Pregled bibliografske jedinice broj: 574456
Degradation of Cellular miR-27 by a Novel, Highly Abundant Viral Transcript Is Important for Efficient Virus Replication In Vivo
Degradation of Cellular miR-27 by a Novel, Highly Abundant Viral Transcript Is Important for Efficient Virus Replication In Vivo // Plos pathogens, 8 (2012), 2; 1-15 doi:10.1371/journal.ppat.1002510 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 574456 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Degradation of Cellular miR-27 by a Novel, Highly Abundant Viral Transcript Is Important for Efficient Virus Replication In Vivo
Autori
Marcinowski, Lisa ; Tanguy, Mélanie ; Krmpotić, Astrid ; Rädle, Bernd ; Juranić Lisnić, Vanda ; Tuddenham, Lee ; Chane-Woon-Ming, Béatrice ; Ruzsics, Zsolt ; Erhard, Florian ; Benkartek, Corinna ; Babić, Marina ; Zimmer, Ralf ; Trgovcich, Joanne ; Koszinowski, Ulrich H. ; Jonjić, Stipan ; Pfeffer, Sébastien ; Dölken, Lars
Izvornik
Plos pathogens (1553-7366) 8
(2012), 2;
1-15
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
miR-27 microRNA virus cytomegalovirus
Sažetak
Cytomegaloviruses express large amounts of viral miRNAs during lytic infection, yet, they only modestly alter the cellular miRNA profile. The most prominent alteration upon lytic murine cytomegalovirus (MCMV) infection is the rapid degradation of the cellular miR-27a and miR-27b. Here, we report that this regulation is mediated by the ∼1.7 kb spliced and highly abundant MCMV m169 transcript. Specificity to miR-27a/b is mediated by a single, apparently optimized, miRNA binding site located in its 3'-UTR. This site is easily and efficiently retargeted to other cellular and viral miRNAs by target site replacement. Expression of the 3'-UTR of m169 by an adenoviral vector was sufficient to mediate its function, indicating that no other viral factors are essential in this process. Degradation of miR-27a/b was found to be accompanied by 3'-tailing and -trimming. Despite its dramatic effect on miRNA stability, we found this interaction to be mutual, indicating potential regulation of m169 by miR-27a/b. Most interestingly, three mutant viruses no longer able to target miR-27a/b, either due to miRNA target site disruption or target site replacement, showed significant attenuation in multiple organs as early as 4 days post infection, indicating that degradation of miR-27a/b is important for efficient MCMV replication in vivo.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
062-0621261-1268 - Uloga imunosubverzivnih citomegalovirusnih gena u latenciji (Krmpotić, Astrid, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Rijeka
Profili:
Vanda Juranić Lisnić
(autor)
Astrid Krmpotić
(autor)
Marina Babić Čač
(autor)
Stipan Jonjić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE