TY - JOUR
T1 - Mitochondrial division, fusion and degradation
AU - Murata, Daisuke
AU - Arai, Kenta
AU - Iijima, Miho
AU - Sesaki, Hiromi
N1 - Funding Information:
This work was supported by National Institutes of Health grants to M.I. (GM131768) and H.S. (GM123266 and GM130695).
Publisher Copyright:
© 2019 The Author(s). Published by Oxford University Press on behalf of the Japanese Biochemical Society. All rights reserved.
PY - 2020/3/1
Y1 - 2020/3/1
N2 - The mitochondrion is an essential organelle for a wide range of cellular processes, including energy production, metabolism, signal transduction and cell death. To execute these functions, mitochondria regulate their size, number, morphology and distribution in cells via mitochondrial division and fusion. In addition, mitochondrial division and fusion control the autophagic degradation of dysfunctional mitochondria to maintain a healthy population. Defects in these dynamic membrane processes are linked to many human diseases that include metabolic syndrome, myopathy and neurodegenerative disorders. In the last several years, our fundamental understanding of mitochondrial fusion, division and degradation has been significantly advanced by high resolution structural analyses, protein-lipid biochemistry, super resolution microscopy and in vivo analyses using animal models. Here, we summarize and discuss this exciting recent progress in the mechanism and function of mitochondrial division and fusion.
AB - The mitochondrion is an essential organelle for a wide range of cellular processes, including energy production, metabolism, signal transduction and cell death. To execute these functions, mitochondria regulate their size, number, morphology and distribution in cells via mitochondrial division and fusion. In addition, mitochondrial division and fusion control the autophagic degradation of dysfunctional mitochondria to maintain a healthy population. Defects in these dynamic membrane processes are linked to many human diseases that include metabolic syndrome, myopathy and neurodegenerative disorders. In the last several years, our fundamental understanding of mitochondrial fusion, division and degradation has been significantly advanced by high resolution structural analyses, protein-lipid biochemistry, super resolution microscopy and in vivo analyses using animal models. Here, we summarize and discuss this exciting recent progress in the mechanism and function of mitochondrial division and fusion.
KW - ER-mitochondria contact
KW - actin
KW - dynamin-related GTPase
KW - lipids
KW - mitophagy
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U2 - 10.1093/jb/mvz106
DO - 10.1093/jb/mvz106
M3 - Review article
C2 - 31800050
AN - SCOPUS:85081076368
SN - 0021-924X
VL - 167
SP - 233
EP - 241
JO - Journal of Biochemistry
JF - Journal of Biochemistry
IS - 3
ER -