메뉴 건너뛰기




Volumn 7, Issue 8, 2008, Pages 1319-1329

Characterization of CHO XPF mutant UV41: Influence of XPF heterozygosity on double-strand break-induced intrachromosomal recombination

Author keywords

Genomic instability; Recombinational repair; UV41; XPF

Indexed keywords

ENDONUCLEASE;

EID: 46649101493     PISSN: 15687864     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.dnarep.2008.04.012     Document Type: Article
Times cited : (7)

References (36)
  • 1
    • 0031023182 scopus 로고    scopus 로고
    • Reconstitution of human excision nuclease with recombinant XPF-ERCC1 complex
    • Bessho T., Sancar A., Thompson L.H., and Thelen M.P. Reconstitution of human excision nuclease with recombinant XPF-ERCC1 complex. J. Biol. Chem. 272 (1997) 3833-3837
    • (1997) J. Biol. Chem. , vol.272 , pp. 3833-3837
    • Bessho, T.1    Sancar, A.2    Thompson, L.H.3    Thelen, M.P.4
  • 2
    • 0034675930 scopus 로고    scopus 로고
    • Role of ERCC1 in removal of long non-homologous tails during targeted homologous recombination
    • Adair G.M., Rolig R.L., Moore-Faver D., Zabelshansky M., Wilson J.H., and Nairn R.S. Role of ERCC1 in removal of long non-homologous tails during targeted homologous recombination. EMBO J. 19 (2000) 5552-5561
    • (2000) EMBO J. , vol.19 , pp. 5552-5561
    • Adair, G.M.1    Rolig, R.L.2    Moore-Faver, D.3    Zabelshansky, M.4    Wilson, J.H.5    Nairn, R.S.6
  • 4
    • 12644303223 scopus 로고    scopus 로고
    • Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1
    • Sargent R.G., Rolig R.L., Kilburn A.E., Adair G.M., Wilson J.H., and Nairn R.S. Recombination-dependent deletion formation in mammalian cells deficient in the nucleotide excision repair gene ERCC1. Proc. Natl. Acad. Sci. U.S.A. 94 (1997) 13122-13127
    • (1997) Proc. Natl. Acad. Sci. U.S.A. , vol.94 , pp. 13122-13127
    • Sargent, R.G.1    Rolig, R.L.2    Kilburn, A.E.3    Adair, G.M.4    Wilson, J.H.5    Nairn, R.S.6
  • 6
    • 0347416975 scopus 로고    scopus 로고
    • ERCC1/XPF removes the 3′ overhang from uncapped telomeres and represses formation of telomeric DNA-containing double minute chromosomes
    • Zhu X.D., Niedernhofer L., Kuster B., Mann M., Hoeijmakers J.H., and de Lange T. ERCC1/XPF removes the 3′ overhang from uncapped telomeres and represses formation of telomeric DNA-containing double minute chromosomes. Mol. Cell 12 (2003) 1489-1498
    • (2003) Mol. Cell , vol.12 , pp. 1489-1498
    • Zhu, X.D.1    Niedernhofer, L.2    Kuster, B.3    Mann, M.4    Hoeijmakers, J.H.5    de Lange, T.6
  • 7
    • 33846210498 scopus 로고    scopus 로고
    • XPF with mutations in its conserved nuclease domain is defective in DNA repair but functions in TRF2-mediated telomere shortening
    • Wu Y., Zacal N.J., Rainbow A.J., and Zhu X.D. XPF with mutations in its conserved nuclease domain is defective in DNA repair but functions in TRF2-mediated telomere shortening. DNA Repair 6 (2007) 157-166
    • (2007) DNA Repair , vol.6 , pp. 157-166
    • Wu, Y.1    Zacal, N.J.2    Rainbow, A.J.3    Zhu, X.D.4
  • 12
    • 0024415769 scopus 로고
    • Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening
    • Busch D., Greiner C., Lewis K., Ford R., Adair G., and Thompson L. Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screening. Mutagenesis 4 (1989) 349-354
    • (1989) Mutagenesis , vol.4 , pp. 349-354
    • Busch, D.1    Greiner, C.2    Lewis, K.3    Ford, R.4    Adair, G.5    Thompson, L.6
  • 13
    • 0027473181 scopus 로고
    • Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics
    • Collins A.R. Mutant rodent cell lines sensitive to ultraviolet light, ionizing radiation and cross-linking agents: a comprehensive survey of genetic and biochemical characteristics. Mutat. Res. 293 (1993) 99-118
    • (1993) Mutat. Res. , vol.293 , pp. 99-118
    • Collins, A.R.1
  • 15
    • 0024763821 scopus 로고
    • Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19
    • Thompson L.H., Bachinski L.L., Stallings R.L., Dolf G., Weber C.A., Westerveld A., and Siciliano M.J. Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19. Genomics 5 (1989) 670-679
    • (1989) Genomics , vol.5 , pp. 670-679
    • Thompson, L.H.1    Bachinski, L.L.2    Stallings, R.L.3    Dolf, G.4    Weber, C.A.5    Westerveld, A.6    Siciliano, M.J.7
  • 16
    • 0030758096 scopus 로고    scopus 로고
    • Survival, mutagenesis, and host cell reactivation in a Chinese hamster ovary cell ERCC1 knock-out mutant
    • Rolig R.L., Layher S.K., Santi B., Adair G.M., Gu F., Rainbow A.J., and Nairn R.S. Survival, mutagenesis, and host cell reactivation in a Chinese hamster ovary cell ERCC1 knock-out mutant. Mutagenesis 12 (1997) 277-283
    • (1997) Mutagenesis , vol.12 , pp. 277-283
    • Rolig, R.L.1    Layher, S.K.2    Santi, B.3    Adair, G.M.4    Gu, F.5    Rainbow, A.J.6    Nairn, R.S.7
  • 17
    • 0031822921 scopus 로고    scopus 로고
    • Characterization and analysis of Chinese hamster ovary cell ERCC1 mutant alleles
    • Rolig R.L., Lowery M.P., Adair G.M., and Nairn R.S. Characterization and analysis of Chinese hamster ovary cell ERCC1 mutant alleles. Mutagenesis 13 (1998) 357-365
    • (1998) Mutagenesis , vol.13 , pp. 357-365
    • Rolig, R.L.1    Lowery, M.P.2    Adair, G.M.3    Nairn, R.S.4
  • 18
    • 38349098477 scopus 로고    scopus 로고
    • The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells
    • Al-Minawi A.Z., Saleh-Gohari N., and Helleday T. The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells. Nucleic Acids Res. 36 (2008) 1-9
    • (2008) Nucleic Acids Res. , vol.36 , pp. 1-9
    • Al-Minawi, A.Z.1    Saleh-Gohari, N.2    Helleday, T.3
  • 19
    • 0037090816 scopus 로고    scopus 로고
    • The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif
    • Enzlin J.H., and Scharer O.D. The active site of the DNA repair endonuclease XPF-ERCC1 forms a highly conserved nuclease motif. EMBO J. 21 (2002) 2045-2053
    • (2002) EMBO J. , vol.21 , pp. 2045-2053
    • Enzlin, J.H.1    Scharer, O.D.2
  • 20
    • 34547810916 scopus 로고    scopus 로고
    • From broken to old: DNA damage, IGF1 endocrine suppression and aging
    • Monnat R.J. From broken to old: DNA damage, IGF1 endocrine suppression and aging. DNA Repair 6 (2007) 1386-1390
    • (2007) DNA Repair , vol.6 , pp. 1386-1390
    • Monnat, R.J.1
  • 21
    • 0029552525 scopus 로고
    • Efficient modification of the APRT gene by FLP/FRT site-specific targeting
    • Merrihew R.V., Sargent R.G., and Wilson J.H. Efficient modification of the APRT gene by FLP/FRT site-specific targeting. Somat. Cell Mol. Genet. 21 (1995) 299-307
    • (1995) Somat. Cell Mol. Genet. , vol.21 , pp. 299-307
    • Merrihew, R.V.1    Sargent, R.G.2    Wilson, J.H.3
  • 22
    • 0021195801 scopus 로고
    • Chromosomal rearrangements and gene expression in CHO cells: mapping of alleles for eight enzyme loci on CHO chromosomes Z3, Z4, Z5, and Z7
    • Adair G.M., Stallings R.L., and Siciliano M.J. Chromosomal rearrangements and gene expression in CHO cells: mapping of alleles for eight enzyme loci on CHO chromosomes Z3, Z4, Z5, and Z7. Somat. Cell Mol. Genet. 10 (1984) 283-295
    • (1984) Somat. Cell Mol. Genet. , vol.10 , pp. 283-295
    • Adair, G.M.1    Stallings, R.L.2    Siciliano, M.J.3
  • 24
    • 1542309071 scopus 로고    scopus 로고
    • Growth retardation, early death, and DNA repair defects in mice deficient for the nucleotide excision repair enzyme XPF
    • Tian M., Shinkura R., Shinkura N., and Alt F.W. Growth retardation, early death, and DNA repair defects in mice deficient for the nucleotide excision repair enzyme XPF. Mol. Cell. Biol. 24 (2004) 1200-1205
    • (2004) Mol. Cell. Biol. , vol.24 , pp. 1200-1205
    • Tian, M.1    Shinkura, R.2    Shinkura, N.3    Alt, F.W.4
  • 25
    • 0034621854 scopus 로고    scopus 로고
    • Frequent chromosomal translocations induced by DNA double-strand breaks
    • Richardson C., and Jasin M. Frequent chromosomal translocations induced by DNA double-strand breaks. Nature 405 (2000) 697-700
    • (2000) Nature , vol.405 , pp. 697-700
    • Richardson, C.1    Jasin, M.2
  • 26
    • 0034600975 scopus 로고    scopus 로고
    • Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells
    • Johnson R.D., and Jasin M. Sister chromatid gene conversion is a prominent double-strand break repair pathway in mammalian cells. EMBO J. 19 (2000) 3398-3407
    • (2000) EMBO J. , vol.19 , pp. 3398-3407
    • Johnson, R.D.1    Jasin, M.2
  • 27
    • 0035801472 scopus 로고    scopus 로고
    • Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences
    • Tutt A., Bertwistle D., Valentine J., Gabriel A., Swift S., Ross G., Griffin C., Thacker J., and Ashworth A. Mutation in Brca2 stimulates error-prone homology-directed repair of DNA double-strand breaks occurring between repeated sequences. EMBO J. 20 (2001) 4704-4716
    • (2001) EMBO J. , vol.20 , pp. 4704-4716
    • Tutt, A.1    Bertwistle, D.2    Valentine, J.3    Gabriel, A.4    Swift, S.5    Ross, G.6    Griffin, C.7    Thacker, J.8    Ashworth, A.9
  • 28
    • 0742323558 scopus 로고    scopus 로고
    • Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics
    • Maquat L.E. Nonsense-mediated mRNA decay: splicing, translation and mRNP dynamics. Nat. Rev. Mol. Cell. Biol. 5 (2004) 89-99
    • (2004) Nat. Rev. Mol. Cell. Biol. , vol.5 , pp. 89-99
    • Maquat, L.E.1
  • 29
    • 0025944309 scopus 로고
    • Direct-repeat analysis of chromatid interactions during intrachromosomal recombination in mouse cells
    • Bollag R.J., and Liskay R.M. Direct-repeat analysis of chromatid interactions during intrachromosomal recombination in mouse cells. Mol. Cell. Biol. 11 (1991) 4839-4845
    • (1991) Mol. Cell. Biol. , vol.11 , pp. 4839-4845
    • Bollag, R.J.1    Liskay, R.M.2
  • 30
    • 0024372735 scopus 로고
    • Yeast intrachromosomal recombination: long gene conversion tracts are preferentially associated with reciprocal exchange and require the RAD1 and RAD3 gene products
    • Aguilera A., and Klein H.L. Yeast intrachromosomal recombination: long gene conversion tracts are preferentially associated with reciprocal exchange and require the RAD1 and RAD3 gene products. Genetics 123 (1989) 683-694
    • (1989) Genetics , vol.123 , pp. 683-694
    • Aguilera, A.1    Klein, H.L.2
  • 31
    • 0035871341 scopus 로고    scopus 로고
    • Loss of Werner syndrome protein function promotes aberrant mitotic recombination
    • Prince P.R., Emond M.J., and Monnat Jr. R.J. 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 Jr., R.J.3
  • 32
    • 0037530653 scopus 로고    scopus 로고
    • Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process
    • Opresko P.L., Cheng W.-H., von Kobbe C., Harrigan J.A., and Bohr V. Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process. Carcinogenesis 24 (2003) 791-802
    • (2003) Carcinogenesis , vol.24 , pp. 791-802
    • Opresko, P.L.1    Cheng, W.-H.2    von Kobbe, C.3    Harrigan, J.A.4    Bohr, V.5
  • 35
    • 84993881991 scopus 로고    scopus 로고
    • New syndrome reconciles theories of ageing
    • Goymer P. New syndrome reconciles theories of ageing. Nat. Rev. Genet. 8 (2007) 90
    • (2007) Nat. Rev. Genet. , vol.8 , pp. 90
    • Goymer, P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.