Literature DB >> 24326103

In vivo functions of Drp1: lessons learned from yeast genetics and mouse knockouts.

Hiromi Sesaki1, Yoshihiro Adachi2, Yusuke Kageyama2, Kie Itoh2, Miho Iijima2.   

Abstract

Mitochondria grow, divide, and fuse in cells. Mitochondrial division is critical for the maintenance of the structure and function of mitochondria. Alterations in this process have been linked to many human diseases, including peripheral neuropathies and aging-related neurological disorders. In this review, we discuss recent progress in mitochondrial division by focusing on molecular and in vivo analyses of the evolutionarily conserved, central component of mitochondrial division, dynamin-related protein 1 (Drp1), in the yeast and mouse model organisms.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Dynamin-related GTPase; Membrane fission; Mitochondrion; Mouse; Neurodegeneration; Yeast

Mesh:

Substances:

Year:  2013        PMID: 24326103      PMCID: PMC4048796          DOI: 10.1016/j.bbadis.2013.11.024

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


  100 in total

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1.  Parkin-independent mitophagy requires Drp1 and maintains the integrity of mammalian heart and brain.

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Review 2.  Proteolytic regulation of mitochondrial dynamics.

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Review 3.  Biosynthesis and roles of phospholipids in mitochondrial fusion, division and mitophagy.

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Review 4.  Causal roles of mitochondrial dynamics in longevity and healthy aging.

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9.  Parkin suppresses Drp1-independent mitochondrial division.

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Review 10.  Endoplasmic Reticulum-Mitochondrial Contactology: Structure and Signaling Functions.

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