Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers

DNA Repair

Volumn 1, Issue 8, 2002, Pages 629-643

  Spivak, Graciela ^a   Itoh, Toshiki ^b   Matsunaga, Tsukasa ^c   Nikaido, Osamu ^c   Hanawalt, Philip ^a   Yamaizumi, Masaru ^d  

^a STANFORD UNIVERSITY   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c KANAZAWA UNIVERSITY   (Japan)

^d KUMAMOTO UNIVERSITY   (Japan)

Author keywords

Cyclobutane pyrimidine dimer; Transcription coupled DNA repair; Ultraviolet light (UV); Ultraviolet sensitive syndrome

Indexed keywords

ALPHA FETOPROTEIN; CYCLOBUTANE; DIHYDROFOLATE REDUCTASE; DNA; PROTEIN P53; PYRIMIDINE DIMER; NEUROFILAMENT PROTEIN; RNA;

ARTICLE; CELL ASSAY; COCKAYNE SYNDROME; CONTROLLED STUDY; DNA DAMAGE; DNA STRAND; GENETIC ANALYSIS; GENETIC TRANSCRIPTION; GENOMIC FRAGMENT; HUMAN; HUMAN CELL; NEUROFILAMENT; OXIDATION; PRIORITY JOURNAL; ULTRAVIOLET RADIATION; CELL CULTURE; DNA REPAIR; FIBROBLAST; GENETICS; METABOLISM; PHYSIOLOGY; RADIATION DOSE; RADIATION EXPOSURE; TUMOR SUPPRESSOR GENE; XERODERMA PIGMENTOSUM;

ALPHA-FETOPROTEINS; CELLS, CULTURED; COCKAYNE SYNDROME; DNA; DNA DAMAGE; DNA REPAIR; FIBROBLASTS; GENES, P53; HUMANS; NEUROFILAMENT PROTEINS; PYRIMIDINE DIMERS; RADIATION TOLERANCE; RNA; TETRAHYDROFOLATE DEHYDROGENASE; TRANSCRIPTION, GENETIC; ULTRAVIOLET RAYS; XERODERMA PIGMENTOSUM;

EID: 0037031218     PISSN: 15687864     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1568-7864(02)00056-3     Document Type: Article

References (67)

1. Heterogeneous DNA damage and repair in the mammalian genome
2. DNA repair in an active gene: Removal of pyrimidine dimers from the DHFR gene of CHO cells is much more efficient that in the genome overall
3. Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene
4. Induction of the Escherichia coli lactose operon selectively increases repair of its transcribed DNA strand
5. Strand-selective repair of DNA damage in the yeast gal7 gene requires RNA polymerase-II
6. Site-specific DNA-repair at the nucleosome level in a yeast minichromosome
7. Preferential repair of cyclobutane pyrimidine dimers in the transcribed strand of a gene in yeast chromosomes and plasmids is dependent on transcription
8. The genetic defect in the Chinese hamster ovary cell mutant UV61 permits moderate selective repair of cyclobutane pyrimidine dimers in an expressed gene
9. Increased UV resistance of a xeroderma pigmentosum revertant cell line is correlated with selective repair of the transcribed strand of an expressed gene
10. (6-4) Photoproducts, (6-4) Photoproducts and not cyclobutane pyrimidine dimers are the main UV-induced mutagenic lesions in Chinese hamster cells
11. Defective repair of ionizing radiation damage in Cockayne's syndrome and xeroderma pigmentosum group G
12. Nucleotide excision repair and human syndromes
13. The genetic defect in Cockayne Syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA
14. Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes
15. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G
16. Transcription-coupled repair of 8-oxoguanine: Requirement for XPG, TFIIH, and CSB and implications for Cockayne syndrome
17. DNA repair: Stranded in an active gene
18. Repair and transcription: Collision or collusion?
19. UV-induced inhibition of transcription involves repression of transription initiation and phosphorylation of RNA polymerase II
20. DNA excision-repair defect of xeroderma pigmentosum prevents removal of a class of oxygen free-radical induced base lesions
21. A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: Siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestations
22. UVs syndrome, a new general category of photosensitive disorder with defective DNA repair, is distinct from xeroderma pigmentosum variant and rodent complementation group I
23. Clinical characteristics of three patients with UVs syndrome, a photosensitive disorder with defective DNA repair
24. Reinvestigation of the classification of five cell strains of xeroderma pigmentosum group E with reclassification of three of them
25. Cockayne syndrome complementation group B associated with xeroderma pigmentosum phenotype
26. High sensitivity of the ultraviolet-induced p53 response in ultraviolet-sensitive syndrome, a photosensitive disorder with a putative defect in deoxyribonucleic acid repair of actively transcribed genes
27. Determination of damage and repair in specific DNA sequences
28. 5-Fluorouracil augmentation of dihydrofolate reductase gene transcripts containing intervening sequences in methotrexate-resistant KB cells
29. Suppresion of human colorectal carcinoma cell growth by wild-type p53
30. The human mid-size neurofilament subunit: A repeated protein sequence and the relationship of its gene to the intermediate filament gene family
31. Simultaneous establishment of monoclonal antibodies specific for either cyclobutane pyrimidine dimer or (6-4) photoproduct from the same mouse immunized with ultraviolet-irradiated DNA
32. Base sequence specificity of a monoclonal antibody binding to (6-4) photoproducts
33. Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A
34. Expression of wild-type p53 is required for efficient global genomic nucleotide excision repair in UV-irradiated human fibroblasts
35. Measurement of the pyrimidine dimer content of DNA in permeabilized bacterial or mammalian cells with endonuclease V of bacteriophage T4
36. Sensitive determination of pyrimidine dimers in DNA of UV-irradiated mammalian cells
37. Deficient repair of the transcribed strand of actives genes in Cockayne's syndrome cells
38. Preferential repair of ultraviolet light-induced DNA damage in the transcribed strand of the human p53 gene
39. Regulation and activities of α-Fetoprotein
40. Intermediate filaments as mechanical integrators of cellular space
41. The molecular biology of intermediate filaments
42. Molecular mechanism of transcription-repair coupling
43. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes
44. Open complex formation around a lesion during nucleotide excision repair provides a structure for cleavage by human XPG protein
45. Isolation of active recombinant XPG protein, a human DNA repair endonuclease
46. Base excision repair of oxidative DNA damage activated by XPG protein
47. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: Implications for a second XPG function
48. Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli
49. Transcription-coupled repair deficiency and mutations in human mismatch repair genes
50. Differential involvement of the human mismatch repair proteins, hMLH1 and hMSH2, in transcription-coupled repair
51. Mismatch repair mutants in yeast are not defective in transcription-coupled DNA repair of UV-induced DNA damage
52. Requirements for DNA mismatch repair proteins in the transcription-coupled repair of thymine glycols in Saccharomyces cerevisiae
53. BRCA1 required for transcription-coupled repair of oxidative DNA damage
54. BRCA1 and BRCA2 are necessary for the transcription-coupled repair of the oxidative 8-oxoguanine lesion in human cells
55. XAB2, a novel tetratricopeptide repeat protein involved in transcription-coupled DNA repair and transcription
56. UV-induced nuclear accumulation of p53 is evoked through DNA damage of actively transcribed genes independent of the cell cycle
57. Blockage of RNA polymerase as a possible trigger for UV light-induced apoptosis
58. Transcription-coupled DNA repair. Which lesions? Which diseases?
59. DNA repair: The bases for Cockayne syndrome
60. Transcription-coupled repair in RNA polymerase I-transcribed genes of yeast
61. Effect of thymine glycol on transcription elongation by T7 RNA polymerase and mammalian RNA polymerase II
62. Regulation of nucleotide excision repair in bacteria and mammalian cells
63. Transcript cleavage by RNA polymerase II arrested by a cyclobutane pyrimidine dimer in the DNA template
64. Structural characterization of RNA polymerase II complexes arrested by a cyclobutane pyrimidine dimer in the transcribed strand of template DNA
65. A compromised yeast RNA polymerase II enhances UV sensitivity in the absence of global genome nucleotide excision repair