Winter C G, Wang B, Ballew A, Royou A, Karess R, Axelrod J D, Luo L
Department of Biological Sciences, Stanford University, Stanford, CA 94305, USA.
Cell. 2001 Apr 6;105(1):81-91. doi: 10.1016/s0092-8674(01)00298-7.
Frizzled (Fz) and Dishevelled (Dsh) are components of an evolutionarily conserved signaling pathway that regulates planar cell polarity. How this signaling pathway directs asymmetric cytoskeletal reorganization and polarized cell morphology remains unknown. Here, we show that Drosophila Rho-associated kinase (Drok) works downstream of Fz/Dsh to mediate a branch of the planar polarity pathway involved in ommatidial rotation in the eye and in restricting actin bundle formation to a single site in developing wing cells. The primary output of Drok signaling is regulating the phosphorylation of nonmuscle myosin regulatory light chain, and hence the activity of myosin II. Drosophila myosin VIIA, the homolog of the human Usher Syndrome 1B gene, also functions in conjunction with this newly defined portion of the Fz/Dsh signaling pathway to regulate the actin cytoskeleton.
卷曲蛋白(Fz)和散乱蛋白(Dsh)是进化保守的信号通路的组成部分,该信号通路调节平面细胞极性。这条信号通路如何指导不对称的细胞骨架重组和极化的细胞形态仍然未知。在这里,我们表明果蝇Rho相关激酶(Drok)在Fz/Dsh的下游起作用,介导平面极性通路的一个分支,该分支参与眼睛小眼的旋转,并将肌动蛋白束的形成限制在发育中的翅细胞的单个位点。Drok信号的主要输出是调节非肌肉肌球蛋白调节轻链的磷酸化,从而调节肌球蛋白II的活性。果蝇肌球蛋白VIIA是人类1B型Usher综合征基因的同源物,它也与Fz/Dsh信号通路的这个新定义部分协同作用,以调节肌动蛋白细胞骨架。