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HIV-1核心启动子缺乏简单的起始元件,但在转录起始位点含有一个双组分激活因子。

HIV-1 core promoter lacks a simple initiator element but contains a bipartite activator at the transcription start site.

作者信息

Zenzie-Gregory B, Sheridan P, Jones K A, Smale S T

机构信息

Howard Hughes Medical Institute, University of California School of Medicine, Los Angeles 90024.

出版信息

J Biol Chem. 1993 Jul 25;268(21):15823-32.

PMID:8340407
Abstract

The human immunodeficiency virus type 1 (HIV-1) core promoter region, extending approximately from nucleotides -40 to +80 relative to the transcription start site, contains a complex array of putative regulatory elements, including a TATA box, an initiator element, an element between the TATA box and start site, binding sites for LBP/UBP, the TAR element, and others. However, because of this elaborate architecture, the precise boundaries and functional roles for the individual regulatory elements have not been defined. To facilitate a detailed analysis of the HIV-1 core promoter, we employed in vitro transcription assays to identify the simplest control elements that activate RNA synthesis in the context of a synthetic, heterologous promoter. Because mutations at the start site previously were shown to diminish transcription, we anticipated finding an initiator as a basic regulator. However, we have demonstrated that the HIV-1 core promoter lacks an initiator that is functionally analogous to those found in the terminal transferase and adenovirus major late promoters. In its place, we identified two elements between -6 and +30, both of which appear to be necessary for significant transcriptional activation. Unlike a strong initiator, the activity of these elements was dependent on the presence of a TATA box and on their position relative to TATA. We have called the region containing these two elements the HIV-1 SSR to distinguish it from the simple transcriptional initiator elements found in other genes.

摘要

人类免疫缺陷病毒1型(HIV-1)核心启动子区域,相对于转录起始位点大约从核苷酸-40延伸至+80,包含一系列复杂的假定调控元件,包括一个TATA盒、一个起始子元件、TATA盒与起始位点之间的一个元件、LBP/UBP的结合位点、TAR元件等。然而,由于这种精细的结构,各个调控元件的确切边界和功能作用尚未明确。为了便于对HIV-1核心启动子进行详细分析,我们采用体外转录试验来鉴定在合成的异源启动子背景下激活RNA合成的最简单调控元件。因为先前已表明起始位点处的突变会减少转录,所以我们预期会发现一个起始子作为基本调控因子。然而,我们已经证明HIV-1核心启动子缺乏一个在功能上类似于末端转移酶和腺病毒主要晚期启动子中发现的起始子。取而代之的是,我们在-6和+30之间鉴定出两个元件,二者对于显著的转录激活似乎都是必需的。与强起始子不同,这些元件的活性依赖于TATA盒的存在以及它们相对于TATA的位置。我们将包含这两个元件的区域称为HIV-1 SSR,以将其与其他基因中发现的简单转录起始子元件区分开来。

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