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Mitochondrial dynamics and disease, OPA1

Authors :
Olichon, Aurélien
Guillou, Emmanuelle
Delettre, Cécile
Landes, Thomas
Arnauné-Pelloquin, Laetitia
Emorine, Laurent J.
Mils, Valérie
Daloyau, Marlène
Hamel, Christian
Amati-Bonneau, Patrizia
Bonneau, Dominique
Reynier, Pascal
Lenaers, Guy
Belenguer, Pascale
Source :
BBA - Molecular Cell Research. May2006, Vol. 1763 Issue 5/6, p500-509. 10p.
Publication Year :
2006

Abstract

Abstract: The mitochondria are dynamic organelles that constantly fuse and divide. An equilibrium between fusion and fission controls the morphology of the mitochondria, which appear as dots or elongated tubules depending the prevailing force. Characterization of the components of the fission and fusion machineries has progressed considerably, and the emerging question now is what role mitochondrial dynamics play in mitochondrial and cellular functions. Its importance has been highlighted by the discovery that two human diseases are caused by mutations in the two mitochondrial pro-fusion genes, MFN2 and OPA1. This review will focus on data concerning the function of OPA1, mutations in which cause optic atrophy, with respect to the underlying pathophysiological processes. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
01674889
Volume :
1763
Issue :
5/6
Database :
Academic Search Index
Journal :
BBA - Molecular Cell Research
Publication Type :
Academic Journal
Accession number :
21492820
Full Text :
https://doi.org/10.1016/j.bbamcr.2006.04.003