Abstract

The HIV-1 (human immunodeficiency virus type 1) and HIV-2 Tat proteins increase the level of transcription from their corresponding long terminal repeats. Tat activates transcription likely by interaction with components of the transcriptional initiation and elongation complexes during different stages of the transcription reaction. In the current study, two approaches were used to address the sites at which Tat becomes stably associated with the HIV transcription complex. First, we isolated column purified HIV-1 and HIV-2 transcription complexes that were competent for in vitro transcription and found that wild-type but not mutant Tat protein was specifically associated with this complex. An intact HIV TATA element and the presence of functional TATA-binding protein were necessary for Tat association. In contrast, the HIV-1 and HIV-2 TAR bulge sequences which serve as binding sites for Tat were not required for its association with the HIV preinitiation complex. A second complementary approach using immobilized HIV-1 and HIV-2 templates also demonstrated a functional association of Tat with HIV-1 and HIV-2 preinitiation complexes. Wild-type but not mutant Tat proteins associated with transcription complexes assembled on immobilized HIV-1 and HIV-2 templates and the association of Tat correlated with increases in the level of in vitro transcription. These results indicate that Tat can associate with HIV-1 and HIV-2 transcription complexes prior to the initiation of transcription by RNA polymerase II.

Highlights

  • HIV-11 and HIV-2 gene expression is regulated by multiple cis-acting sequences in the LTR and the transactivator protein Tat

  • Tat Is Associated with the HIV-2 Transcription Complex—Our previous in vitro transcription analysis indicated that the HIV-2 LTR could be strongly activated by both the HIV-1 and HIV-2 Tat proteins [5]

  • The HIV-2 LTR template resulted in higher overall levels of basal and Tat-induced transcription than the HIV-1 LTR so that it was a useful template with which to perform in vitro studies to analyze the assembly of preinitiation complexes

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Summary

Introduction

HIV-11 and HIV-2 gene expression is regulated by multiple cis-acting sequences in the LTR and the transactivator protein Tat (reviewed in Refs. 1 and 2). The TAR RNA loop and bulge structures are critical for the binding of RNA polymerase II [24] Both the TAR element and upstream regulatory elements are important in regulating the activation of gene expression by the HIV-1 and HIV-2 Tat proteins. One potential mechanism to explain Tat activation is that the structure of TAR RNA serves to pause the elongating RNA polymerase II and that Tat in conjunction with cellular transcription factors and kinases act on this paused polymerase to increase its processivity Consistent with this model, a recent study demonstrated that Tat was stably associated with components of the HIV-1 transcriptional elongation complex [33]. One of the major questions in understanding HIV-1 and HIV-2 Tat function is what point during HIV transcriptional

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