Amyloid-β peptide induces mitochondrial dysfunction by inhibition of preprotein maturation.
Most mitochondrial proteins possess N-terminal presequences that are required for targeting and import into the organelle. Upon import, presequences are cleaved off by matrix processing peptidases and subsequently degraded by the peptidasome Cym1/PreP, which also degrades Amyloid-beta peptides (Aβ). Here we find that impaired turnover of presequence peptides results in ... feedback inhibition of presequence processing enzymes. Moreover, Aβ inhibits degradation of presequence peptides by PreP, resulting in accumulation of mitochondrial preproteins and processing intermediates. Dysfunctional preprotein maturation leads to rapid protein degradation and an imbalanced organellar proteome. Our findings reveal a general mechanism by which Aβ peptide can induce the multiple diverse mitochondrial dysfunctions accompanying Alzheimer's disease.
Mesh Terms:
Alzheimer Disease, Amyloid beta-Peptides, Animals, Brain, Humans, Metalloproteases, Mice, Mice, Inbred C57BL, Mitochondria, Mitochondrial Proteins, Mutation, Proto-Oncogene Proteins, Reactive Oxygen Species, Receptors, G-Protein-Coupled, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Serine Endopeptidases, Superoxide Dismutase
Alzheimer Disease, Amyloid beta-Peptides, Animals, Brain, Humans, Metalloproteases, Mice, Mice, Inbred C57BL, Mitochondria, Mitochondrial Proteins, Mutation, Proto-Oncogene Proteins, Reactive Oxygen Species, Receptors, G-Protein-Coupled, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins, Serine Endopeptidases, Superoxide Dismutase
Cell Metab.
Date: Oct. 07, 2014
PubMed ID: 25176146
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