Asymmetric colocalization of Flamingo, a seven-pass transmembrane cadherin, and Dishevelled in planar cell polarization

被引:147
作者
Shimada, Y
Usui, T
Yanagawa, S
Takeichi, M
Uemura, T [1 ]
机构
[1] Kyoto Univ, Genet Mol Lab, Inst Virus Res, Kyoto 6068507, Japan
[2] Kyoto Univ, Lab Gene Anal, Inst Virus Res, Kyoto 6068507, Japan
[3] Kyoto Univ, Grad Sch Biostudies, Dept Cell & Dev Biol, Sakyo Ku, Kyoto 6068502, Japan
[4] Japan Sci & Technol, CREST, Yokohama, Kanagawa, Japan
关键词
D O I
10.1016/S0960-9822(01)00233-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Drosophila wing provides an appropriate model system for studying genetic programming of planar cell polarity (PCP) [1-4], Each wing cell respects the proximodistal (PD) axis; i.e., it localizes an assembly of actin bundles to its distalmost vertex and produces a single prehair, This PD polarization requires the redistribution of Flamingo (Fmi), a seven-pass transmembrane cadherin, to proximal/ distal cell boundaries; otherwise, the cell mislocalizes the prehair [5], Achievement of the biased Fmi pattern depends on two upstream components in the PCP signaling pathway: Frizzled (Fz), a receptor for a hypothetical polarity signal, and an intracellular protein, Dishevelled (Dsh) [6-8]. Here, we visualized endogenous Dsh in the developing wing. A portion of Dsh colocalized with Fmi, and the distributions of both proteins were interdependent. Furthermore, Fz controlled the association of Dsh with cell boundaries, which association was correlated with the presence of hyperphosphorylated forms of Dsh, Our results, together with a recent study on Fz distribution [9], support the possibility that Fz, Dsh, and Fmi constitute a signaling complex and that its restricted localization directs cytoskeletal reorganization only at the distal cell edge.
引用
收藏
页码:859 / 863
页数:5
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