PUBLICATION
            Inhibition of endogenous MTF-1 signaling in zebrafish embryos identifies novel roles for MTF-1 in development
- Authors
- O'Shields, B., McArthur, A.G., Holowiecki, A., Kamper, M., Tapley, J., Jenny, M.J.
- ID
- ZDB-PUB-140513-107
- Date
- 2014
- Source
- Biochimica et biophysica acta. Molecular cell research 1843(9): 1818-33 (Journal)
- Registered Authors
- Keywords
- Embryonic development, MTF-1, Metal, Zebrafish, Zinc homeostasis
- Datasets
- GEO:GSE51298
- MeSH Terms
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                - Female
- Mutation/genetics
- Mice
- Cloning, Molecular
- Molecular Sequence Data
- Gene Expression Profiling
- Amino Acid Sequence
- Zebrafish/embryology*
- Zebrafish/genetics*
- Cadmium/toxicity
- Embryo, Nonmammalian/drug effects
- Embryo, Nonmammalian/metabolism*
- Gene Ontology
- Male
- Transcription Factors/chemistry
- Transcription Factors/genetics
- Transcription Factors/metabolism*
- Hemopexin/genetics
- Hemopexin/metabolism
- Humans
- Embryonic Development/drug effects
- Embryonic Development/genetics
- Oligonucleotide Array Sequence Analysis
- Reproducibility of Results
- Transcriptional Activation/drug effects
- Transcriptional Activation/genetics
- Gene Expression Regulation, Developmental/drug effects
- Models, Biological
- Animals
- DNA-Binding Proteins/chemistry
- DNA-Binding Proteins/genetics
- DNA-Binding Proteins/metabolism*
- RNA, Messenger/genetics
- RNA, Messenger/metabolism
- Signal Transduction*/drug effects
- Signal Transduction*/genetics
 
- PubMed
- 24751692 Full text @ BBA Molecular Cell Research
            Citation
        
        
            O'Shields, B., McArthur, A.G., Holowiecki, A., Kamper, M., Tapley, J., Jenny, M.J. (2014) Inhibition of endogenous MTF-1 signaling in zebrafish embryos identifies novel roles for MTF-1 in development. Biochimica et biophysica acta. Molecular cell research. 1843(9):1818-33.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The metal responsive element-binding transcription factor-1 (MTF-1) responds to changes in cellular zinc levels caused by zinc exposure or disruption of endogenous zinc homeostasis by heavy metals or oxygen-related stress. Here we report the functional characterization of a complete zebrafish MTF-1 in comparison with the previously identified isoform lacking the highly conserved cysteine-rich motif (Cys-X-Cys-Cys-X-Cys) found in all other vertebrate MTF-1 orthologs. In an effort to develop novel molecular tools, a constitutively nuclear dominant-negative MTF-1 (dnMTF-1) was generated as tool for inhibiting endogenous MTF-1 signaling. The in vivo efficacy of the dnMTF-1 was determined by microinjecting in vitro transcribed dnMTF-1 mRNA into zebrafish embryos (1-2 cell stage) followed by transcriptomic profiling using an Agilent 4x44K array on 28- and 36-hpf embryos. A total of 594 and 560 probes were identified as differentially expressed at 28hpf and 36hpf, respectively, with interesting overlaps between timepoints. The main categories of genes affected by the inhibition of MTF-1 signaling were: nuclear receptors and genes involved in stress signaling, neurogenesis, muscle development and contraction, eye development, and metal homeostasis, including novel observations in iron and heme homeostasis. Finally, we investigate both the transcriptional activator and transcriptional repressor role of MTF-1 in potential novel target genes identified by transcriptomic profiling during early zebrafish development.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    