Examination of the subcellular localization of Dishevelled (Dsh) in fertilized Xenopus eggs revealed that Dsh is associated with vesicle-like organelles that are enriched on the prospective dorsal side of the embryo after cortical rotation. Dorsal enrichment of Dsh is blocked by UV irradiation of the vegetal pole, a treatment that inhibits development of dorsal cell fates, linking accumulation of Dsh and specification of dorsal cell fates. Investigation of the dynamics of Dsh localization using Dsh tagged with green fluorescent protein (Dsh-GFP) demonstrated that Dsh-GFP associates with small vesicle-like organelles that are directionally transported along the parallel array of microtubules towards the prospective dorsal side of the embryo during cortical rotation. Perturbing the assembly of the microtubule array with D2O, a treatment that promotes the random assembly of the array and the dorsalization of embryos, randomizes translocation of Dsh-GFP. Conversely, UV irradiation of the vegetal pole abolishes movement of Dsh-GFP. Finally, we demonstrate that overexpression of Dsh can stabilize β-catenin in Xenopus. These data suggest that the directional translocation of Dsh along microtubules during cortical rotation and its subsequent enrichment on the prospective dorsal side of the embryo play a role in locally activating a maternal Wnt pathway responsible for establishing dorsal cell fates in Xenopus.
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26 July 1999
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July 26 1999
Establishment of the Dorsal–Ventral Axis inXenopus Embryos Coincides with the Dorsal Enrichment of Dishevelled That Is Dependent on Cortical Rotation
Jeffrey R. Miller,
Jeffrey R. Miller
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
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Brian A. Rowning,
Brian A. Rowning
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
bLawrence Berkeley National Laboratory, University of California at Berkeley, Berkeley, California 94720
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Carolyn A. Larabell,
Carolyn A. Larabell
bLawrence Berkeley National Laboratory, University of California at Berkeley, Berkeley, California 94720
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Julia A. Yang-Snyder,
Julia A. Yang-Snyder
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
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Rebecca L. Bates,
Rebecca L. Bates
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
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Randall T. Moon
Randall T. Moon
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
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Jeffrey R. Miller
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
Brian A. Rowning
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
bLawrence Berkeley National Laboratory, University of California at Berkeley, Berkeley, California 94720
Carolyn A. Larabell
bLawrence Berkeley National Laboratory, University of California at Berkeley, Berkeley, California 94720
Julia A. Yang-Snyder
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
Rebecca L. Bates
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
Randall T. Moon
aHoward Hughes Medical Institute, Department of Pharmacology, and Center for Developmental Biology, University of Washington School of Medicine, Seattle, Washington 98195
1.used in this paper: Dsh, Dishevelled; Dsh-GFP, Dsh tagged with green fluorescent protein; GSK-3, glycogen synthase kinase 3; MR, modified ringers; RFz1, Rat Frizzled-1
The first two authors contributed equally to this paper.
Received:
January 27 1999
Revision Requested:
June 14 1999
Accepted:
June 17 1999
Online ISSN: 1540-8140
Print ISSN: 0021-9525
© 1999 The Rockefeller University Press
1999
The Rockefeller University Press
J Cell Biol (1999) 146 (2): 427–438.
Article history
Received:
January 27 1999
Revision Requested:
June 14 1999
Accepted:
June 17 1999
Citation
Jeffrey R. Miller, Brian A. Rowning, Carolyn A. Larabell, Julia A. Yang-Snyder, Rebecca L. Bates, Randall T. Moon; Establishment of the Dorsal–Ventral Axis inXenopus Embryos Coincides with the Dorsal Enrichment of Dishevelled That Is Dependent on Cortical Rotation. J Cell Biol 26 July 1999; 146 (2): 427–438. doi: https://doi.org/10.1083/jcb.146.2.427
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