Interaction of Alzheimer's beta -amyloid precursor family proteins with scaffold proteins of the JNK signaling cascade.
We have isolated a novel protein based on its association with Drosophila APP-like protein (APPL), a homolog of the beta-amyloid precursor protein (APP) that is implicated in Alzheimer's disease. This novel APPL-interacting protein 1 (APLIP1) contains a Src homology 3 domain and a phosphotyrosine interaction domain and is expressed abundantly in neural tissues. The phosphotyrosine interaction domain of APLIP1 interacts with a sequence containing GYENPTY in the cytoplasmic domain of APPL. APLIP1 is highly homologous to the carboxyl-terminal halves of mammalian c-Jun NH(2)-terminal kinase (JNK)-interacting protein 1b (JIP1b) and 2 (JIP2), which also contain Src homology 3 and phosphotyrosine interaction domains. The similarity of APLIP1 to JIP1b and JIP2 includes interaction with component(s) of the JNK signaling pathway and with the motor protein kinesin and the formation of homo-oligomers. JIP1b interacts strongly with the cytoplasmic domain of APP (APPcyt), as APLIP1 does with APPL, but the interaction of JIP2 with APPcyt is weak. Overexpression of JIP1b slightly enhances the JNK-dependent threonine phosphorylation of APP in cultured cells, but that of JIP2 suppresses it. These observations suggest that the interactions of APP family proteins with APLIP1, JIP1b, and JIP2 are conserved and play important roles in the metabolism and/or the function of APPs including the regulation of APP phosphorylation by JNK. Analysis of APP family proteins and their associated proteins is expected to contribute to understanding the molecular process of neural degeneration in Alzheimer's disease.
Pubmed ID: 11912189 RIS Download
Adaptor Proteins, Signal Transducing | Alzheimer Disease | Amino Acid Sequence | Amyloid beta-Protein Precursor | Animals | Blotting, Northern | COS Cells | Carrier Proteins | Cloning, Molecular | Cytoplasm | Drosophila Proteins | Glutathione Transferase | Humans | JNK Mitogen-Activated Protein Kinases | Mice | Mitogen-Activated Protein Kinases | Models, Biological | Molecular Sequence Data | Plasmids | Protein Binding | Protein Structure, Tertiary | Recombinant Fusion Proteins | Reverse Transcriptase Polymerase Chain Reaction | Sequence Homology, Amino Acid | Tumor Cells, Cultured | Two-Hybrid System Techniques