Jansen-Durr P, Boeuf H, Kédinger C
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire et de Génie Génetique de l'INSERM, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, France.
Nucleic Acids Res. 1988 May 11;16(9):3771-86. doi: 10.1093/nar/16.9.3771.
The sequence requirements for transcriptional stimulation of the adenovirus major late promoter (MLP) by the products of the early transcription unit Ela and by the replication of viral DNA were analyzed by in vitro transcription. Sequences upstream of +33 are involved in the moderate Ela-responsiveness of the MLP, while sequences between +33 and +131 are required for its major replication-induced transcriptional activation. Dnase I footprinting experiments delineate a sequence component, extending from +76 to +120, which binds protein(s) only in extracts of cells where viral DNA replication occurred. Taken together, these results suggest that the replication-dependent stimulation of the MLP is mediated by the increased binding of this protein(s).
通过体外转录分析了腺病毒主要晚期启动子(MLP)受早期转录单元E1a产物和病毒DNA复制的转录刺激的序列要求。+33上游的序列参与MLP的中度E1a反应性,而+33和+131之间的序列是其主要复制诱导的转录激活所必需的。DNA酶I足迹实验确定了一个从+76延伸到+120的序列成分,该成分仅在发生病毒DNA复制的细胞提取物中与蛋白质结合。综上所述,这些结果表明MLP的复制依赖性刺激是由这种蛋白质结合增加介导的。