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Requirement for intracellular calcium modulation in zebrafish dorsal–ventral patterning
Journal article   Open access   Peer reviewed

Requirement for intracellular calcium modulation in zebrafish dorsal–ventral patterning

Trudi A Westfall, Beth Hjertos and Diane C Slusarski
Developmental biology, Vol.259(2), pp.380-391
2003
DOI: 10.1016/S0012-1606(03)00209-4
PMID: 12871708
url
https://doi.org/10.1016/S0012-1606(03)00209-4View
Published (Version of record) Open Access

Abstract

The phosphoinositide (PI) cycle is an important signal transduction pathway that, upon activation, generates intracellular second messengers and leads to calcium release. To determine whether PI cycle-mediated intracellular calcium release is required for body plan formation, we systematically dissect PI cycle function in the zebrafish ( Danio rerio). We inhibit PI cycle function at three different steps and deplete internal calcium stores, demonstrating an impact on endogenous calcium release and Wnt/β-catenin signaling. Inhibition of endogenous calcium modulation induces hyperdorsalized phenotypes in a dose-dependent manner. Ectopic dorsal-signaling centers are generated in PI cycle-inhibited embryos as demonstrated by altered β-catenin subcellular localization and ectopic expression of β-catenin target genes. These results provide evidence that modulation of calcium release is critical for early embryonic patterning and acts by influencing the stabilization of β-catenin protein.
Calcium β-Catenin Zebrafish Dorsal–ventral patterning Phospholipase C (PLC) Wnt Phosphatidylinositol cycle Inositol 1,4,5-trisphosphate receptor (IP 3R)

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