Repair in ribosomal RNA genes is deficient in xeroderma pigmentosum group C and in Cockayne's syndrome cells

Mutation Research Letters

Volumn 323, Issue 4, 1994, Pages 179-187

  Christians, Fred C ^a   Hanawalt, Philip C ^a  

^a STANFORD UNIVERSITY   (United States)

Author keywords

Dihydrofolate reductase; DNA excision repair; Preferential repair; rDNA; Transcription

Indexed keywords

CYCLOBUTANE DERIVATIVE; DIHYDROFOLATE REDUCTASE; RIBOSOME DNA;

ARTICLE; COCKAYNE SYNDROME; CONTROLLED STUDY; EXCISION REPAIR; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; PRIORITY JOURNAL; XERODERMA PIGMENTOSUM;

ANIMAL; CELLS, CULTURED; COCKAYNE SYNDROME; DNA REPAIR; GENETIC COMPLEMENTATION TEST; HUMAN; MICE; RNA POLYMERASE I; RNA, RIBOSOMAL; SUPPORT, U.S. GOV'T, P.H.S.; XERODERMA PIGMENTOSUM;

EID: 0028178058     PISSN: 01657992     EISSN: None     Source Type: Journal    
DOI: 10.1016/0165-7992(94)90031-0     Document Type: Article

References (32)

1. Excision repair in ataxia telangiectasia, Fanconi's anemia, Cockayne syndrome, and Bloom's syndrome after treatment with ultraviolet radiation and N-acetoxy-2-acetylaminfluorene
2. DNA repair in the c-myc proto-oncogene locus: possible involvement in susceptibility or resistance to plasmacytoma induction in BALB/c mice
3. DNA repair in an active gene: removal of pyrimmidine dimers from the DHFR gene of CHO cells is much more efficient than in the genome overall
4. Survival of UV-irradiated mammalian cells correlates with efficient DNA repair in an essential gene
5. Transcription-dependent and independent DNA excision repair pathways in human cells
6. Relationship between transcription and DNA repair
7. Inhibition of transcription and strand-specific DNA repair by α-amanitin in Chinese hamster ovary cells
8. Lack of transcription-coupled repair in mammalian ribosomal RNA genes
9. Gene-specific DNA repair in xeroderma pigmentosum complementation groups A, C, D and F
10. Transcription-dependent and transcription-coupled DNA repair responses
11. Biological significance of domain-oriented DNA repair in xeroderma pigmentosum cells
12. The rate of removal of pyrimidine dimers in quiescent cultures of normal human and xeroderma pigmentosum cells
13. Selective repair of specific chromatin domains in UV-irradiated cells from xeroderma pigmentosum complementation group C
14. Preferential repair of DNA damage on the transcribed strand of the human metallothionein genes requires RNA polymerase II
15. Increased UV resistance of a xeroderma pigmentosum revertant cell line is correlated with selective repair of the transcribed strand of an expressed gene
16. Domain-limited repair of DNA in ultraviolet irradiated fibroblasts from xeroderma pigmentosum complementation group C
17. Failure of RNA synthesis to recover after UV irradiation: an early defect in cells from individuals with Cockayne's syndrome and xeroderma pigmentosum
18. Excision repair in Cockayne syndrome
19. Selective removal of transcription blocking DNA damage from the transcribed strand of the mammalian DHFR gene
20. The biology of the (6-4) photoproduct
21. Nuclear matrix associated DNA is preferentially repaired in normal human fibroblasts, exposed to a low dose of ultraviolet light but not in Cockayne's syndrome fibroblasts
22. Physical association of pyrimidine dimer DNA glycosylase and apurinic/apyrimidinic DNA endonuclease essential for repair of ultraviolet-damaged DNA
23. Formation and enzymatic properties of the UvrB-DNA complex
24. Gene- and strand-specific repair in vitro: Partial purification of a transcription-repair coupling factor
25. Molecular mechanism of transcription-repair coupling
26. ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active gene
27. Mechanism of action of the Escherichia coli UvrABC nuclease: Clues to the damage recognition problem
28. Gene specific repair of UV-induced DNA damage in mammalian cells
29. The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA
30. The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNA
31. Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes
32. Effects of DNA damaging agents on cultured fibroblasts derived from patients with Cockayne syndrome