Kristie T M, Sharp P A
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
J Biol Chem. 1993 Mar 25;268(9):6525-34.
The assembly of specific multiprotein complexes on the herpes simplex virus alpha/IE (immediate early) enhancer elements requires the interactions of the Oct-1 POU homeodomain, the viral alpha TIF (alpha-trans-induction factor) (VP16), and at least one additional cellular factor, the C1 factor. The C1 factor interacts directly with alpha TIF, likely forming an intermediate protein complex that recognizes the Oct-1 homeodomain-DNA complex. The biochemical purification of the mammalian C1 factor suggests that it is composed of multiple subunits of related, but heterogeneous, polypeptides. The interaction of a subset of these polypeptides with alpha TIF is stimulated by post-translational modifications of the C1 proteins, suggesting that this factor may be a critical target for the regulation of the herpes simplex virus alpha/IE transcription.
在单纯疱疹病毒α/IE(立即早期)增强子元件上组装特定的多蛋白复合物需要Oct-1 POU同源结构域、病毒α TIF(α反式诱导因子)(VP16)以及至少一种其他细胞因子C1因子之间的相互作用。C1因子直接与α TIF相互作用,可能形成一种中间蛋白复合物,该复合物可识别Oct-1同源结构域-DNA复合物。哺乳动物C1因子的生化纯化表明,它由相关但异质的多肽的多个亚基组成。这些多肽的一个子集与α TIF的相互作用受到C1蛋白翻译后修饰的刺激,这表明该因子可能是单纯疱疹病毒α/IE转录调控的关键靶点。