Vol.30 No.3 (2008 June): 297-300
Antagonistic Effect of Virion Infectivity Factor and APOBEC3G in the Intrinsic Antiretroviral Defense
Yun-Hua Wang, Yao-Zhou Zhang*
(Institute of Biochemistry, College of Life Science, Zhejiang Sci-Tec University, Hangzhou 310018, China)
Abstract The virion infectivity factor (Vif) is one of the six human immunodeficiency virus (HIV) accessory proteins. It is essential for efficient viral replication. For a long time, the progress in Vif function is limited because the complexity of its function and correspondingly complex systems are not clear. Until 2002, some studies have revealed the apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3G (APOBEC3G) is a potent intrinsic inhibitor of retroviral replication. Vif function has been rapidly elucidated. APOBEC3G blocks the productive infection of HIV-1 mainly through cytidine deaminase activity. APOBEC3G effectively halts HIV replication by lethal dC to dU editing and dG to dA hypermutation during the reverse transcription. Retroviruses have evolved Vif to counter the antiretroviral action of APOBEC3G. Firstly, Vif can directly induce APOBEC3G rapid degradation via the ubiquitin-proteasomal pathway. Secondly, Vif inhibits the translation of APOBEC3G mRNA, further reducing the enzyme within the cell. In addition, Vif might promote the transition of APOBEC3G from low molecular mass (LMM) to high molecular mass (HMM) conformations, thereby defeats the antiviral activity of APOBEC3G. The further research on the reaction of Vif/APOBEC3G will provide the theoretical basis for the antiviral drug development.
Key words human immunodeficiency virus; virion infectivity factor; apolipoprotein B mRNA-editing enzyme catalytic polypeptide-like 3G
Received: November 19, 2007 Accepted: February 21, 2008
This work was supported by the National Basic Research Program of China (973 Program) (No.2005CB121006), the National Key Technologies R&D Program (No.2006BAI01B04), the National Natural Science Foundation of China (No.30740015, No.30600323, No.30670447), and the Natural Science Foundation of Zhejiang Province (No.Y205449, No.Y304122)
*Corresponding author. Tel/Fax: 86-571-86843198, E-mail: yaozhou@chinagene.com