Expression of the Anti-amyloidogenic Secretase ADAM10 Is Suppressed by Its 5′-Untranslated Region*

Autor: Christian Haass, Sonja Zilow, Claudia Prinzen, Ann-Katrin Ludwig, Dominik Buell, Stefan F. Lichtenthaler, Brigitte Nuscher, Sven Lammich, Falk Fahrenholz
Jazyk: angličtina
Rok vydání: 2010
Předmět:
Five prime untranslated region
enzymology [Brain]
ADAM10
ADAM10 protein
human

BACE1-AS
genetics [Amyloid Precursor Protein Secretases]
genetics [Alzheimer Disease]
genetics [ADAM Proteins]
Biochemistry
Gene Expression Regulation
Enzymologic

biosynthesis [Membrane Proteins]
ADAM10 Protein
Alzheimer Disease
Chlorocebus aethiops
Amyloid precursor protein
Protein biosynthesis
biosynthesis [Amyloid beta-Peptides]
genetics [Amyloid beta-Peptides]
Animals
Humans
Gene Regulation
Molecular Biology
Sequence Deletion
biosynthesis [ADAM Proteins]
Amyloid beta-Peptides
biology
Base Sequence
P3 peptide
enzymology [Alzheimer Disease]
Brain
Membrane Proteins
Cell Biology
Molecular biology
Biochemistry of Alzheimer's disease
genetics [Membrane Proteins]
ADAM Proteins
biosynthesis [Amyloid Precursor Protein Secretases]
Protein Biosynthesis
ddc:540
COS Cells
biology.protein
Amyloid Precursor Protein Secretases
5' Untranslated Regions
Amyloid precursor protein secretase
Zdroj: The journal of biological chemistry 285(21), 15753-15760 (2010). doi:10.1074/jbc.M110.110742
Popis: Proteolytic processing of the amyloid precursor protein by alpha-secretase prevents formation of the amyloid beta-peptide (Abeta), which is the main constituent of amyloid plaques in brains of Alzheimer disease (AD) patients. alpha-Secretase activity is decreased in AD, and overexpression of the alpha-secretase ADAM10 (a disintegrin and metalloprotease 10) in an AD animal model prevents amyloid pathology. ADAM10 has a 444-nucleotide-long, very GC-rich 5'-untranslated region (5'-UTR) with two upstream open reading frames. Because similar properties of 5'-UTRs are found in transcripts of many genes, which are regulated by translational control mechanisms, we asked whether ADAM10 expression is translationally controlled by its 5'-UTR. We demonstrate that the 5'-UTR of ADAM10 represses the rate of ADAM10 translation. In the absence of the 5'-UTR, we observed a significant increase of ADAM10 protein levels in HEK293 cells, whereas mRNA levels were not changed. Moreover, the 5'-UTR of ADAM10 inhibits translation of a luciferase reporter in an in vitro transcription/translation assay. Successive deletion of the first half of the ADAM10 5'-UTR revealed a striking increase in ADAM10 protein expression in HEK293 cells, suggesting that this part of the 5'-UTR contains inhibitory elements for translation. Moreover, we detect an enhanced alpha-secretase activity and consequently reduced Abeta levels in the conditioned medium of HEK293 cells expressing both amyloid precursor protein and a 5'-UTR-ADAM10 deletion construct lacking the first half of the 5'-UTR. Thus, we provide evidence that the 5'-UTR of ADAM10 may have an important role for post-transcriptional regulation of ADAM10 expression and consequently Abeta production.
Databáze: OpenAIRE