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The different activities of RNA G-quadruplex structures are controlled by flanking sequences
AJ. Zheng, A. Thermou, P. Guixens Gallardo, L. Malbert-Colas, C. Daskalogianni, N. Vaudiau, P. Brohagen, A. Granzhan, M. Blondel, MP. Teulade-Fichou, RP. Martins, R. Fahraeus
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2018
Freely Accessible Science Journals
od 2018
PubMed Central
od 2018
ROAD: Directory of Open Access Scholarly Resources
od 2018
PubMed
34785537
DOI
10.26508/lsa.202101232
Knihovny.cz E-zdroje
- MeSH
- G-kvadruplexy * MeSH
- intergenová DNA chemie genetika MeSH
- lidé MeSH
- regulace genové exprese MeSH
- RNA virová MeSH
- RNA chemie genetika MeSH
- transport RNA MeSH
- virus Epsteinův-Barrové - jaderné antigeny chemie genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The role of G-quadruplex (G4) RNA structures is multifaceted and controversial. Here, we have used as a model the EBV-encoded EBNA1 and the Kaposi's sarcoma-associated herpesvirus (KSHV)-encoded LANA1 mRNAs. We have compared the G4s in these two messages in terms of nucleolin binding, nuclear mRNA retention, and mRNA translation inhibition and their effects on immune evasion. The G4s in the EBNA1 message are clustered in one repeat sequence and the G4 ligand PhenDH2 prevents all G4-associated activities. The RNA G4s in the LANA1 message take part in similar multiple mRNA functions but are spread throughout the message. The different G4 activities depend on flanking coding and non-coding sequences and, interestingly, can be separated individually. Together, the results illustrate the multifunctional, dynamic and context-dependent nature of G4 RNAs and highlight the possibility to develop ligands targeting specific RNA G4 functions. The data also suggest a common multifunctional repertoire of viral G4 RNA activities for immune evasion.
CNRS UMR9187 INSERM U1196 Institut Curie PSL Research University Orsay France
CNRS UMR9187 INSERM U1196 Université Paris Sud Université Paris Saclay Orsay France
Department of Medical Biosciences Umeå University Umeå Sweden
ICCVS University of Gdańsk Science Gdańsk Poland
Inserm UMR1078 Université de Bretagne Occidentale Bretagne CHRU Brest Brest France
Inserm UMRS1131 Institut de Génétique Moléculaire Université Paris 7 Hôpital St Louis Paris France
ISP INRAE Université de Tours UMR1282 Tours France
RECAMO Masaryk Memorial Cancer Institute Brno Czech Republic
Citace poskytuje Crossref.org
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