Pomiès Pascal, Pashmforoush Mohammad, Vegezzi Cristina, Chien Kenneth R, Auffray Charles, Beckerle Mary C
Centre National de la Recherche Scientifique Unité Mixte de Recherche 5237, Centre de Recherches de Biochimie Macromoléculaire, 34293 Montpellier, France.
Mol Biol Cell. 2007 May;18(5):1723-33. doi: 10.1091/mbc.e06-09-0815. Epub 2007 Mar 1.
In this report, an antisense RNA strategy has allowed us to show that disruption of ALP expression affects the expression of the muscle transcription factors myogenin and MyoD, resulting in the inhibition of muscle differentiation. Introduction of a MyoD expression construct into ALP-antisense cells is sufficient to restore the capacity of the cells to differentiate, illustrating that ALP function occurs upstream of MyoD. It is known that MyoD is under the control of serum response factor (SRF), a transcriptional regulator whose activity is modulated by actin dynamics. A dramatic reduction of actin filament bundles is observed in ALP-antisense cells and treatment of these cells with the actin-stabilizing drug jasplakinolide stimulates SRF activity and restores the capacity of the cells to differentiate. Furthermore, we show that modulation of ALP expression influences SRF activity, the level of its coactivator, MAL, and muscle differentiation. Collectively, these results suggest a critical role of ALP on muscle differentiation, likely via cytoskeletal regulation of SRF.
在本报告中,一种反义RNA策略使我们能够证明碱性磷酸酶(ALP)表达的破坏会影响肌肉转录因子肌细胞生成素(myogenin)和肌分化因子(MyoD)的表达,从而导致肌肉分化受到抑制。将MyoD表达构建体导入ALP反义细胞足以恢复细胞的分化能力,这表明ALP的功能发生在MyoD的上游。已知MyoD受血清反应因子(SRF)的控制,SRF是一种转录调节因子其活性受肌动蛋白动力学调节。在ALP反义细胞中观察到肌动蛋白丝束显著减少,用肌动蛋白稳定药物茉莉酮酸甲酯处理这些细胞可刺激SRF活性并恢复细胞的分化能力。此外,我们表明ALP表达的调节会影响SRF活性、其共激活因子MAL的水平以及肌肉分化。总的来说,这些结果表明ALP在肌肉分化中起关键作用,可能是通过对SRF的细胞骨架调节来实现的。