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RAD26, the functional S. cerevisiae homolog of the Cockayne syndrome B gene ERCC6.
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- معلومة اضافية
- Publisher Information:
1994-01-01
- نبذة مختصرة :
Transcription-coupled repair (TCR) is a universal sub-pathway of the nucleotide excision repair (NER) system that is limited to the transcribed strand of active structural genes. It accomplishes the preferential elimination of transcription-blocking DNA lesions and permits rapid resumption of the vital process of transcription. A defect in TCR is responsible for the rare hereditary disorder Cockayne syndrome (CS). Recently we found that mutations in the ERCC6 repair gene, encoding a putative helicase, underly the repair defect of CS complementation group B. Here we report the cloning and characterization of the Saccharomyces cerevisiae homolog of CSB/ERCC6, which we designate RAD26. A rad26 disruption mutant appears viable and grows normally, indicating that the gene does not have an essential function. In analogy with CS, preferential repair of UV-induced cyclobutane pyrimidine dimers in the transcribed strand of the active RBP2 gene is severely impaired. Surprisingly, in contrast to the human CS mutant, yeast RAD26 disruption does not induce any UV-, cisPt- or X-ray sensitivity, explaining why it was not isolated as a mutant before. Recovery of growth after UV exposure was somewhat delayed in rad26. These findings suggest that TCR in lower eukaryotes is not very important for cell survival and that the global genome repair pathway of NER is the major determinant of cellular resistance to genotoxicity.
- الموضوع:
- Availability:
Open access content. Open access content
info:eu-repo/semantics/openAccess
- Note:
application/pdf
EMBO Journal vol. 13, pp. 5361-5369
English
- Other Numbers:
QGQ oai:repub.eur.nl:3071
urn:hdl:1765/3071
929962688
- Contributing Source:
ERASMUS UNIVERSITEIT ROTTERDAM
From OAIster®, provided by the OCLC Cooperative.
- الرقم المعرف:
edsoai.ocn929962688
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