Journal article
Requirement for intracellular calcium modulation in zebrafish dorsal–ventral patterning
Developmental biology, Vol.259(2), pp.380-391
2003
DOI: 10.1016/S0012-1606(03)00209-4
PMID: 12871708
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.
Details
- Title: Subtitle
- Requirement for intracellular calcium modulation in zebrafish dorsal–ventral patterning
- Creators
- Trudi A Westfall - Department of Biological Sciences, University of Iowa, Iowa City, IA 52242, USABeth Hjertos - Department of Biological Sciences, University of Iowa, Iowa City, IA 52242, USADiane C Slusarski - Department of Biological Sciences, University of Iowa, Iowa City, IA 52242, USA
- Resource Type
- Journal article
- Publication Details
- Developmental biology, Vol.259(2), pp.380-391
- DOI
- 10.1016/S0012-1606(03)00209-4
- PMID
- 12871708
- NLM abbreviation
- Dev Biol
- ISSN
- 0012-1606
- eISSN
- 1095-564X
- Publisher
- Elsevier Inc
- Language
- English
- Date published
- 2003
- Academic Unit
- Iowa Neuroscience Institute; Biology
- Record Identifier
- 9983992089802771
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