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Volumn 124, Issue 8-9, 2003, Pages 921-930

The N-terminal domain of the large subunit of human replication protein A binds to Werner syndrome protein and stimulates helicase activity

Author keywords

DNA helicase; Genetic instability; Premature aging; Replication protein A; Werner syndrome

Indexed keywords

HELICASE; REPLICATION PROTEIN A;

EID: 0141853230     PISSN: 00476374     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0047-6374(03)00164-7     Document Type: Article
Times cited : (54)

References (66)
  • 1
    • 0032832195 scopus 로고    scopus 로고
    • Physical and functional interaction between p53 and the Werner's syndrome protein
    • Blander G., Kipnis J., Leal J.F., Yu C.E., Schellenberg G.D., Oren M. Physical and functional interaction between p53 and the Werner's syndrome protein. J. Biol. Chem. 274:1999;29 463-29 469.
    • (1999) J. Biol. Chem. , vol.274 , pp. 29463-29469
    • Blander, G.1    Kipnis, J.2    Leal, J.F.3    Yu, C.E.4    Schellenberg, G.D.5    Oren, M.6
  • 2
    • 0031030449 scopus 로고    scopus 로고
    • Structure of the single-stranded-DNA-binding domain of replication protein A bound to DNA
    • Bochkarev A., Pfuetzner R.A., Edwards A.M., Frappier L. Structure of the single-stranded-DNA-binding domain of replication protein A bound to DNA. Nature. 385:1997;176-181.
    • (1997) Nature , vol.385 , pp. 176-181
    • Bochkarev, A.1    Pfuetzner, R.A.2    Edwards, A.M.3    Frappier, L.4
  • 3
    • 0032579254 scopus 로고    scopus 로고
    • The herpes simplex virus type-1 single-strand DNA-binding protein, ICP8, increases the processivity of the UL9 protein DNA helicase
    • Boehmer P.E. The herpes simplex virus type-1 single-strand DNA-binding protein, ICP8, increases the processivity of the UL9 protein DNA helicase. J. Biol. Chem. 273:1998;2676-2683.
    • (1998) J. Biol. Chem. , vol.273 , pp. 2676-2683
    • Boehmer, P.E.1
  • 4
    • 0030848209 scopus 로고    scopus 로고
    • Role of protein-protein interactions in the function of replication protein A (RPA): RPA modulates the activity of DNA polymerase alpha by multiple mechanisms
    • Braun K.A., Lao Y., He Z., Ingles C.J., Wold M.S. Role of protein-protein interactions in the function of replication protein A (RPA): RPA modulates the activity of DNA polymerase alpha by multiple mechanisms. Biochemistry. 36:1997;8443-8454.
    • (1997) Biochemistry , vol.36 , pp. 8443-8454
    • Braun, K.A.1    Lao, Y.2    He, Z.3    Ingles, C.J.4    Wold, M.S.5
  • 5
    • 0036161562 scopus 로고    scopus 로고
    • Roles of the Werner syndrome protein in pathways required for maintenance of genome stability
    • Brosh R.M. Jr., Bohr V.A. Roles of the Werner syndrome protein in pathways required for maintenance of genome stability. Exp. Gerontol. 37:2002;491-506.
    • (2002) Exp. Gerontol. , vol.37 , pp. 491-506
    • Brosh R.M., Jr.1    Bohr, V.A.2
  • 8
    • 0032109778 scopus 로고    scopus 로고
    • Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair
    • Chen C., Umezu K., Kolodner R.D. Chromosomal rearrangements occur in S. cerevisiae rfa1 mutator mutants due to mutagenic lesions processed by double-strand-break repair. Mol. Cell. 2:1998;9-22.
    • (1998) Mol. Cell , vol.2 , pp. 9-22
    • Chen, C.1    Umezu, K.2    Kolodner, R.D.3
  • 9
    • 0025613567 scopus 로고
    • Homologous recombination is elevated in some Werner-like syndromes but not during normal in vitro or in vivo senescence of mammalian cells
    • Cheng R.Z., Murano S., Kurz B., Shmookler-Reis R.J. Homologous recombination is elevated in some Werner-like syndromes but not during normal in vitro or in vivo senescence of mammalian cells. Mutat. Res. 237:1990;259-269.
    • (1990) Mutat. Res. , vol.237 , pp. 259-269
    • Cheng, R.Z.1    Murano, S.2    Kurz, B.3    Shmookler-Reis, R.J.4
  • 10
    • 0034231844 scopus 로고    scopus 로고
    • Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest
    • Constantinou A., Tarsounas M., Karow J.K., Brosh R.M., Bohr V.A., Hickson I.D., West S.C. Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest. EMBO Rep. 1:2000;80-84.
    • (2000) EMBO Rep. , vol.1 , pp. 80-84
    • Constantinou, A.1    Tarsounas, M.2    Karow, J.K.3    Brosh, R.M.4    Bohr, V.A.5    Hickson, I.D.6    West, S.C.7
  • 12
    • 0032740855 scopus 로고    scopus 로고
    • RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli
    • Courcelle J., Hanawalt P.C. RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli. Mol. Gen. Genet. 262:1999;543-551.
    • (1999) Mol. Gen. Genet. , vol.262 , pp. 543-551
    • Courcelle, J.1    Hanawalt, P.C.2
  • 13
    • 0026583949 scopus 로고
    • Interaction of DNA polymerase alpha-primase with cellular replication protein A and SV40 T antigen
    • Dornreiter I., Erdile L.F., Gilbert I.U., von Winkler D., Kelly T.J., Fanning E. Interaction of DNA polymerase alpha-primase with cellular replication protein A and SV40 T antigen. EMBO J. 11:1992;769-776.
    • (1992) EMBO J. , vol.11 , pp. 769-776
    • Dornreiter, I.1    Erdile, L.F.2    Gilbert, I.U.3    Von Winkler, D.4    Kelly, T.J.5    Fanning, E.6
  • 15
    • 0024465870 scopus 로고
    • Mutator phenotype of Werner syndrome is characterized by extensive deletions
    • Fukuchi K., Martin G.M., Monnat R.J. Jr. Mutator phenotype of Werner syndrome is characterized by extensive deletions. Proc. Natl. Acad. Sci. USA. 86:1989;5893-5897.
    • (1989) Proc. Natl. Acad. Sci. USA , vol.86 , pp. 5893-5897
    • Fukuchi, K.1    Martin, G.M.2    Monnat R.J., Jr.3
  • 16
    • 0028033989 scopus 로고
    • The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: A potential eukaryotic reverse gyrase
    • Gangloff S., McDonald J.P., Bendixen C., Arthur L., Rothstein R. The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase. Mol. Cell Biol. 14:1994;8391-8398.
    • (1994) Mol. Cell Biol. , vol.14 , pp. 8391-8398
    • Gangloff, S.1    McDonald, J.P.2    Bendixen, C.3    Arthur, L.4    Rothstein, R.5
  • 17
    • 0032527973 scopus 로고    scopus 로고
    • Rad52 associates with RPA and functions with rad55 and rad57 to assemble meiotic recombination complexes
    • Gasior S.L., Wong A.K., Kora Y., Shinohara A., Bishop D.K. Rad52 associates with RPA and functions with rad55 and rad57 to assemble meiotic recombination complexes. Genes Dev. 12:1998;2208-2221.
    • (1998) Genes Dev. , vol.12 , pp. 2208-2221
    • Gasior, S.L.1    Wong, A.K.2    Kora, Y.3    Shinohara, A.4    Bishop, D.K.5
  • 18
    • 0029798240 scopus 로고    scopus 로고
    • Functional domains of the 70-kDa subunit of human replication protein A
    • Gomes X.V., Wold M.S. Functional domains of the 70-kDa subunit of human replication protein A. Biochemistry. 35:1996;10 558-10 568.
    • (1996) Biochemistry , vol.35 , pp. 10558-10568
    • Gomes, X.V.1    Wold, M.S.2
  • 20
    • 0026502062 scopus 로고
    • Genetic linkage of Werner's syndrome to five markers on chromosome 8
    • Goto M., Rubenstein M., Weber J., Woods K., Drayne D. Genetic linkage of Werner's syndrome to five markers on chromosome 8. Nature. 355:1992;735-758.
    • (1992) Nature , vol.355 , pp. 735-758
    • Goto, M.1    Rubenstein, M.2    Weber, J.3    Woods, K.4    Drayne, D.5
  • 23
    • 0032522789 scopus 로고    scopus 로고
    • RecQ helicase, in concert with RecA and SSB proteins, initiates and disrupts DNA recombination
    • Harmon F.G., Kowalczykowski S.C. RecQ helicase, in concert with RecA and SSB proteins, initiates and disrupts DNA recombination. Genes Dev. 12:1998;1134-1144.
    • (1998) Genes Dev. , vol.12 , pp. 1134-1144
    • Harmon, F.G.1    Kowalczykowski, S.C.2
  • 24
    • 0027299244 scopus 로고
    • The transactivator proteins VP16 and GAL4 bind replication factor A
    • He Z., Brinton B.T., Greenblatt J., Hassell J.A., Ingles C.J. The transactivator proteins VP16 and GAL4 bind replication factor A. Cell. 73:1993;1223-1232.
    • (1993) Cell , vol.73 , pp. 1223-1232
    • He, Z.1    Brinton, B.T.2    Greenblatt, J.3    Hassell, J.A.4    Ingles, C.J.5
  • 25
    • 0028929611 scopus 로고
    • RPA involvement in the damage-recognition and incision steps of nucleotide excision repair
    • He Z., Henricksen L.A., Wold M.S., Ingles C.J. RPA involvement in the damage-recognition and incision steps of nucleotide excision repair. Nature. 374:1995;566-569.
    • (1995) Nature , vol.374 , pp. 566-569
    • He, Z.1    Henricksen, L.A.2    Wold, M.S.3    Ingles, C.J.4
  • 26
    • 0031686571 scopus 로고    scopus 로고
    • The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease [letter]
    • Huang S., Li B., Gray M.D., Oshima J., Mian I.S., Campisi J. The premature ageing syndrome protein, WRN, is a 3′→5′ exonuclease [letter]. Nat. Genet. 20:1998;114-116.
    • (1998) Nat. Genet. , vol.20 , pp. 114-116
    • Huang, S.1    Li, B.2    Gray, M.D.3    Oshima, J.4    Mian, I.S.5    Campisi, J.6
  • 29
    • 0027939024 scopus 로고
    • Interactions of human replication protein A with oligonucleotides
    • Kim C., Paulus B.F., Wold M.S. Interactions of human replication protein A with oligonucleotides. Biochemistry. 33:1994;14 197-14 206.
    • (1994) Biochemistry , vol.33 , pp. 14197-14206
    • Kim, C.1    Paulus, B.F.2    Wold, M.S.3
  • 30
    • 0032535661 scopus 로고    scopus 로고
    • Cloning of two new human helicase genes of the RecQ family: Biological significance of multiple species in higher eukaryotes
    • Kitao S., Ohsugi I., Ichikawa K., Goto M., Furuichi Y., Shimamoto A. Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes. Genomics. 54:1998;443-452.
    • (1998) Genomics , vol.54 , pp. 443-452
    • Kitao, S.1    Ohsugi, I.2    Ichikawa, K.3    Goto, M.4    Furuichi, Y.5    Shimamoto, A.6
  • 33
    • 0034953044 scopus 로고    scopus 로고
    • Werner syndrome: Genetic and molecular basis of a premature aging disorder
    • Lebel M. Werner syndrome: genetic and molecular basis of a premature aging disorder. Cell Mol. Life Sci. 58:2001;857-867.
    • (2001) Cell Mol. Life Sci. , vol.58 , pp. 857-867
    • Lebel, M.1
  • 34
    • 0033621354 scopus 로고    scopus 로고
    • The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I
    • Lebel M., Spillare E.A., Harris C.C., Leder P. The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I. J. Biol. Chem. 274:1999;37 795-37 799.
    • (1999) J. Biol. Chem. , vol.274 , pp. 37795-37799
    • Lebel, M.1    Spillare, E.A.2    Harris, C.C.3    Leder, P.4
  • 35
    • 0027195936 scopus 로고
    • The acidic transcriptional activation domains of VP16 and p53 bind the cellular replication protein A and stimulate in vitro BPV-1 DNA replication
    • Li R., Botchan M.R. The acidic transcriptional activation domains of VP16 and p53 bind the cellular replication protein A and stimulate in vitro BPV-1 DNA replication. Cell. 73:1993;1207-1221.
    • (1993) Cell , vol.73 , pp. 1207-1221
    • Li, R.1    Botchan, M.R.2
  • 37
    • 0031204917 scopus 로고    scopus 로고
    • Impaired nuclear localization of defective DNA helicases in Werner's syndrome
    • Matsumoto T., Shimamoto A., Goto M., Furuichi Y. Impaired nuclear localization of defective DNA helicases in Werner's syndrome. Nat. Genet. 16:1997;335-336.
    • (1997) Nat. Genet. , vol.16 , pp. 335-336
    • Matsumoto, T.1    Shimamoto, A.2    Goto, M.3    Furuichi, Y.4
  • 38
    • 0031574363 scopus 로고    scopus 로고
    • The proofreading domain of Escherichia coli DNA polymerase I and other DNA and/or RNA exonuclease domains
    • Moser M.J., Holley W.R., Chatterjee A., Mian I.S. The proofreading domain of Escherichia coli DNA polymerase I and other DNA and/or RNA exonuclease domains. Nucleic Acids Res. 25:1997;5110-5118.
    • (1997) Nucleic Acids Res. , vol.25 , pp. 5110-5118
    • Moser, M.J.1    Holley, W.R.2    Chatterjee, A.3    Mian, I.S.4
  • 39
    • 0030699088 scopus 로고    scopus 로고
    • Role of Schizosaccharomyces pombe RecQ homolog, recombination, and checkpoint genes in UV damage tolerance
    • Murray J.M., Lindsay H.D., Munday C.A., Carr A.M. Role of Schizosaccharomyces pombe RecQ homolog, recombination, and checkpoint genes in UV damage tolerance. Mol. Cell Biol. 17:1997;6868-6875.
    • (1997) Mol. Cell Biol. , vol.17 , pp. 6868-6875
    • Murray, J.M.1    Lindsay, H.D.2    Munday, C.A.3    Carr, A.M.4
  • 40
    • 0030915681 scopus 로고    scopus 로고
    • Positionally cloned human disease genes: Patterns of evolutionary conservation and functional motifs
    • Mushegian A.R., Bassett D.E. Jr., Boguski M.S., Bork P., Koonin E.V. Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs. Proc. Natl. Acad. Sci. USA. 94:1997;5831-5836.
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , pp. 5831-5836
    • Mushegian, A.R.1    Bassett D.E., Jr.2    Boguski, M.S.3    Bork, P.4    Koonin, E.V.5
  • 41
    • 0021185614 scopus 로고
    • Isolation and genetic characterization of a thymineless death-resistant mutant of Escherichia coli K12: Identification of a new mutation (recQ1) that blocks the recF recombination pathway
    • Nakayama H., Nakayama K., Nakayama R., Irino N., Nakayama Y., Hanawalt P.C. Isolation and genetic characterization of a thymineless death-resistant mutant of Escherichia coli K12: identification of a new mutation (recQ1) that blocks the recF recombination pathway. Mol. Gen. Genet. 195:1984;474-480.
    • (1984) Mol. Gen. Genet. , vol.195 , pp. 474-480
    • Nakayama, H.1    Nakayama, K.2    Nakayama, R.3    Irino, N.4    Nakayama, Y.5    Hanawalt, P.C.6
  • 42
    • 0032556870 scopus 로고    scopus 로고
    • Rad52 protein stimulates DNA strand exchange by Rad51 and replication protein A
    • New J.H., Sugiyama T., Zaitseva E., Kowalczykowski S.C. Rad52 protein stimulates DNA strand exchange by Rad51 and replication protein A. Nature. 391:1998;407-410.
    • (1998) Nature , vol.391 , pp. 407-410
    • New, J.H.1    Sugiyama, T.2    Zaitseva, E.3    Kowalczykowski, S.C.4
  • 43
    • 0037175018 scopus 로고    scopus 로고
    • Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases
    • Opresko P.L., von Kobbe C., Laine J.-P., Harrigan J., Hickson I.D., Bohr V.A. Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases. J. Biol. Chem. 277:2002;41 110-41 119.
    • (2002) J. Biol. Chem. , vol.277 , pp. 41110-41119
    • Opresko, P.L.1    Von Kobbe, C.2    Laine, J.-P.3    Harrigan, J.4    Hickson, I.D.5    Bohr, V.A.6
  • 45
    • 0035871341 scopus 로고    scopus 로고
    • Loss of Werner syndrome protein function promotes aberrant mitotic recombination
    • Prince P.R., Emond M.J., Monnat R.J. Jr. Loss of Werner syndrome protein function promotes aberrant mitotic recombination. Genes Dev. 15:2001;933-938.
    • (2001) Genes Dev. , vol.15 , pp. 933-938
    • Prince, P.R.1    Emond, M.J.2    Monnat R.J., Jr.3
  • 46
    • 0027942415 scopus 로고
    • Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ
    • Puranam K.L., Blackshear P.J. Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ. J. Biol. Chem. 269:1994;29 838-29 845.
    • (1994) J. Biol. Chem. , vol.269 , pp. 29838-29845
    • Puranam, K.L.1    Blackshear, P.J.2
  • 47
    • 0035009356 scopus 로고    scopus 로고
    • Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51
    • Sakamoto S., Nishikawa K., Heo S.-J., Goto M., Furuichi Y., Shimamoto A. Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51. Genes Cells. 6:2001;421-430.
    • (2001) Genes Cells , vol.6 , pp. 421-430
    • Sakamoto, S.1    Nishikawa, K.2    Heo, S.-J.3    Goto, M.4    Furuichi, Y.5    Shimamoto, A.6
  • 48
    • 0019440557 scopus 로고
    • Cytogenetics of Werner's syndrome cultured skin fibroblasts: Variegated translocation mosaicism
    • Salk D., Au K., Hoehn H., Martin G.M. Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism. Cytogenet. Cell Genet. 30:1981;92-107.
    • (1981) Cytogenet. Cell Genet. , vol.30 , pp. 92-107
    • Salk, D.1    Au, K.2    Hoehn, H.3    Martin, G.M.4
  • 50
    • 0028061993 scopus 로고
    • Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli RecQ helicase and localization of the gene at chromosome 12p12
    • Seki M., Miyazawa H., Tada S., Yanagisawa J., Yamaoka T., Hoshino S., Ozawa K., Eki T., Nogami M., Okumura K. Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli RecQ helicase and localization of the gene at chromosome 12p12. Nucleic Acids Res. 22:1994;4566-4573.
    • (1994) Nucleic Acids Res. , vol.22 , pp. 4566-4573
    • Seki, M.1    Miyazawa, H.2    Tada, S.3    Yanagisawa, J.4    Yamaoka, T.5    Hoshino, S.6    Ozawa, K.7    Eki, T.8    Nogami, M.9    Okumura, K.10
  • 51
    • 0032545515 scopus 로고    scopus 로고
    • Werner syndrome protein I. DNA helicase and DNA exonuclease reside on the same polypeptide
    • Shen J.-C., Gray M.D., Oshima J., Kamath-Loeb A.S., Fry M., Loeb L.A. Werner syndrome protein I. DNA helicase and DNA exonuclease reside on the same polypeptide. J. Biol. Chem. 273:1998;34 139-34 144.
    • (1998) J. Biol. Chem. , vol.273 , pp. 31439-34144
    • Shen, J.-C.1    Gray, M.D.2    Oshima, J.3    Kamath-Loeb, A.S.4    Fry, M.5    Loeb, L.A.6
  • 52
    • 0032526583 scopus 로고    scopus 로고
    • Characterization of Werner syndrome protein DNA helicase activity: Directionality, substrate dependence, and stimulation by replication protein A
    • Shen J.-C., Gray M.D., Oshima J., Loeb L.A. Characterization of Werner syndrome protein DNA helicase activity: directionality, substrate dependence, and stimulation by replication protein A. Nucleic Acids Res. 26:1998;2879-2885.
    • (1998) Nucleic Acids Res. , vol.26 , pp. 2879-2885
    • Shen, J.-C.1    Gray, M.D.2    Oshima, J.3    Loeb, L.A.4
  • 53
    • 0034192020 scopus 로고    scopus 로고
    • The Werner syndrome gene. The molecular basis of RecQ helicase-deficiency diseases
    • Shen J.-C., Loeb L.A. The Werner syndrome gene. The molecular basis of RecQ helicase-deficiency diseases. Trends Genet. 16:2000;213-220.
    • (2000) Trends Genet. , vol.16 , pp. 213-220
    • Shen, J.-C.1    Loeb, L.A.2
  • 54
    • 0032497368 scopus 로고    scopus 로고
    • The 32- and 14-kilodalton subunits of replication protein A are responsible for species-specific interactions with single-stranded DNA
    • Sibenaller Z.A., Sorensen B.R., Wold M.S. The 32- and 14-kilodalton subunits of replication protein A are responsible for species-specific interactions with single-stranded DNA. Biochemistry. 37:1998;12 496-12 506.
    • (1998) Biochemistry , vol.37 , pp. 12496-12506
    • Sibenaller, Z.A.1    Sorensen, B.R.2    Wold, M.S.3
  • 56
    • 0030994386 scopus 로고    scopus 로고
    • Rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest
    • Stewart E., Chapman C.R., Al-Khodairy F., Carr A.M., Enoch T. rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest. EMBO J. 16:1997;2682-2692.
    • (1997) EMBO J. , vol.16 , pp. 2682-2692
    • Stewart, E.1    Chapman, C.R.2    Al-Khodairy, F.3    Carr, A.M.4    Enoch, T.5
  • 58
    • 0027158626 scopus 로고
    • RecQ DNA helicase of Escherichia coli
    • Umezu K., Nakayama H. RecQ DNA helicase of Escherichia coli. J. Mol. Biol. 230:1993;1145-1150.
    • (1993) J. Mol. Biol. , vol.230 , pp. 1145-1150
    • Umezu, K.1    Nakayama, H.2
  • 60
    • 0033616816 scopus 로고    scopus 로고
    • Replication protein A interactions with DNA 1. Functions of the DNA-binding and zinc-finger domains of the 70-kDa subunit
    • Walther A.P., Gomes X.V., Lao Y., Lee C.G., Wold M.S. Replication protein A interactions with DNA 1. Functions of the DNA-binding and zinc-finger domains of the 70-kDa subunit. Biochemistry. 38:1999;3963-3973.
    • (1999) Biochemistry , vol.38 , pp. 3963-3973
    • Walther, A.P.1    Gomes, X.V.2    Lao, Y.3    Lee, C.G.4    Wold, M.S.5
  • 61
    • 0029657781 scopus 로고    scopus 로고
    • SGS1, a homologue of the Bloom's and Wernr's syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae
    • Watt P.M., Hickson I.D., Borts R.H., Louis E.J. SGS1, a homologue of the Bloom's and Wernr's syndrome genes, is required for maintenance of genome stability in Saccharomyces cerevisiae. Genetics. 144:1996;935-945.
    • (1996) Genetics , vol.144 , pp. 935-945
    • Watt, P.M.1    Hickson, I.D.2    Borts, R.H.3    Louis, E.J.4
  • 62
    • 0029002965 scopus 로고
    • Sgs1: A eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation
    • Watt P.M., Louis E.J., Borts R.H., Hickson I.D. Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation. Cell. 81:1995;253-260.
    • (1995) Cell , vol.81 , pp. 253-260
    • Watt, P.M.1    Louis, E.J.2    Borts, R.H.3    Hickson, I.D.4
  • 63
    • 0030908093 scopus 로고    scopus 로고
    • Replication protein A: A heterotrimeric single-stranded DNA-binding protein required for eukaryotic DNA metabolism
    • Wold M.S. Replication protein A: a heterotrimeric single-stranded DNA-binding protein required for eukaryotic DNA metabolism. Annu. Rev. Biochem. 66:1997;61-92.
    • (1997) Annu. Rev. Biochem. , vol.66 , pp. 61-92
    • Wold, M.S.1
  • 64
    • 0032555220 scopus 로고    scopus 로고
    • Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: Implication for genomic instability in human diseases
    • Yamagata K., Kato J., Shimamoto A., Goto M., Furuichi Y., Ikeda H. Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases. Proc. Natl. Acad. Sci. USA. 95:1998;8733-8738.
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 8733-8738
    • Yamagata, K.1    Kato, J.2    Shimamoto, A.3    Goto, M.4    Furuichi, Y.5    Ikeda, H.6
  • 65
    • 0031848284 scopus 로고    scopus 로고
    • Replication focus-forming activity 1 and the Werner syndrome gene product [see comments]
    • Yan H., Chen C.Y., Kobayashi R., Newport J. Replication focus-forming activity 1 and the Werner syndrome gene product [see comments]. Nat. Genet. 19:1998;375-378.
    • (1998) Nat. Genet. , vol.19 , pp. 375-378
    • Yan, H.1    Chen, C.Y.2    Kobayashi, R.3    Newport, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.