Vpx

Vpx is a virion-associated protein encoded by human immunodeficiency virus type 2 HIV-2 and most simian immunodeficiency virus (SIV) strains, but that is absent from HIV-1.[1] It is similar in structure to the protein Vpr that is carried by SIV and HIV-2 as well as HIV-1.[2] Vpx is one of five accessory proteins (Vif, Vpx, Vpr, Vpu, and Nef) carried by lentiviruses that enhances viral replication by inhibiting host antiviral factors.[2]

This article is about protein. For the computer bus standard, see VPX. For the video coding format series, see On2 Technologies.
Vpx
Identifiers
OrganismHuman immunodeficiency virus type 2 subtype A (isolate ROD)
Symbol?
UniProtP06939

Vpx enhances HIV-2 replication in humans by counteracting the host factor SAMHD1.[3] SAMHD1 is a host factor found in human myeloid cells, such as dendritic cells and macrophages, that restricts HIV-1 replication by depleting the cytoplasmic pool of deoxynucleoside triphosphates needed for viral DNA production.[4] SAMHD1 does not, however, restrict HIV-2 replication in myeloid cells due to the presence of viral Vpx. Vpx counteracts restriction by inducing the ubiquitin-proteasome-dependent degradation of SAMHD1.[3] Vpx-mediated degradation of SAMHD1 therefore decreases deoxynucleoside triphosphate hydrolysis, thereby increasing the availability of dNTPs for viral reverse transcription in the cytoplasm. It has been postulated that SAMHD1 degradation is required for HIV-2 replication because the HIV-2 reverse transcriptase (RT) is less active than the HIV-1 RT, which would be the reason for the absence of Vpx from HIV-1.[2] Because Vpx is required for HIV-2 reverse transcription and the early stages of the viral life cycle, it is packaged into virions in significant amounts.[5][6]

Vpx is also involved in the nuclear import of the HIV-2/SIV genomes and associated proteins,[7] but the specific mechanisms and interactions are currently unknown. Although Vpr and Vpx are similar in size (both are ~100 amino acids with 20-25% sequence similarity) and structure (both are predicted to have similar tertiary structure with three major helices), they serve very different roles in viral replication.[2] Vpx targets a host restriction factor for proteasomal degradation, while Vpr arrests the host cell cycle in the G2 phase.[2] However, they are both involved in the import of the viral preintegration complex into the host nucleus.[7]

References
  1. Vicenzi E, Poli G (February 2013). "Novel factors interfering with human immunodeficiency virus-type 1 replication in vivo and in vitro". Tissue Antigens. 81 (2): 61–71. doi:10.1111/tan.12047. PMID 23330719.
  2. Fujita M, Nomaguchi M, Adachi A, Otsuka M (2012). "SAMHD1-Dependent and -Independent Functions of HIV-2/SIV Vpx Protein". Frontiers in Microbiology. 3: 297. doi:10.3389/fmicb.2012.00297. PMC 3415948. PMID 22908011.
  3. Laguette N, Rahm N, Sobhian B, Chable-Bessia C, Münch J, Snoeck J, et al. (February 2012). "Evolutionary and functional analyses of the interaction between the myeloid restriction factor SAMHD1 and the lentiviral Vpx protein". Cell Host & Microbe. 11 (2): 205–17. doi:10.1016/j.chom.2012.01.007. PMC 3595996. PMID 22305291.
  4. Lahouassa H, Daddacha W, Hofmann H, Ayinde D, Logue EC, Dragin L, et al. (February 2012). "SAMHD1 restricts the replication of human immunodeficiency virus type 1 by depleting the intracellular pool of deoxynucleoside triphosphates". Nature Immunology. 13 (3): 223–228. doi:10.1038/ni.2236. PMC 3771401. PMID 22327569.
  5. Wu X, Conway JA, Kim J, Kappes JC (October 1994). "Localization of the Vpx packaging signal within the C terminus of the human immunodeficiency virus type 2 Gag precursor protein". Journal of Virology. 68 (10): 6161–9. doi:10.1128/JVI.68.10.6161-6169.1994. PMC 237035. PMID 8083957.
  6. Fujita M, Otsuka M, Miyoshi M, Khamsri B, Nomaguchi M, Adachi A (August 2008). "Vpx is critical for reverse transcription of the human immunodeficiency virus type 2 genome in macrophages". Journal of Virology. 82 (15): 7752–6. doi:10.1128/JVI.01003-07. PMC 2493314. PMID 18495778.
  7. Bouzar AB, Guiguen F, Morin T, Villet S, Fornazero C, Garnier C, et al. (April 2003). "Specific G2 arrest of caprine cells infected with a caprine arthritis encephalitis virus expressing vpr and vpx genes from simian immunodeficiency virus". Virology. 309 (1): 41–52. doi:10.1016/S0042-6822(03)00014-X. PMID 12726725.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.