Shaping mitochondria: The complex posttranslational regulation of the mitochondrial fission protein DRP1

被引:133
作者
Santel, Ansgar [2 ]
Frank, Stephan [1 ]
机构
[1] Univ Basel Hosp, Dept Neuropathol, Inst Pathol, CH-4031 Basel, Switzerland
[2] Silence Therapeut AG, D-13125 Berlin, Germany
关键词
fusion; fission; mitochondria; dynamin; apoptosis;
D O I
10.1002/iub.71
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria are essential and dynamic cellular organelles differing in size, subcellular distribution, and internal structure. These aspects of mitochondrial morphology are intimately controlled by a growing number of mitochondrial morphology shaping proteins. The past decade has revealed remarkable and often unexpected new insights into the molecular regulation and physiological impact of mitochondrial morphology maintenance. Obviously, proper mitochondrial dynamics, resulting from a tightly regulated equilibrium between opposing mitochondrial fusion and fission activities, is a prerequisite for normal organelle function. Consequently, a disturbance of these activities results in mitochondrial dysfunction and, thus, can lay the foundation for human disorders. Here we specifically focus on recent advances in our understanding of the regulation, activity, and function of dynamin-related protein 1, the main factor for controlled mitochondrial fission. (c) 2008 IUBMB.
引用
收藏
页码:448 / 455
页数:8
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