Schönichen André, Geyer Matthias
Max-Planck-Institut für Molekulare Physiologie, Abteilung Physikalische Biochemie, Otto-Hahn-Str. 11, 44227 Dortmund, Germany.
Biochim Biophys Acta. 2010 Feb;1803(2):152-63. doi: 10.1016/j.bbamcr.2010.01.014. Epub 2010 Jan 25.
The regulation of the actin cytoskeleton is a key process for the stability and motility of eukaryotic cells. Besides the Arp2/3 complex and its nucleation promoting factors, WH2 domain-containing proteins and a diverse family of formin proteins have recently been recognized as actin nucleators and potent polymerization factors of actin filaments. Formins are defined by the presence of a catalytic formin homology 2 (FH2) domain, yet, the modular domain architecture appears significantly different for the eight formin families identified in humans. A diverse picture of protein localization, interaction partners and cell specific regulation emerged, suggesting various functions of formins in the building and maintenance of actin filaments. This review focuses on the domain architecture of human formins, the regulation mechanisms of their activation and the diversity in formin cellular functions.
肌动蛋白细胞骨架的调控是真核细胞稳定性和运动性的关键过程。除了Arp2/3复合体及其成核促进因子外,含WH2结构域的蛋白质和多种formin蛋白家族最近被认为是肌动蛋白成核剂和肌动蛋白丝的有效聚合因子。Formin由催化性的formin同源结构域2(FH2)的存在来定义,然而,在人类中鉴定出的八个formin家族的模块化结构域架构似乎有显著差异。出现了关于蛋白质定位、相互作用伙伴和细胞特异性调控的多样化情况,这表明formin在肌动蛋白丝的构建和维持中具有多种功能。本综述重点关注人类formin的结构域架构、其激活的调控机制以及formin细胞功能的多样性。