一种直接调节类视黄醛受体转录激活的神经元特异性分化蛋白。

Kenneth W Henry II, Michael L Spencer, Maria Theodosiou, Dingyuan Lou, Daniel J Noonan
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引用次数: 6

摘要

背景:核受体调节基因表达能力的特异性在于其结合特定亲脂配体的能力,与特定二聚化伙伴结合的能力,以及结合基因启动子区域特定DNA序列的能力。这一系列事件似乎是靶向由多种蛋白质和RNA组分组成的额外调节复合体的基础,该复合体可传递促进或抑制RNA聚合酶复合体的信号。这些共调节复合物的组织和细胞特异性组分的表征似乎是我们理解核受体调控转录的组成部分。结果:一种对类视黄酸x受体(RXR)转录激活敏感的新型酵母筛选分离到了小鼠NPDC-1基因的大鼠同源物。NPDC-1可能通过与细胞周期促进转录因子E2F-1的相互作用参与神经细胞增殖和分化的控制。尽管NPDC-1的氨基酸序列在小鼠、大鼠和人类同源物之间高度保守,但它们的组织特异性表达有所不同。在体外实验中观察到NPDC-1、RXR和视黄酸受体β (rrbeta)之间可能存在直接蛋白:蛋白相互作用,NPDC-1促进了RXR同型二聚体和RAR-RXR异源二聚体的DNA结合。NPDC-1的表达也被观察到抑制由类视黄醛受体以及其他几个核受体家族成员介导的转录,尽管不是普遍的方式。结论:NPDC-1通过与类视黄醛受体的直接相互作用,增强了类视黄醛受体转录复合物的形成和DNA结合功能,但最终抑制了类视黄醛受体介导的基因表达。与NPDC-1一样,类维甲酸及其受体与大脑发育有关,这些数据为NPDC-1和类维甲酸介导神经元分化提供了一个趋同点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A neuronal-specific differentiation protein that directly modulates retinoid receptor transcriptional activation.

A neuronal-specific differentiation protein that directly modulates retinoid receptor transcriptional activation.

A neuronal-specific differentiation protein that directly modulates retinoid receptor transcriptional activation.

A neuronal-specific differentiation protein that directly modulates retinoid receptor transcriptional activation.

BACKGROUND: The specificity of a nuclear receptor's ability to modulate gene expression resides in its ability to bind a specific lipophilic ligand, associate with specific dimerization partners and bind specific DNA sequences in the promoter regions of genes. This sequence of events appears to be the basis for targeting an additional regulatory complex composed of a variety of protein and RNA components that deliver signals for facilitation or inhibition of the RNA polymerase complex. Characterization of the tissue and cell-specific components of these coregulatory complexes appear to be integral to our understanding of nuclear receptor regulation of transcription. RESULTS: A novel yeast screen sensitive to retinoid-X receptor (RXR) transcriptional activation resulted in the isolation of the rat homologue of the mouse NPDC-1 gene. NPDC-1 has been shown to be involved in the control of neural cell proliferation and differentiation, possibly through interactions with the cell cycle promoting transcription factor E2F-1. Although the amino acid sequence of NPDC-1 is highly conserved between mouse, rat and human homologues, their tissue specific expression was seen to vary. A potential for direct protein:protein interaction between NPDC-1, RXR and retinoic acid receptor beta (RARbeta) was observed in vitro and NPDC-1 facilitated RXR homodimer and RAR-RXR heterodimer DNA binding in vitro. Expression of NPDC-1 was also observed to repress transcription mediated by retinoid receptors as well as by several other nuclear receptor family members, although not in a universal manner. CONCLUSIONS: These results suggest that NPDC-1, through direct interaction with retinoid receptors, functions to enhance the transcription complex formation and DNA binding function of retinoid receptors, but ultimately repress retinoid receptor-mediated gene expression. As with NPDC-1, retinoids and their receptors have been implicated in brain development and these data provide a point of convergence for NPDC-1 and retinoid mediation of neuronal differentiation.

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