Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Molecular and cellular biology - 1 Dec 1997

Tantin D, Kansal A, Carey M

Abstract excerpt

Cockayne's syndrome (CS) is a disease characterized by developmental and growth defects, sunlight sensitivity, and a defect in transcription-coupled nucleotide excision repair. The two principle proteins involved in CS, CSA and CSB/ERCC6, have been hypothesized to bind RNA polymerase II (Pol II) and link transcription to DNA repair. We have tested CSA and CSB in assays designed to determine their role in...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Base Sequence
Share to Molecular Sequence Data
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Protein Binding

Share to Proteins

Share to Recombinant Proteins

Share to Transcription Factors

Share to Transcription, Genetic

Source

Open in PubMed Open full text

Identifiers

PMID: 9372911
DOI: 10.1128/MCB.17.12.6803
PMCID: PMC232536

Genes

ERCC6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes.PMID 9372911Read ↗

Mechanistic insights into the regulation of transcription and transcription-coupled DNA repair by Cockayne syndrome protein B.Semantic proximity Read ↗

ATP-Dependent Chromatin Remodeler CSB Couples DNA Repair Pathways to Transcription with Implications for Cockayne Syndrome and Cancer TherapySemantic proximity Read ↗

ATP-dependent chromatin remodeling by the Cockayne syndrome B DNA repair-transcription-coupling factor.Semantic proximity Read ↗

Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair.Semantic proximity Read ↗

Mechanism of Rad26-assisted rescue of stalled RNA polymerase II in transcription-coupled repair.Semantic proximity Read ↗

Cockayne syndrome B protein acts as an ATP-dependent processivity factor that helps RNA polymerase II overcome nucleosome barriers.Semantic proximity Read ↗

Cockayne syndrome: the expanding clinical and mutational spectrum.Semantic proximity Read ↗

Cockayne syndrome group B protein has novel strand annealing and exchange activitiesSemantic proximity Read ↗

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

A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair.Semantic proximity Read ↗

Transcription-coupled repair of DNA–protein crosslinksSemantic proximity Read ↗

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 IISemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.