| Literature DB >> 26779410 |
Théophile Ohlmann1, Chloé Mengardi1, Marcelo López-Lastra2.
Abstract
Translation initiation of the full-length mRNA of the human immunodeficiency virus can occur via several different mechanisms to maintain production of viral structural proteins throughout the replication cycle. HIV-1 viral protein synthesis can occur by the use of both a cap-dependant and IRES-driven mechanism depending on the physiological conditions of the cell and the status of the ongoing infection. For both of these mechanisms there is a need for several viral and cellular co-factors for optimal translation of the viral mRNA. In this review we will describe the mechanism used by the full-length mRNA to initiate translation highlighting the role of co-factors within this process. A particular emphasis will be given to the role of the DDX3 RNA helicase in HIV-1 mRNA translation initiation.Entities:
Year: 2014 PMID: 26779410 PMCID: PMC4696476 DOI: 10.4161/2169074X.2014.960242
Source DB: PubMed Journal: Translation (Austin) ISSN: 2169-0731