DNA damage stabilizes interaction of CSB with the transcription elongation machinery. - Wikidata - awgldk - TriplyDB

DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

http://www.wikidata.org/entity/Q33204356

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Dynamic interaction of TTDA with TFIIH is stabilized by nucleotide excision repair in living cells Replication factor C recruits DNA polymerase delta to sites of nucleotide excision repair but is not required for PCNA recruitment UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repair Scale-free flow of life: on the biology, economics, and physics of the cell Functional TFIIH is required for UV-induced translocation of CSA to the nuclear matrix Cockayne syndrome group B protein has novel strand annealing and exchange activities.Structure, function and regulation of CSB: a multi-talented gymnast Mammalian transcription-coupled excision repair Identification of a common subnuclear localization signal UVSSA and USP7, a new couple in transcription-coupled DNA repair Cockayne syndrome B protein stimulates apurinic endonuclease 1 activity and protects against agents that introduce base excision repair intermediates Regulation of ubiquitin ligase dynamics by the nucleolus Rad26, the transcription-coupled repair factor in yeast, is required for removal of stalled RNA polymerase-II following UV irradiation Initiation of DNA repair mediated by a stalled RNA polymerase IIO.NAP1L1 accelerates activation and decreases pausing to enhance nucleosome remodeling by CSB The p53 tumor suppressor protein represses human snRNA gene transcription by RNA polymerases II and III independently of sequence-specific DNA binding Stochastic and reversible assembly of a multiprotein DNA repair complex ensures accurate target site recognition and efficient repair.Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane.Quantitative nucleolar proteomics reveals nuclear re-organization during stress- induced senescence in mouse fibroblast.The contribution of mitochondrial thymidylate synthesis in preventing the nuclear genome stress Tethering of the conserved piggyBac transposase fusion protein CSB-PGBD3 to chromosomal AP-1 proteins regulates expression of nearby genes in humans.Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease NOA36 protein contains a highly conserved nucleolar localization signal capable of directing functional proteins to the nucleolus, in mammalian cells DNA repair mechanisms in dividing and non-dividing cells.Regulation of the Rhp26ERCC6/CSB chromatin remodeler by a novel conserved leucine latch motif Reciprocally regulated chromatin association of Cockayne syndrome protein B and p53 protein Checking on DNA damage in S phase.Self-organization versus Watchmaker: stochastic dynamics of cellular organization.Cockayne syndrome exhibits dysregulation of p21 and other gene products that may be independent of transcription-coupled repair.The Nucleotide Excision Repair Pathway Limits L1 Retrotransposition Nucleotide excision repair-initiating proteins bind to oxidative DNA lesions in vivo.Valosin-containing Protein (VCP)/p97 Segregase Mediates Proteolytic Processing of Cockayne Syndrome Group B (CSB) in Damaged Chromatin.Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress Multiple interaction partners for Cockayne syndrome proteins: implications for genome and transcriptome maintenance Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects.UV-induced proteolysis of RNA polymerase II is mediated by VCP/p97 segregase and timely orchestration by Cockayne syndrome B protein Navigating the nucleotide excision repair threshold.DNA damage response.Molecular basis of transcriptional fidelity and DNA lesion-induced transcriptional mutagenesis.Gearing up chromatin: A role for chromatin remodeling during the transcriptional restart upon DNA damage

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P2860

DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

http://www.wikidata.org/entity/Q33204356

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2004 nî lūn-bûn

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2004 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2004 թվականի հունիսին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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name

DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

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DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

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type

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DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

@ast

DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

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prefLabel

DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

@ast

DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

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Journal of Cell Biology

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DNA damage stabilizes interaction of CSB with the transcription elongation machinery.

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P2093

Adriaan B Houtsmuller

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Angelika Zotter

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Deborah Hoogstraten

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Jan H J Hoeijmakers

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Vincent van den Boom

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Wiggert A van Cappellen

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Wim Vermeulen

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P2860

Cockayne syndrome group B protein enhances elongation by RNA polymerase II

DSIF, a novel transcription elongation factor that regulates RNA polymerase II processivity, is composed of human Spt4 and Spt5 homologs

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

UV-induced ubiquitination of RNA polymerase II: a novel modification deficient in Cockayne syndrome cells

Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes

A Rad26-Def1 complex coordinates repair and RNA pol II proteolysis in response to DNA damage.

Evidence that Spt4, Spt5, and Spt6 control transcription elongation by RNA polymerase II in Saccharomyces cerevisiae

Genome maintenance mechanisms for preventing cancer

Activation of p53 or loss of the Cockayne syndrome group B repair protein causes metaphase fragility of human U1, U2, and 5S genes

ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes

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27-36

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scholarly article

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10.1083/JCB.200401056

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1

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166

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Elisabetta Citterio

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2004-06-28T00:00:00Z

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8482776

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15226310

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2172148

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