PUBLICATION
Cold-inducible expression of the cell division cycle gene CDC48 and its promotion of cell proliferation during cold acclimation in zebrafish cells
- Authors
- Imamura, S., Ojima, N., and Yamashita, M.
- ID
- ZDB-PUB-030826-23
- Date
- 2003
- Source
- FEBS letters 549(1-3): 14-20 (Journal)
- Registered Authors
- Yamashita, Michiaki
- Keywords
- none
- MeSH Terms
-
- Molecular Sequence Data
- RNA, Messenger/analysis
- Transcription, Genetic
- Cold Temperature*
- Cell Cycle Proteins/genetics*
- Cell Cycle Proteins/physiology*
- Cell Division
- Animals
- Zebrafish
- Sequence Alignment
- DNA, Complementary/isolation & purification
- Cloning, Molecular
- Gene Expression Regulation/physiology*
- Acclimatization/genetics*
- Transfection
- Phosphorylation
- Adenosine Triphosphatases
- Amino Acid Sequence
- PubMed
- 12914916 Full text @ FEBS Lett.
Citation
Imamura, S., Ojima, N., and Yamashita, M. (2003) Cold-inducible expression of the cell division cycle gene CDC48 and its promotion of cell proliferation during cold acclimation in zebrafish cells. FEBS letters. 549(1-3):14-20.
Abstract
A member of the ATPases associated with diverse cellular activities (AAA) family, the cell division cycle gene CDC48/VCP (valosin-containing protein)/p97, was cloned from zebrafish and found to be a major cold-inducible protein in fish cells. CDC48 mRNA levels increased significantly after reducing the temperature from 30 to 15 degrees C for 25 days. CDC48 protein levels also increased 2.5-fold after 30 days at cold temperatures. When fish cells overexpressing CDC48 were exposed to a temperature of 15 degrees C, cell proliferation was markedly enhanced in comparison with control cells. By contrast, expression of a mutant molecule with a tyrosine-805 to alanine substitution at the C-terminal phosphorylation site inhibited cell proliferation and induced apoptosis at low temperatures. Therefore, CDC48 may promote cell cycling and cell proliferation via C-terminal tyrosine phosphorylation during cold acclimation in fish cells.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping