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来自干扰素-α基因的一段46个核苷酸的启动子片段可使一个不相关的启动子具有病毒诱导性。

A 46-nucleotide promoter segment from an IFN-alpha gene renders an unrelated promoter inducible by virus.

作者信息

Ryals J, Dierks P, Ragg H, Weissmann C

出版信息

Cell. 1985 Jun;41(2):497-507. doi: 10.1016/s0092-8674(85)80023-4.

Abstract

A hybrid gene consisting of the human IFN-alpha 1 promoter and a beta-globin transcription unit is expressed correctly only after viral induction. To determine the region required for inducibility, 25 hybrid promoters consisting of varying upstream IFN-alpha 1 and downstream beta-globin promoter moieties were analyzed, and 5'-deletion analysis was performed on an inducible hybrid promoter. An IFN promoter region from position -109 to -64 conferred maximal inducibility on downstream beta-globin promoter segments and even on the intact beta-globin promoter. This region is strikingly conserved among human IFN-alpha and -beta genes. As constitutive expression of the beta-globin gene was not diminished by placing IFN promoter fragments in various positions, induction is attributed largely to positive, rather than to negative control.

摘要

由人干扰素α1启动子和β-珠蛋白转录单元组成的杂种基因只有在病毒诱导后才能正确表达。为了确定诱导性所需的区域,分析了由不同的上游干扰素α1和下游β-珠蛋白启动子部分组成的25个杂种启动子,并对一个可诱导的杂种启动子进行了5'端缺失分析。从-109位到-64位的干扰素启动子区域赋予下游β-珠蛋白启动子片段甚至完整的β-珠蛋白启动子最大的诱导性。该区域在人干扰素α和β基因中极为保守。由于将干扰素启动子片段置于不同位置时β-珠蛋白基因的组成型表达并未减弱,因此诱导主要归因于正调控而非负调控。

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