PUBLICATION
Udu deficiency activates DNA damage checkpoint
- Authors
- Lim, C.H., Chong, S.W., and Jiang, Y.J.
- ID
- ZDB-PUB-100105-1
- Date
- 2009
- Source
- Molecular biology of the cell 20(19): 4183-4193 (Journal)
- Registered Authors
- Chong, Shang Wei, Jiang, Yun-Jin, Lim, Chiaw Hwee
- Keywords
- none
- MeSH Terms
-
- Zebrafish/embryology
- Zebrafish/genetics
- In Situ Hybridization
- Tumor Suppressor Protein p53/genetics
- Tumor Suppressor Protein p53/metabolism
- Flow Cytometry
- Embryo, Nonmammalian/embryology
- Embryo, Nonmammalian/metabolism*
- Two-Hybrid System Techniques
- Bromodeoxyuridine/metabolism
- Microscopy, Fluorescence
- Reverse Transcriptase Polymerase Chain Reaction
- Protein Serine-Threonine Kinases/genetics
- Protein Serine-Threonine Kinases/metabolism
- Mutation*
- Zebrafish Proteins/deficiency
- Zebrafish Proteins/genetics*
- Zebrafish Proteins/metabolism
- Heterochromatin/metabolism
- DNA Damage*
- Animals
- Gene Expression Regulation, Developmental
- DNA Replication/drug effects
- Chlorocebus aethiops
- Protein Binding
- Erythroid-Specific DNA-Binding Factors/deficiency
- Erythroid-Specific DNA-Binding Factors/genetics*
- Erythroid-Specific DNA-Binding Factors/metabolism
- Apoptosis/genetics
- Checkpoint Kinase 2
- COS Cells
- Cell Cycle/genetics
- Body Patterning/genetics
- Immunohistochemistry
- PubMed
- 19656853 Full text @ Mol. Biol. Cell
Citation
Lim, C.H., Chong, S.W., and Jiang, Y.J. (2009) Udu deficiency activates DNA damage checkpoint. Molecular biology of the cell. 20(19):4183-4193.
Abstract
Udu has been shown to play an essential role during blood cell development; however, its roles in other cellular processes remain largely unexplored. In addition, ugly duckling (udu) mutants exhibited somite and myotome boundary defects. Our fluorescence-activated cell sorting analysis also showed that the loss of udu function resulted in defective cell cycle progression and comet assay indicated the presence of increased DNA damage in udu(tu24) mutants. We further showed that the extensive p53-dependent apoptosis in udu(tu24) mutants is a consequence of activation in the Atm-Chk2 pathway. Udu seems not to be required for DNA repair, because both wild-type and udu embryos similarly respond to and recover from UV treatment. Yeast two-hybrid and coimmunoprecipitation data demonstrated that PAH-L repeats and SANT-L domain of Udu interacts with MCM3 and MCM4. Furthermore, Udu is colocalized with 5-bromo-2'-deoxyuridine and heterochromatin during DNA replication, suggesting a role in maintaining genome integrity.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping