메뉴 건너뛰기




Volumn 59, Issue 14, 1999, Pages 3489-3494

Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition

Author keywords

[No Author keywords available]

Indexed keywords

7,12 DIMETHYLBENZ[A]ANTHRACENE; DNA; HELICASE; RNA;

EID: 0033565649     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (64)

References (44)
  • 2
    • 0029892791 scopus 로고    scopus 로고
    • DNA in eukaryotes
    • Wood, R. D. DNA in eukaryotes. Ann. Rev. Biochem., 65: 135-167, 1996.
    • (1996) Ann. Rev. Biochem. , vol.65 , pp. 135-167
    • Wood, R.D.1
  • 3
    • 0003095801 scopus 로고    scopus 로고
    • Nucleotide excision repair syndromes: Xeroderma Pigmentosum, Cockayne syndrome and Trichothiodystrophy
    • B. Vogelstein, and K. W. Kinzler (eds.), New York: McGraw-Hill
    • Bootsma, D., Kraemer, K. H., Cleaver, J. E., and Hoeijmakers, J. H. J. Nucleotide excision repair syndromes: Xeroderma Pigmentosum, Cockayne syndrome and Trichothiodystrophy. In: B. Vogelstein, and K. W. Kinzler (eds.), The Genetic Basis of Human Cancer, pp. 245-274. New York: McGraw-Hill, 1998.
    • (1998) The Genetic Basis of Human Cancer , pp. 245-274
    • Bootsma, D.1    Kraemer, K.H.2    Cleaver, J.E.3    Hoeijmakers, J.H.J.4
  • 4
    • 0031022619 scopus 로고    scopus 로고
    • Sunlight and skin cancer: Another link revealed
    • Kraemer, K. H. Sunlight and skin cancer: another link revealed. Proc. Nail. Acad. Sci. USA, 94: 11-14, 1997.
    • (1997) Proc. Nail. Acad. Sci. USA , vol.94 , pp. 11-14
    • Kraemer, K.H.1
  • 5
    • 0025341294 scopus 로고
    • The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA
    • Venema, J., Mullenders, L. H. F., Natarajan, A. T., Van Zeeland, A. A., and Mayne, L. V. The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA. Proc. Natl. Acad. Sci. USA, 87: 4707-4711, 1990.
    • (1990) Proc. Natl. Acad. Sci. USA , vol.87 , pp. 4707-4711
    • Venema, J.1    Mullenders, L.H.F.2    Natarajan, A.T.3    Van Zeeland, A.A.4    Mayne, L.V.5
  • 6
    • 0025158110 scopus 로고
    • A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome
    • Weeda, G., Van Ham, R. C. A., Vermeulen, W., Bootsma, D., Van der Eb, A. J., and Hoeijmakers, J. H. J. A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome. Cell, 62:777-791, 1990.
    • (1990) Cell , vol.62 , pp. 777-791
    • Weeda, G.1    Van Ham, R.C.A.2    Vermeulen, W.3    Bootsma, D.4    Van Der Eb, A.J.5    Hoeijmakers, J.H.J.6
  • 9
    • 0022868911 scopus 로고
    • Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity
    • Stefanini, M., Lagomarsini, P., Arlett, C. F., Marinoni, S., Borrone, C., Crovato, F., Trevisan, G., Cordone, G., and Nuzzo, F. Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity. Hum. Genet., 74: 107-112, 1986.
    • (1986) Hum. Genet. , vol.74 , pp. 107-112
    • Stefanini, M.1    Lagomarsini, P.2    Arlett, C.F.3    Marinoni, S.4    Borrone, C.5    Crovato, F.6    Trevisan, G.7    Cordone, G.8    Nuzzo, F.9
  • 11
    • 0020692904 scopus 로고
    • A comparison of the proteins of normal and trichothiodystrophic human hair
    • Gillespie, J., and Marshall, R. A comparison of the proteins of normal and trichothiodystrophic human hair. J. Invest. Dermatol., 80: 195-202, 1983.
    • (1983) J. Invest. Dermatol. , vol.80 , pp. 195-202
    • Gillespie, J.1    Marshall, R.2
  • 17
    • 0027489079 scopus 로고
    • The Saccharomyces cerevisiae DNA repair gene RAD25 is required for transcription by RNA polymerase II
    • Qiu, H., Park, E., Prakash, L., and Prakash, S. The Saccharomyces cerevisiae DNA repair gene RAD25 is required for transcription by RNA polymerase II. Genes Dev., 7: 2161-2171, 1993.
    • (1993) Genes Dev. , vol.7 , pp. 2161-2171
    • Qiu, H.1    Park, E.2    Prakash, L.3    Prakash, S.4
  • 18
    • 0028140494 scopus 로고
    • DNA repair gene RAD3 of S. Cerevisiae is essential for transcription by RNA polymerase II
    • Guzder, S. N., Qiu, H., Sommers, C. H., Sung, P., Prakash, L., and Prakash, S. DNA repair gene RAD3 of S. cerevisiae is essential for transcription by RNA polymerase II. Nature (Lond.), 367: 91-94, 1994.
    • (1994) Nature (Lond.) , vol.367 , pp. 91-94
    • Guzder, S.N.1    Qiu, H.2    Sommers, C.H.3    Sung, P.4    Prakash, L.5    Prakash, S.6
  • 19
    • 0027967644 scopus 로고
    • Human nucleotide excision repair syndromes: Molecular clues to unexpected intricacies
    • Hoeijmakers, J. H. J. Human nucleotide excision repair syndromes: molecular clues to unexpected intricacies. Eur. J. Cancer, 30A: 1912-1921, 1994.
    • (1994) Eur. J. Cancer , vol.30 A , pp. 1912-1921
    • Hoeijmakers, J.H.J.1
  • 21
    • 0028358988 scopus 로고
    • Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy
    • Broughton, B. C., Steingrimsdottir, H., Weber, C. A., and Lehmann, A. R. Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy. Nat. Genet., 7: 189-194, 1994.
    • (1994) Nat. Genet. , vol.7 , pp. 189-194
    • Broughton, B.C.1    Steingrimsdottir, H.2    Weber, C.A.3    Lehmann, A.R.4
  • 22
    • 0028832388 scopus 로고
    • Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D
    • Takayama, K., Salazar, E. P., Lehmann, A. R., Stefanini, M., Thompson, L. H., and Weber, C. A. Defects in the DNA repair and transcription gene ERCC2 in the cancer-prone disorder xeroderma pigmentosum group D. Cancer Res., 55: 5656-5663, 1995.
    • (1995) Cancer Res. , vol.55 , pp. 5656-5663
    • Takayama, K.1    Salazar, E.P.2    Lehmann, A.R.3    Stefanini, M.4    Thompson, L.H.5    Weber, C.A.6
  • 25
    • 0032231836 scopus 로고    scopus 로고
    • Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: Site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity
    • Botta, E., Nardo, T., Broughton, B. C., Marinoni, S., Lehmann, A. R., and Stefanini, M. Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity. Am. J. Hum. Genet., 63: 1036-1048, 1998.
    • (1998) Am. J. Hum. Genet. , vol.63 , pp. 1036-1048
    • Botta, E.1    Nardo, T.2    Broughton, B.C.3    Marinoni, S.4    Lehmann, A.R.5    Stefanini, M.6
  • 26
    • 0031964151 scopus 로고    scopus 로고
    • Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality
    • de Boer, J., Donker, I., de Wit, J., Hoeijmakers, J. H. J., and Weeda, G. Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality. Cancer Res., 58: 89-94, 1998.
    • (1998) Cancer Res. , vol.58 , pp. 89-94
    • De Boer, J.1    Donker, I.2    De Wit, J.3    Hoeijmakers, J.H.J.4    Weeda, G.5
  • 29
    • 0028978672 scopus 로고
    • High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC
    • Sands, A. T., Abuin, A., Sanchez, A., Conti, C. J., and Bradley, A. High susceptibility to ultraviolet-induced carcinogenesis in mice lacking XPC. Nature (Lond.), 377: 162-165, 1995.
    • (1995) Nature (Lond.) , vol.377 , pp. 162-165
    • Sands, A.T.1    Abuin, A.2    Sanchez, A.3    Conti, C.J.4    Bradley, A.5
  • 32
    • 0020066520 scopus 로고
    • Failure of RNA synthesis to recover after UV irradiation: An early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum
    • Mayne, L. V., and Lehmann, A. R. Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum. Cancer Res., 42: 1473-1478, 1982.
    • (1982) Cancer Res. , vol.42 , pp. 1473-1478
    • Mayne, L.V.1    Lehmann, A.R.2
  • 33
    • 0028289952 scopus 로고
    • Ultraviolet radiation-induced impairment of the early initiating and the late effector phases of contact hypersensitivity to picrylchloride: Regulation by different mechanisms
    • Sontag, Y., Garssen, J., de Gruijl, F. R., van der Leun, J. C., van Vloten, W. A., and van Loveren, H. Ultraviolet radiation-induced impairment of the early initiating and the late effector phases of contact hypersensitivity to picrylchloride: regulation by different mechanisms. J. Invest. Dermatol., 102: 923-927, 1994.
    • (1994) J. Invest. Dermatol. , vol.102 , pp. 923-927
    • Sontag, Y.1    Garssen, J.2    De Gruijl, F.R.3    Van Der Leun, J.C.4    Van Vloten, W.A.5    Van Loveren, H.6
  • 34
    • 0031920594 scopus 로고    scopus 로고
    • Defective global genome repair in XPC mice is associated with skin cancer susceptibility but not with sensitivity to UVB induced erythema and edema
    • Berg, R. J. W., Ruven, H. J., Sands, A. T., de Gruijl, F. R., and Mullenders, L. H. Defective global genome repair in XPC mice is associated with skin cancer susceptibility but not with sensitivity to UVB induced erythema and edema. J. Invest. Dermatol., 110: 405-409, 1998.
    • (1998) J. Invest. Dermatol. , vol.110 , pp. 405-409
    • Berg, R.J.W.1    Ruven, H.J.2    Sands, A.T.3    De Gruijl, F.R.A.4    Mullenders, L.H.5
  • 35
    • 0029096805 scopus 로고
    • Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells
    • Marionnet, C., Benoit, A., Benhamou, S., Sarasin, A., and Stary, A. Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells. J. Mol. Biol., 252: 550-562, 1995.
    • (1995) J. Mol. Biol. , vol.252 , pp. 550-562
    • Marionnet, C.1    Benoit, A.2    Benhamou, S.3    Sarasin, A.4    Stary, A.5
  • 36
    • 0025276699 scopus 로고
    • Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias
    • Itin, P. H., and Pittelkow, M. R. Trichothiodystrophy: review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasias. J. Am. Acad. Dermatol., 22: 705-717, 1990.
    • (1990) J. Am. Acad. Dermatol. , vol.22 , pp. 705-717
    • Itin, P.H.1    Pittelkow, M.R.2
  • 37
    • 0032128389 scopus 로고    scopus 로고
    • Ultraviolet-B induced hyperplasia and squamous cell carcinomas in the cornea of XPA-deficient mice
    • de Vries, A., Gorgels, T. G., Berg, R. J. W., Jansen, G. H., and van Steeg, H. Ultraviolet-B induced hyperplasia and squamous cell carcinomas in the cornea of XPA-deficient mice. Exp. Eye Res., 67: 53-59, 1998.
    • (1998) Exp. Eye Res. , vol.67 , pp. 53-59
    • De Vries, A.1    Gorgels, T.G.2    Berg, R.J.W.3    Jansen, G.H.4    Van Steeg, H.5
  • 38
    • 0027317209 scopus 로고
    • UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum
    • Madzak, C., Armier, J., Stary, A., Daya-Grosjean, L., and Sarasin, A. UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum. Carcinogenesis (Lond.), 14: 1255-1260, 1993.
    • (1993) Carcinogenesis (Lond.) , vol.14 , pp. 1255-1260
    • Madzak, C.1    Armier, J.2    Stary, A.3    Daya-Grosjean, L.4    Sarasin, A.5
  • 41
    • 0031974425 scopus 로고    scopus 로고
    • Cyclobutane pyrimidine dimers are the main mutagenic DNA photoproducts in DNA repair-deficient trichothiodystrophy cells
    • Marionnet, C., Armier, J., Sarasin, A., and Stary, A. Cyclobutane pyrimidine dimers are the main mutagenic DNA photoproducts in DNA repair-deficient trichothiodystrophy cells. Cancer Res., 58: 102-108, 1998.
    • (1998) Cancer Res. , vol.58 , pp. 102-108
    • Marionnet, C.1    Armier, J.2    Sarasin, A.3    Stary, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.