The bovine leukemia virus (BLV) p34tax (also called tat, p34, XLOR gene product) is a 34-kDa polypeptide encoded in the 3'-terminal region of the virus. This protein is responsible for positive transcriptional trans-activation of promoter elements located within the BLV long-terminal repeat. We introduced the protein-coding region of BLV p34tax into the genome of the baculovirus Autographa californica nuclear polyhedrosis virus. After infection of the insect Spodoptera frugiperda (SF9) cell line, this recombinant strain of baculovirus produced approximately 100 to 150 mg of p34tax per 2 X 10(9) cells. This protein, when introduced into mammalian fibroblasts by using a cell-to-cell fusion technique, functionally trans-activated the BLV long-terminal repeat. Analysis of 32P-labeled proteins of SF9 cells expressing BLV tax by two-dimensional gel electrophoresis indicated that the BLV p34tax was phosphorylated.
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http://dx.doi.org/10.1016/0042-6822(89)90254-7 | DOI Listing |
Cytokine
November 1994
Department of Molecular Biology, University of Brussels (ULB), Rhode-St-Genèse, Belgium.
Bovine leukaemia virus (BLV) is the aetiologic agent of bovine leucosis. The virus induces malignancies of the B-cell lineage (leukaemia/lymphoma). The role played by interleukin 6 (IL-6) in the BLV-induced leukemogenesis process was evaluated.
View Article and Find Full Text PDFBiochem Biophys Res Commun
August 1994
Bay Zoltán Biotechnological Institute, Szeged, Hungary.
Recent studies demonstrated, that the R/U5 region of the Bovine Leukemia Virus (BLV) long terminal repeat (LTR) up-regulates the virus promoter. It is also known that this effect is independent from the BLV trans activator protein, p34tax, encoded by the virus genome. Deletions were constructed in the R/U5 region to localize the sequences responsible for this effect.
View Article and Find Full Text PDFJ Gen Virol
October 1991
Biophysics Laboratory, National Institute of Animal Health, Ibaraki, Japan.
The p34tax protein [p38tax, p34, p38(XBL), XBL-I] of bovine leukaemia virus (BLV) activates transcription from the BLV long terminal repeat (LTR) promoter. To analyse the functional properties of this protein, inframe insertions and internal deletions were systematically introduced in a plasmid-encoded copy of the p34tax gene. The abilities of wild-type and mutant genes to activate gene expression from the LTR promoter linked to the chloramphenicol acetyltransferase gene and to inhibit trans-activation by the wild-type protein were studied.
View Article and Find Full Text PDFOncogene
January 1991
Department of Molecular Biology, Faculty of Agronomy, Gembloux-Belgium.
The specific DNA-binding Gal4 amino-terminal portion (amino acids 1 to 147) was fused to protein segments of BLV transactivator p34tax and tested for its capacity to activate CAT-gene expression in mammalian cells. The p34tax peptide segment 157 to 197 encompasses an activating region. The segment is approximately located in the middle of p34tax and is globally neutral (net charge zero).
View Article and Find Full Text PDFEMBO J
May 1990
Faculty of Agronomy, Gembloux, Belgium.
Human T-lymphotropic viruses (HTLV-I and -II) and bovine leukaemia virus (BLV) express transactivator proteins able to increase long terminal repeat (LTR) directed viral expression. These transacting factors are though to be involved in the induction of leukaemia by these viruses. Transfection of BLV transactivator p34tax together with Ha-ras immortalizes and transforms rat embryo fibroblasts, in vitro.
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