World Library  
Flag as Inappropriate
Email this Article

Tat (HIV)

Article Id: WHEBN0020938024
Reproduction Date:

Title: Tat (HIV)  
Author: World Heritage Encyclopedia
Language: English
Subject: Syndecan 1, Protein phosphatase 1, IRF1, Respiratory syncytial virus G protein, E2 (HCV)
Collection:
Publisher: World Heritage Encyclopedia
Publication
Date:
 

Tat (HIV)

Tat
Bovine immunodeficiency virus tat–tar complex, nmr, 5 structures
Identifiers
Symbol Tat
Pfam PF00539
InterPro IPR001831
PROSITE PDOC00836
SCOP 1tvs
SUPERFAMILY 1tvs
TCDB 2.A.64
In molecular biology, tat is a protein that is encoded for by the tat gene in HIV-1.[1][2] Tat is a regulatory protein that drastically enhances the efficiency of viral transcription.[2]

Tat stands for "Trans-Activator of Transcription."The protein consists of between 86 and 101 amino acids depending on the subtype.[3]==Function==Tat vastly increases the level of transcription of the HIV dsDNA. Before Tat is present, a small number of RNA transcripts will be made, which allow the Tat protein to be produced. Tat then binds to cellular factors and mediates their phosphorylation, resulting in increased transcription of all HIV genes,[4] providing a positive feedback cycle. This in turn allows HIV to have an explosive response once a threshold amount of Tat is produced, a useful tool for defeating the body's response.

Tat also appears to play a more direct role in the HIV disease process. The protein is released by infected cells in culture, and is found in the blood of HIV-1 infected patients.[5]

It can be absorbed by cells that are not infected with HIV, and can act directly as a toxin producing cell death via apoptosis in uninfected "bystander" T cells, assisting in progression toward AIDS.[6]

By antagonizing the CXCR4 receptor, Tat also appears to selectively encourage the reproduction of less virulent M-tropic (macrophage-tropic) strains of HIV (which use the CCR5 receptor) early in the course of infection, allowing the more rapidly pathogenic T-tropic (T-cell-tropic) strains (which use the CXCR4 receptor) to emerge later after mutating from M-tropic strains.[5]

Function and mechanism

Like other lentiviruses, HIV-1 encodes a trans-activating regulatory protein (Tat), which is essential for efficient transcription of the viral genome.[7][8] Tat acts by binding to an RNA stem-loop structure, the trans-activating response element (TAR), found at the 5′ ends of nascent HIV-1 transcripts. In binding to TAR, Tat alters the properties of the transcription complex, recruits the positive transcription elongation complex (P-TEFb) of cellular CDK9 and cyclin T1, and hence increases the production of full-length viral RNA.[8]

Tat protein also associates with RNA polymerase II complexes during early transcription elongation after the promoter clearance and before the synthesis of full-length TAR RNA transcript. This interaction of Tat with RNA polymerase II elongation complexes is P-TEFb-independent. There are two Tat binding sites on each transcription elongation complex; one is located on TAR RNA and the other one on RNA polymerase II near the exit site for nascent mRNA transcripts which suggests that two Tat molecules are involved in performing various functions during a single round of HIV-1 mRNA synthesis.[9]

The minimum Tat sequence that can mediate specific TAR binding in vitro has been mapped to a basic domain of 10 amino acids, comprising mostly Arg and Lys residues. Regulatory activity, however, also requires the 47 N-terminal residues, which interact with components of the transcription complex and function as a transcriptional activation domain.[8][10][11]

Tat also uses an unusual transcellular transport pathway. Firstly, it binds with high affinity to phosphatidylinositol (4,5) bisphosphate (PI(4,5)P2), found on the inner surface of the cell membrane, this enables Tat recruitment at this level. Tat then crosses the plasma membrane to reach the extracellular space. Tat secretion by infected cells is highly active, and export is the major destination for HIV-1 Tat.[12]

Structure

The basic region of HIV-Tat protein is suggested to form an alpha helix. The basic region is involved in RNA (TAR, trans-activation response element) binding and Tat proteins thus belong to the family of arginine-rich motif (ARM) RNA binding proteins.[13]

Protein transduction domain

Tat contains a protein transduction domain, and is therefore known as a cell-penetrating peptide.[14] Originally[15] characterised by Frankel and Pabo (1988)[16] and Green and Loewenstein (1988),[17] this domain allows Tat to enter cells by crossing the cell membrane. The amino acid sequence of the protein transduction domain is YGRKKRRQRRR.[14] The nuclear localisation signal found within the domain, GRKKR, mediates further translocation of Tat into the cell nucleus.[18][19] As of 2000 The biological role of this domain and exact mechanism of transfer is unknown.[14]

Clinical significance

Inhibition of Tat has been investigated.[20] It has been suggested that Tat antagonists may be of use in the treatment of HIV infections.[21]

References

  1. ^ Genes, tat at the US National Library of Medicine Medical Subject Headings (MeSH)
  2. ^ a b Debaisieux S, Rayne F, Yezid H, Beaumelle B (2012). "The ins and outs of HIV-1 Tat.". Traffic 13 (3): 355–63.  
  3. ^ Jeang, K. T. (1996) In: Human Retroviruses and AIDS: "A Compilation and Analysis of Nucleic Acid and Amino Acid Sequences". Los Alamos National Laboratory (Ed.) pp. III-3–III-18
  4. ^ Kim JB, Sharp PA (April 2001). "Positive transcription elongation factor B phosphorylates hSPT5 and RNA polymerase II carboxyl-terminal domain independently of cyclin-dependent kinase-activating kinase". J. Biol. Chem. 276 (15): 12317–23.  
  5. ^ a b Xiao H, Neuveut C, Tiffany HL, et al. (October 2000). expansion of coreceptor use by HIV-1"in vivo"Selective CXCR4 antagonism by Tat: implications for . Proc. Natl. Acad. Sci. U.S.A. 97 (21): 11466–71.  
  6. ^ Campbell GR, Pasquier E, Watkins J, Bourgarel-Rey V, Peyrot V, Esquieu D, Barbier P, de Mareuil J, Braguer D, Kaleebu P, Yirrell DL, Loret EP (November 2004). "The glutamine-rich region of the HIV-1 Tat protein is involved in T-cell apoptosis". J. Biol. Chem. 279 (46): 48197–204.  
  7. ^ Vaishnav YN, Wong-Staal F (1991). "The biochemistry of AIDS". Annu. Rev. Biochem. 60: 577–630.  
  8. ^ a b c Mujeeb A, Bishop K, Peterlin BM, Turck C, Parslow TG, James TL (August 1994). "NMR structure of a biologically active peptide containing the RNA-binding domain of human immunodeficiency virus type 1 Tat". Proc. Natl. Acad. Sci. U.S.A. 91 (17): 8248–52.  
  9. ^ Zhou C, Rana TM (July 2002). "A bimolecular mechanism of HIV-1 Tat protein interaction with RNA polymerase II transcription elongation complexes". J. Mol. Biol. 320 (5): 925–42.  
  10. ^ Selby MJ, Peterlin BM (August 1990). "Trans-activation by HIV-1 Tat via a heterologous RNA binding protein". Cell 62 (4): 769–76.  
  11. ^ Kashanchi F, Piras G, Radonovich MF, Duvall JF, Fattaey A, Chiang CM, Roeder RG, Brady JN (January 1994). "Direct interaction of human TFIID with the HIV-1 transactivator Tat". Nature 367 (6460): 295–9.  
  12. ^ Debaisieux S, Rayne F, Yezid H, Beaumelle B (2012). "The ins and outs of HIV-1 Tat.". Traffic 13 (3): 355–63.  
  13. ^ Tahirov TH, Babayeva ND, Varzavand K, Cooper JJ, Sedore SC, Price DH (June 2010). "Crystal structure of HIV-1 Tat complexed with human P-TEFb". Nature 465 (7299): 747–51.  
  14. ^ a b c Schwarze SR, Hruska KA, Dowdy SF (July 2000). "Protein transduction: unrestricted delivery into all cells?". Trends Cell Biol. 10 (7): 290–5.  
  15. ^ Dietz GP, Bähr M (October 2004). "Delivery of bioactive molecules into the cell: the Trojan horse approach".  
  16. ^ Frankel AD, Pabo CO (December 1988). "Cellular uptake of the tat protein from human immunodeficiency virus".  
  17. ^ Green M, Loewenstein PM (December 1988). "Autonomous functional domains of chemically synthesized human immunodeficiency virus tat trans-activator protein". Cell 55 (6): 1179–88.  
  18. ^ Ruben S, Perkins A, Purcell R, et al. (January 1989). "Structural and functional characterization of human immunodeficiency virus Tat protein".  
  19. ^ Hauber J, Malim MH, Cullen BR (March 1989). "Mutational analysis of the conserved basic domain of human immunodeficiency virus tat protein".  
  20. ^ Cook JA, August A, Henderson AJ (July 2002). "Recruitment of phosphatidylinositol 3-kinase to CD28 inhibits HIV transcription by a Tat-dependent mechanism". J. Immunol. 169 (1): 254–60.  
  21. ^ Bedoya LM, Beltrán M, Sancho R, et al. (October 2005). "4-Phenylcoumarins as HIV transcription inhibitors". Bioorg. Med. Chem. Lett. 15 (20): 4447–50.  
This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and USA.gov, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for USA.gov and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
 
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
 
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.
 



Copyright © World Library Foundation. All rights reserved. eBooks from World eBook Library are sponsored by the World Library Foundation,
a 501c(4) Member's Support Non-Profit Organization, and is NOT affiliated with any governmental agency or department.