Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pgen.1006221
DC Field | Value | |
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dc.title | FACT Assists Base Excision Repair by Boosting the Remodeling Activity of RSC | |
dc.contributor.author | Charles Richard J.L. | |
dc.contributor.author | Shukla M.S. | |
dc.contributor.author | Menoni H. | |
dc.contributor.author | Ouararhni K. | |
dc.contributor.author | Lone I.N. | |
dc.contributor.author | Roulland Y. | |
dc.contributor.author | Papin C. | |
dc.contributor.author | Ben Simon E. | |
dc.contributor.author | Kundu T. | |
dc.contributor.author | Hamiche A. | |
dc.contributor.author | Angelov D. | |
dc.contributor.author | Dimitrov S. | |
dc.date.accessioned | 2020-03-13T05:23:30Z | |
dc.date.available | 2020-03-13T05:23:30Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | Charles Richard J.L., Shukla M.S., Menoni H., Ouararhni K., Lone I.N., Roulland Y., Papin C., Ben Simon E., Kundu T., Hamiche A., Angelov D., Dimitrov S. (2016). FACT Assists Base Excision Repair by Boosting the Remodeling Activity of RSC. PLoS Genetics 12 (7) : e1006221. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1006221 | |
dc.identifier.issn | 15537390 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/165384 | |
dc.description.abstract | FACT, in addition to its role in transcription, is likely implicated in both transcription-coupled nucleotide excision repair and DNA double strand break repair. Here, we present evidence that FACT could be directly involved in Base Excision Repair and elucidate the chromatin remodeling mechanisms of FACT during BER. We found that, upon oxidative stress, FACT is released from transcription related protein complexes to get associated with repair proteins and chromatin remodelers from the SWI/SNF family. We also showed the rapid recruitment of FACT to the site of damage, coincident with the glycosylase OGG1, upon the local generation of oxidized DNA. Interestingly, FACT facilitates uracil-DNA glycosylase in the removal of uracil from nucleosomal DNA thanks to an enhancement in the remodeling activity of RSC. This discloses a novel property of FACT wherein it has a co-remodeling activity and strongly enhances the remodeling capacity of the chromatin remodelers. Altogether, our data suggest that FACT may acts in concert with RSC to facilitate excision of DNA lesions during the initial step of BER. © 2016 Charles Richard et al. | |
dc.publisher | Public Library of Science | |
dc.source | Unpaywall 20200320 | |
dc.subject | nucleoplasmin | |
dc.subject | uracil DNA glycosidase | |
dc.subject | chromatin | |
dc.subject | DNA binding protein | |
dc.subject | high mobility group protein | |
dc.subject | histone | |
dc.subject | nonhistone protein | |
dc.subject | nucleosome | |
dc.subject | RSC complex, S cerevisiae | |
dc.subject | Saccharomyces cerevisiae protein | |
dc.subject | SSRP1 protein, human | |
dc.subject | SWI-SNF-B chromatin-remodeling complex | |
dc.subject | transcription elongation factor | |
dc.subject | transcription factor | |
dc.subject | uracil | |
dc.subject | antibody affinity | |
dc.subject | Article | |
dc.subject | centrifugation | |
dc.subject | chromatin assembly and disassembly | |
dc.subject | controlled study | |
dc.subject | dissociation | |
dc.subject | DNA histone interaction | |
dc.subject | DNA repair | |
dc.subject | excision repair | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | hydrolysis | |
dc.subject | immunoprecipitation | |
dc.subject | in vivo study | |
dc.subject | mass spectrometry | |
dc.subject | molecular docking | |
dc.subject | molecular dynamics | |
dc.subject | nucleosome | |
dc.subject | oxidative stress | |
dc.subject | protein analysis | |
dc.subject | protein domain | |
dc.subject | protein footprinting | |
dc.subject | protein function | |
dc.subject | protein protein interaction | |
dc.subject | protein purification | |
dc.subject | Western blotting | |
dc.subject | animal | |
dc.subject | biosynthesis | |
dc.subject | chromatin | |
dc.subject | DNA damage | |
dc.subject | genetic transcription | |
dc.subject | genetics | |
dc.subject | HeLa cell line | |
dc.subject | metabolism | |
dc.subject | Saccharomyces cerevisiae | |
dc.subject | Xenopus laevis | |
dc.subject | Animals | |
dc.subject | Chromatin | |
dc.subject | Chromatin Assembly and Disassembly | |
dc.subject | Chromosomal Proteins, Non-Histone | |
dc.subject | DNA Damage | |
dc.subject | DNA Repair | |
dc.subject | DNA-Binding Proteins | |
dc.subject | HeLa Cells | |
dc.subject | High Mobility Group Proteins | |
dc.subject | Histones | |
dc.subject | Humans | |
dc.subject | Nucleosomes | |
dc.subject | Oxidative Stress | |
dc.subject | Saccharomyces cerevisiae | |
dc.subject | Saccharomyces cerevisiae Proteins | |
dc.subject | Transcription Factors | |
dc.subject | Transcription, Genetic | |
dc.subject | Transcriptional Elongation Factors | |
dc.subject | Uracil | |
dc.subject | Xenopus laevis | |
dc.type | Article | |
dc.contributor.department | CANCER SCIENCE INSTITUTE OF SINGAPORE | |
dc.description.doi | 10.1371/journal.pgen.1006221 | |
dc.description.sourcetitle | PLoS Genetics | |
dc.description.volume | 12 | |
dc.description.issue | 7 | |
dc.description.page | e1006221 | |
dc.published.state | Published | |
Appears in Collections: | Staff Publications Elements |
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