HIV-I TAT Inhibits PKR Activity by Both RNA-Dependent and RNA-Independent Mechanisms

• Published in: Archives of biochemistry and biophysics Vol. 373; no. 2; pp. 361 - 367
• Main Authors: Cai, Ruorong, Carpick, Bruce, Chun, Rene F., Jeang, Kuan-Teh, Williams, Bryan R.G.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.01.2000
• Subjects: AIDS/HIV; Amino Acid Sequence; Animals; COS Cells; eIF-2 Kinase - antagonists & inhibitors; Enzyme Activation; Eukaryotic Initiation Factor-2 - chemistry; Gene Products, tat - genetics; Gene Products, tat - pharmacology; Heparin - pharmacology; HIV-1; Humans; Molecular Sequence Data; Phosphorylation; Protein Binding; Recombinant Fusion Proteins; RNA, Double-Stranded - pharmacology; Sequence Alignment; tat Gene Products, Human Immunodeficiency Virus; Viral Proteins - pharmacology
• ISSN: 0003-9861; 1096-0384
• DOI: 10.1006/abbi.1999.1583

Replication of the human immunodeficiency virus type 1 (HIV-1) is inhibited by interferons (IFNs), in part through activity of the IFN-inducible protein kinase PKR. To escape this antiviral effect, HIV-1 has developed strategies for blocking PKR function. We have previously shown that the HIV-1 Tat protein can associate with PKR in vitro and in vivo and inhibit PKR activity. Here we present evidence that Tat can inhibit PKR activity by both RNA-dependent and RNA-independent mechanisms. Tat inhibited PKR activation by the non-RNA activator heparin, and also suppressed PKR basal level autophosphorylation in the absence of RNA. However, when Tat and dsRNA were preincubated, the amount of Tat required to inhibit PKR activation by dsRNA depended on the dsRNA concentration. In addition to its function in vitro, Tat can also reverse translation inhibition mediated by PKR in COS cells. The Tat amino acid sequence required for interaction with PKR was mapped to residues 40–58, overlapping the hydrophobic core and basic region of HIV-1 Tat. Alignment of amino acid sequences of Tat and eIF-2α indicates similarity between the Tat-PKR binding region and the residues around the eIF-2α phosphorylation site, suggesting that Tat and eIF-2α may bind to the same site on PKR.