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大鼠肝脏肉碱棕榈酰转移酶I(CPT-Iα)基因的表达受Sp1和核因子Y调控:染色体定位及启动子特征分析

Expression of the rat liver carnitine palmitoyltransferase I (CPT-Ialpha) gene is regulated by Sp1 and nuclear factor Y: chromosomal localization and promoter characterization.

作者信息

Steffen M L, Harrison W R, Elder F F, Cook G A, Park E A

机构信息

Department of Pharmacology, College of Medicine, University of Tennessee, 874 Union Avenue, Memphis, TN 38163, USA.

出版信息

Biochem J. 1999 Jun 1;340 ( Pt 2)(Pt 2):425-32.

Abstract

Carnitine palmitoyltransferase (CPT)-I catalyses the transfer of long-chain fatty acids from CoA to carnitine for translocation across the mitochondrial inner membrane. Expression of the 'liver' isoform of the CPT-I gene (CPT-Ialpha) is subject to developmental, hormonal and tissue-specific regulation. To understand the basis for control of CPT-Ialpha gene expression, we have characterized the proximal promoter of the CPT-Ialpha gene. Here, we report the sequence of 6839 base pairs of the promoter and the localization of the rat CPT-Ialpha gene to region q43 on chromosome 1. Our studies show that the first 200 base pairs of the promoter are sufficient to drive transcription of the CPT-Ialpha gene. Within this region are two sites that bind both Sp1 and Sp3 transcription factors. In addition, nuclear factor Y (NF-Y) binds the proximal promoter. Mutation at the Sp1 or NF-Y sites severely decreases transcription from the CPT-Ialpha promoter. Other protein binding sites were identified within the first 200 base pairs of the promoter by DNase I footprinting, and these elements contribute to CPT-Ialpha gene expression. Our studies demonstrate that CPT-Ialpha is a TATA-less gene which utilizes NF-Y and Sp proteins to drive basal expression.

摘要

肉碱棕榈酰转移酶(CPT)-I催化长链脂肪酸从辅酶A转移至肉碱,以便跨线粒体内膜转运。CPT-I基因的“肝脏”同工型(CPT-Iα)的表达受到发育、激素和组织特异性调控。为了解CPT-Iα基因表达的调控基础,我们对CPT-Iα基因的近端启动子进行了特征分析。在此,我们报告该启动子6839个碱基对的序列以及大鼠CPT-Iα基因在1号染色体q43区域的定位。我们的研究表明,启动子的前200个碱基对足以驱动CPT-Iα基因的转录。在该区域内有两个同时结合Sp1和Sp3转录因子的位点。此外,核因子Y(NF-Y)结合近端启动子。Sp1或NF-Y位点的突变会严重降低CPT-Iα启动子的转录。通过DNase I足迹法在启动子的前200个碱基对内鉴定出其他蛋白质结合位点,这些元件有助于CPT-Iα基因的表达。我们的研究表明,CPT-Iα是一个无TATA盒的基因,它利用NF-Y和Sp蛋白来驱动基础表达。

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