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Previous studies have demonstrated the molecular linkage of three causative genes for early-onset Alzheimer's disease: the presenilin 1 gene on chromosome 14, the presenilin 2 gene on chromosome 1, and the amyloid precursor protein gene on chromosome 21. In the present study, we have investigated the distributions of the approximately 20-kDa C-terminal and approximately 30-kDa N-terminal fragments of presenilin 1 and the amyloid precursor protein in rat brain and compared them with the distribution of several marker proteins. The fragments of presenilin 1 are present in synaptic plasma membranes, neurite growth cone membranes, and small synaptic vesicles of rat brain. Both proteolytic fragments are coenriched in the corresponding tissue fractions. Based on this observation, it seems likely that N- and C-terminal presenilin 1 fragments form a functional unit while remaining associated. In contrast to a predominant subcellular localization of presenilin 1 to the endoplasmic reticulum and Golgi apparatus in different cell lines, our results indicate that rat brain presenilin 1 fragments exit from these biosynthetic compartments to reach synaptic organelles in neurons.


Journal article


J Neurochem

Publication Date





1564 - 1573


Alzheimer Disease, Amyloid beta-Protein Precursor, Animals, Antibodies, Biological Transport, Cell Membrane, Cerebral Cortex, Female, Growth Cones, Membrane Proteins, Neuroblastoma, Peptide Fragments, Presenilin-1, Rats, Rats, Wistar, Receptors, N-Methyl-D-Aspartate, Subcellular Fractions, Synapses, Synaptic Vesicles, Synaptophysin, Tumor Cells, Cultured