Xie Heidi Q, Leung K Wing, Chen Vicky P, Lau Faye T C, Liu Lois S, Choi Roy C Y, Tsim Karl W K
Department of Biology and Center for Chinese Medicine, The Hong Kong University of Science and Technology, Clear Water Bay Road, Kowloon, Hong Kong SAR, China.
Chem Biol Interact. 2008 Sep 25;175(1-3):79-82. doi: 10.1016/j.cbi.2008.04.028. Epub 2008 May 2.
The tetrameric globular form of acetylcholinesterase (G(4) AChE) is present and precisely controlled in muscles. The assembly and membrane targeting of G(4) AChE are directed by a proline-rich membrane anchor (PRiMA). It has been demonstrated that in muscle cells, the expression of PRiMA mRNA, as well as the level of G(4) AChE was suppressed by myogenesis and innervating nerve. A human PRiMA promoter-driven luciferase reporter was employed in this study to further reveal the activity of PRiMA transcription during myogenic differentiation and the influence of innervation. In parallel with PRiMA mRNA, the PRiMA promoter activity was suppressed by both myogenic regulatory factor(s) (MRFs) and nerve-derived factor(s). These results suggest that the regulation of PRiMA mRNA expression in muscle by MRFs and nerve-derived factors is due to a control system at the transcriptional level.
乙酰胆碱酯酶的四聚体球状形式(G(4) AChE)存在于肌肉中且受到精确调控。G(4) AChE的组装和膜靶向由富含脯氨酸的膜锚定蛋白(PRiMA)指导。已经证明,在肌肉细胞中,PRiMA mRNA的表达以及G(4) AChE的水平受到肌生成和支配神经的抑制。本研究采用人PRiMA启动子驱动的荧光素酶报告基因,以进一步揭示PRiMA转录在肌源性分化过程中的活性以及神经支配的影响。与PRiMA mRNA平行,PRiMA启动子活性受到肌源性调节因子(MRFs)和神经源性因子的抑制。这些结果表明,MRFs和神经源性因子对肌肉中PRiMA mRNA表达的调节是由于转录水平的控制系统。