PUBLICATION

Molecular Cloning and Characterization of the Catalytic Domain of Zebrafish Homologue of the Ataxia-Telangiectasia Mutated Gene

Authors
Garg, R., Geng, C.D., Miller, J.L., Callens, S., Tang, X., Appel, B., and Xu, B.
ID
ZDB-PUB-040706-11
Date
2004
Source
Molecular cancer research : MCR   2(6): 348-353 (Journal)
Registered Authors
Appel, Bruce
Keywords
none
MeSH Terms
  • Amino Acid Sequence
  • Animals
  • Ataxia Telangiectasia Mutated Proteins
  • Catalytic Domain*
  • Cell Cycle Proteins
  • Cell Line
  • Cloning, Molecular
  • DNA-Binding Proteins
  • Embryo, Nonmammalian/metabolism
  • Genes, Dominant/genetics
  • Humans
  • Molecular Sequence Data
  • Mutation/genetics
  • Protein Serine-Threonine Kinases/antagonists & inhibitors
  • Protein Serine-Threonine Kinases/chemistry*
  • Protein Serine-Threonine Kinases/genetics*
  • Protein Serine-Threonine Kinases/metabolism
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • S Phase/radiation effects
  • Sequence Homology, Amino Acid
  • Transfection
  • Tumor Suppressor Proteins
  • Zebrafish/embryology
  • Zebrafish/genetics*
  • Zebrafish Proteins/antagonists & inhibitors
  • Zebrafish Proteins/chemistry*
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/metabolism
PubMed
15235110
Abstract
Inherited biallelic mutations of the ATM (ataxia-telangiectasia mutated) gene in humans cause ataxia-telangiectasia, a rare autosomal recessive disorder associated with progressive neuro-degeneration, cancer predisposition, immunodeficiency, and hypersensitivity to ionizing radiation. The ATM gene is highly conserved across a wide range of species. In an attempt to establish a zebrafish (Danio rerio) model of ataxia-telangiectasia, we cloned the coding sequence of the catalytic domain of the zebrafish homologue of ATM and found it to contain an open reading frame encoding 907 amino acids at the carboxyl terminus of the zebrafish ATM (zATM). The catalytic domain of zATM shares 67% and 66% homology with human ATM (hATM) and mouse ATM (mATM), respectively. The full-length mRNA encoding zATM is found to be approximately 11 kb by Northern hybridization, and the expression of zATM is observed in different adult and embryonic tissues. Overexpression of a kinase-inactive zATM domain in human cells has a dominant-negative effect against hATM function. Expression of the altered zATM in ZF4 cells leads to an A-T-like phenotype in response to ionizing radiation. These results taken together indicate that zATM is the homologue of hATM. Furthermore, using the kinase-inactive form of zATM should allow manipulation of zATM function in fish cells.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping