LONP1 Is Required for Maturation of a Subset of Mitochondrial Proteins, and Its Loss Elicits an Integrated Stress Response
Author:
Affiliation:
1. Montreal Neurological Institute, McGill University, Montreal, QC, Canada
2. Department of Human Genetics, McGill University, Montreal, QC, Canada
Abstract
Funder
Consejo Nacional de Ciencia y Tecnología
Gouvernement du Canada | Canadian Institutes of Health Research
Fonds de Recherche du Québec-Nature et Technologies
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Link
https://journals.asm.org/doi/pdf/10.1128/MCB.00412-17
Reference41 articles.
1. The m-AAA Protease Defective in Hereditary Spastic Paraplegia Controls Ribosome Assembly in Mitochondria
2. Multitasking in the mitochondrion by the ATP-dependent Lon protease
3. Crystal Structures of Bacillus subtilis Lon Protease
4. The N-terminal domain plays a crucial role in the structure of a full-length human mitochondrial Lon protease
5. The Human LON Protease Binds to Mitochondrial Promoters in a Single-Stranded, Site-Specific, Strand-Specific Manner
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