Literature DB >> 20385089

NER factors are recruited to active promoters and facilitate chromatin modification for transcription in the absence of exogenous genotoxic attack.

Nicolas Le May1, David Mota-Fernandes, Renier Vélez-Cruz, Izarn Iltis, Denis Biard, Jean Marc Egly.   

Abstract

Upon gene activation, we found that RNA polymerase II transcription machinery assembles sequentially with the nucleotide excision repair (NER) factors at the promoter. This recruitment occurs in absence of exogenous genotoxic attack, is sensitive to transcription inhibitors, and depends on the XPC protein. The presence of these repair proteins at the promoter of activated genes is necessary in order to achieve optimal DNA demethylation and histone posttranslational modifications (H3K4/H3K9 methylation, H3K9/14 acetylation) and thus efficient RNA synthesis. Deficiencies in some NER factors impede the recruitment of others and affect nuclear receptor transactivation. Our data suggest that there is a functional difference between the presence of the NER factors at the promoters (which requires XPC) and the NER factors at the distal regions of the gene (which requires CSB). While the latter may be a repair function, the former is a function with respect to transcription unveiled in the current study. 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20385089     DOI: 10.1016/j.molcel.2010.03.004

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  101 in total

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Review 3.  The intertwined roles of transcription and repair proteins.

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Journal:  Mol Cell       Date:  2013-11-07       Impact factor: 17.970

4.  Assembly of the Elongin A Ubiquitin Ligase Is Regulated by Genotoxic and Other Stresses.

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Journal:  J Biol Chem       Date:  2015-04-15       Impact factor: 5.157

5.  Functional and mechanistic studies of XPC DNA-repair complex as transcriptional coactivator in embryonic stem cells.

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6.  Transcription-coupled nucleotide excision repair factors promote R-loop-induced genome instability.

Authors:  Julie Sollier; Caroline Townsend Stork; María L García-Rubio; Renee D Paulsen; Andrés Aguilera; Karlene A Cimprich
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Review 7.  Vitamin D receptor and RXR in the post-genomic era.

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8.  ARCH domain of XPD, an anchoring platform for CAK that conditions TFIIH DNA repair and transcription activities.

Authors:  Wassim Abdulrahman; Izarn Iltis; Laura Radu; Cathy Braun; Anne Maglott-Roth; Christophe Giraudon; Jean-Marc Egly; Arnaud Poterszman
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

9.  Defective mitophagy in XPA via PARP-1 hyperactivation and NAD(+)/SIRT1 reduction.

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Journal:  Cell       Date:  2014-05-08       Impact factor: 41.582

10.  DDB2 suppresses epithelial-to-mesenchymal transition in colon cancer.

Authors:  Nilotpal Roy; Prashant V Bommi; Uppoor G Bhat; Shaumick Bhattacharjee; Indira Elangovan; Jing Li; Krushna C Patra; Dragana Kopanja; Adam Blunier; Richard Benya; Srilata Bagchi; Pradip Raychaudhuri
Journal:  Cancer Res       Date:  2013-04-22       Impact factor: 12.701

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