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- antioxidant1
- cell culture1
- cell signaling1
- ChIP-sequencing (ChIP-seq)1
- Cockayne syndrome WD repeat protein (CSA)1
- CSB1
- cyclobutane pyrimidine dimers1
- Drosophila1
- excision repair sequencing (XR-Seq)1
- gene transcription1
- nuclear factor 2 (erythroid-derived 2-like factor) (NFE2L2) (Nrf2)1
- nucleotide excision repair1
- oxidative stress1
- Rad261
- Rad281
- RNA polymerase II1
- signal transduction1
- transcription-coupled repair (TCR)1
- transcriptomics1
- UV DNA damage1
Genomics and Proteomics
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. - Gene RegulationOpen Access
Differential and overlapping targets of the transcriptional regulators NRF1, NRF2, and NRF3 in human cells
Journal of Biological ChemistryVol. 294Issue 48p18131–18149Published online: October 18, 2019- Pengfei Liu
- Michael J. Kerins
- Wang Tian
- Durga Neupane
- Donna D. Zhang
- Aikseng Ooi
Cited in Scopus: 38The nuclear factor (erythroid 2)-like (NRF) transcription factors are a subset of cap'n'collar transcriptional regulators. They consist of three members, NRF1, NRF2, and NRF3, that regulate the expression of genes containing antioxidant-response elements (AREs) in their promoter regions. Although all NRF members regulate ARE-containing genes, each is associated with distinct roles. A comprehensive study of differential and overlapping DNA-binding and transcriptional activities of the NRFs has not yet been conducted.