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PMID: 12228233 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Processing of beta-amyloid precursor-like protein-1 and -2 by gamma-secretase regulates transcription.

The Journal of biological chemistry ·Vol. 277 ·No. 46 ·2002-11-15 ·页码 44195-201

Scheinfeld MH, Ghersi E, Laky K, Fowlkes BJ, D'Adamio L

Abstract

The familial Alzheimer's disease gene product beta-amyloid (Abeta) precursor protein (APP) is processed by the beta- and gamma-secretases to produce Abeta as well as AID (APP Intracellular Domain) which is derived from the extreme carboxyl terminus of APP. AID was originally shown to lower the cellular threshold to apoptosis and more recently has been shown to modulate gene expression such that it represses Notch-dependent gene expression while in combination with Fe65 it enhances gene activation. Here we report that the two other members of the APP family, beta-amyloid precursor-like protein-1 and -2 (APLP1 and APLP2), are also processed by the gamma-secretase in a Presenilin 1-dependent manner. Furthermore, the extreme carboxyl-terminal fragments produced by this processing (here termed APP-like Intracellular Domain or ALID1 and ALID2) are able to enhance Fe65-dependent gene activation, similar to what has been reported for AID. Considering that only APP and not the APLPs have been linked to familial Alzheimer's disease (AD), this data should help in understanding the physiologic roles of the APP family members and in differentiating these functions from the pathologic role of APP in Alzheimer's disease.

MeSH 主题词
Alzheimer Disease/metabolism Amino Acid Motifs Amyloid Precursor Protein Secretases Amyloid beta-Protein Precursor/analogs & derivatives,chemistry,metabolism Animals Aspartic Acid Endopeptidases Blotting, Western Brain/metabolism Cell Differentiation Cell Line Cell Nucleus/metabolism Cells, Cultured Cytoplasm/metabolism Endopeptidases/metabolism Glutathione Transferase/metabolism Humans Immunohistochemistry Luciferases/metabolism Membrane Proteins/metabolism Mice Mice, Knockout Microscopy, Fluorescence Nerve Tissue Proteins/metabolism Point Mutation Precipitin Tests Protein Binding Protein Structure, Tertiary Receptors, Notch Transcription, Genetic Transcriptional Activation Tyrosine/metabolism
化学物质
APLP1 protein, human APLP2 protein, human Amyloid beta-Protein Precursor Aplp1 protein, mouse Aplp2 protein, mouse Membrane Proteins Nerve Tissue Proteins Receptors, Notch Tyrosine Luciferases Glutathione Transferase Amyloid Precursor Protein Secretases Endopeptidases Aspartic Acid Endopeptidases BACE1 protein, human Bace1 protein, mouse
作者与单位
共 5 位作者,点击展开单位 / ORCID
Scheinfeld Meir H
Albert Einstein College of Medicine, Department of Microbiology and Immunology, Bronx, New York 10461, USA.
Ghersi Enrico
Laky Karen
Fowlkes B J
D'Adamio Luciano
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2002-11-15
电子出版
2002-00-12
页码
44195-201
Language
English
Country/Region
United States
NLM ID
2985121R
基金资助
NIGMS NIH HHS · T32GM07288 · United States
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