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首页> 外文期刊>The biochemical journal >Thyroid hormones directly activate the expression of the human and mouse uncoupling protein-3 genes through a thyroid response element in the proximal promoter region
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Thyroid hormones directly activate the expression of the human and mouse uncoupling protein-3 genes through a thyroid response element in the proximal promoter region

机译:甲状腺激素通过近端启动子区域中的甲状腺反应元件直接激活人和小鼠解偶联蛋白3基因的表达

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pThe transcription of the human iUCP3/i (uncoupling protein-3) gene in skeletal muscle is tightly regulated by metabolic signals related to fatty acid availability. However, changes in thyroid status also modulate iUCP3/i gene expression, albeit by unknown mechanisms. We created transgenic mice bearing the entire human iUCP3/i gene to investigate the effect of thyroid hormones on human iUCP3/i gene expression. Treatment of human iUCP3/i transgenic mice with thyroid hormones induced the expression of the human gene in skeletal muscle. In addition, transient transfection experiments demonstrate that thyroid hormones activate the transcription of the human iUCP3/i gene promoter when MyoD and the TR (thyroid hormone receptor) were co-transfected. The action of thyroid hormones on iUCP3/i gene transcription is mediated by the binding of the TR to a proximal region in the iUCP3/i gene promoter that contains a direct repeat structure. An intact DNA sequence of this site is required for thyroid hormone responsiveness and TR binding. Chromatin immunoprecipitation assays revealed that the TR binds this element iin vivo/i. The murine iUcp3/i gene promoter was also dependent on MyoD and responsive to thyroid hormone in transient transfection assays. However, it was much less sensitive to thyroid hormone than the human iUCP3/i promoter. In summary, iUCP3/i gene transcription is activated by thyroid hormone treatment iin vivo/i, and this activation is mediated by a TRE (thyroid hormone response element) in the proximal promoter region. Such regulation suggests a link between iUCP3/i gene expression and the effects of thyroid hormone on mitochondrial function in skeletal muscle./p
机译:>人类 UCP3 (解偶联蛋白3)基因在骨骼肌中的转录受到与脂肪酸利用相关的代谢信号的严格调控。然而,尽管机制未知,甲状腺状态的改变也会调节 UCP3 基因的表达。我们创建了带有整个人类 UCP3 基因的转基因小鼠,以研究甲状腺激素对人类 UCP3 基因表达的影响。用甲状腺激素处理人 UCP3 转基因小鼠可诱导人基因在骨骼肌中的表达。另外,瞬时转染实验表明,当MyoD和TR(甲状腺激素受体)被共转染时,甲状腺激素激活人 UCP3 基因启动子的转录。甲状腺激素对 UCP3 基因转录的作用是通过TR与 UCP3 基因启动子中包含直接重复结构的近端区域的结合而介导的。甲状腺激素反应性和TR结合需要该位点的完整DNA序列。染色质免疫沉淀分析表明TR在体内结合了该元素。在瞬时转染试验中,鼠 Ucp3 基因启动子也依赖于MyoD,并对甲状腺激素有反应。但是,它对甲状腺激素的敏感性远低于人类 UCP3 启动子。总之,UCP3基因的转录在体内通过甲状腺激素治疗被激活,并且这种激活是由近端启动子区域的TRE(甲状腺激素反应元件)介导的。这种调控表明 UCP3 基因表达与甲状腺激素对骨骼肌线粒体功能的影响之间存在联系。

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