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A disease-associated Aifm1 variant induces severe myopathy in knockin mice
OBJECTIVE: Mutations in the AIFM1 gene have been identified in recessive X-linked mitochondrial diseases. Functional and molecular consequences of these pathogenic AIFM1 mutations have been poorly studied in vivo. METHODS/RESULTS: Here we provide evidence that the disease-associated apoptosis-induci...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026322/ https://www.ncbi.nlm.nih.gov/pubmed/29780003 http://dx.doi.org/10.1016/j.molmet.2018.05.002 |
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author | Wischhof, Lena Gioran, Anna Sonntag-Bensch, Dagmar Piazzesi, Antonia Stork, Miriam Nicotera, Pierluigi Bano, Daniele |
author_facet | Wischhof, Lena Gioran, Anna Sonntag-Bensch, Dagmar Piazzesi, Antonia Stork, Miriam Nicotera, Pierluigi Bano, Daniele |
author_sort | Wischhof, Lena |
collection | PubMed |
description | OBJECTIVE: Mutations in the AIFM1 gene have been identified in recessive X-linked mitochondrial diseases. Functional and molecular consequences of these pathogenic AIFM1 mutations have been poorly studied in vivo. METHODS/RESULTS: Here we provide evidence that the disease-associated apoptosis-inducing factor (AIF) deletion arginine 201 (R200 in rodents) causes pathology in knockin mice. Within a few months, posttranslational loss of the mutant AIF protein induces severe myopathy associated with a lower number of cytochrome c oxidase-positive muscle fibers. At a later stage, Aifm1 (R200 del) knockin mice manifest peripheral neuropathy, but they do not show neurodegenerative processes in the cerebellum, as observed in age-matched hypomorphic Harlequin (Hq) mutant mice. Quantitative proteomic and biochemical data highlight common molecular signatures of mitochondrial diseases, including aberrant folate-driven one-carbon metabolism and sustained Akt/mTOR signaling. CONCLUSION: Our findings indicate metabolic defects and distinct tissue-specific vulnerability due to a disease-causing AIFM1 mutation, with many pathological hallmarks that resemble those seen in patients. |
format | Online Article Text |
id | pubmed-6026322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-60263222018-07-06 A disease-associated Aifm1 variant induces severe myopathy in knockin mice Wischhof, Lena Gioran, Anna Sonntag-Bensch, Dagmar Piazzesi, Antonia Stork, Miriam Nicotera, Pierluigi Bano, Daniele Mol Metab Original Article OBJECTIVE: Mutations in the AIFM1 gene have been identified in recessive X-linked mitochondrial diseases. Functional and molecular consequences of these pathogenic AIFM1 mutations have been poorly studied in vivo. METHODS/RESULTS: Here we provide evidence that the disease-associated apoptosis-inducing factor (AIF) deletion arginine 201 (R200 in rodents) causes pathology in knockin mice. Within a few months, posttranslational loss of the mutant AIF protein induces severe myopathy associated with a lower number of cytochrome c oxidase-positive muscle fibers. At a later stage, Aifm1 (R200 del) knockin mice manifest peripheral neuropathy, but they do not show neurodegenerative processes in the cerebellum, as observed in age-matched hypomorphic Harlequin (Hq) mutant mice. Quantitative proteomic and biochemical data highlight common molecular signatures of mitochondrial diseases, including aberrant folate-driven one-carbon metabolism and sustained Akt/mTOR signaling. CONCLUSION: Our findings indicate metabolic defects and distinct tissue-specific vulnerability due to a disease-causing AIFM1 mutation, with many pathological hallmarks that resemble those seen in patients. Elsevier 2018-05-08 /pmc/articles/PMC6026322/ /pubmed/29780003 http://dx.doi.org/10.1016/j.molmet.2018.05.002 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Wischhof, Lena Gioran, Anna Sonntag-Bensch, Dagmar Piazzesi, Antonia Stork, Miriam Nicotera, Pierluigi Bano, Daniele A disease-associated Aifm1 variant induces severe myopathy in knockin mice |
title | A disease-associated Aifm1 variant induces severe myopathy in knockin mice |
title_full | A disease-associated Aifm1 variant induces severe myopathy in knockin mice |
title_fullStr | A disease-associated Aifm1 variant induces severe myopathy in knockin mice |
title_full_unstemmed | A disease-associated Aifm1 variant induces severe myopathy in knockin mice |
title_short | A disease-associated Aifm1 variant induces severe myopathy in knockin mice |
title_sort | disease-associated aifm1 variant induces severe myopathy in knockin mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026322/ https://www.ncbi.nlm.nih.gov/pubmed/29780003 http://dx.doi.org/10.1016/j.molmet.2018.05.002 |
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