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CCAAT/增强子结合蛋白是胎盘细胞系中人二型脱碘酶表达的关键调节因子。

CCAAT/enhancer-binding proteins are key regulators of human type two deiodinase expression in a placenta cell line.

机构信息

Laboratory of Molecular Oncology Department of Molecular Medicine, “Sapienza” University of Rome, I-00161 Rome and I-04100 Latina, Italy.

出版信息

Endocrinology. 2012 Aug;153(8):4030-8. doi: 10.1210/en.2011-2113. Epub 2012 Jun 11.

Abstract

An appropriate concentration of intracellular T(3) is a critical determinant of placenta development and function and is mainly controlled by the activity of type II deiodinase (D2). The levels of this enzyme are finely regulated in different tissues by coordinated transcriptional mechanisms, which rely on dedicated promoter sequences (e.g. cAMP response element and TATA elements) that impart inducibility and tissue specificity to Dio2 mRNA expression. Here we show that CCAAT enhancer-binding proteins α and β (C/EBPα and C/EBPβ) promote Dio2 expression in the trophoblastic cell line JEG3 through a conserved CCAAT element, which is a novel key component of the Dio2 promoter code that confers tissue-specific expression of D2 in these cells. Increased C/EBPs levels potently induce Dio2 transcription, whereas their ablation results in loss of Dio2 mRNA. By measuring the activity of several deletion and point mutant promoter constructs, we have identified the functional CCAAT element responsible for this effect, which is located in close proximity to the most 5' TATA box. Notably, this newly identified sequence is highly conserved throughout the species and binds in vivo and in vitro C/EBP, indicating the relevance of this regulatory mechanism. Together, our results unveil a novel mechanism of regulation of D2 expression in a trophoblastic cell line, which may play a relevant role during placenta development.

摘要

细胞内 T(3) 的适当浓度是胎盘发育和功能的关键决定因素,主要由 II 型脱碘酶 (D2) 的活性控制。该酶的水平在不同组织中通过协调的转录机制进行精细调节,这些机制依赖于专用启动子序列(例如 cAMP 反应元件和 TATA 元件),这些序列赋予 Dio2 mRNA 表达的诱导性和组织特异性。在这里,我们表明 CCAAT 增强子结合蛋白 α 和 β(C/EBPα 和 C/EBPβ)通过保守的 CCAAT 元件促进滋养层细胞系 JEG3 中的 Dio2 表达,该元件是 Dio2 启动子编码中的一个新的关键组成部分,赋予这些细胞中 D2 的组织特异性表达。增加 C/EBP 的水平可有力地诱导 Dio2 转录,而它们的缺失导致 Dio2 mRNA 的丢失。通过测量几个缺失和点突变启动子构建体的活性,我们确定了负责这种效应的功能性 CCAAT 元件,该元件位于最靠近 5' TATA 盒的位置。值得注意的是,这个新鉴定的序列在整个物种中高度保守,并且在体内和体外与 C/EBP 结合,表明这种调节机制的相关性。总之,我们的结果揭示了滋养层细胞系中 D2 表达的一种新的调节机制,该机制可能在胎盘发育过程中发挥重要作用。

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