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Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

http://www.wikidata.org/entity/Q34590427

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True lies: the double life of the nucleotide excision repair factors in transcription and DNA repair A new connection of mRNP biogenesis and export with transcription-coupled repair The cockayne syndrome B protein is essential for neuronal differentiation and neuritogenesis Identification of two missense mutations of ERCC6 in three Chinese sisters with Cockayne syndrome by whole exome sequencing p38 MAPK- and Akt-mediated p300 phosphorylation regulates its degradation to facilitate nucleotide excision repair.Decreased transcription-coupled nucleotide excision repair capacity is associated with increased p53- and MLH1-independent apoptosis in response to cisplatin.Caffeine prevents transcription inhibition and P-TEFb/7SK dissociation following UV-induced DNA damage.UVB induces a genome-wide acting negative regulatory mechanism that operates at the level of transcription initiation in human cells.Interaction between the Cockayne syndrome B and p53 proteins: implications for aging Dysregulation of gene expression as a cause of Cockayne syndrome neurological disease.Cockayne syndrome protein A is a transcription factor of RNA polymerase I and stimulates ribosomal biogenesis and growth Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease DNA repair mechanisms in dividing and non-dividing cells.Histone methyltransferase DOT1L drives recovery of gene expression after a genotoxic attack.Testicular nuclear receptor 4 (TR4) regulates UV light-induced responses via Cockayne syndrome B protein-mediated transcription-coupled DNA repair Identification of Novel Proteins Co-Purifying with Cockayne Syndrome Group B (CSB) Reveals Potential Roles for CSB in RNA Metabolism and Chromatin Dynamics.ATP-dependent chromatin remodeling factors and DNA damage repair Mfd is required for rapid recovery of transcription following UV-induced DNA damage but not oxidative DNA damage in Escherichia coli.Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression A Chromatin-Focused siRNA Screen for Regulators of p53-Dependent Transcription.Regulation of active genome integrity and expression by Rad26p.E2F1 and p53 transcription factors as accessory factors for nucleotide excision repair.Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells.A possible cranio-oro-facial phenotype in Cockayne syndrome.Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?The involvement of DNA-damage and -repair defects in neurological dysfunction Multiple mechanisms contribute to inhibit transcription in response to DNA damage.The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging.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.The molecular basis of chromatin dynamics during nucleotide excision repair.Yeast RAD2, a homolog of human XPG, plays a key role in the regulation of the cell cycle and actin dynamics.Cockayne Syndrome group B protein stimulates NEIL2 DNA glycosylase activity.Molecular mechanisms of ultraviolet radiation-induced DNA damage and repair.Genome maintenance and transcription integrity in aging and disease.RNA polymerase between lesion bypass and DNA repair.Cockayne syndrome B protein regulates recruitment of the Elongin A ubiquitin ligase to sites of DNA damage.UV Irradiation Induces a Non-coding RNA that Functionally Opposes the Protein Encoded by the Same Gene Transcription factors that influence RNA polymerases I and II: To what extent is mechanism of action conserved?

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P2860

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

http://www.wikidata.org/entity/Q34590427

description

2006 nî lūn-bûn

@nan

2006 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի ապրիլին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

@zh-mo

2006年論文

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2006年论文

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name

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

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Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

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type

label

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

@en

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

@nl

prefLabel

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

@en

Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

@nl

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SJ.EMBOJ.7601071

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The EMBO Journal

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Cockayne syndrome B protein regulates the transcriptional program after UV irradiation

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Luca Proietti-De-Santis

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Pascal Drané

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P2860

Recognition of RNA polymerase II and transcription bubbles by XPG, CSB, and TFIIH: insights for transcription-coupled repair and Cockayne Syndrome

Functional consequences of mutations in the conserved SF2 motifs and post-translational phosphorylation of the CSB protein

Human transcription-repair coupling factor CSB/ERCC6 is a DNA-stimulated ATPase but is not a helicase and does not disrupt the ternary transcription complex of stalled RNA polymerase II

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

Acetylation of histone H4 by Esa1 is required for DNA double-strand break repair.

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

Different phosphorylated forms of RNA polymerase II and associated mRNA processing factors during transcription

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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1915-1923

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scholarly article

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10.1038/SJ.EMBOJ.7601071

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9

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25

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16601682

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1456931

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