Document 0901 DOCN M9650901 TI The protein tyrosine kinase Fyn activates transcription from the HIV promoter via activation of NF kappa B-like DNA-binding proteins. DT 9605 AU Hohashi N; Hayashi T; Fusaki N; Takeuchi M; Higurashi M; Okamoto T; Semba K; Yamamoto T; Department of Oncology, University of Tokyo, Japan. SO Int Immunol. 1995 Nov;7(11):1851-9. Unique Identifier : AIDSLINE MED/96162443 AB Protein tyrosine kinase p59fyn (Fyn) associates with the TCR-CD3 complex, which suggests that Fyn plays a significant role in the signal transduction involving TCR complex. In addition to cellular genes, viral promoters such as the HIV long terminal repeat (LTR) are also activated upon T cell activation. To elucidate the functional significance of Fyn in the expression of viral promoters, we transfected a Fyn-expression vector together with a reporter plasmid containing the chloramphenicol acetyltransferase gene driven by HIV LTR into a human T cell line, Jurkat. In this assay, Fyn stimulated the promoter in HIV LTR when the transfected cells were treated with both concanavalin A and PMA as an antigen-mimic stimulation. This activation required the intact SH2 domain of Fyn. Mutational analysis of HIV LTR showed that the NF kappa B binding sites were responsible for this effect. Electrophoretic mobility shift assays and UV cross-linking experiments showed that activation of T cells by anti-CD3 antibody induced four kappa B-binding proteins (50, 60, 65 and 100 kDa) in Fyn-overexpressing cells more efficiently than in the parental cells. Our results suggested that Fyn was able to regulate expression of a subset of genes via kappa B-binding proteins upon T cell activation. DE Base Sequence Binding Sites/GENETICS DNA-Binding Proteins/BIOSYNTHESIS/*GENETICS *Gene Expression Regulation Human HIV/*GENETICS Leukemia, T-Cell Molecular Sequence Data NF-kappa B/BIOSYNTHESIS/*GENETICS Promoter Regions (Genetics)/*DRUG EFFECTS Protein-Tyrosine Kinase/*GENETICS/PHYSIOLOGY Proto-Oncogene Proteins/*GENETICS/PHYSIOLOGY Repetitive Sequences, Nucleic Acid/DRUG EFFECTS Support, Non-U.S. Gov't Trans-Activation (Genetics)/DRUG EFFECTS Transcription, Genetic/*DRUG EFFECTS Tumor Cells, Cultured JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).