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大鼠XDH/XO无TATA启动子多个转录起始位点的正确使用以及C/EBP依赖的转录激活需要位于基因编码区域的下游元件。

Correct usage of multiple transcription initiation sites and C/EBP-dependent transcription activation of the rat XDH/XO TATA-less promoter requires downstream elements located in the coding region of the gene.

作者信息

Clark M P, Chow C W, Rinaldo J E, Chalkley R

机构信息

Department of Medicine, School of Medicine, Vanderbilt University, Nashville, TN 37232, USA.

出版信息

Nucleic Acids Res. 1998 Apr 1;26(7):1801-6. doi: 10.1093/nar/26.7.1801.

Abstract

In the present study, we have shown that a downstream element located in the coding region of the TATA-less rat xanthine dehydrogenase/oxidase (XDH/XO) gene (-7 to +42) plays an important role in transcription initiation and C/EBP transcriptional activation. Previous work from our laboratory has shown that the promoter is organized with multiple initiator elements (Inr 1, 2, 3 and 4) which are important for transcription initiation. Additionally, we had identified two C/EBP binding sites upstream of this promoter. Deletional and mutational studies revealed that C/EBP binding was not essential for the basal level of transcriptional initation. However when XO-luciferase constructs include downstream sequence extending to +42 there is development of C/EBP sensitivity as well as a shift in the initiator usage. In the absence of the downstream element, primer extension analyses reveals Inr 3 and 4 to be the major start sites but in the presence of this additional sequence the usage is shifted to Inr 1 and 2. This shift in Inr usage more closely resembles that seen in intact macrophages or liver cells. Gel mobility shift assays indicate the presence of several binding factors located in this downstream region, one of which has been identified as YY-1. We postulate that YY-1 allows DNA bending which permits the upstream C/EBP elements to exhibit a transcriptional activation which is not seen when the downstream element is absent. This study presents a potential model for regulation of the XDH/XO promoter.

摘要

在本研究中,我们已经表明位于无TATA盒的大鼠黄嘌呤脱氢酶/氧化酶(XDH/XO)基因编码区(-7至+42)的一个下游元件在转录起始和C/EBP转录激活中起重要作用。我们实验室之前的工作表明,该启动子由多个起始子元件(Inr 1、2、3和4)组成,这些元件对转录起始很重要。此外,我们在该启动子上游鉴定出两个C/EBP结合位点。缺失和突变研究表明,C/EBP结合对于转录起始的基础水平并非必需。然而,当XO-荧光素酶构建体包含延伸至+42的下游序列时,会出现C/EBP敏感性以及起始子使用的转变。在没有下游元件的情况下,引物延伸分析显示Inr 3和4是主要起始位点,但在存在该额外序列时,起始子使用转变为Inr 1和2。这种起始子使用的转变更类似于在完整巨噬细胞或肝细胞中观察到的情况。凝胶迁移率变动分析表明在该下游区域存在几种结合因子,其中之一已被鉴定为YY-1。我们推测YY-1允许DNA弯曲,这使得上游C/EBP元件表现出转录激活,而当不存在下游元件时则看不到这种激活。本研究提出了一个XDH/XO启动子调控的潜在模型。

相似文献

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Identification of the rat xanthine dehydrogenase/oxidase promoter.
Nucleic Acids Res. 1994 May 25;22(10):1846-54. doi: 10.1093/nar/22.10.1846.

本文引用的文献

6
Identification of the rat xanthine dehydrogenase/oxidase promoter.
Nucleic Acids Res. 1994 May 25;22(10):1846-54. doi: 10.1093/nar/22.10.1846.

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