Abstract
HIV-1 requires the cellular transcription factor CBFβ to stabilize its accessory protein Vif and promote APOBEC3G degradation. Here, we demonstrate that both isoforms of CBFβ allow for increased steady-state levels of Vif, enhanced APOBEC3G degradation, and increased viral infectivity. This conserved functional interaction enhances the steady-state levels of Vif proteins from multiple HIV-1 subtypes and is required for the degradation of all human and rhesus Vif-sensitive APOBEC3 proteins by their respective lentiviral Vif proteins.
Original language | English |
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Pages (from-to) | 2874-2877 |
Number of pages | 4 |
Journal | Journal of Virology |
Volume | 86 |
Issue number | 5 |
DOIs | |
State | Published - Mar 2012 |