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TR4孤儿受体对人睫状神经营养因子受体(CNTFRα)基因内含子增强子的诱导作用。类固醇受体超家族的一个成员。

Induction of the intronic enhancer of the human ciliary neurotrophic factor receptor (CNTFRalpha) gene by the TR4 orphan receptor. A member of steroid receptor superfamily.

作者信息

Young W J, Smith S M, Chang C

机构信息

Endocrinology-Reproductive Physiology Program, Comprehensive Cancer Center, University of Wisconsin, Madison, Wisconsin 53792, USA.

出版信息

J Biol Chem. 1997 Jan 31;272(5):3109-16. doi: 10.1074/jbc.272.5.3109.

Abstract

A conserved hormone response element, CNTFR-DR1 (5'-AGGTCAGAGGTCAGG-3'), has been identified in the 5th intron of the alpha component of the ciliary neurotrophic factor receptor (CNTFRalpha) gene for the human TR4 orphan receptor (TR4). Electrophoretic mobility shift assay showed a specific binding with high affinity (Kd = 0.066 nM) between TR4 and the CNTFR-DR1. A reporter gene assay using chloramphenicol acetyltransferase demonstrated that the 5th intron of CNTFRalpha has an enhancer activity which could be induced by TR4 in a dose-dependent manner. Furthermore, our in situ hybridization data showed that abundant TR4 transcripts were detected in adult brain, in regions of cortical and hippocampal neurons, as well as in many developing neural structures, including brain, spinal cord, ganglia (sympathetic and sensory), and neuronal epithelia (retinal, otic, olfactory, and gustatory). The striking similarities in the expression patterns of TR4 and CNTFRalpha in the developing and postnatal nervous systems further support the potential role of TR4 in neurogenesis. Collectively, these data suggest that the human CNTFRalpha gene could represent the first identified neural-specific gene induced by TR4.

摘要

在人类TR4孤儿受体(TR4)的睫状神经营养因子受体(CNTFRα)基因α亚基的第5内含子中,已鉴定出一个保守的激素反应元件CNTFR - DR1(5'-AGGTCAGAGGTCAGG-3')。电泳迁移率变动分析显示TR4与CNTFR - DR1之间存在高亲和力的特异性结合(Kd = 0.066 nM)。使用氯霉素乙酰转移酶的报告基因分析表明,CNTFRα的第5内含子具有增强子活性,该活性可被TR4以剂量依赖的方式诱导。此外,我们的原位杂交数据显示,在成人大脑中,在皮质和海马神经元区域以及许多发育中的神经结构中,包括脑、脊髓、神经节(交感神经和感觉神经节)和神经上皮(视网膜、耳、嗅觉和味觉上皮)中,均检测到丰富的TR4转录本。TR4和CNTFRα在发育中和出生后神经系统中的表达模式惊人相似,这进一步支持了TR4在神经发生中的潜在作用。总体而言,这些数据表明人类CNTFRα基因可能是首个被TR4诱导的神经特异性基因。

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