PUBLICATION
Zebrafish cdc25a is expressed during early development and limiting for post-blastoderm cell cycle progression
- Authors
- Nogare, D.E., Arguello, A., Sazer, S., and Lane, M.E.
- ID
- ZDB-PUB-071118-15
- Date
- 2007
- Source
- Developmental Dynamics : an official publication of the American Association of Anatomists 236(12): 3427-3435 (Journal)
- Registered Authors
- Lane, Mary Ellen
- Keywords
- zebrafish, cell cycle, Cdc25, mitotic domain, mitosis
- MeSH Terms
-
- Amino Acid Sequence
- Animals
- Base Sequence
- Cell Cycle/genetics
- Cloning, Molecular
- DNA Primers/genetics
- Gastrulation/genetics
- Gene Expression Regulation, Developmental
- Genes, Fungal
- Genetic Complementation Test
- Molecular Sequence Data
- Phylogeny
- Schizosaccharomyces/cytology
- Schizosaccharomyces/enzymology
- Schizosaccharomyces/genetics
- Sequence Homology, Amino Acid
- Zebrafish/embryology*
- Zebrafish/genetics*
- cdc25 Phosphatases/genetics*
- PubMed
- 17969147 Full text @ Dev. Dyn.
Citation
Nogare, D.E., Arguello, A., Sazer, S., and Lane, M.E. (2007) Zebrafish cdc25a is expressed during early development and limiting for post-blastoderm cell cycle progression. Developmental Dynamics : an official publication of the American Association of Anatomists. 236(12):3427-3435.
Abstract
Cdc25 phosphatases are required for eukaryotic cell cycle progression. To investigate mechanisms governing spatiotemporal dynamics of cell cycle progression during vertebrate development, we isolated two cdc25 genes from the zebrafish, Danio rerio, cdc25a, and cdc25d. We propose that Zebrafish cdc25a is the zebrafish orthologue of the tetrapod Cdc25A genes, while cdc25d is of indeterminate origin. We show that both genes have proliferation promoting activity, but that only cdc25d can complement a Schizosaccharomyces pombe loss of function cdc25 mutation. We present expression data demonstrating that cdc25d expression is very limited during early development, while cdc25a is widely expressed and consistent with the mitotic activity in previously identified mitotic domains of the post-blastoderm zebrafish embryo. Finally, we show that cdc25a can accelerate the entry of post-blastoderm cells into mitosis, suggesting that levels of cdc25a are rate limiting for cell cycle progression during gastrulation.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping