Bernard Frédéric, Kasherov Petar, Grenetier Sabrina, Dutriaux Annie, Zider Alain, Silber Joël, Lalouette Alexis
Equipe Génétique Moléculaire de la Différenciation, Institut Jacques Monod, CNRS-Université Paris Diderot, Paris, France.
Dev Biol. 2009 Aug 15;332(2):258-72. doi: 10.1016/j.ydbio.2009.05.573. Epub 2009 Jun 3.
The gene vestigial (vg) plays a key role in indirect flight muscle (IFM) development. We show here that vg is controlled by the Notch anti-myogenic signaling pathway in myoblasts and is regulated by a novel 822 bp enhancer during IFM differentiation. Interestingly, this muscle enhancer is activated in developing fibers and in a small number of myoblasts before the fusion of myoblasts with the developing muscle fibers. Moreover, we show that this enhancer is activated by Drosophila Myocyte enhancing factor 2 (MEF2), Scalloped (SD) and VG but repressed by Twist, demonstrating a sensitivity to differentiation in vivo. In vitro experiments reveal that SD can directly bind this enhancer and MEF2 can physically interact with both SD and TWI. Cumulatively, our data reveal the interplay between different myogenic factors responsible for the expression of an enhancer activated during muscle differentiation.
基因“痕迹”(vg)在间接飞行肌(IFM)发育中起关键作用。我们在此表明,vg在成肌细胞中受Notch抗肌生成信号通路控制,并且在IFM分化过程中受一个新的822 bp增强子调控。有趣的是,这个肌肉增强子在发育中的纤维以及成肌细胞与发育中的肌纤维融合之前的少数成肌细胞中被激活。此外,我们表明这个增强子被果蝇肌细胞增强因子2(MEF2)、扇贝状蛋白(SD)和VG激活,但被扭曲蛋白(Twist)抑制,这表明其在体内对分化敏感。体外实验表明,SD能直接结合这个增强子,且MEF2能与SD和TWI发生物理相互作用。总体而言,我们的数据揭示了负责肌肉分化过程中激活的增强子表达的不同肌生成因子之间的相互作用。