Suppr超能文献

小鼠Gabpα/ATP合酶偶联因子6双向启动子中功能元件的鉴定

Identification of functional elements in the murine Gabp alpha/ATP synthase coupling factor 6 bi-directional promoter.

作者信息

Patton John, Block Scott, Coombs Chris, Martin Mark E

机构信息

Department of Biochemistry, University of Missouri, Columbia, MO 65212, USA.

出版信息

Gene. 2006 Mar 15;369:35-44. doi: 10.1016/j.gene.2005.10.009. Epub 2005 Nov 23.

Abstract

The GA-repeat binding protein (GABP) is a ubiquitous transcription factor involved in transcriptional regulation of genes encoding proteins involved in a variety of cellular processes including adipocyte differentiation, mitochondrial respiration, and neuromuscular signaling. GABP is composed of two subunits; the GABP alpha subunit is a member of the Ets-family of transcription factors, and the unrelated ankyrin repeat containing GABP beta subunit. We previously identified a bidirectional promoter directing the expression of Gabpa (GAA) gene in one direction and ATP Synthase Coupling Factor 6 (Atp5j) (CF6) gene in the other [Chinenov, Y., Coombs, C. and Martin, M. E., 2000a. "Isolation of a bi-directional promoter directing the expression of the mouse GABP alpha and ATP Synthase Coupling Factor 6 genes. Gene 261:311-320.]. In this study we characterize sequence elements and regulatory factors contributing to the promoter activities of the GAA/CF6 bidirectional promoter. The core of the GAA/CF6 bidirectional promoter is retained within a 400 bp sequence and contains four GABP binding sites, a Sp1/3 binding site and an YY1 binding site. Site-directed mutagenesis demonstrated that while no single factor binding site was essential for promoter activity in either direction, the GA1 site located proximal to the previously mapped transcription start sites functioned cooperatively with the other GABP binding sites and with the Sp1/3 and YY1 sites to provide transcriptional activation of the GAA and CF6 promoters. The other GABP sites and the Sp1/3 and YY1 binding sites were functionally redundant for basal promoter activities in both directions. Electrophoretic mobility shift assays identified multiple DNA-protein complexes containing GABP alpha, GABP beta, Sp1, Sp3 or YY1 proteins, including one ternary complex containing GABP alpha, GABP beta and Sp1 proteins. Binding of GABP to the GAA/CF6 bi-directional promoter provides the potential for autoregulation of GABP alpha expression and confirms the importance of GABP in the coordinate expression of respiratory chain components.

摘要

GA 重复序列结合蛋白(GABP)是一种普遍存在的转录因子,参与多种细胞过程中相关蛋白编码基因的转录调控,这些细胞过程包括脂肪细胞分化、线粒体呼吸和神经肌肉信号传导。GABP 由两个亚基组成;GABPα亚基是 Ets 家族转录因子的成员,而不相关的含锚蛋白重复序列的 GABPβ亚基。我们之前鉴定了一个双向启动子,它在一个方向上指导 Gabpa(GAA)基因的表达,在另一个方向上指导 ATP 合酶偶联因子 6(Atp5j)(CF6)基因的表达[Chinenov, Y., Coombs, C. 和 Martin, M. E., 2000a. “分离一个双向启动子,指导小鼠 GABPα和 ATP 合酶偶联因子 6 基因的表达。基因 261:311 - 320。”]。在本研究中,我们对有助于 GAA/CF6 双向启动子启动子活性的序列元件和调控因子进行了表征。GAA/CF6 双向启动子的核心保留在一个 400 bp 的序列内,包含四个 GABP 结合位点、一个 Sp1/3 结合位点和一个 YY1 结合位点。定点诱变表明,虽然没有单个因子结合位点对任一方向的启动子活性是必需的,但位于先前定位的转录起始位点近端的 GA1 位点与其他 GABP 结合位点以及 Sp1/3 和 YY1 位点协同作用,以提供 GAA 和 CF6 启动子的转录激活。其他 GABP 位点以及 Sp1/3 和 YY1 结合位点在两个方向上对基础启动子活性在功能上是冗余的。电泳迁移率变动分析鉴定了多种包含 GABPα、GABPβ、Sp1、Sp3 或 YY1 蛋白的 DNA - 蛋白质复合物,包括一种包含 GABPα、GABPβ和 Sp1 蛋白的三元复合物。GABP 与 GAA/CF6 双向启动子的结合为 GABPα表达的自动调节提供了可能性,并证实了 GABP 在呼吸链成分协同表达中的重要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验