Identification of transactivation-response sequences in the long terminal repeat of bovine immunodeficiency-like virus
Susan Carpenter, Susan A. Nadin‐Davis, Yvonne Wannemuehler, James A. Roth
Abstract
Susan Carpenter, Susan A. Nadin‐Davis, Yvonne Wannemuehler, James A. Roth
Abstract
Transient expression assays using the reporter gene that encodes chloramphenicol acetyltransferase were used to identify cis-acting sequences necessary for bovine immunodeficiency-like virus (BIV) transactivation. Computer analyses identified two RNA stem-loop structures located immediately downstream of the transcription start site in the long terminal repeat. Deletion analysis of the long terminal repeat indicated that sequences containing the proximal stem-loop structure located between +4 and +31 are required for virus-specific transactivation. Therefore, BIV likely utilizes a mechanism of transactivation similar to that of the human and simian lentiviruses.
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Transient expression assays using the reporter gene that encodes chloramphenicol acetyltransferase were used to identify cis-acting sequences necessary for bovine immunodeficiency-like virus (BIV) transactivation. Computer analyses identified two RNA stem-loop structures located immediately downstream of the transcription start site in the long terminal repeat. Deletion analysis of the long terminal repeat indicated that sequences containing the proximal stem-loop structure located between +4 and +31 are required for virus-specific transactivation. Therefore, BIV likely utilizes a mechanism of transactivation similar to that of the human and simian lentiviruses.
Key concepts: Transactivation, Biology, Long terminal repeat, Chloramphenicol acetyltransferase, HIV Long Terminal Repeat, Reporter gene, Virology, Gene