Abstract
Missense substitutions in the presenilin 1 (PS1) and presenilin 2 (PS2) proteins are associated with early-onset familial Alzheimer's disease. We have used yeast-two-hybrid and coimmunoprecipitation methods to show that the large cytoplasmic loop domains of PS1 and PS2 interact specifically with three members of the armadillo protein family, including beta-catenin, p0071, and a novel neuronal-specific armadillo protein--neural plakophilin-related armadillo protein (NPRAP). The PS1:NPRAP interaction occurs between the arm repeats of NPRAP and residues 372-399 at the C-terminal end of the large cytoplasmic loop of PS1. The latter residues contain a single arm-like domain and are highly conserved in the presenilins, suggesting that they form a functional armadillo protein binding site for the presenilins.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alzheimer Disease / genetics
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Amino Acid Sequence
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Animals
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Armadillo Domain Proteins
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Catenins
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Cell Adhesion Molecules
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Cells, Cultured
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Chromatography, Affinity
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Cytoskeletal Proteins / metabolism*
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Delta Catenin
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Humans
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Immunohistochemistry
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Membrane Proteins / genetics
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Membrane Proteins / metabolism*
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Mice
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Microscopy, Confocal
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Molecular Sequence Data
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Nerve Tissue Proteins / genetics
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Nerve Tissue Proteins / metabolism*
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Phosphoproteins
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Plakophilins
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Precipitin Tests
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Presenilin-1
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Presenilin-2
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Protein Binding
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Trans-Activators*
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Transfection
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beta Catenin
Substances
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Armadillo Domain Proteins
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CTNNB1 protein, human
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CTNNB1 protein, mouse
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Catenins
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Cell Adhesion Molecules
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Cytoskeletal Proteins
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Membrane Proteins
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Nerve Tissue Proteins
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PKP4 protein, human
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PSEN1 protein, human
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PSEN2 protein, human
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Phosphoproteins
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Plakophilins
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Presenilin-1
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Presenilin-2
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Trans-Activators
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beta Catenin
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Delta Catenin