Literature DB >> 33632269

Dominant mutations in MIEF1 affect mitochondrial dynamics and cause a singular late onset optic neuropathy.

Majida Charif1,2, Yvette C Wong3, Soojin Kim3, Agnès Guichet4, Catherine Vignal5, Xavier Zanlonghi6, Philippe Bensaid7, Vincent Procaccio1,4, Dominique Bonneau1,4, Patrizia Amati-Bonneau1,4, Pascal Reynier1,4, Dimitri Krainc3, Guy Lenaers8.   

Abstract

Inherited optic neuropathies are the most common mitochondrial diseases, leading to neurodegeneration involving the irreversible loss of retinal ganglion cells, optic nerve degeneration and central visual loss. Importantly, properly regulated mitochondrial dynamics are critical for maintaining cellular homeostasis, and are further regulated by MIEF1 (mitochondrial elongation factor 1) which encodes for MID51 (mitochondrial dynamics protein 51), an outer mitochondrial membrane protein that acts as an adaptor protein to regulate mitochondrial fission. However, dominant mutations in MIEF1 have not been previously linked to any human disease. Using targeted sequencing of genes involved in mitochondrial dynamics, we report the first heterozygous variants in MIEF1 linked to disease, which cause an unusual form of late-onset progressive optic neuropathy characterized by the initial loss of peripheral visual fields. Pathogenic MIEF1 variants linked to optic neuropathy do not disrupt MID51's localization to the outer mitochondrial membrane or its oligomerization, but rather, significantly disrupt mitochondrial network dynamics compared to wild-type MID51 in high spatial and temporal resolution confocal microscopy live imaging studies. Together, our study identifies dominant MIEF1 mutations as a cause for optic neuropathy and further highlights the important role of properly regulated mitochondrial dynamics in neurodegeneration.

Entities:  

Keywords:  Dominant optic atrophy (DOA); Inherited optic neuropathy (ION); MIEF1; Mid51; Mitochondria dynamics; Mitochondrial disease; Neurodegeneration; Peripheral visual field

Year:  2021        PMID: 33632269      PMCID: PMC7905578          DOI: 10.1186/s13024-021-00431-w

Source DB:  PubMed          Journal:  Mol Neurodegener        ISSN: 1750-1326            Impact factor:   14.195


  34 in total

Review 1.  Mitochondrial fusion/fission dynamics in neurodegeneration and neuronal plasticity.

Authors:  A M Bertholet; T Delerue; A M Millet; M F Moulis; C David; M Daloyau; L Arnauné-Pelloquin; N Davezac; V Mils; M C Miquel; M Rojo; P Belenguer
Journal:  Neurobiol Dis       Date:  2015-10-19       Impact factor: 5.996

2.  Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion.

Authors:  Rahma Felhi; Lamia Sfaihi; Majida Charif; Valerie Desquiret-Dumas; Céline Bris; David Goudenège; Leila Ammar-Keskes; Mongia Hachicha; Dominique Bonneau; Vincent Procaccio; Pascal Reynier; Patrizia Amati-Bonneau; Guy Lenaers; Faiza Fakhfakh
Journal:  Clin Chim Acta       Date:  2018-11-03       Impact factor: 3.786

3.  Non-syndromic isolated dominant optic atrophy caused by the p.R468C mutation in the AFG3 like matrix AAA peptidase subunit 2 gene.

Authors:  Davide Colavito; Veronica Maritan; Agnese Suppiej; Elda Del Giudice; Monica Mazzarolo; Stefania Miotto; Sofia Farina; Maurizio Dalle Carbonare; Stefano Piermarocchi; Alberta Leon
Journal:  Biomed Rep       Date:  2017-09-22

4.  Interchangeable adaptors regulate mitochondrial dynamin assembly for membrane scission.

Authors:  Sajjan Koirala; Qian Guo; Raghav Kalia; Huyen T Bui; Debra M Eckert; Adam Frost; Janet M Shaw
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-25       Impact factor: 11.205

5.  Rapid three-dimensional isotropic imaging of living cells using Bessel beam plane illumination.

Authors:  Thomas A Planchon; Liang Gao; Daniel E Milkie; Michael W Davidson; James A Galbraith; Catherine G Galbraith; Eric Betzig
Journal:  Nat Methods       Date:  2011-03-04       Impact factor: 28.547

6.  Compound heterozygosity for severe and hypomorphic NDUFS2 mutations cause non-syndromic LHON-like optic neuropathy.

Authors:  Sylvie Gerber; Martina G Ding; Xavier Gérard; Klaus Zwicker; Xavier Zanlonghi; Marlène Rio; Valérie Serre; Sylvain Hanein; Arnold Munnich; Agnès Rotig; Lucas Bianchi; Patrizia Amati-Bonneau; Orly Elpeleg; Josseline Kaplan; Ulrich Brandt; Jean-Michel Rozet
Journal:  J Med Genet       Date:  2016-12-28       Impact factor: 6.318

7.  Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical data.

Authors:  Marc Ferré; Angélique Caignard; Dan Milea; Stéphanie Leruez; Julien Cassereau; Arnaud Chevrollier; Patrizia Amati-Bonneau; Christophe Verny; Dominique Bonneau; Vincent Procaccio; Pascal Reynier
Journal:  Hum Mutat       Date:  2014-12-01       Impact factor: 4.878

8.  Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.

Authors:  Daniela Di Bella; Federico Lazzaro; Alfredo Brusco; Massimo Plumari; Giorgio Battaglia; Annalisa Pastore; Adele Finardi; Claudia Cagnoli; Filippo Tempia; Marina Frontali; Liana Veneziano; Tiziana Sacco; Enrica Boda; Alessandro Brussino; Florian Bonn; Barbara Castellotti; Silvia Baratta; Caterina Mariotti; Cinzia Gellera; Valentina Fracasso; Stefania Magri; Thomas Langer; Paolo Plevani; Stefano Di Donato; Marco Muzi-Falconi; Franco Taroni
Journal:  Nat Genet       Date:  2010-03-07       Impact factor: 38.330

9.  Quantitation of mitochondrial dynamics by photolabeling of individual organelles shows that mitochondrial fusion is blocked during the Bax activation phase of apoptosis.

Authors:  Mariusz Karbowski; Damien Arnoult; Hsiuchen Chen; David C Chan; Carolyn L Smith; Richard J Youle
Journal:  J Cell Biol       Date:  2004-02-09       Impact factor: 10.539

10.  Mutations in the m-AAA proteases AFG3L2 and SPG7 are causing isolated dominant optic atrophy.

Authors:  Majida Charif; Arnaud Chevrollier; Naïg Gueguen; Céline Bris; David Goudenège; Valérie Desquiret-Dumas; Stéphanie Leruez; Estelle Colin; Audrey Meunier; Catherine Vignal; Vasily Smirnov; Sabine Defoort-Dhellemmes; Isabelle Drumare Bouvet; Cyril Goizet; Marcela Votruba; Neringa Jurkute; Patrick Yu-Wai-Man; Francesca Tagliavini; Leonardo Caporali; Chiara La Morgia; Valerio Carelli; Vincent Procaccio; Xavier Zanlonghi; Isabelle Meunier; Pascal Reynier; Dominique Bonneau; Patrizia Amati-Bonneau; Guy Lenaers
Journal:  Neurol Genet       Date:  2020-05-20
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  4 in total

1.  High-throughput screening identifies suppressors of mitochondrial fragmentation in OPA1 fibroblasts.

Authors:  Emma Cretin; Priscilla Lopes; Elodie Vimont; Takashi Tatsuta; Thomas Langer; Anastasia Gazi; Martin Sachse; Patrick Yu-Wai-Man; Pascal Reynier; Timothy Wai
Journal:  EMBO Mol Med       Date:  2021-05-20       Impact factor: 12.137

2.  Mid51/Fis1 mitochondrial oligomerization complex drives lysosomal untethering and network dynamics.

Authors:  Yvette C Wong; Soojin Kim; Jasmine Cisneros; Catherine G Molakal; Pingping Song; Steven J Lubbe; Dimitri Krainc
Journal:  J Cell Biol       Date:  2022-09-01       Impact factor: 8.077

3.  Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy.

Authors:  Yuri Seo; Tae Young Kim; Dongju Won; Saeam Shin; Jong Rak Choi; Seung-Tae Lee; Byung Joo Lee; Hyun Taek Lim; Sueng-Han Han; Jinu Han
Journal:  Front Neurol       Date:  2022-08-22       Impact factor: 4.086

Review 4.  Molecular Mechanisms behind Inherited Neurodegeneration of the Optic Nerve.

Authors:  Alessandra Maresca; Valerio Carelli
Journal:  Biomolecules       Date:  2021-03-25
  4 in total

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