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90K免疫刺激基因的表达受具有独特特征的启动子控制。

Expression of the 90K immunostimulator gene is controlled by a promoter with unique features.

作者信息

Brakebusch C, Jallal B, Fusco O, Iacobelli S, Ullrich A

机构信息

Max-Planck-Institute of Biochemistry, Department of Molecular Biology, Am Klopferspitz 18A, 82152 Martinsried, Federal Republic of Germany.

出版信息

J Biol Chem. 1997 Feb 7;272(6):3674-82. doi: 10.1074/jbc.272.6.3674.

Abstract

90K is a secreted glycoprotein with tumor suppressive functions, which is up-regulated in various types of cancer and in AIDS. In order to understand the regulation of its expression, the mouse 90K gene was isolated and analyzed. The gene spans about 8.8-kilobase pairs and consists of 6 exons and was localized on chromosome 11, region E. RNase protection identified one major transcription start site (+1) and three minor ones (-3, +32, +34). The mouse 90K gene was found to have a TATA-less promoter of unusual structure. The 2. 3-kilobase pair 5'-flanking region exhibited strong promoter activity in NIH 3T3 cells; however, it contained neither a TATA-box nor a SP1 site and was not GC-rich. No known initiator motif was found around the transcription start site. 5'- and 3'-deletions defined a minimal promoter of 51 base pairs (-66 --> -16), not including the start site, essential and sufficient for promoter activity. This minimal promoter showed increased activity after stimulation with interferon-gamma or poly(I.C), a substance mimicking viral infection. Essential for both inductions was the integrity of an interferon regulatory factor element within this sequence, a potential binding site for the anti-oncogenic transcription factor interferon regulatory factor-1.

摘要

90K是一种具有肿瘤抑制功能的分泌型糖蛋白,在各种类型的癌症和艾滋病中表达上调。为了了解其表达调控机制,对小鼠90K基因进行了分离和分析。该基因跨度约8.8千碱基对,由6个外显子组成,定位于11号染色体E区域。核糖核酸酶保护实验确定了一个主要转录起始位点(+1)和三个次要转录起始位点(-3、+32、+34)。发现小鼠90K基因具有结构异常的无TATA框启动子。2.3千碱基对的5'侧翼区域在NIH 3T3细胞中表现出较强的启动子活性;然而,它既不包含TATA框也不包含SP1位点,且富含GC。在转录起始位点周围未发现已知的起始子基序。5'和3'缺失确定了一个51个碱基对(-66 --> -16)的最小启动子,不包括起始位点,对启动子活性至关重要且足够。该最小启动子在受到干扰素-γ或聚肌苷酸胞苷酸(一种模拟病毒感染的物质)刺激后活性增强。两种诱导作用所必需的是该序列内干扰素调节因子元件的完整性,它是抗癌转录因子干扰素调节因子-1的潜在结合位点。

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