Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wischhof, Lena, Gioran, Anna, Sonntag-Bensch, Dagmar, Piazzesi, Antonia, Stork, Miriam, Nicotera, Pierluigi, Bano, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
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
_version_ 1783336420844240896
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
work_keys_str_mv AT wischhoflena adiseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT giorananna adiseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT sonntagbenschdagmar adiseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT piazzesiantonia adiseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT storkmiriam adiseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT nicoterapierluigi adiseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT banodaniele adiseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT wischhoflena diseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT giorananna diseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT sonntagbenschdagmar diseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT piazzesiantonia diseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT storkmiriam diseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT nicoterapierluigi diseaseassociatedaifm1variantinducesseveremyopathyinknockinmice
AT banodaniele diseaseassociatedaifm1variantinducesseveremyopathyinknockinmice