TY - JOUR
T1 - The Elav-like protein HuR exerts translational control of viral internal ribosome entry sites
AU - Rivas-Aravena, Andrea
AU - Ramdohr, Pablo
AU - Vallejos, Maricarmen
AU - Valiente-Echeverría, Fernando
AU - Dormoy-Raclet, Virginie
AU - Rodríguez, Felipe
AU - Pino, Karla
AU - Holzmann, Cristian
AU - Huidobro-Toro, J. Pablo
AU - Gallouzi, Imed Eddine
AU - López-Lastra, Marcelo
N1 - Generated from Scopus record by KAUST IRTS on 2022-09-13
PY - 2009/9/30
Y1 - 2009/9/30
N2 - The human embryonic-lethal abnormal vision (ELAV)-like protein, HuR, has been recently found to be involved in the regulation of protein synthesis. In this study we show that HuR participates in the translational control of the HIV-1 and HCV IRES elements. HuR functions as a repressor of HIV-1 IRES activity and acts as an activator of the HCV IRES. The effect of HuR was evaluated in three independent experimental systems, rabbit reticulocyte lysate, HeLa cells, and Xenopus laevis oocytes, using both overexpression and knockdown approaches. Furthermore, results suggest that HuR mediated regulation of HIV-1 and HCV IRESes does not require direct binding of the protein to the RNA nor does it need the nuclear translocation of the IRES-containing RNAs. Finally, we show that HuR has a negative impact on post-integration steps of the HIV-1 replication cycle. Thus, our observations yield novel insights into the role of HuR in the post-transcriptional regulation of HCV and HIV-1 gene expression. © 2009 Elsevier Inc. All rights reserved.
AB - The human embryonic-lethal abnormal vision (ELAV)-like protein, HuR, has been recently found to be involved in the regulation of protein synthesis. In this study we show that HuR participates in the translational control of the HIV-1 and HCV IRES elements. HuR functions as a repressor of HIV-1 IRES activity and acts as an activator of the HCV IRES. The effect of HuR was evaluated in three independent experimental systems, rabbit reticulocyte lysate, HeLa cells, and Xenopus laevis oocytes, using both overexpression and knockdown approaches. Furthermore, results suggest that HuR mediated regulation of HIV-1 and HCV IRESes does not require direct binding of the protein to the RNA nor does it need the nuclear translocation of the IRES-containing RNAs. Finally, we show that HuR has a negative impact on post-integration steps of the HIV-1 replication cycle. Thus, our observations yield novel insights into the role of HuR in the post-transcriptional regulation of HCV and HIV-1 gene expression. © 2009 Elsevier Inc. All rights reserved.
UR - https://linkinghub.elsevier.com/retrieve/pii/S0042682209004127
UR - http://www.scopus.com/inward/record.url?scp=69949148795&partnerID=8YFLogxK
U2 - 10.1016/j.virol.2009.06.050
DO - 10.1016/j.virol.2009.06.050
M3 - Article
SN - 0042-6822
VL - 392
SP - 178
EP - 185
JO - Virology
JF - Virology
IS - 2
ER -