PUBLICATION
            Leukemia-associated transcription factor mllt3 is important for primitive erythroid development in zebrafish embryogenesis
- Authors
- Germano, G., Porazzi, P., Felix, C.
- ID
- ZDB-PUB-220419-12
- Date
- 2022
- Source
- Developmental Dynamics : an official publication of the American Association of Anatomists 251(10): 1728-1740 (Journal)
- Registered Authors
- Keywords
- gene expression, intermediate cell mass, mutants, primitive hematopoiesis
- MeSH Terms
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                - Leukemia*
- Embryonic Development/genetics
- Nuclear Proteins
- Gene Expression Regulation, Developmental
- Humans
- Transcription Factors/genetics
- Phylogeny
- Zebrafish*/genetics
- Animals
 
- PubMed
- 35429189 Full text @ Dev. Dyn.
            Citation
        
        
            Germano, G., Porazzi, P., Felix, C. (2022) Leukemia-associated transcription factor mllt3 is important for primitive erythroid development in zebrafish embryogenesis. Developmental Dynamics : an official publication of the American Association of Anatomists. 251(10):1728-1740.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
Background MLLT3 (AF9) is a nuclear transcription factor crucial for hematopoietic stem cell and progenitor cell maintenance, but its role during embryonic hematopoiesis remains uncertain. Here, we examine the role of mllt3 in developmental hematopoiesis during embryogenesis using zebrafish.
Results Cloning, sequencing, phylogenetic and synteny analyses showed high evolutionary conservation between important functional domains of the zebrafish orthologue of mllt3 and MLLT3 in humans. Quantitative RT-PCR and in situ hybridization analyses revealed that mllt3 is maternally supplied and zygotically expressed throughout embryonic development, and that expression is highest between 10 to 24 h post fertilization (hpf) coincident with enrichment in the intermediate cell mass (ICM) and posterior blood island, which are the sites of the primitive and transient definitive hematopoiesis in zebrafish, respectively. Further, we found co-expression of mllt3 with the early hematopoietic progenitor markers tal1, gata2 and gata1a in the posterior ICM. By investigating zebrafish hematopoietic mutants, we discovered that mllt3 is involved in erythroid precursor formation. By 48 to 72 hpf, mllt3 expression proved to be restricted to non-hematopoietic tissues including head structures, pronephric tubules and liver primordium.
Conclusions These findings establish a link between mllt3 and primitive erythropoiesis and provide the basis for future functional investigations. This article is protected by copyright. All rights reserved.
            
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    