4.6 Article

Polyubiquitination of APOBEC3G Is Essential for Its Degradation by HIV-1 Vif

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JOURNAL OF VIROLOGY
卷 84, 期 9, 页码 4840-4844

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AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.01911-09

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  1. NIH [5U54RR019192, 5G12RR003032, 5P30AI054999]
  2. NATIONAL CENTER FOR RESEARCH RESOURCES [U54RR019192, G12RR003032] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [P30AI054999] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [SC1GM089269] Funding Source: NIH RePORTER

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Proteasomal degradation of APOBEC3G is a critical step for human immunodeficiency virus type 1 (HIV-1) replication. However, the necessity for polyubiquitination of APOBEC3G in this process is still controversial. In this study, we showed that although macaque simian immunodeficiency virus (SIVmac) Vif is more stable than HIV-1 Vif in human cells, SIVmac Vif induces degradation of APBOEC3G as efficiently as HIV-1 Vif. Overexpression of APOBEC3G or lysine-free APOBEC3G stabilized HIV-1 Vif, indicating that APOBEC3G degradation is independent of the degradation of Vif. Furthermore, an in vivo polyubiquitination assay showed that lysine-free APOBEC3G was also polyubiquitinated. These data suggest that polyubiquitination of APOBEC3G, not that of HIV-1 Vif, is crucial for APOBEC3G degradation.

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