PUBLICATION

Temporal control over the initiation of cell motility by a regulator of G-protein signaling

Authors
Hartwig, J., Tarbashevich, K., Seggewiß, J., Stehling, M., Bandemer, J., Grimaldi, C., Paksa, A., Groß-Thebing, T., Meyen, D., Raz, E.
ID
ZDB-PUB-140723-6
Date
2014
Source
Proceedings of the National Academy of Sciences of the United States of America   111(31): 11389-94 (Journal)
Registered Authors
Bandemer, Jan, Grimaldi, Cecilia, Hartwig, Johannes, Meyen, Dana, Paksa, Azadeh, Raz, Erez, Tarbashevich, Katsiyarina
Keywords
cell adhesion, rgs protein
MeSH Terms
  • Animals
  • Cadherins/metabolism
  • Cell Movement*/genetics
  • Cell Polarity/genetics
  • Gene Expression Regulation, Developmental
  • Germ Cells/cytology
  • Germ Cells/metabolism
  • RGS Proteins/genetics
  • RGS Proteins/metabolism*
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Signal Transduction*/genetics
  • Time Factors
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Zebrafish/metabolism*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism*
PubMed
25049415 Full text @ Proc. Natl. Acad. Sci. USA
Abstract
The control over the acquisition of cell motility is central for a variety of biological processes in development, homeostasis, and disease. An attractive in vivo model for investigating the regulation of migration initiation is that of primordial germ cells (PGCs) in zebrafish embryos. In this study, we show that, following PGC specification, the cells can polarize but do not migrate before the time chemokine-encoded directional cues are established. We found that the regulator of G-protein signaling 14a protein, whose RNA is a newly identified germ plasm component, regulates the temporal relations between the appearance of the guidance molecules and the acquisition of cellular motility by regulating E-cadherin levels.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping