|Apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 3G|
Rendering based on PDB .
|Symbols||APOBEC3G (; A3G; ARCD; ARP-9; ARP9; CEM-15; CEM15; bK150C2.7; dJ494G10.1)|
APOBEC3G (apolipoprotein B mRNA-editing, enzyme-catalytic, polypeptide-like 3G) is a human enzyme encoded by the APOBEC3G gene that belongs to the APOBEC superfamily of proteins. This family of proteins has been suggested to play an important role in innate anti-viral immunity. APOBEC3G is a cytidine deaminase enzyme, which turns cytidine into uridine. 
APOBEC3G exerts innate antiretroviral immune activity against retroviruses, most notably HIV, by interfering with proper replication. However, lentiviruses such as HIV have evolved the Viral infectivity factor (Vif) protein in order to counteract this effect. Vif interacts with APOBEC3G and triggers the ubiquitination and degradation of APOBEC3G via the proteasomal pathway.
It was first identified by Jarmuz et al. as a member of family of proteins APOBEC3A to 3G on chromosome 22 in 2002 and later also as a cellular factor able to restrict replication of HIV-1 lacking the viral accessory protein Vif. Soon after, it was shown that APOBEC3G belonged to a family of proteins grouped together due to their homology with the cytidine deaminase APOBEC1.
APOBEC3G has a symmetric structure, resulting in 2 homologous catalytic domains, the N-terminal (CD1) and C-terminal (CD2) domains, each of which contains a Zn2+
coordination site. Each domain also has the typical His/Cys-X-Glu-X23–28-Pro-Cys-X2-Cys motif for cytidine deaminases. However, unlike the typical cytidine deaminases, APOBEC3G contains a unique alpha helix between two beta sheets in the catalytic domain that could be a cofactor binding site. (Figure 1)
CD2 is catalytically active and vital for deamination and motif specificity. CD1 is catalytically inactive, but very important for binding to DNA and RNA and is key to defining the 5’->3’ processivity of APOBEC3G deamination. Interestingly, CD2 is unable to exert deaminase activity without the presence of CD1.
Native APOBEC3G is composed of monomers, dimers, trimers, tetramers, and higher order oligomers. While it is thought that APOBEC3G functions as a dimer, it is possible that it actually functions as a mix of monomers and oligomers.
The D128 amino acid residue, which lies within CD1 (Figure 1), appears to be particularly important for APOBEC3G interactions with Vif because a D128K point mutation prevents Vif-dependent depletion of APOBEC3G. Additionally, amino acids 128-130 on APOBEC3G form a negatively charged motif that is critical for interactions with Vif and the formation of APOBEC3G-Vif complexes. Furthermore, residues 124-127 are important for encapsidation of APOBEC3G into HIV-1 virions and the resulting antiretroviral activity.
Mechanism of Action
APOBEC3G has been widely studied and several mechanisms that negatively affect HIV-1 replication have been identified.
Cytidine Deamination and Hypermutation
APOBEC3G and other proteins in the same family are able to act as Activation-Induced (Cytidine) Deaminases (AID). APOBEC3G interferes with reverse transcription by inducing numerous deoxycytidine to deoxyuridine mutations in the negative strand of the HIV DNA primarily expressed as complementary DNA (cDNA) in a 3’->5’processive manner. Because APOBEC3G is part of the APOBEC superfamily and acts as an AID, it is likely that the mechanism mediated by APOBEC3G for cytidine deamination is similar to that of an E. coli cytidine deaminase that is known to be highly homologous to APOBEC1 and AID around the nucleotide and zinc binding region. The predicted deamination reaction is driven by a direct nucleophilic attack on position 4 of the cytidine pyrimidine ring by the zinc-coordinated enzyme. Water is needed as both a hydrogen ion and hydroxyl group donor (Figure 2). The deamination (and resulting oxidation) at position 4 yields a carbonyl group and results in a change from cytidine to uridine.
The deamination activity ultimately results in G→A hypermutations at “hot spots” of the proviral DNA. Such hypermutation ultimately destroys the coding and replicative capacity of the virus, resulting in many nonviable virions. APOBEC3G has a much weaker antiviral effect when its active site has been mutated to the point that the protein can no longer mutate retroviral DNA. It was originally thought that the APOBEC3G-mediated deamination can also indirectly lead to viral DNA degradation by DNA repair systems attracted to the mutated residues. However, this has been discounted because Human APOBEC3G reduces viral cDNA levels independently of DNA repair enzymes UNG and SMUG1. 
Interference with Reverse Transcription
APOBEC3G interferes with reverse transcription of HIV-1 independent of DNA deamination. tRNA3Lys typically binds to the HIV-1 primer binding site to initiate reverse transcription. APOBEC3G can inhibit tRNA3Lys priming, thereby negatively affecting viral ssDNA production and virus infectivity. It is predicted that reverse transcription is also negatively affected by APOBEC3G binding to viral RNA and causing steric alterations.
APOBEC3G was associated with interference of viral DNA integration into the host genome in a manner dependent on functional catalytic domains and deaminase activity. Mbisa et al. saw that APOBEC3G interferes with the processing and removal of primer tRNA from the DNA minus strand, thus leading to aberrant viral 3’ long terminal repeat (LTR) DNA ends. These viral DNA ends are inefficient substrates for integration and plus-strand DNA transfer. As a result, HIV-1 provirus formation is inhibited.
APOBEC3G mRNA is expressed in certain cells, referred to as non-permissive cells, in which HIV-1 cannot properly infect and replicate in the absence of Vif. Such cells include physiologically relevant primary CD4 T lymphocytes and macrophages. The encapsidation of APOBEC3G into HIV-1 virions is very important for the spread of APOBEC3G and the exertion of anti-retroviral activity. Encapsidation of APOBEC3G may occur by at least the following four proposed mechanisms (Figure 3): 1. Non-specific packaging of APOBEC3G 2. APOBEC3G interaction with host RNA 3. APOBEC3G interaction with viral RNA 4. Interaction of APOBEC3G with HIV-1 Gag proteins. Only the latter two mechanisms have been extensively confirmed.
The amount that is incorporated into virions is dependent on the level of APOBEC3G expression within the cell producing the virion. Xu et al. conducted studies with PBMC cells and found that, in the absence of Vif, 7±4 APOBEC3G molecules were incorporated into the virions and resulted in potent inhibition of HIV-1 replication.
APOBEC3G is expressed within the non-permissive cells and is a key inhibitory factor of HIV-1 replication and infectivity. However, Vif counteracts this antiretroviral factor, enabling production of viable and infective HIV-1 virions in the presence of APOBEC3G activity . In particular, Vif prevents incorporation of APOBEC3G into HIV-1 virions and promotes destruction of the enzyme in a manner independent of all other HIV-1 proteins.
While APOBEC3G has typically been studied as a vital protein exhibiting potent antiviral effects on HIV-1, recent studies have elucidated the potential of APOBEC3G-mediated mutation to help to facilitate the propagation HIV-1. The number of deaminations in the preferred regions varies from one to many, possibly dependent on the time of exposure to APOBEC3G. Additionally, it has been shown that there is a dose response between intracellular APOBEC3G concentration and degree of viral hypermutation. Some HIV-1 proviruses with APOBEC3G-mediated mutation have been shown to thrive because they carry too few mutations at APOBEC3G hotspots or because recombination between a lethally APOBEC3G-restricted provirus and a viable provirus has occurred. Such sublethal mutagenesis contributes to greater genetic diversity among the HIV-1 virus population, demonstrating the potential for APOBEC3G to enhance HIV-1’s ability to adapt and propagate.
- Sheehy AM, Gaddis NC, Choi JD, Malim MH (August 2002). "Isolation of a human gene that inhibits HIV-1 infection and is suppressed by the viral Vif protein". Nature 418 (6898): 646–50. doi:10.1038/nature00939. PMID 12167863.
- Takaori A (December 2005). "[Antiviral defense by APOBEC3 family proteins]". Uirusu (in Japanese) 55 (2): 267–72. doi:10.2222/jsv.55.267. PMID 16557012.
- Donahue JP, Vetter ML, Mukhtar NA, D'Aquila RT (July 2008). "The HIV-1 Vif PPLP motif is necessary for human APOBEC3G binding and degradation". Virology 377 (1): 49–53. doi:10.1016/j.virol.2008.04.017. PMC 2474554. PMID 18499212.
- Jarmuz A, Chester A, Bayliss J, Gisbourne J, Dunham I, Scott J, Navaratnam N (March 2002). "An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22". Genomics 79 (3): 285–96. doi:10.1006/geno.2002.6718. PMID 11863358.
- Huthoff H, Malim MH (2007). "Identification of amino acid residues in APOBEC3G required for regulation by human immunodeficiency virus type 1 Vif and Virion encapsidation". Journal of Virology 81 (8): 3807–15. doi:10.1128/JVI.02795-06. PMC 1866099. PMID 17267497.
- Greene WC, Debyser Z, Ikda Y, Freed EO, Stephens E, Yonemoto W, Buckheit RW, Este JA, Cihlar T (2008). "Novel targets for HIV therapy". Antiviral Research 80 (3): 251–265. doi:10.1016/j.antiviral.2008.08.003. PMID 18789977.
- Huthoff H, Malim MH (2005). "Cytidine deamination and resistance to retroviral infection: towards a structural understanding of the APOBEC proteins". Virology 334 (2): 147–153. doi:10.1016/j.virol.2005.01.038. PMID 15780864.
- Chelico L, Prochnow C, Erie DA, Chen XS, Goodman MF (2011). "Structural model for deoxycytidine deaminaton mechanism of the HIV-1 inactivation enzyme APOBEC3G". The Journal of Biological Chemistry 285 (21): 16195–205. doi:10.1074/jbc.M110.107987. PMC 2871487. PMID 20212048.
- Li X, Ma J, Zhang Q, Yin X, Zhai C, You X, Yu L, Guo F, Zhao L, Li Z, Zeng Y, Cen S (2011). "Functional analysis of the two cytidine deaminase domains in APOBEC3G". Virology 414 (2): 130–136. doi:10.1016/j.virol.2011.03.014. PMID 21489586.
- Xu H, Svarovskaia ES, Barr R, Zhang Y, Khan MA, Strebel K, Pathak VK (2004). "A single amino acid substitution in human APOBEC3G antiretroviral enzyme confers resistance to HIV-1 virion infectivity factor-induced depletion". PNAS 101 (15): 5652–7. doi:10.1073/pnas.0400830101. PMC 397464. PMID 15054139.
- Strebel K, Khan MA (2008). "APOBEC3Gencapsidation into HIV-1 virions: which RNA is it?". Retrovirology 5 (55). doi:10.1186/1742-4690-5-55. PMC 2491656. PMID 18597677.
- Mbisa JL, Barr R, Thomas JA, Vandegraaff N, Dorweiler IJ, Svarovskaia ES, Brown WL, Mansky LM, Gorelick RJ, Harris RS, Engelman A, Pathak VK (2007). "Human immunodeficiency virus type 1 cDNAs produced in the presence of APOBEC3G exhibit defects in plus-strand DNA transfer and integration". Journal of Virology 81 (13): 7099–110. doi:10.1128/JVI.00272-07. PMC 1933301. PMID 17428871.
- Neuberger MS, Harris RS, Di Noia J, Petersen-Mahrt SK (2003). "Imunity through DNA deamination". Trends in Biochemical Sciences 28 (6): 305–12. doi:10.1016/S0968-0004(03)00111-7. PMID 12826402.
- Sadler HA, Stenglein MD, Harris RS, Mansky LM (2010). "APOBEC3G vontributes to HIV-1 variation through sublethal mutagenesis". Journal of Virology 84 (14): 7396–404. doi:10.1128/JVI.00056-10. PMC 2898230. PMID 20463080.
- Goila-Gaur R, Strebel K (2008). "HIV-1 Vif, APOBEC, and intrinsic immunity". Retrovirology 5 (1): 51. doi:10.1186/1742-4690-5-51. PMC 2443170. PMID 18577210.
- Guo F, Cen S, Niu M, Saadatmand J, Kleiman L (2006). "Inhibition of tRNA3Lys-primed reverse transcription by human APOBEC3G during human Immunodeficiency virus type 1 replication". Journal of Virology 80 (23): 11710–22. doi:10.1128/JVI.01038-06. PMC 1642613. PMID 16971427.
- Langlois M.A, Neuberger M.S (2008). "Human APOBEC3G can restrict retroviral infection in avian cells and acts independently of both UNG and SMUG1.". journal of virology 82: 4660–4664. doi:10.1128/JVI.02469-07.
- Wissing S, Galloway NL, Greene WC (2010). "HIV-1 Vif versus the APOBEC3 cytidine deaminases: an intracellular duel between pathogen and host restriction factors". Molecular Aspects of Medicine 31 (5): 383–397. doi:10.1016/j.mam.2010.06.001. PMC 2967609. PMID 20538015.
- Xu H, Chertova E, Chen J, Ott DE, Roser JD, Hu WS, Pathak VK (2007). "Stoichiometry of the antiviral protein APOBEC3G in HIV-1 virions". Virology 360 (2): 247–256. doi:10.1016/j.virol.2006.10.036. PMID 17126871.
- Joao G, Mariana SM (2004). "HIV-1 Vif and APOBEC3G: Multiple roads to one goal". Retrovirology 1 (28). doi:10.1186/1742-4690-1-28. PMC 521195. PMID 15383144.
- Stopak K, de Noronha C, Yonemoto W, Greene WC (2003). "HIV-1 Vif blocks the antiviral activity of APOBEC3G by impairing both its translation and intracellular stability". Molecular Cell 12 (3): 591–601. doi:10.1016/S1097-2765(03)00353-8. PMID 14527406.
- Pillai SK, Wong JK, Barbour JD (2008). "Turning up the volume on mutational pressure: is more of a good thing always better? (A case study of HIV-1 Vif and APOBEC3)". Retrovirology 5 (26). doi:10.1186/1742-2690-5-26. PMC 2323022. PMID 18339206.
- Mulder LC, Harari A, Simon V (2008). "Cytidine deamination induced HIV-1 drug resistance". PNAS 105 (14): 5501–6. doi:10.1073/pnas.0710190105. PMC 2291111. PMID 18391217.
- Prochnow C, Bransteitter R, Klein MG, Goodman MF, Chen XS (January 2007). "The APOBEC-2 crystal structure and functional implications for the deaminase AID". Nature 445 (7126): 447–51. doi:10.1038/nature05492. PMID 17187054.
- Iwabu Y, Kinomoto M, Tatsumi M, Fujita H, Shimura M, Tanaka Y, Ishizaka Y, Nolan D, Mallal S, Sata T, Tokunaga K. (2010). "Differential anti-APOBEC3G activity of HIV-1 Vif proteins derived from different subtypes". J Biol Chem. 285 (46): 35350–8. doi:10.1074/jbc.M110.173286. PMID 20833716.