IDENTIFICATION OF A NOVEL DOWNSTREAM BINDING-PROTEIN IMPLICATED IN LATE-PHASE-SPECIFIC ACTIVATION OF THE ADENOVIRUS MAJOR LATE PROMOTER

被引:30
|
作者
MONDESERT, G [1 ]
TRIBOULEY, C [1 ]
KEDINGER, C [1 ]
机构
[1] FAC MED STRASBOURG,CHIM BIOL LAB,CNRS,UNITE 184,GENET MOLEC EUCARYOTES LAB,INSERM,11 RUE HUMANN,F-67085 STRASBOURG,FRANCE
关键词
D O I
10.1093/nar/20.15.3881
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The adenovirus major late promoter (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 + 1 00 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., 1 989, 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.
引用
收藏
页码:3881 / 3889
页数:9
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