The host-cell architectural protein HMG I(Y) modulates binding of herpes simplex virus type 1 ICP4 to its cognate promoter.

The host-cell architectural protein HMG I(Y) modulates binding of herpes simplex virus type 1 ICP4 to its cognate promoter.
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宿主细胞结构蛋白 HMG I(Y) 调节 1 型单纯疱疹病毒 ICP4 与其同源启动子的结合。

DOI:
10.1006/viro.1999.9607
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发表时间:
1999
期刊:
Virology.
影响因子:
--
通讯作者:
Silverstein,SJ
Silverstein,SJ
中科院分区:
--
文献类型:
--
作者:
Panagiotidis,CA;Silverstein,SJ

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The productive infection cycle of herpes simplex virus is controlled in part by the action of ICP4, an immediate-early gene product that acts as both an activator and repressor of transcription. ICP4 is autoregulatory, and IE-3, the gene that encodes it, contains a high-affinity binding site for the protein at its cap site. Previously, we had demonstrated that this site could be occupied by proteins found in nuclear extracts from uninfected cells. A HeLa cell cDNA expression library was screened with a DNA probe containing the IE-3 gene cap site, and clones expressing the architectural chromatin proteins HMG I and HMG Y were identified by this technique. HMG I is shown to augment binding of ICP4 to its cognate site inin vitroassays and to enhance the activity of this protein in short-term transient expression assays.
ICP4 与细胞/感染细胞因子的相互作用及其磷酸化状态调节单纯疱疹病毒 DNA 中前导序列的差异识别。
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