Gildor Boaz, Massarwa R'ada, Shilo Ben-Zion, Schejter Eyal D
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Fly (Austin). 2010 Apr-Jun;4(2):145-8. doi: 10.4161/fly.4.2.10954. Epub 2010 Apr 15.
In Drosophila embryos, muscle fiber formation via myoblast fusion relies on essential contributions made by the conserved Arp2/3 microfilament nucleation machinery. Two key nucleation promoting factors (NPFs), SCAR and WASp, have been shown to mediate this aspect of Arp2/3 function. We have used these unique circumstances, to study the requirements and coordination of distinct NPF activities, within a common developmental setting. Our results suggest that, although operating within close spatial and temporal proximity, the two regulators of actin polymerization are used in a step-wise manner and perform separate functional roles. Our approach also allows us to assess the involvement of the Arp2/3 machinery in formation of a distinct, fusion-associated actin structure.
在果蝇胚胎中,成肌细胞融合形成肌纤维依赖于保守的Arp2/3微丝成核机制的重要作用。已证实两种关键的成核促进因子(NPFs),即SCAR和WASp,介导Arp2/3功能的这一方面。我们利用这些独特的情况,在共同的发育环境中研究不同NPF活性的要求和协调。我们的结果表明,尽管在空间和时间上紧密相邻发挥作用,但肌动蛋白聚合的这两种调节因子是以逐步方式使用的,并发挥各自独立的功能作用。我们的方法还使我们能够评估Arp2/3机制在形成一种独特的、与融合相关的肌动蛋白结构中的作用。