首页> 美国卫生研究院文献>Journal of Virology >A Short cis-Acting Motif in the M112-113 Promoter Region Is Essential for IE3 To Activate M112-113 Gene Expression and Is Important for Murine Cytomegalovirus Replication
【2h】

A Short cis-Acting Motif in the M112-113 Promoter Region Is Essential for IE3 To Activate M112-113 Gene Expression and Is Important for Murine Cytomegalovirus Replication

机译:M112-113启动子区域中的短顺式作用基序对于IE3激活M112-113基因表达至关重要并且对于鼠巨细胞病毒复制很重要

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Immediate-early 3 (IE3) gene products are required to activate early (E)-stage gene expression of murine cytomegaloviruses (MCMV). The first early gene activated by IE3 is the M112-113 gene (also called E1), although a complete understanding of the activation mechanism is still lacking. In this paper, we identify a 10-bp cis-regulating motif upstream of the M112-113 TATA box as important for IE3 activation of M112-113 expression. Results from DNA affinity assays and chromatin immunoprecipitation assays show that the association of IE3 with the M112-113 gene promoter was eliminated by deletion of the 10-bp DNA sequence, now named IE3AM (for IE3 activating motif). In addition, IE3 interacts with TATA box binding protein (TBP), a core protein of TFIID (transcription initiation) complexes. Finally, we created an IE3AM-deleted MCMV (MCMVdIE3AM) using a bacterial artificial chromosome system. The mutant virus can still replicate in NIH 3T3 cells but at a significantly lower level. The defectiveness of the MCMVdIE3AM infection can be rescued in an M112-113-complemented cell line. Our results suggest that the interactions of IE3 with IE3AM and with TBP stabilize the TFIID complex at the M112-113 promoter such that M112-113 gene expression can be activated and/or enhanced.
机译:需要立即早期3(IE3)基因产物来激活鼠巨细胞病毒(MCMV)的早期(E)期基因表达。 IE3激活的第一个早期基因是M112-113基因(也称为E1),尽管仍然缺乏对激活机制的完整理解。在本文中,我们确定了M112-113 TATA盒上游10 bp的顺式调控基序对于IE3激活M112-113表达很重要。 DNA亲和力测定法和染色质免疫沉淀测定法的结果表明,通过删除10 bp DNA序列(现在称为IE3AM(用于IE3激活基序)),可以消除IE3与M112-113基因启动子的联系。另外,IE3与TATA盒结合蛋白(TBP)相互作用,后者是TFIID(转录起始)复合物的核心蛋白。最后,我们使用细菌人工染色体系统创建了一个删除IE3AM的MCMV(MCMVdIE3AM)。突变病毒仍可以在NIH 3T3细胞中复制,但水平要低得多。可以在M112-113互补细胞系中挽救MCMVdIE3AM感染的缺陷。我们的结果表明,IE3与IE3AM以及与TBP的相互作用稳定了M112-113启动子上的TFIID复合物,从而可以激活和/或增强M112-113基因的表达。

著录项

相似文献

  • 外文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号