Document 0051 DOCN M95B0051 TI Identification of the Tax interaction region of serum response factor that mediates the aberrant induction of immediate early genes through CArG boxes by HTLV-I Tax. DT 9511 AU Fujii M; Chuhjo T; Minamino T; Masaaki N; Miyamoto K; Seiki M; Department of Molecular Virology and Oncology, Kanazawa; University, Ishikawa, Japan. SO Oncogene. 1995 Jul 6;11(1):7-14. Unique Identifier : AIDSLINE MED/95349938 AB Tax of human T-cell leukemia virus type I (HTLV-I) activates transcription at a CArG box of various immediate early genes such as the proto-oncogene c-fos. To do this, Tax does not directly bind to the CArG box, but instead binds to the CArG binding factor SRF. In this study, we investigated the domain of SRF required for the activation by Tax and studied the role of this domain on transcriptional regulation at the CArG box. Using a fusion protein of SRF with a yeast transcription factor GAL4, the 14 amino acid (aa) portion (aa 422-435) of SRF was identified as the domain required for Tax activation [Tax-responsive region of SRF (TRRS)]. By means of a two hybrid system, we showed that TRRS was essential for the interaction of SRF with Tax in vivo. The over-expression of SRF with a deletion of TRRS inhibited the Tax activation at the CArG box. Thus, TRRS is the domain of SRF that is essential for Tax activation at the CArG box. Unlike to Tax activation, TRRS was not required for TPA (12-o-tetradecanoylphobol-13-acetate) induction at the CArG box, but a TRRS deletion enhanced the basal activity at the CArG box both under serum-starved and TPA-stimulated conditions. These results suggest that TRRS negatively regulates the transcriptional activation function of SRF, and consequently contributes to the low basal activity at the CArG box before TPA induction. DE Amino Acid Sequence Base Sequence DNA-Binding Proteins/*CHEMISTRY/PHYSIOLOGY *Gene Expression Regulation Gene Products, tax/*CHEMISTRY/PHYSIOLOGY Genes, fos *Genes, Immediate-Early Hela Cells Human Molecular Sequence Data Nuclear Proteins/*CHEMISTRY/PHYSIOLOGY Oligodeoxyribonucleotides Support, Non-U.S. Gov't Transcription Factors/CHEMISTRY/PHYSIOLOGY Transcription, Genetic JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).