Latimer, J.J.3    Thull, D.4    Burke, L.W.5
  • 105
    • 4344685225 scopus 로고    scopus 로고
    • Separase-mediated cleavage of cohesin at interphase is required for DNA repair
    • Nagao K., Adachi Y., and Yanagida M. Separase-mediated cleavage of cohesin at interphase is required for DNA repair. Nature 430 (2004) 1044-1048
    • (2004) Nature , vol.430 , pp. 1044-1048
    • Nagao, K.1    Adachi, Y.2    Yanagida, M.3
  • 106
    • 0035912183 scopus 로고    scopus 로고
    • Degradation of a cohesin subunit by the N-end rule pathway is essential for chromosome stability
    • Rao H., Uhlmann F., Nasmyth K., and Varshavsky A. Degradation of a cohesin subunit by the N-end rule pathway is essential for chromosome stability. Nature 410 (2001) 955-959
    • (2001) Nature , vol.410 , pp. 955-959
    • Rao, H.1    Uhlmann, F.2    Nasmyth, K.3    Varshavsky, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.