期刊
BRAIN RESEARCH
卷 1265, 期 -, 页码 13-23出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.brainres.2009.01.065
关键词
AChE; PRiMA; G(4) enzyme; Promoter regulation; Neuron differentiation
资金
- Research Grants Council of Hong Kong [HKUST 6283/03M, 6237/04M, 6404/05M, 662407]
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 AChET 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 AChET transcripts were induced by the over expression of an active mutant of Raf in the cultured neurons. The treatment of a MAP 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. (C) 2009 Elsevier B.V. All rights reserved.
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