Abstract
The trans-activator (Tat) proteins of the related but distinct type 1 and type 2 human immunodeficiency viruses (HIV-1 and HIV-2) display incomplete functional reciprocity. One possible explanation of this observation, suggested by computer analysis of potential RNA secondary structures within the viral trans-activation response (TAR) elements, is that HIV-2 Tat requires the presentation of two viral RNA stem-loop sequences for full activity whereas HIV-1 Tat is maximally active upon presentation of a single stem-loop structure. Here, we demonstrate that the HIV-2 long terminal repeat indeed contains two functionally independent TAR elements. However, the second (3') TAR element of HIV-2 is significantly less active than the 5' TAR element and is functionally masked in the context of an intact HIV-2 long terminal repeat. Evidence is presented suggesting that the activities of these two HIV-2 TAR elements reflect, at least in part, their relative distances from the site of transcription initiation. Although the HIV-2 TAR element proximal to the viral mRNA cap site appears to be sufficient for effective trans activation by HIV-2 Tat in vitro, this functional redundancy may nevertheless serve to enhance HIV-2 replication in infected cells in vivo.
MeSH Terms
Animals
Base Sequence
Cell Line
Chromosome Deletion
Cloning, Molecular
Gene Products, tat/genetics
Genes, tat
HIV-2/genetics,growth & development
Humans
Molecular Sequence Data
Mutation
Nucleic Acid Conformation
Trans-Activators/genetics
Transfection
Virus Activation/genetics
Virus Replication
tat Gene Products, Human Immunodeficiency Virus
Chemicals
Gene Products, tat
Trans-Activators
tat Gene Products, Human Immunodeficiency Virus
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Fenrick R
Howard Hughes Medical Institute, Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.
Malim M H
Hauber J
Le S Y
Maizel J
Cullen B R
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