Literature DB >> 16574259

Get the balance right: mitofusins roles in health and disease.

Ansgar Santel1.   

Abstract

Mitochondria are highly dynamic organelles exhibiting an elaborate morphology and fine structure. Fusion and fission processes contribute to the maintenance and dynamics of mitochondrial morphology. The Mitofusins, a class of evolutionary conserved GTPases of the mitochondrial outer membrane, are essential for the controlled fusion of mitochondrial membranes. Genetic and biochemical data propose a model in which functional domains, such as the GTPase domain and the C-terminally located coiled coil structure, act in an orchestrated manner to coordinate the tethering and mitochondrial outer membrane fusion. In addition, recent reports shed new light on the physiological importance of Mitofusin function suggesting a role in mitochondrial metabolism, apoptosis as well as cellular signalling. Mutations identified in the human Mfn2 gene from patients with the peripheral neuropathy Charcot-Marie-Tooth Type 2A invoke a direct correlation between mitochondrial morphology and function.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16574259     DOI: 10.1016/j.bbamcr.2006.02.004

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  14 in total

1.  Proteasome Impairment Induces Recovery of Mitochondrial Membrane Potential and an Alternative Pathway of Mitochondrial Fusion.

Authors:  Ryohei Shirozu; Hideki Yashiroda; Shigeo Murata
Journal:  Mol Cell Biol       Date:  2015-11-09       Impact factor: 4.272

2.  Adult skeletal muscle deletion of Mitofusin 1 and 2 impedes exercise performance and training capacity.

Authors:  Margaret B Bell; Zachary Bush; Graham R McGinnis; Glenn C Rowe
Journal:  J Appl Physiol (1985)       Date:  2018-09-27

Review 3.  Mitochondrial dynamics in cell death and neurodegeneration.

Authors:  Dong-Hyung Cho; Tomohiro Nakamura; Stuart A Lipton
Journal:  Cell Mol Life Sci       Date:  2010-06-25       Impact factor: 9.261

4.  Abnormalities in mitochondrial structure in cells from patients with bipolar disorder.

Authors:  Anne M Cataldo; Donna L McPhie; Nicholas T Lange; Steven Punzell; Sarah Elmiligy; Nancy Z Ye; Michael P Froimowitz; Linda C Hassinger; Emily B Menesale; Laura W Sargent; David J Logan; Anne E Carpenter; Bruce M Cohen
Journal:  Am J Pathol       Date:  2010-06-21       Impact factor: 4.307

5.  A designed point mutant in Fis1 disrupts dimerization and mitochondrial fission.

Authors:  Jonathan P B Lees; Cara Marie Manlandro; Lora K Picton; Alexandra Z Ebie Tan; Salvador Casares; John M Flanagan; Karen G Fleming; R Blake Hill
Journal:  J Mol Biol       Date:  2012-07-09       Impact factor: 5.469

Review 6.  Mitochondrial fragmentation in neurodegeneration.

Authors:  Andrew B Knott; Guy Perkins; Robert Schwarzenbacher; Ella Bossy-Wetzel
Journal:  Nat Rev Neurosci       Date:  2008-07       Impact factor: 34.870

7.  MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families.

Authors:  Geir J Braathen; Jette C Sand; Ana Lobato; Helle Høyer; Michael B Russell
Journal:  BMC Med Genet       Date:  2010-03-29       Impact factor: 2.103

Review 8.  Structural and functional link between the mitochondrial network and the endoplasmic reticulum.

Authors:  Carlotta Giorgi; Diego De Stefani; Angela Bononi; Rosario Rizzuto; Paolo Pinton
Journal:  Int J Biochem Cell Biol       Date:  2009-04-21       Impact factor: 5.085

9.  Effects of mitofusin-2 gene on cell proliferation and chemotherapy sensitivity of MCF-7.

Authors:  Yun Xia; Yaqun Wu; Xiaojun He; Jianping Gong; Fazu Qiu
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2008-05-15

Review 10.  Charcot-Marie-Tooth disease and intracellular traffic.

Authors:  Cecilia Bucci; Oddmund Bakke; Cinzia Progida
Journal:  Prog Neurobiol       Date:  2012-03-22       Impact factor: 11.685

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.