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腺病毒主要晚期启动子的复制依赖性激活是由转录因子与第一个内含子中的序列结合增加所介导的。

Replication-dependent activation of the adenovirus major late promoter is mediated by the increased binding of a transcription factor to sequences in the first intron.

作者信息

Jansen-Durr P, Mondésert G, Kédinger C

机构信息

Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Unité 184 de Biologie Moléculaire et de Génie, Génétique de l'INSERM, Faculté de Médecine, Strasbourg, France.

出版信息

J Virol. 1989 Dec;63(12):5124-32. doi: 10.1128/JVI.63.12.5124-5132.1989.

Abstract

During lytic infection, the adenovirus major late promoter (MLP) is primarily activated after the onset of viral DNA replication. Using a combination of DNA binding and in vitro transcription assays, we delineated a discrete MLP element spanning positions +80 to +106 which is essential for the replication-dependent activation of this promoter. We also identified a 40-kilodalton protein (the downstream element factor [DEF]) which binds to the +86-TTGTCAGTTT-+95 motif within this element. Whereas the DEF-binding activity is barely detectable in uninfected cells, it is readily visualized in adenovirus-infected cells, but only after the onset of viral DNA replication. Preventing the interaction of DEF with the MLP template impairs the in vitro transcriptional stimulation. We conclude that this replication-dependent activation of the MLP is, at least in part, mediated by induction of the specific binding of DEF to the MLP downstream element.

摘要

在裂解感染期间,腺病毒主要晚期启动子(MLP)主要在病毒DNA复制开始后被激活。通过结合DNA结合和体外转录分析,我们确定了一个跨越+80至+106位的离散MLP元件,该元件对于该启动子的复制依赖性激活至关重要。我们还鉴定出一种40千道尔顿的蛋白质(下游元件因子[DEF]),它与该元件内的+86-TTGTCAGTTT-+95基序结合。虽然在未感染的细胞中几乎检测不到DEF结合活性,但在腺病毒感染的细胞中很容易观察到,不过仅在病毒DNA复制开始后。阻止DEF与MLP模板的相互作用会损害体外转录刺激。我们得出结论,MLP的这种复制依赖性激活至少部分是由DEF与MLP下游元件的特异性结合的诱导介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37d3/251175/0bdf5e0ee425/jvirol00079-0148-a.jpg

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