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单纯疱疹病毒1型晚期基因的表达需要一个特定的15碱基对的TATA盒启动子元件。

A specific 15-bp TATA box promoter element is required for expression of a herpes simplex virus type 1 late gene.

作者信息

Homa F L, Glorioso J C, Levine M

机构信息

Department of Human Genetics, University of Michigan Medical School, Ann Arbor 48109-0618.

出版信息

Genes Dev. 1988 Jan;2(1):40-53. doi: 10.1101/gad.2.1.40.

DOI:10.1101/gad.2.1.40
PMID:2833425
Abstract

The herpes simplex virus type 1 (HSV-1) glycoprotein C (gC) gene is a true late or gamma 2 gene in that its expression shows a strict requirement for viral DNA replication. Elements required for regulated expression of this gene were previously shown to consist of the gC TATA box, transcription start site and a large portion of the leader sequence of the gC gene. In this paper we show that transcription of the gC gene requires a 15-bp sequence, GGGTATAAATTCCGG, which contains the gC TATA box. This sequence contains specific promoter elements because replacement of this sequence with either the TATA box of the HSV-1 early thymidine kinase (tk) gene or two random TATA-like elements results in a transcriptionally inactive gC gene. In addition, we show that temporal expression of HSV beta and gamma genes at early and late times during infection are controlled by separate and distinct regulatory elements; regulatory signals distal to the TATA box are needed for early expression, whereas a gC-like TATA box is needed for late expression. These signals were identified by construction of a chimeric HSV gene that contained the distal control signals of the beta tk gene fused upstream of the TATA sequence of the gamma 2 gC gene. When RNA was isolated at various times postinfection from cells infected with a virus whose genome contained this chimeric tk-gC gene, synthesis of gC mRNA showed both early and late kinetics.

摘要

单纯疱疹病毒1型(HSV - 1)糖蛋白C(gC)基因是一个真正的晚期或γ2基因,因为其表达对病毒DNA复制有严格要求。先前已表明,该基因调控表达所需的元件包括gC TATA框、转录起始位点和gC基因前导序列的一大部分。在本文中,我们表明gC基因的转录需要一个15碱基对的序列GGGTATAAATTCCGG,其中包含gC TATA框。该序列包含特定的启动子元件,因为用HSV - 1早期胸苷激酶(tk)基因的TATA框或两个随机的类TATA元件替换该序列会导致gC基因转录失活。此外,我们表明HSVβ和γ基因在感染早期和晚期的时序表达由单独且不同的调控元件控制;TATA框远端的调控信号是早期表达所必需的,而晚期表达则需要一个类似gC的TATA框。这些信号是通过构建一个嵌合HSV基因来鉴定的,该基因包含βtk基因的远端控制信号,融合在γ2 gC基因TATA序列的上游。当从感染了基因组包含这种嵌合tk - gC基因的病毒的细胞中在感染后的不同时间分离RNA时,gC mRNA的合成显示出早期和晚期动力学。

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