Document 0497 DOCN M9550497 TI HTLV-1 Tax enhances NF-kappa B2 expression and binds to the products p52 and p100, but does not suppress the inhibitory function of p100. DT 9505 AU Murakami T; Hirai H; Suzuki T; Fujisawa J; Yoshida M; Department of Cellular and Molecular Biology, University of; Tokyo, Japan. SO Virology. 1995 Feb 1;206(2):1066-74. Unique Identifier : AIDSLINE MED/95159418 AB Tax protein of HTLV-1 triggers transcriptional activation through enhancers, NF-kappa B binding site, 21-bp enhancer, and serum response element. Previously, we demonstrated binding of Tax to transcription factors NF-kappa B1 p105 and p50. Here, we report that Tax enhances expression of NF-kappa B2 at the mRNA level and proteins; the effect was more apparent on the p52 expression than on its precursor p100, suggesting post-translational regulation. Consistent with these observations, HTLV-1-infected T-cell lines expressed higher levels of p52. Tax binds to the protein products p52 and p100 which inhibits NF-kappa B proteins forming cytoplasmic complexes; the binding to p100 was preferential over NF-kappa B1 p105. However, Tax did not induce efficient dissociation of the cytoplasmic complexes p100/c-Rel or p100/p65, and thus did not induce nuclear translocation of c-Rel or p65. This was in sharp contrast to the previous observation that Tax dissociated the p105/c-Rel and I kappa B-gamma/p65 complexes. These results indicate that HTLV-1 Tax interacts with NF-kappa B2 p100 and p52 and upregulate the NF-kappa B function, but their contribution to Tax-mediated transcriptional regulation differs from those of NF-kappa B1. DE Base Sequence Binding Sites Cell Line Cell Line, Transformed Cell Nucleus/METABOLISM Enhancer Elements (Genetics) Gene Expression Regulation Gene Products, tax/BIOSYNTHESIS/*METABOLISM Hela Cells Human HTLV-I/GENETICS/*METABOLISM Kidney Macromolecular Systems Molecular Sequence Data NF-kappa B/*BIOSYNTHESIS Polymerase Chain Reaction Promoter Regions (Genetics) Protein Binding Proto-Oncogene Proteins/BIOSYNTHESIS Support, Non-U.S. Gov't T-Lymphocytes Transcription, Genetic Transfection Tumor Cells, Cultured JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).