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在单纯疱疹病毒1型α基因调控域内,将定义基础表达的序列与赋予α基因识别能力的序列分开。

Separation of sequences defining basal expression from those conferring alpha gene recognition within the regulatory domains of herpes simplex virus 1 alpha genes.

作者信息

Kristie T M, Roizman B

出版信息

Proc Natl Acad Sci U S A. 1984 Jul;81(13):4065-9. doi: 10.1073/pnas.81.13.4065.

Abstract

The genes of herpes simplex virus 1 form three major groups--alpha, beta, and gamma--whose expression is coordinately regulated and sequentially ordered in a cascade fashion. To determine how the infected cell differentiates between these gene groups, alpha-regulated chimeric genes were constructed in earlier studies by fusing the structural sequences of the thymidine kinase (TK) gene, a beta gene, to the 5' noncoding sequences of alpha genes. These studies showed that (i) one or more structural components of the virion act in trans to increase alpha gene expression and (ii) the 5' noncoding sequences of alpha genes contain cis-acting domains that promote gene expression and confer alpha-gene regulation. These two domains could be moved independently, but the regulatory domain required a promoter for its function. We report here the properties of three sequences containing features common to the regulatory regions of all alpha genes. Sequence 1, containing (G + C)-rich inverted repeats, increased the basal level of TK expression when fused 5' to either the alpha gene 4 promoter or the truncated beta TK promoter. The effect was to some extent orientation dependent. Moreover, sequence 1 restored beta regulation to the truncated beta TK promoter but did not confer alpha-specific regulation on any of the chimeric genes tested. Sequences 2 (49 base pairs) and 3 (29 base pairs), containing an (A + T)-rich homolog from alpha gene 27 and alpha gene 0, respectively, restored alpha-specific regulation to the alpha promoter gene but only sequence 2 conferred alpha regulation on the truncated beta promoter gene. Our results indicate that (i) in natural beta TK the promoter and regulatory domains overlap, (ii) sequence 1 determines basal level of expression and substitutes for a promoter component that is essential for beta but not alpha regulation, and (iii) conversion of a gene with a promoter into an alpha gene requires two elements. Sequence 2 may contain both whereas sequence 3 contains only one.

摘要

单纯疱疹病毒1型的基因形成三个主要组——α、β和γ——它们的表达以级联方式进行协调调节并按顺序排列。为了确定受感染细胞如何区分这些基因组,在早期研究中通过将β基因胸苷激酶(TK)基因的结构序列与α基因的5'非编码序列融合,构建了α调节的嵌合基因。这些研究表明:(i)病毒体的一个或多个结构成分反式作用以增加α基因表达;(ii)α基因的5'非编码序列包含促进基因表达并赋予α基因调节作用的顺式作用结构域。这两个结构域可以独立移动,但调节结构域需要启动子才能发挥功能。我们在此报告三个序列的特性,这些序列包含所有α基因调节区域共有的特征。序列1含有富含(G + C)的反向重复序列,当与α基因4启动子或截短的β TK启动子5'端融合时,可提高TK表达的基础水平。这种效应在一定程度上依赖于方向。此外,序列1将β调节恢复到截短的β TK启动子,但未赋予所测试的任何嵌合基因α特异性调节作用。序列2(49个碱基对)和序列3(29个碱基对)分别含有来自α基因27和α基因0的富含(A + T)的同源序列,它们将α特异性调节恢复到α启动子基因,但只有序列2赋予截短的β启动子基因α调节作用。我们的结果表明:(i)在天然β TK中,启动子和调节结构域重叠;(ii)序列1决定表达的基础水平,并替代对β调节而非α调节必不可少的启动子成分;(iii)将具有启动子的基因转化为α基因需要两个元件。序列2可能同时包含这两个元件,而序列3只包含其中一个。

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