IFITM proteins inhibit HIV-1 protein synthesis.
Wing-Yiu Jason LeeRebecca Menhua FuChen LiangRichard D SloanPublished in: Scientific reports (2018)
Interferon induced transmembrane proteins (IFITMs) inhibit the cellular entry of a broad range of viruses, but it has been suspected that for HIV-1 IFITMs may also inhibit a post-integration replicative step. We show that IFITM expression reduces HIV-1 viral protein synthesis by preferentially excluding viral mRNA transcripts from translation and thereby restricts viral production. Codon-optimization of proviral DNA rescues viral translation, implying that IFITM-mediated restriction requires recognition of viral RNA elements. In addition, we find that expression of the viral accessory protein Nef can help overcome the IFITM-mediated inhibition of virus production. Our studies identify a novel role for IFITMs in inhibiting HIV replication at the level of translation, but show that the effects can be overcome by the lentiviral protein Nef.
Keyphrases
- antiretroviral therapy
- sars cov
- hiv positive
- hiv infected
- hiv testing
- human immunodeficiency virus
- hepatitis c virus
- hiv aids
- men who have sex with men
- poor prognosis
- binding protein
- south africa
- pulmonary embolism
- immune response
- small molecule
- high glucose
- dendritic cells
- signaling pathway
- oxidative stress
- cell free
- gene therapy
- endothelial cells
- stress induced
- case control