Linking mitochondrial dynamics to mitochondrial protein quality control
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Wallace, 2005, A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine, Annu Rev Genet, 39, 359, 10.1146/annurev.genet.39.110304.095751
McBride, 2006, Mitochondria: more than just a powerhouse, Curr Biol, 16, R551, 10.1016/j.cub.2006.06.054
Frederick, 2007, Moving mitochondria: establishing distribution of an essential organelle, Traffic, 8, 1668, 10.1111/j.1600-0854.2007.00644.x
Mootha, 2003, Integrated analysis of protein composition, tissue diversity, and gene regulation in mouse mitochondria, Cell, 115, 629, 10.1016/S0092-8674(03)00926-7
Rhee, 2013, Proteomic mapping of mitochondria in living cells via spatially restricted enzymatic tagging, Science, 339, 1328, 10.1126/science.1230593
Schmidt, 2010, Mitochondrial protein import: from proteomics to functional mechanisms, Nat Rev Mol Cell Biol, 11, 655, 10.1038/nrm2959
Frazier, 2006, Mitochondrial morphology and distribution in mammalian cells, Biol Chem, 387, 1551, 10.1515/BC.2006.193
Chan, 2012, Fusion and fission: interlinked processes critical for mitochondrial health, Annu Rev Genet, 46, 265, 10.1146/annurev-genet-110410-132529
Mishra, 2014, Mitochondrial dynamics and inheritance during cell division, development and disease, Nat Rev Mol Cell Biol, 15, 634, 10.1038/nrm3877
Santel, 2001, Control of mitochondrial morphology by a human mitofusin, J Cell Sci, 114, 867, 10.1242/jcs.114.5.867
Rojo, 2002, Membrane topology and mitochondrial targeting of mitofusins, ubiquitous mammalian homologs of the transmembrane GTPase Fzo, J Cell Sci, 115, 1663, 10.1242/jcs.115.8.1663
Alexander, 2000, OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28, Nat Genet, 26, 211, 10.1038/79944
Delettre, 2000, Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy, Nat Genet, 26, 207, 10.1038/79936
Cipolat, 2004, OPA1 requires mitofusin 1 to promote mitochondrial fusion, Proc Natl Acad Sci U S A, 101, 15927, 10.1073/pnas.0407043101
Detmer, 2007, Functions and dysfunctions of mitochondrial dynamics, Nat Rev Mol Cell Biol, 8, 870, 10.1038/nrm2275
Richter, 2015, Splitting up the powerhouse: structural insights into the mechanism of mitochondrial fission, Cell Mol Life Sci, 72, 3695, 10.1007/s00018-015-1950-y
Bleazard, 1999, The dynamin-related GTPase Dnm1 regulates mitochondrial fission in yeast, Nat Cell Biol, 1, 298, 10.1038/13014
Sesaki, 1999, Division versus fusion: Dnm1p and Fzo1p antagonistically regulate mitochondrial shape, J Cell Biol, 147, 699, 10.1083/jcb.147.4.699
Labrousse, 1999, C. elegans dynamin-related protein DRP-1 controls severing of the mitochondrial outer membrane, Mol Cell, 4, 815, 10.1016/S1097-2765(00)80391-3
Yoon, 2003, The mitochondrial protein hFis1 regulates mitochondrial fission in mammalian cells through an interaction with the dynamin-like protein DLP1, Mol Cell Biol, 23, 5409, 10.1128/MCB.23.15.5409-5420.2003
Stojanovski, 2004, Levels of human Fis1 at the mitochondrial outer membrane regulate mitochondrial morphology, J Cell Sci, 117, 1201, 10.1242/jcs.01058
Gandre-Babbe, 2008, The novel tail-anchored membrane protein Mff controls mitochondrial and peroxisomal fission in mammalian cells, Mol Biol Cell, 19, 2402, 10.1091/mbc.E07-12-1287
Otera, 2010, Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells, J Cell Biol, 191, 1141, 10.1083/jcb.201007152
Palmer, 2011, MiD49 and MiD51, new components of the mitochondrial fission machinery, EMBO Rep, 12, 565, 10.1038/embor.2011.54
Palmer, 2013, Adaptor proteins MiD49 and MiD51 can act independently of Mff and Fis1 in Drp1 recruitment and are specific for mitochondrial fission, J Biol Chem, 288, 27584, 10.1074/jbc.M113.479873
Zhao, 2011, Human MIEF1 recruits Drp1 to mitochondrial outer membranes and promotes mitochondrial fusion rather than fission, EMBO J, 30, 2762, 10.1038/emboj.2011.198
Chen, 2005, Disruption of fusion results in mitochondrial heterogeneity and dysfunction, J Biol Chem, 280, 26185, 10.1074/jbc.M503062200
Chen, 2007, Mitochondrial fusion protects against neurodegeneration in the cerebellum, Cell, 130, 548, 10.1016/j.cell.2007.06.026
Chen, 2010, Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations, Cell, 141, 280, 10.1016/j.cell.2010.02.026
Tait, 2010, Mitochondria and cell death: outer membrane permeabilization and beyond, Nat Rev Mol Cell Biol, 11, 621, 10.1038/nrm2952
Lee, 2004, Roles of the mammalian mitochondrial fission and fusion mediators Fis1, Drp1, and Opa1 in apoptosis, Mol Biol Cell, 15, 5001, 10.1091/mbc.E04-04-0294
Frank, 2001, The role of dynamin-related protein 1, a mediator of mitochondrial fission, in apoptosis, Dev Cell, 1, 515, 10.1016/S1534-5807(01)00055-7
Gegg, 2010, Mitofusin 1 and mitofusin 2 are ubiquitinated in a PINK1/parkin-dependent manner upon induction of mitophagy, Hum Mol Genet, 19, 4861, 10.1093/hmg/ddq419
Chan, 2011, Broad activation of the ubiquitin-proteasome system by Parkin is critical for mitophagy, Hum Mol Genet, 20, 1726, 10.1093/hmg/ddr048
Tanaka, 2010, Proteasome and p97 mediate mitophagy and degradation of mitofusins induced by Parkin, J Cell Biol, 191, 1367, 10.1083/jcb.201007013
Poole, 2008, The PINK1/Parkin pathway regulates mitochondrial morphology, Proc Natl Acad Sci U S A, 105, 1638, 10.1073/pnas.0709336105
Deng, 2008, The Parkinson's disease genes pink1 and parkin promote mitochondrial fission and/or inhibit fusion in Drosophila, Proc Natl Acad Sci U S A, 105, 14503, 10.1073/pnas.0803998105
Tondera, 2009, SLP-2 is required for stress-induced mitochondrial hyperfusion, EMBO J, 28, 1589, 10.1038/emboj.2009.89
Gomes, 2011, During autophagy mitochondria elongate, are spared from degradation and sustain cell viability, Nat Cell Biol, 13, 589, 10.1038/ncb2220
Chen, 2003, Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development, J Cell Biol, 160, 189, 10.1083/jcb.200211046
Yu-Wai-Man, 2010, Multi-system neurological disease is common in patients with OPA1 mutations, Brain, 133, 771, 10.1093/brain/awq007
Zuchner, 2004, Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A, Nat Genet, 36, 449, 10.1038/ng1341
Itoh, 2013, Mitochondrial dynamics in neurodegeneration, Trends Cell Biol, 23, 64, 10.1016/j.tcb.2012.10.006
Chen, 2009, Mitochondrial dynamics – fusion, fission, movement, and mitophagy – in neurodegenerative diseases, Hum Mol Genet, 18, R169, 10.1093/hmg/ddp326
Narendra, 2008, Parkin is recruited selectively to impaired mitochondria and promotes their autophagy, J Cell Biol, 183, 795, 10.1083/jcb.200809125
Pickrell, 2015, The roles of PINK1, parkin, and mitochondrial fidelity in Parkinson's disease, Neuron, 85, 257, 10.1016/j.neuron.2014.12.007
Buhlman, 2014, Functional interplay between Parkin and Drp1 in mitochondrial fission and clearance, Biochim Biophys Acta, 1843, 2012, 10.1016/j.bbamcr.2014.05.012
Twig, 2008, Fission and selective fusion govern mitochondrial segregation and elimination by autophagy, EMBO J, 27, 433, 10.1038/sj.emboj.7601963
Houtkooper, 2013, Mitonuclear protein imbalance as a conserved longevity mechanism, Nature, 497, 451, 10.1038/nature12188
Jovaisaite, 2015, The mitochondrial unfolded protein response-synchronizing genomes, Curr Opin Cell Biol, 33, 74, 10.1016/j.ceb.2014.12.003
Kim, 2013, Molecular chaperone functions in protein folding and proteostasis, Annu Rev Biochem, 82, 323, 10.1146/annurev-biochem-060208-092442
Zhao, 2002, A mitochondrial specific stress response in mammalian cells, EMBO J, 21, 4411, 10.1093/emboj/cdf445
Schulz, 2015, UPR(mt)-mediated cytoprotection and organismal aging, Biochim Biophys Acta, 1847, 1448, 10.1016/j.bbabio.2015.03.008
Martinus, 1996, Selective induction of mitochondrial chaperones in response to loss of the mitochondrial genome, Eur J Biochem, 240, 98, 10.1111/j.1432-1033.1996.0098h.x
Pulliam, 2014, Complex IV-deficient Surf1(−/−) mice initiate mitochondrial stress responses, Biochem J, 462, 359, 10.1042/BJ20140291
Baker, 2011, Mitochondrial protein quality control during biogenesis and aging, Trends Biochem Sci, 36, 254, 10.1016/j.tibs.2011.01.004
Yoneda, 2004, Compartment-specific perturbation of protein handling activates genes encoding mitochondrial chaperones, J Cell Sci, 117, 4055, 10.1242/jcs.01275
Arnould, 2015, Mitochondria retrograde signaling and the UPR mt: where are we in mammals?, Int J Mol Sci, 16, 18224, 10.3390/ijms160818224
Horibe, 2007, The chop gene contains an element for the positive regulation of the mitochondrial unfolded protein response, PLoS ONE, 2, e835, 10.1371/journal.pone.0000835
Aldridge, 2007, Discovery of genes activated by the mitochondrial unfolded protein response (mtUPR) and cognate promoter elements, PLoS ONE, 2, e874, 10.1371/journal.pone.0000874
Papa, 2014, SirT3 regulates the mitochondrial unfolded protein response, Mol Cell Biol, 34, 699, 10.1128/MCB.01337-13
Papa, 2011, Estrogen receptor mediates a distinct mitochondrial unfolded protein response, J Cell Sci, 124, 1396, 10.1242/jcs.078220
Radke, 2008, Mitochondrial protein quality control by the proteasome involves ubiquitination and the protease Omi, J Biol Chem, 283, 12681, 10.1074/jbc.C800036200
Mouchiroud, 2013, The NAD(+)/sirtuin pathway modulates longevity through activation of mitochondrial UPR and FOXO signaling, Cell, 154, 430, 10.1016/j.cell.2013.06.016
Jovaisaite, 2014, The mitochondrial unfolded protein response, a conserved stress response pathway with implications in health and disease, J Exp Biol, 217, 137, 10.1242/jeb.090738
Durieux, 2011, The cell-non-autonomous nature of electron transport chain-mediated longevity, Cell, 144, 79, 10.1016/j.cell.2010.12.016