The molecular mechanisms by which a cell becomes polarized for directional migration remains poorly understood. The non-canonical Wnt pathway has recently been shown to play important roles in cell polarization and migration which are required for gastrulation and neural fold closure during vertebrate embryogenesis. Importantly defects in Wnt signaling are implicated in neural fold closure disorders in humans includingspina bifida and also in cancer metastasis. To date, how the Wnt signaling pathway mediates changes to the actin cytoskeleton remains at best poorly defined. Our previous studies have established that the Dishevelled-associated activator of morphogenesis protein (Daaml) provides a crucial link between Dishevelled (Dvl)and the small GTPase Rho for gastrulation. Importantly, our studies demonstrate Daaml is required for Wnt-dependent cytoskeletal changes, although the underlying biochemical details are not known. To further identify factors required downstream of Daaml for cytoskeletal changes, we performed a yeast two-hybrid screen and isolated the protein Profilin, in addition to others. Profilin can induce actin polymerization and thus provides a direct link between Daaml and the actin cytoskeleton. Co-immunoprecipitation and GST-pulldown assays confirm that Profilin is a bona-fide Daaml- interacting factor and upon Wnt-stimulationco-localizes with Daaml at the cellular membrane. Furthermore, over-expression or depletion of Profilin,similar to Daaml, blocks gastrulation cell movements in Xenopus and results in an open neural tube phenotype characteristic of spina bifida In buildinga model for how non-canonical Wnt signaling through Daaml regulates cytoskeletal changes, we hypothesize Daaml and Profilinl are key modulators of the actin cytoskeleton for cellular motility. In this proposal, we will investigate how Daaml functions to mediate cytoskeletal changes for cell motility using the individual advantages of both mammaliancells and Xenopus embryos in two specific aims. First, we will examine how Daaml is activated by Dvl and define the role of its domains in Rho activation, cytoskeletal changes and gastrulation. Second, we will investigate how Profilin functions in non-canonical Wntsignaling as an effector for Daaml for cytoskeletal reorganization. These studies will employ gain-of-function and loss- of-function approaches utilizing biochemical, cell biological and embryological approaches. These studies together will advance our knowledgeof how non-canonical Wnt signalingregulates cell polarity and cell motility required duringgastrulation cell movements and neural fold closure.
Seo, Hwa-Seon; Habas, Raymond; Chang, Chenbei et al. (2017) Bimodal regulation of Dishevelled function by Vangl2 during morphogenesis. Hum Mol Genet 26:2053-2061 |
Komiya, Yuko; Bai, Zhiyong; Cai, Na et al. (2017) A Nonredundant Role for the TRPM6 Channel in Neural Tube Closure. Sci Rep 7:15623 |
Overton, Jeffrey D; Komiya, Yuko; Mezzacappa, Courtney et al. (2015) Hepatocystin is Essential for TRPM7 Function During Early Embryogenesis. Sci Rep 5:18395 |
Ajima, Rieko; Bisson, Joseph A; Helt, Jay-Christian et al. (2015) DAAM1 and DAAM2 are co-required for myocardial maturation and sarcomere assembly. Dev Biol 408:126-39 |
Kiechel, Marjorie A; Beringer, Laura T; Donius, Amalie E et al. (2015) Osteoblast biocompatibility of premineralized, hexamethylene-1,6-diaminocarboxysulfonate crosslinked chitosan fibers. J Biomed Mater Res A 103:3201-11 |
Beringer, Laura T; Kiechel, Marjorie A; Komiya, Yuko et al. (2015) Osteoblast biocompatibility of novel chitosan crosslinker, hexamethylene-1,6-diaminocarboxysulfonate. J Biomed Mater Res A 103:3026-33 |
Mezzacappa, Courtney; Komiya, Yuko; Habas, Raymond (2012) Activation and function of small GTPases Rho, Rac, and Cdc42 during gastrulation. Methods Mol Biol 839:119-31 |
Liu, Wei; Komiya, Yuko; Mezzacappa, Courtney et al. (2011) MIM regulates vertebrate neural tube closure. Development 138:2035-47 |
Miller, Rachel K; Canny, Sol Gomez de la Torre; Jang, Chuan-Wei et al. (2011) Pronephric tubulogenesis requires Daam1-mediated planar cell polarity signaling. J Am Soc Nephrol 22:1654-64 |
Su, Li-Ting; Liu, Wei; Chen, Hsiang-Chin et al. (2011) TRPM7 regulates polarized cell movements. Biochem J 434:513-21 |
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