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PMID: 9224802 Published · ppublish English Journal Article

Different effects of Alzheimer-associated mutations of presenilin 1 on its processing.

Neuroscience letters ·Vol. 229 ·No. 1 ·1997-06-20 ·Pages 61-4

Murayama O, Honda T, Mercken M, Murayama M, Yasutake K, Nihonmatsu N, Nakazato Y, Michel G, Song S, Sato K, Takahashi H, Takashima A

Abstract

Presenilin 1 (PS 1) shows missense mutations in most early-onset familial Alzheimer's disease (FAD). Transfection of cDNA for wild type PS 1 into rat pheochromocytoma PC12 cells generated a 47 kDa full-size PS 1 protein, which was processed into a 28 kDa N-terminal fragment and a 19 kDa C-terminal fragment. We prepared selected Alzheimer-associated mutations (Gly384Ala, Leu392Val, and Cys410Tyr) of PS 1, which localized after a possible cleavage site. By transient expression in PC12 cells and rat glioma cell line, C6, we examined their influence on the processing of PS 1. Cys410Tyr inhibited proteolytic processing of PS 1, while Gly384Ala and Leu392Val did not. Thus, the Alzheimer related mutations can be divided into two groups in terms of their effect on the proteolytic cleavage of PS 1.

MeSH Terms
Alzheimer Disease/genetics Animals Blotting, Western Humans Membrane Proteins/biosynthesis,genetics,metabolism PC12 Cells Point Mutation Presenilin-1 Protein Processing, Post-Translational Rats Transfection
Chemicals
Membrane Proteins PSEN1 protein, human Presenilin-1
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Murayama O
Mitsubishi Kasei Institute of Life Sciences, Machida-shi, Tokyo, Japan.
Honda T
Mercken M
Murayama M
Yasutake K
Nihonmatsu N
Nakazato Y
Michel G
Song S
Sato K
Takahashi H
Takashima A
Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
1997-06-20
Pages
61-4
Language
English
Region
Ireland
NLM ID
7600130
Subset
IM
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