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大鼠钙/钙调蛋白依赖性蛋白激酶IV基因5'侧翼区域中的一个复杂脱氧核糖核酸反应元件介导甲状腺激素诱导和鸡卵清蛋白上游启动子转录因子1抑制。

A complex deoxyribonucleic acid response element in the rat Ca(2+)/calmodulin-dependent protein kinase IV gene 5'-flanking region mediates thyroid hormone induction and chicken ovalbumin upstream promoter transcription factor 1 repression.

作者信息

Liu Yan-Yun, Brent Gregory A

机构信息

Molecular Endocrinology Laboratory, Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, California 90073, USA.

出版信息

Mol Endocrinol. 2002 Nov;16(11):2439-51. doi: 10.1210/me.2001-0324.

Abstract

Ca(2+)/calmodulin-dependent protein kinase IV (CaMKIV) is regulated by T(3) in a time- and concentration-dependent manner in the developing rat brain and plays an important role in neuronal-specific gene regulation. T(3) treatment, but not retinoic acid (RA), stimulated endogenous CaMKIV mRNA 5-fold in mouse embryonic stem (ES) cells differentiated into neurons. We localized a region -750 to -700 in the CaMKIV gene 5'-flanking region that conferred T(3) responsiveness and bound thyroid hormone receptor (TR), retinoic acid receptor (RAR), and chicken ovalbumin upstream promoter-transcription factor 1 (COUP-TF1). T(3) and RA treatment stimulated the CaMKIV hormone response element. Cotransfection of a COUP-TF1 expression vector repressed the T(3) response and augmented the RA response. Mutational analysis identified three half-sites arranged in a direct repeat (AB) and overlapping inverted repeat (BC), required for functional induction and receptor binding. TR and RAR bound predominantly to the BC portion of the element and COUP-TF1 to the AB region, with a close correlation of binding and functional studies. COUP-TF1 binding did not influence TR/retinoid X receptor binding but modestly augmented RAR/retinoid X receptor binding. A single element confers T(3) and COUP-TF1 regulation of CaMKIV expression.

摘要

在发育中的大鼠脑中,钙/钙调蛋白依赖性蛋白激酶IV(CaMKIV)受三碘甲状腺原氨酸(T₃)的时间和浓度依赖性调节,并在神经元特异性基因调控中起重要作用。在分化为神经元的小鼠胚胎干细胞(ES细胞)中,T₃处理而非视黄酸(RA)处理能使内源性CaMKIV mRNA增加5倍。我们在CaMKIV基因5'侧翼区域定位了一个-750至-700的区域,该区域赋予T₃反应性,并与甲状腺激素受体(TR)、视黄酸受体(RAR)和鸡卵清蛋白上游启动子转录因子1(COUP-TF1)结合。T₃和RA处理可刺激CaMKIV激素反应元件。COUP-TF1表达载体的共转染可抑制T₃反应并增强RA反应。突变分析确定了三个以直接重复(AB)和重叠反向重复(BC)排列的半位点,它们是功能诱导和受体结合所必需的。TR和RAR主要与元件的BC部分结合,而COUP-TF1与AB区域结合,结合研究与功能研究密切相关。COUP-TF1结合不影响TR/视黄酸X受体结合,但适度增强RAR/视黄酸X受体结合。单个元件赋予T₃和COUP-TF1对CaMKIV表达的调控。

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