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Keyword
- carcinogenesis1
- chemotherapy1
- Cockayne syndrome WD repeat protein (CSA)1
- CSB1
- cyclobutane pyrimidine dimers1
- damage mapping1
- damage recognition1
- DNA transcription1
- Drosophila1
- excision repair sequencing (XR-Seq)1
- kinetic proofreading1
- nucleotide excision repair1
- Rad261
- Rad281
- repair mapping1
- RNA polymerase II1
- transcription-coupled repair (TCR)1
- UV DNA damage1
DNA and Chromosomes
2 Results
- Accelerated CommunicationsOpen Access
Drosophila, which lacks canonical transcription-coupled repair proteins, performs transcription-coupled repair
Journal of Biological ChemistryVol. 294Issue 48p18092–18098Published online: October 17, 2019- Nazli Deger
- Yanyan Yang
- Laura A. Lindsey-Boltz
- Aziz Sancar
- Christopher P. Selby
Cited in Scopus: 20Previous work with the classic T4 endonuclease V digestion of DNA from irradiated Drosophila cells followed by Southern hybridization led to the conclusion that Drosophila lacks transcription-coupled repair (TCR). This conclusion was reinforced by the Drosophila Genome Project, which revealed that Drosophila lacks Cockayne syndrome WD repeat protein (CSA), CSB, or UV-stimulated scaffold protein A (UVSSA) homologs, whose orthologs are present in eukaryotes ranging from Arabidopsis to humans that carry out TCR. - MinireviewsOpen Access
Molecular mechanisms and genomic maps of DNA excision repair in Escherichia coli and humans
Journal of Biological ChemistryVol. 292Issue 38p15588–15597Published online: August 10, 2017- Jinchuan Hu
- Christopher P. Selby
- Sheera Adar
- Ogun Adebali
- Aziz Sancar
Cited in Scopus: 51Nucleotide excision repair is a major DNA repair mechanism in all cellular organisms. In this repair system, the DNA damage is removed by concerted dual incisions bracketing the damage and at a precise distance from the damage. Here, we review the basic mechanisms of excision repair in Escherichia coli and humans and the recent genome-wide mapping of DNA damage and repair in these organisms at single-nucleotide resolution.