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首页> 外文期刊>Brain research >Transcriptional regulation of proline-rich membrane anchor (PRiMA) of globular form acetylcholinesterase in neuron: an inductive effect of neuron differentiation.
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Transcriptional regulation of proline-rich membrane anchor (PRiMA) of globular form acetylcholinesterase in neuron: an inductive effect of neuron differentiation.

机译:神经元中球状乙酰胆碱酯酶的富含脯氨酸的膜锚(PRiMA)的转录调控:神经元分化的诱导作用。

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摘要

The transcriptional regulation of proline-rich membrane anchor (PRiMA), an anchoring protein of tetrameric globular form of acetylcholinesterase (G(4) AChE), was revealed in cultured cortical neurons during differentiation. The level of AChE(T) protein, total enzymatic activity and the amount of G(4) AChE were dramatically increased during the neuron differentiation. RT-PCR analyses revealed that the transcript encoding PRiMA was significantly up-regulated in the differentiated neurons. To investigate the transcriptional mechanism on PRiMA regulation, a reporter construct of human PRiMA promoter-tagged luciferase was employed in this study. Upon the neuronal differentiation in cortical neurons, a mitogen-activated protein (MAP) kinase-dependent pathway was stimulated: this signaling cascade was shown to regulate the transcriptional activity of PRiMA. In addition, both PRiMA and AChE(T) transcripts were induced by the over expression of an active mutant of Raf in the cultured neurons. The treatment of aMAP kinase inhibitor (U0126) significantly blocked the expression of PRiMA transcript and promoter-driven luciferase activity as induced by the differentiation of cortical neurons. These results suggested that a MAP kinase signaling pathway served as one of the transcriptional regulators in controlling PRiMA gene expression during the neuronal differentiation process.
机译:富含脯氨酸的膜锚(PRiMA),乙酰胆碱酯酶(G(4)AChE)的四聚球状形式的锚定蛋白的转录调控,在分化过程中被显示在皮质神经元中。在神经元分化过程中,AChE(T)蛋白的水平,总酶活性和G(4)AChE的量均显着增加。 RT-PCR分析显示,在分化的神经元中,编码PRiMA的转录物显着上调。为了研究PRiMA调控的转录机制,本研究使用了人PRiMA启动子标签的荧光素酶的报告基因构建体。在皮层神经元的神经元分化后,有丝分裂原激活蛋白(MAP)激酶依赖性途径受到刺激:该信号级联反应可调节PRiMA的转录活性。另外,通过培养的神经元中Raf的活性突变体的过表达诱导PRiMA和AChE(T)转录物。 aMAP激酶抑制剂(U0126)的治疗可显着阻断PRiMA转录物的表达以及由皮层神经元分化诱导的启动子驱动的荧光素酶活性。这些结果表明,MAP激酶信号通路在神经元分化过程中作为控制PRiMA基因表达的转录调节因子之一。

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