PUBLICATION
            Functional and molecular features of the calmodulin-interacting protein IQCG required for haematopoiesis in zebrafish
- Authors
 - Chen, L.T., Liang, W.X., Chen, S., Li, R.K., Tan, J.L., Xu, P.F., Luo, L.F., Wang, L., Yu, S.H., Meng, G., Li, K.K., Liu, T.X., Chen, Z., Chen, S.J.
 - ID
 - ZDB-PUB-140513-54
 - Date
 - 2014
 - Source
 - Nature communications 5: 3811 (Journal)
 - Registered Authors
 - Chen, Zhu, Liu, Ting Xi, Xu, Peng-Fei
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Calcium-Calmodulin-Dependent Protein Kinase Type 4/metabolism
 - Calmodulin/metabolism*
 - Hematopoiesis
 - Cell Proliferation
 - Zebrafish
 - Animals
 - Zebrafish Proteins/genetics
 - Zebrafish Proteins/metabolism*
 - Gene Knockdown Techniques
 - HSP70 Heat-Shock Proteins/metabolism
 
 - PubMed
 - 24787902 Full text @ Nat. Commun.
 
            Citation
        
        
            Chen, L.T., Liang, W.X., Chen, S., Li, R.K., Tan, J.L., Xu, P.F., Luo, L.F., Wang, L., Yu, S.H., Meng, G., Li, K.K., Liu, T.X., Chen, Z., Chen, S.J. (2014) Functional and molecular features of the calmodulin-interacting protein IQCG required for haematopoiesis in zebrafish. Nature communications. 5:3811.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                We previously reported a fusion protein NUP98-IQCG in an acute leukaemia, which functions as an aberrant regulator of transcriptional expression, yet the structure and function of IQCG have not been characterized. Here we use zebrafish to investigate the role of iqcg in haematopoietic development, and find that the numbers of haematopoietic stem cells and multilineage-differentiated cells are reduced in iqcg-deficient embryos. Mechanistically, IQCG binds to calmodulin (CaM) and acts as a molecule upstream of CaM-dependent kinase IV (CaMKIV). Crystal structures of complexes between CaM and IQ domain of IQCG reveal dual CaM-binding footprints in this motif, and provide a structural basis for a higher CaM-IQCG affinity when deprived of calcium. The results collectively allow us to understand IQCG-mediated calcium signalling in haematopoiesis, and propose a model in which IQCG stores CaM at low cytoplasmic calcium concentrations, and releases CaM to activate CaMKIV when calcium level rises.
            
    
        
        
    
    
    
                
                    
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                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
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