PUBLICATION
            CCSer2 gates dynein activity at the cell periphery
- Authors
 - Zang, J.L., Gibson, D., Zheng, A.M., Shi, W., Gillies, J.P., Stein, C., Drerup, C.M., DeSantis, M.E.
 - ID
 - ZDB-PUB-250423-2
 - Date
 - 2025
 - Source
 - The Journal of cell biology 224: (Journal)
 - Registered Authors
 - Drerup, Katie (Catherine)
 - Keywords
 - none
 - MeSH Terms
 - 
    
        
        
            
                
- Protein Transport
 - Cytoplasmic Dyneins*/genetics
 - Cytoplasmic Dyneins*/metabolism
 - Cell Movement
 - Zebrafish Proteins*/genetics
 - Zebrafish Proteins*/metabolism
 - Macrophages/metabolism
 - Humans
 - Zebrafish/embryology
 - Zebrafish/genetics
 - Zebrafish/metabolism
 - Dyneins*/genetics
 - Dyneins*/metabolism
 - Carrier Proteins/genetics
 - Carrier Proteins/metabolism
 - Animals
 
 - PubMed
 - 40261303 Full text @ J. Cell Biol.
 
            Citation
        
        
            Zang, J.L., Gibson, D., Zheng, A.M., Shi, W., Gillies, J.P., Stein, C., Drerup, C.M., DeSantis, M.E. (2025) CCSer2 gates dynein activity at the cell periphery. The Journal of cell biology. 224:.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Cytoplasmic dynein-1 (dynein) is a microtubule-associated, minus end-directed motor that traffics hundreds of different cargos. Dynein must discriminate between cargos and traffic them at the appropriate time from the correct cellular region. How dynein's trafficking activity is regulated in time or cellular space remains poorly understood. Here, we identify CCSer2 as the first known protein to gate dynein activity in the spatial dimension. CCSer2 promotes the migration of developing zebrafish primordium cells, macrophages, and cultured human cells by facilitating the trafficking of cargos that are acted on by peripherally localized dynein. Our data suggest that CCSer2 disfavors the interaction between dynein and its regulator Ndel1 at the cell edge, resulting in localized dynein activation. These findings support a model where the spatial specificity of dynein is achieved by the localization of proteins that trigger Ndel1's release from dynein. We propose that CCSer2 defines a broader class of proteins that activate dynein in distinct microenvironments via regulating Ndel1-dynein interaction.
            
    
        
        
    
    
    
                
                    
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