Mondesert G, Tribouley C, Kedinger C
Laboratoire de Génétique Moléculaire des Eucaryotes (CNRS), Unité 184 (INSERM), Laboratoire de Chimie Biologique, Faculté de Médecine, Strasbourg, France.
Nucleic Acids Res. 1992 Aug 11;20(15):3881-9. doi: 10.1093/nar/20.15.3881.
The adenovirus major late promotor (MLP) is induced to very high levels after the onset of the viral DNA replication. Previous studies have identified sequence elements located downstream of the MLP startsite (DE1, between +85 and +98; DE2, between +100 and +120) implicated, together with the upstream promoter element, in this late-phase-specific transcriptional activation. One protein (DEF, now renamed DEF-A), induced during the late phase of viral infection, has been identified and shown to bind to the DE1 element (Jansen-Durr et al., 1989, J. Virol. 63, 5124-5132). Here we report about a distinct late-phase-specific protein (DEF-B) and its interactions with DEF-A. DNA-binding studies reveal that DEF-B interacts with the 5' part of DE2 (DE2b), whereas DEF-A, besides its interaction with DE1, also binds to the 3' portion of DE2 (DE2a), but with a lower affinity than for DE1. Furthermore, when added together, DEF-A and DEF-B cooperatively assemble onto the DE2 element as a heteromeric complex which is substantially more stable than the complexes formed by each protein alone. Using an in vivo transcriptional assay of the MLP, we show that DEF-A and DEF-B both have intrinsic transactivating properties.
腺病毒主要晚期启动子(MLP)在病毒DNA复制开始后被诱导至非常高的水平。先前的研究已经确定了位于MLP起始位点下游的序列元件(DE1,在+85至+98之间;DE2,在+100至+120之间),连同上游启动子元件一起,参与了这种晚期特异性转录激活。一种在病毒感染晚期诱导产生的蛋白质(DEF,现重新命名为DEF-A)已被鉴定出来,并显示与DE1元件结合(Jansen-Durr等人,1989年,《病毒学杂志》63卷,5124 - 5132页)。在这里,我们报告一种不同的晚期特异性蛋白质(DEF-B)及其与DEF-A的相互作用。DNA结合研究表明,DEF-B与DE2的5'部分(DE2b)相互作用,而DEF-A除了与DE1相互作用外,也与DE2的3'部分(DE2a)结合,但亲和力低于与DE1的结合。此外,当一起添加时,DEF-A和DEF-B作为异源复合物协同组装到DE2元件上,该复合物比每种蛋白质单独形成的复合物稳定得多。使用MLP的体内转录测定,我们表明DEF-A和DEF-B都具有内在的反式激活特性。