PUBLICATION

The centrosome neither persistently leads migration nor determines the site of axonogenesis in migrating neurons in vivo

Authors
Distel, M., Hocking, J.C., Volkmann, K., and Köster, R.W.
ID
ZDB-PUB-101115-10
Date
2010
Source
The Journal of cell biology   191(4): 875-890 (Journal)
Registered Authors
Distel, Martin, Hocking, Jennifer, Köster, Reinhard W., Volkmann, Katrin
Keywords
none
MeSH Terms
  • Animals
  • Animals, Genetically Modified
  • Axons*/physiology
  • Axons*/ultrastructure
  • Biomarkers/metabolism
  • Cell Movement/physiology*
  • Cell Nucleus/metabolism
  • Centrosome/metabolism*
  • Cerebellum*/cytology
  • Cerebellum*/embryology
  • Neurogenesis/physiology*
  • Neurons*/cytology
  • Neurons*/physiology
  • Recombinant Fusion Proteins/genetics
  • Recombinant Fusion Proteins/metabolism
  • Stem Cells/cytology
  • Stem Cells/physiology
  • Tubulin/genetics
  • Tubulin/metabolism
  • Zebrafish*/anatomy & histology
  • Zebrafish*/embryology
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
PubMed
21059852 Full text @ J. Cell Biol.
Abstract
The position of the centrosome ahead of the nucleus has been considered crucial for coordinating neuronal migration in most developmental situations. The proximity of the centrosome has also been correlated with the site of axonogenesis in certain differentiating neurons. Despite these positive correlations, accumulating experimental findings appear to negate a universal role of the centrosome in determining where an axon forms, or in leading the migration of neurons. To further examine this controversy in an in vivo setting, we have generated cell type-specific multi-cistronic gene expression to monitor subcellular dynamics in the developing zebrafish cerebellum. We show that migration of rhombic lip-derived neurons is characterized by a centrosome that does not persistently lead the nucleus, but which is instead regularly overtaken by the nucleus. In addition, axonogenesis is initiated during the onset of neuronal migration and occurs independently of centrosome proximity. These in vivo data reveal a new temporal orchestration of organelle dynamics and provide important insights into the variation in intracellular processes during vertebrate brain differentiation.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping