Gravin regulates mesodermal cell behavior changes required for axis elongation during zebrafish gastrulation
- Weiser, D.C., Pyati, U.J., and Kimelman, D.
- Genes & Development 21(12): 1559-1571 (Journal)
- Registered Authors
- Kimelman, David, Pyati, Ujwal, Weiser, Douglas C.
- AKAP, convergence and extension, gastrulation, Gravin, Rho, zebrafish
- MeSH Terms
- A Kinase Anchor Proteins/genetics
- A Kinase Anchor Proteins/physiology*
- Amino Acid Sequence
- Base Sequence
- Body Patterning
- Cell Cycle Proteins
- Cell Movement
- Cell Shape
- Gene Expression Regulation, Developmental
- Models, Biological
- Molecular Sequence Data
- Myosin Type II/metabolism
- RNA, Messenger/genetics
- RNA, Messenger/metabolism
- Sequence Homology, Amino Acid
- Zebrafish Proteins/genetics
- Zebrafish Proteins/physiology*
- rhoA GTP-Binding Protein/metabolism
- 17575056 Full text @ Genes & Dev.
Weiser, D.C., Pyati, U.J., and Kimelman, D. (2007) Gravin regulates mesodermal cell behavior changes required for axis elongation during zebrafish gastrulation. Genes & Development. 21(12):1559-1571.
Convergent extension of the mesoderm is the major driving force of vertebrate gastrulation. During this process, mesodermal cells move toward the future dorsal side of the embryo, then radically change behavior as they initiate extension of the body axis. How cells make this transition in behavior is unknown. We have identified the scaffolding protein and tumor suppressor Gravin as a key regulator of this process in zebrafish embryos. We show that Gravin is required for the conversion of mesodermal cells from a highly migratory behavior to the medio-laterally intercalative behavior required for body axis extension. In the absence of Gravin, paraxial mesodermal cells fail to shut down the protrusive activity mediated by the Rho/ROCK/Myosin II pathway, resulting in embryos with severe extension defects. We propose that Gravin functions as an essential scaffold for regulatory proteins that suppress the migratory behavior of the mesoderm during gastrulation, and suggest that this function also explains how Gravin inhibits invasive behaviors in metastatic cells.
Genes / Markers
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Engineered Foreign Genes
Errata and Notes