Literature DB >> 33578638

Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic Approaches.

Michela Di Nottia1, Daniela Verrigni1, Alessandra Torraco1, Teresa Rizza1, Enrico Bertini1, Rosalba Carrozzo1.   

Abstract

Mitochondria do not exist as individual entities in the cell-conversely, they constitute an interconnected community governed by the constant and opposite process of fission and fusion. The mitochondrial fission leads to the formation of smaller mitochondria, promoting the biogenesis of new organelles. On the other hand, following the fusion process, mitochondria appear as longer and interconnected tubules, which enhance the communication with other organelles. Both fission and fusion are carried out by a small number of highly conserved guanosine triphosphatase proteins and their interactors. Disruption of this equilibrium has been associated with several pathological conditions, ranging from cancer to neurodegeneration, and mutations in genes involved in mitochondrial fission and fusion have been reported to be the cause of a subset of neurogenetic disorders.

Entities:  

Keywords:  mitochondrial diseases; mitochondrial dynamics; therapeutic approaches

Mesh:

Substances:

Year:  2021        PMID: 33578638      PMCID: PMC7916359          DOI: 10.3390/genes12020247

Source DB:  PubMed          Journal:  Genes (Basel)        ISSN: 2073-4425            Impact factor:   4.096


  214 in total

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Authors:  Aurélien Olichon; Laurent J Emorine; Eric Descoins; Laetitia Pelloquin; Laetitia Brichese; Nicole Gas; Emmanuelle Guillou; Cécile Delettre; Annie Valette; Christian P Hamel; Bernard Ducommun; Guy Lenaers; Pascale Belenguer
Journal:  FEBS Lett       Date:  2002-07-17       Impact factor: 4.124

2.  Mitofusin2 mutations disrupt axonal mitochondrial positioning and promote axon degeneration.

Authors:  Albert L Misko; Yo Sasaki; Elizabeth Tuck; Jeffrey Milbrandt; Robert H Baloh
Journal:  J Neurosci       Date:  2012-03-21       Impact factor: 6.167

3.  Whole exome sequencing revealed mutations in FBXL4, UNC80, and ADK in Thai patients with severe intellectual disabilities.

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Journal:  Gene       Date:  2019-02-14       Impact factor: 3.688

4.  MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A.

Authors:  Agostinho G Rocha; Antonietta Franco; Andrzej M Krezel; Jeanne M Rumsey; Justin M Alberti; William C Knight; Nikolaos Biris; Emmanouil Zacharioudakis; James W Janetka; Robert H Baloh; Richard N Kitsis; Daria Mochly-Rosen; R Reid Townsend; Evripidis Gavathiotis; Gerald W Dorn
Journal:  Science       Date:  2018-04-20       Impact factor: 47.728

5.  Mitofusin 2 tethers endoplasmic reticulum to mitochondria.

Authors:  Olga Martins de Brito; Luca Scorrano
Journal:  Nature       Date:  2008-12-04       Impact factor: 49.962

6.  SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease.

Authors:  Carina Fischer; Slave Trajanoski; Lea Papić; Christian Windpassinger; Günther Bernert; Michael Freilinger; Maria Schabhüttl; Mine Arslan-Kirchner; Poupak Javaher-Haghighi; Barbara Plecko; Jan Senderek; Christian Rauscher; Wolfgang N Löscher; Thomas R Pieber; Andreas R Janecke; Michaela Auer-Grumbach
Journal:  J Neurol       Date:  2011-09-04       Impact factor: 4.849

7.  Multiple dynamin family members collaborate to drive mitochondrial division.

Authors:  Jason E Lee; Laura M Westrate; Haoxi Wu; Cynthia Page; Gia K Voeltz
Journal:  Nature       Date:  2016-10-31       Impact factor: 49.962

8.  A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathies.

Authors:  Marina Bartsakoulia; Angela Pyle; Diego Troncoso-Chandía; Josefa Vial-Brizzi; Marysol V Paz-Fiblas; Jennifer Duff; Helen Griffin; Veronika Boczonadi; Hanns Lochmüller; Stephanie Kleinle; Patrick F Chinnery; Sarah Grünert; Janbernd Kirschner; Verónica Eisner; Rita Horvath
Journal:  Hum Mol Genet       Date:  2018-04-01       Impact factor: 6.150

Review 9.  Structure, function, and regulation of mitofusin-2 in health and disease.

Authors:  Gursimran Chandhok; Michael Lazarou; Brent Neumann
Journal:  Biol Rev Camb Philos Soc       Date:  2017-10-25

10.  Loss of Mfn2 results in progressive, retrograde degeneration of dopaminergic neurons in the nigrostriatal circuit.

Authors:  Anh H Pham; Shuxia Meng; Quynh N Chu; David C Chan
Journal:  Hum Mol Genet       Date:  2012-07-31       Impact factor: 6.150

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Review 4.  Influence of Age and Dose on the Effect of Resveratrol for Glycemic Control in Type 2 Diabetes Mellitus: Systematic Review and Meta-Analysis.

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6.  Pathogenic DNM1L Variant (1085G>A) Linked to Infantile Progressive Neurological Disorder: Evidence of Maternal Transmission by Germline Mosaicism and Influence of a Contemporary in cis Variant (1535T>C).

Authors:  Claudia Piccoli; Rosella Scrima; Annamaria D'Aprile; Massimiliano Chetta; Olga Cela; Consiglia Pacelli; Maria Ripoli; Giovanna D'Andrea; Maurizio Margaglione; Nenad Bukvic; Nazzareno Capitanio
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Review 7.  Mitochondrial Implications in Cardiovascular Aging and Diseases: The Specific Role of Mitochondrial Dynamics and Shifts.

Authors:  Anastasia V Poznyak; Tatiana V Kirichenko; Evgeny E Borisov; Nikolay K Shakhpazyan; Andrey G Kartuesov; Alexander N Orekhov
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  7 in total

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