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RECQ5 helicase promotes resolution of conflicts between replication and transcription in human cells
V. Urban, J. Dobrovolna, D. Hühn, J. Fryzelkova, J. Bartek, P. Janscak,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
NLK
Free Medical Journals
od 1962 do Před 6 měsíci
Freely Accessible Science Journals
od 1962 do Před 6 měsíci
Europe PubMed Central
od 1962 do Před 6 měsíci
Open Access Digital Library
od 1955-01-25
Open Access Digital Library
od 1959-01-01
Open Access Digital Library
od 1962-01-01
PubMed
27502483
DOI
10.1083/jcb.201507099
Knihovny.cz E-zdroje
- MeSH
- biologické modely MeSH
- DNA řízené RNA-polymerasy metabolismus MeSH
- DNA vazebné proteiny metabolismus MeSH
- DNA-dependentní DNA-polymerasy metabolismus MeSH
- elongace genetické transkripce MeSH
- fyziologický stres genetika MeSH
- genetická transkripce * MeSH
- HEK293 buňky MeSH
- helikasy RecQ metabolismus MeSH
- interakční proteinové domény a motivy MeSH
- lidé MeSH
- multienzymové komplexy metabolismus MeSH
- otevřené čtecí rámce genetika MeSH
- prekurzory RNA genetika MeSH
- proliferační antigen buněčného jádra metabolismus MeSH
- protein BRCA1 metabolismus MeSH
- rekombinasa Rad51 metabolismus MeSH
- replikace DNA * MeSH
- ribozomální DNA metabolismus MeSH
- ubikvitinace MeSH
- ubikvitinligasy metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
Collisions between replication and transcription machineries represent a significant source of genomic instability. RECQ5 DNA helicase binds to RNA-polymerase (RNAP) II during transcription elongation and suppresses transcription-associated genomic instability. Here, we show that RECQ5 also associates with RNAPI and enforces the stability of ribosomal DNA arrays. We demonstrate that RECQ5 associates with transcription complexes in DNA replication foci and counteracts replication fork stalling in RNAPI- and RNAPII-transcribed genes, suggesting that RECQ5 exerts its genome-stabilizing effect by acting at sites of replication-transcription collisions. Moreover, RECQ5-deficient cells accumulate RAD18 foci and BRCA1-dependent RAD51 foci that are both formed at sites of interference between replication and transcription and likely represent unresolved replication intermediates. Finally, we provide evidence for a novel mechanism of resolution of replication-transcription collisions wherein the interaction between RECQ5 and proliferating cell nuclear antigen (PCNA) promotes RAD18-dependent PCNA ubiquitination and the helicase activity of RECQ5 promotes the processing of replication intermediates.
Citace poskytuje Crossref.org
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