4.4 Article

TRPM7 regulates gastrulation during vertebrate embryogenesis

Journal

DEVELOPMENTAL BIOLOGY
Volume 350, Issue 2, Pages 348-357

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2010.11.034

Keywords

Gastrulation; TRPM7; Ion channel; Kinase; Magnesium; Rat

Funding

  1. National Institutes of Health [GM080753, GM078172]
  2. March of Dimes [1-FY07-522]

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During gastrulation. cells in the dorsal marginal zone polarize, elongate, align and intercalate to establish the physical body axis of the developing embryo. Here we demonstrate that the bifunctional channel-kinase TRPM7 is specifically required for vertebrate gastrulation. TRPM7 is temporally expressed maternally and throughout development, and is spatially enriched in tissues undergoing convergent extension during gastrulation. Functional studies reveal that TRPM7's ion channel, but not its kinase domain, specifically affects cell polarity and convergent extension movements during gastrulation, independent of mesodermal specification. During gastrulation. the non-canonical Wnt pathway via Dishevelled (DvI) orchestrates the activities of the GTPases Rho and Rat to control convergent extension movements. We find that TRPM7 functions synergistically with non-canonical Wnt signaling to regulate Rat activity. The phenotype caused by depletion of the Ca2+- and Mg2+-permeant TRPM7 is suppressed by expression of a dominant negative form of Rac, as well as by Mg2+ supplementation or by expression of the Mg2+ transporter SLC41A2. Together. these studies demonstrate an essential role for the ion channel TRPM7 and Mg2+ in Rac-dependent polarized cell movements during vertebrate gastrulation. (C) 2010 Elsevier Inc. All rights reserved.

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