作者: L Huang , C L Malone , M F Stinski
DOI: 10.1128/JVI.68.4.2108-2117.1994
关键词: Biology 、 Transcription factor 、 Plasma protein binding 、 DNA-binding protein 、 CAAT box 、 Molecular biology 、 Viral protein 、 Immediate early protein 、 Dyad symmetry 、 Viral envelope
摘要: The human cytomegalovirus early promoter for the UL4 gene, which codes an viral envelope glycoprotein designated gpUL4, requires immediate-early protein two (IE2) synthesis to be activated (C.-P. Chang, C. L. Malone, and M. F. Stinski, J. Virol. 63:281, 1989). We investigated cis-acting trans-acting factors that regulate transcription from this promoter. In transient transfection assays, IE2 negated effect of upstream negative element enhanced downstream gene expression. A positive contributed activity when was deleted or present. cellular protein(s) binds further investigation. characterized. Two DNA sequence-specific complexes were detected with probes spanning region containing cytomegalovirus-infected fibroblast cell nuclear extracts. more slowly migrating complex labeled A, faster B. Only B mock-infected Competition experiments confirmed specificity complexes. bound in both contacts a CCAAT box imperfect dyad symmetry (5'CCAATCACTGG3'). Either within could compete binding factor. Mutation resulted decrease transcriptional factor, antigenically related factor-Y (NF-Y), found Events associated infection caused phosphorylation A. Dephosphorylation DNA-binding converts NF-Y is not known.