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大鼠CCAAT/增强子结合蛋白α基因启动子区域的特性及其在大鼠永生化棕色脂肪细胞中受甲状腺激素的调控

Characterization of the promoter region of the rat CCAAT/enhancer-binding protein alpha gene and regulation by thyroid hormone in rat immortalized brown adipocytes.

作者信息

Menéndez-Hurtado A, Santos A, Pérez-Castillo A

机构信息

Instituto de Investigaciones Biomédicas, Consejo Superior de Investigaciones Cientificas-Universidad Autónoma de Madrid, Spain.

出版信息

Endocrinology. 2000 Nov;141(11):4164-70. doi: 10.1210/endo.141.11.7756.

Abstract

CCAAT/enhancer binding proteins (C/EBP) are a family of transcription factors with a highly conserved basic/leucine zipper (bZIP) domain that has been implicated in the transcriptional control of genes involved in cell growth and differentiation. We have previously demonstrated that the expression of C/EBPalpha and C/EBPbeta genes is regulated by thyroid hormone in rat liver during development. The aim of the present study was to explore the molecular mechanisms underlying the control of C/EBPalpha gene expression by thyroid hormone. To achieve this goal, we isolated and characterized a genomic clone containing 1171 bp of the 5'-flanking region of the rat C/EBPalpha gene. This fragment was an active promoter in MB492 cells, an immortalized brown adipocyte cell line that expresses the endogenous C/EBPalpha gene in a T3-dependent manner. Sequence analysis suggested the presence of three thyroid hormone response elements, TRE-1 (-602/-589), TRE2 (-411/-396), and TRE3 (-376/-350). The results of deletion, mutagenesis, and gel mobility shift analysis disclosed that only TRE-1, an ER2-type response element, represented a functional T3 response element. Our results demonstrate that T3 is a factor that positively regulates C/EBPalpha gene expression in a direct fashion.

摘要

CCAAT/增强子结合蛋白(C/EBP)是一类转录因子家族,具有高度保守的碱性/亮氨酸拉链(bZIP)结构域,该结构域与参与细胞生长和分化的基因的转录调控有关。我们之前已经证明,在发育过程中,大鼠肝脏中C/EBPα和C/EBPβ基因的表达受甲状腺激素调控。本研究的目的是探索甲状腺激素调控C/EBPα基因表达的分子机制。为实现这一目标,我们分离并鉴定了一个基因组克隆,该克隆包含大鼠C/EBPα基因5'侧翼区的1171 bp。该片段在MB492细胞中是一个活性启动子,MB492细胞是一种永生化的棕色脂肪细胞系,以T3依赖的方式表达内源性C/EBPα基因。序列分析表明存在三个甲状腺激素反应元件,即TRE-1(-602/-589)、TRE2(-411/-396)和TRE3(-376/-350)。缺失、诱变和凝胶迁移率变动分析结果表明,只有TRE-1(一种ER2型反应元件)代表功能性T3反应元件。我们的结果表明,T3是一种以直接方式正向调节C/EBPα基因表达的因子。

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