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宿主细胞结构蛋白HMG I(Y)调节单纯疱疹病毒1型ICP4与其同源启动子的结合。

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

作者信息

Panagiotidis C A, Silverstein S J

机构信息

College of Physicians and Surgeons, Columbia University, New York, New York 10032, USA.

出版信息

Virology. 1999 Mar 30;256(1):64-74. doi: 10.1006/viro.1999.9607.

DOI:10.1006/viro.1999.9607
PMID:10087227
Abstract

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 in in vitro assays and to enhance the activity of this protein in short-term transient expression assays.

摘要

单纯疱疹病毒的增殖感染周期部分受ICP4作用的控制,ICP4是一种立即早期基因产物,它既是转录激活因子又是转录抑制因子。ICP4是自我调节的,编码它的基因IE-3在其帽位点含有该蛋白的高亲和力结合位点。此前,我们已经证明该位点可被未感染细胞核提取物中的蛋白质占据。用含有IE-3基因帽位点的DNA探针筛选HeLa细胞cDNA表达文库,通过该技术鉴定出表达结构染色质蛋白HMG I和HMG Y的克隆。在体外试验中,HMG I可增强ICP4与其同源位点的结合,并在短期瞬时表达试验中增强该蛋白的活性。

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