首页> 美国卫生研究院文献>Molecular and Cellular Biology >The Paired-Domain Transcription Factor Pax8 Binds to the Upstream Enhancer of the Rat Sodium/Iodide Symporter Gene and Participates in Both Thyroid-Specific and Cyclic-AMP-Dependent Transcription
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The Paired-Domain Transcription Factor Pax8 Binds to the Upstream Enhancer of the Rat Sodium/Iodide Symporter Gene and Participates in Both Thyroid-Specific and Cyclic-AMP-Dependent Transcription

机译:配对域转录因子Pax8绑定到大鼠钠/碘化物转运体基因的上游增强子并参与甲状腺特异性和依赖环AMP的转录。

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摘要

The gene encoding the Na/I symporter (NIS) is expressed at high levels only in thyroid follicular cells, where its expression is regulated by the thyroid-stimulating hormone via the second messenger, cyclic AMP (cAMP). In this study, we demonstrate the presence of an enhancer that is located between nucleotides −2264 and −2495 in the 5′-flanking region of the NIS gene and that recapitulates the most relevant aspects of NIS regulation. When fused to either its own or a heterologous promoter, the NIS upstream enhancer, which we call NUE, stimulates transcription in a thyroid-specific and cAMP-dependent manner. The activity of NUE depends on the four most relevant sites, identified by mutational analysis. The thyroid-specific transcription factor Pax8 binds at two of these sites. Mutations that interfere with Pax8 binding also decrease transcriptional activity of the NUE. Furthermore, expression of Pax8 in nonthyroid cells results in transcriptional activation of NUE, strongly suggesting that the paired-domain protein Pax8 plays an important role in NUE activity. The NUE responds to cAMP in both protein kinase A-dependent and -independent manners, indicating that this enhancer could represent a novel type of cAMP responsive element. Such a cAMP response requires Pax8 but also depends on the integrity of a cAMP responsive element (CRE)-like sequence, thus suggesting a functional interaction between Pax8 and factors binding at the CRE-like site.
机译:编码Na / I转运蛋白(NIS)的基因仅在甲状腺滤泡细胞中以高水平表达,而其表达受促甲状腺激素通过第二信使环状AMP(cAMP)调节。在这项研究中,我们证明了存在增强子,该增强子位于NIS基因5'侧翼区域的核苷酸-2264和-2495之间,概括了NIS调节的最相关方面。当与自身或异源启动子融合时,我们称为NUE的NIS上游增强子以甲状腺特异性和cAMP依赖性方式刺激转录。 NUE的活性取决于通过突变分析确定的四个最相关的位点。甲状腺特异性转录因子Pax8在其中两个位点结合。干扰Pax8结合的突变也会降低NUE的转录活性。此外,Pax8在非甲状腺细胞中的表达导致NUE的转录激活,强烈暗示配对域蛋白Pax8在NUE活性中起重要作用。 NUE以蛋白激酶A依赖性和非依赖性方式对cAMP响应,表明该增强子可以代表新型的cAMP响应元件。这种cAMP反应需要Pax8,但也取决于cAMP响应元件(CRE)样序列的完整性,因此表明Pax8与在CRE样位点结合的因子之间存在功能性相互作用。

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