Sequential assembly of the nucleotide excision repair factors in vivo

Molecular Cell

Volumn 8, Issue 1, 2001, Pages 213-224

  Volker, Marcel ^a   Moné, Martijn J ^b   Karmakar, Parimal ^a   Van Hoffen, Anneke ^a   Schul, Wouter ^b   Vermeulen, Wim ^c   Hoeijmakers, Jan H J ^c   Van Driel, Roel ^b   Van Zeeland, Albert A ^a   Mullenders, Leon H F ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^b UNIVERSITY OF AMSTERDAM   (Netherlands)

^c ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ENDONUCLEASE; EXCISION REPAIR CROSS COMPLEMENTING PROTEIN 1; NUCLEOTIDE EXCISION REPAIR PROTEIN; PROTEIN; PROTEIN XPA; PROTEIN XPG; TRANSCRIPTION FACTOR IIH; UNCLASSIFIED DRUG; XERODERMA PIGMENTOSUM GROUP C PROTEIN;

ARTICLE; COMPLEX FORMATION; CONTROLLED STUDY; DNA DAMAGE; DNA SYNTHESIS; ENZYME ACTIVATION; ENZYME BINDING; EXCISION REPAIR; FLUORESCENT ANTIBODY TECHNIQUE; HUMAN; HUMAN CELL; IN VIVO STUDY; PROTEIN LOCALIZATION; ULTRAVIOLET IRRADIATION; XERODERMA PIGMENTOSUM;

EID: 17944361949     PISSN: 10972765     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1097-2765(01)00281-7     Document Type: Article

References (45)

1. The XPA protein is a zinc metalloprotein with an ability to recognize various kinds of DNA damage
2. Damage recognition in nucleotide excision repair of DNA
3. Stable binding of human XPC complex to irradiated DNA confers strong discrimination for damaged sites
4. Reconstitution of human excision nuclease with recombinant XPF-ERCC1 complex
5. Nucleotide excision repair syndromes: Xeroderma pigmentosum, Cockayne syndrome, and trichothiodystrophy
6. Enzymatic activities involved in the DNA resynthesis step of nucleotide excision repair are firmly attached to chromatin
7. Xeroderma pigmentosum group E cells lack a nuclear factor that binds to damaged DNA
8. DNA-binding polarity of human replication protein A positions nucleases in nucleotide excision repair
9. Molecular mechanism of nucleotide excision repair
10. Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II
11. Recovery of growth-arrested human fibroblasts from UV-induced lethal damage is inhibited by low cell density or sodium butyrate
12. Mechanism of open complex and dual incision formation by human nucleotide excision repair factors
13. Dual roles of a multiprotein complex from S. cerevisiae in transcription and DNA repair
14. Nuclear distribution of transcription factors in relation to sites of transcription and RNA polymerase II
15. Nucleotide excision repair in yeast is mediated by sequential assembly of repair factors and not by a pre-assembled repairosome
16. DNA repair comes of age
17. Action of DNA repair endonuclease ERCC1-XPF in living cells
18. Interactions involving the human RNA polymerase II transcription/nucleotide excision repair complex TFIIH, the nucleotide excision repair protein XPG, and Cockayne syndrome group B (CSB) protein
19. Sites in human nuclei where DNA damaged by ultraviolet light is repaired: Visualization and localization relative to the nucleoskeleton
20. Preferential repair of DNA damage on the transcribed strand of the human metallothionein genes requires RNA polymerase II
21. Mutations in XPA that prevent association with ERCC1 are defective in nucleotide excision repair
22. An interaction between the DNA repair factor XPA and replication protein A appears essential for nucleotide excision repair
23. Characterization of molecular defects in xeroderma pigmentosum group F in relation to its clinically mild symptoms
24. Failure of RNA synthesis to recover after UV-irradiation: An early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum
25. Simultaneous establishment of monoclonal antibodies specific for either cyclobutane pyrimidine dimer or (6-4) photoproduct from the same mouse immunized with ultraviolet-irradiated DNA
26. Reaction mechanism of human DNA repair excision nuclease
27. DNA damage recognition by XPA protein promotes efficient recruitment of transcription factor II H
28. A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: Implications for a second XPG function
29. The general transcription-repair factor TFIIH is recruited to the excision repair complex by the XPA protein independent of the TFIIE transcription factor
30. Overproduction, purification and characterization of the XPC subunit of the human DNA repair excision nuclease
31. DNA repair helicase: A component of BTF2 (TFIIH) basic transcription factor
32. Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease
33. Different forms of TFIIH for transcription and DNA repair: Holo-TFIIH and a nucleotide excision repairosome
34. Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair
35. A multistep damage recognition mechanism for global genomic nucleotide excision repair
36. Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain
37. Xeroderma pigmentosum p48 gene enhances global genomic repair and suppresses UV-induced mutagenesis
38. XPC and human homologs of RAD23: Intracellular localization and relationship to other nucleotide excision repair complexes
39. Deficient repair of the transcribed strand of active genes in Cockayne syndrome cells
40. Transcription-coupled repair removes both cyclobutane pyrimidine dimers and 6-4 photoproducts with equal efficiency and in a sequential way from transcribed DNA in xeroderma pigmentosum group C fibroblasts
41. The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA
42. Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes
43. Transcription affects the rate but not the extent of repair of cyclobutane pyrimidine dimers in the human adenosine deaminase gene
44. Order of assembly of human DNA repair excision nuclease
45. The xeroderma pigmentosum group C protein complex XPC-HR23B plays an important role in the recruitment of transcription factor IIH to damaged DNA