PUBLICATION
            NIPSNAP1 and NIPSNAP2 Act as "Eat Me" Signals for Mitophagy
- Authors
- Princely Abudu, Y., Pankiv, S., Mathai, B.J., Håkon Lystad, A., Bindesbøll, C., Brenne, H.B., Yoke Wui Ng, M., Thiede, B., Yamamoto, A., Mutugi Nthiga, T., Lamark, T., Esguerra, C.V., Johansen, T., Simonsen, A.
- ID
- ZDB-PUB-190416-9
- Date
- 2019
- Source
- Developmental Cell 49(4): 509-525.e12 (Journal)
- Registered Authors
- Esguerra, Camila V., Johansen, Terje
- Keywords
- ALFY, NDP52, NIPSNAP1, NIPSNAP2, Parkin, TAX1BP1, autophagy, mitophagy, optineurin, p62/SQSTM1
- MeSH Terms
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                - Protein Binding
- Neurons/metabolism
- Animals
- Autophagy/physiology
- Autophagy-Related Protein 8 Family/metabolism
- Carrier Proteins/metabolism
- Mitochondria/metabolism
- Sequestosome-1 Protein/metabolism
- Transcription Factors/metabolism
- Mitochondrial Proteins/metabolism
- Membrane Proteins/metabolism*
- Zebrafish Proteins/metabolism*
- Microtubule-Associated Proteins/metabolism
- Adaptor Proteins, Signal Transducing/metabolism
- HEK293 Cells
- Mitophagy/physiology*
- Zebrafish
- RNA-Binding Proteins/metabolism
- Intercellular Signaling Peptides and Proteins/metabolism*
- HeLa Cells
- Humans
- Intracellular Signaling Peptides and Proteins/metabolism*
- Ubiquitin-Protein Ligases/metabolism
 
- PubMed
- 30982665 Full text @ Dev. Cell
            Citation
        
        
            Princely Abudu, Y., Pankiv, S., Mathai, B.J., Håkon Lystad, A., Bindesbøll, C., Brenne, H.B., Yoke Wui Ng, M., Thiede, B., Yamamoto, A., Mutugi Nthiga, T., Lamark, T., Esguerra, C.V., Johansen, T., Simonsen, A. (2019) NIPSNAP1 and NIPSNAP2 Act as "Eat Me" Signals for Mitophagy. Developmental Cell. 49(4):509-525.e12.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                The clearance of damaged or dysfunctional mitochondria by selective autophagy (mitophagy) is important for cellular homeostasis and prevention of disease. Our understanding of the mitochondrial signals that trigger their recognition and targeting by mitophagy is limited. Here, we show that the mitochondrial matrix proteins 4-Nitrophenylphosphatase domain and non-neuronal SNAP25-like protein homolog 1 (NIPSNAP1) and NIPSNAP2 accumulate on the mitochondria surface upon mitochondrial depolarization. There, they recruit proteins involved in selective autophagy, including autophagy receptors and ATG8 proteins, thereby functioning as an "eat me" signal for mitophagy. NIPSNAP1 and NIPSNAP2 have a redundant function in mitophagy and are predominantly expressed in different tissues. Zebrafish lacking a functional Nipsnap1 display reduced mitophagy in the brain and parkinsonian phenotypes, including loss of tyrosine hydroxylase (Th1)-positive dopaminergic (DA) neurons, reduced motor activity, and increased oxidative stress.
            
    
        
        
    
    
    
                
                    
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                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    