PUBLICATION
Cell mixing during early epiboly in the zebrafish embryo
- Authors
- Wilson, E.T., Cretekos, C.J., and Helde, K.A.
- ID
- ZDB-PUB-961014-1260
- Date
- 1995
- Source
- Developmental genetics 17: 6-15 (Journal)
- Registered Authors
- Cretekos, Chris, Helde, Kathryn, Wilson, Ellen
- Keywords
- none
- MeSH Terms
-
- Animals
- Blastoderm/cytology
- Blastomeres/cytology
- Cell Movement
- Gastrula/cytology
- Models, Biological
- Time Factors
- Zebrafish/embryology*
- PubMed
- 7554496 Full text @ Dev. Genet.
Citation
Wilson, E.T., Cretekos, C.J., and Helde, K.A. (1995) Cell mixing during early epiboly in the zebrafish embryo. Developmental genetics. 17:6-15.
Abstract
Descendants of early blastomeres in the zebrafish come to populate distinctive regions of the fate map. We present a model suggesting that the distribution of cells in the early gastrula (the fate map stage) results from the passive response of cells to reproducible forces that change the overall shape of the blastoderm just prior to gastrulation. We suggest that one of the morphogenetic changes that accompanies epiboly, the upward doming of the yolk cell into the overlying blastoderm, could be responsible for cell mixing. In support of the model, we show that the timing, extent, and directions of cell mixing in the embryo accurately reflect the expectations of the model. Finally, we show that one portion of the gastrula, a marginal region that later gives rise to many of the mesendodermal derivatives, experiences little cell mixing during the doming process. As a result, this region in the gastrula is populated by the descendants of the subset of the early blastomeres that were originally at the margin. The finding that cytoplasm initially at the edge of the 1-celled blastodisc is transmitted specifically to mesendodermal precursors at the fate map stage raises the possibility that maternal determinants may contribute to initiation of embryonic patterning in the zebrafish embryo.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping