The machines that divide and fuse mitochondria
By J. Nunnari. Annual Review of Biochemistry, 2007
810 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/93830fbe895e0ce3fec1f8a7dcd097f53b3ab33d
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In Molecular Biology
- D. C. Chan
- R. Youle
- B. Westermann
- J. Nunnari
- Hsiuchen Chen
- A. M. van der Bliek
- D. Suen
- Angelika S. Rambold
Citations in the corpus
- Mechanics of membrane fusion (2008, background): “; and intracellular fusion reactions in exocytosis, protein trafficking, mitochondrial remodeling and resealing of plasma membrane”
- Reversible phosphorylation of Drp1 by cyclic AMP‐dependent protein kinase and calcineurin regulates mitochondrial fission and cell death (2007, background): “However, opposite regulation of enzymes by neighbouring phosphorylation sites is well documented (Hudmon & Schulman, 2002).”
- SLP‐2 is required for stress‐induced mitochondrial hyperfusion (2009, positive): “Mitochondrial fission due to impaired mitochondrial fusion is often accompanied by bioenergetics defects due to a loss of mitochondrial DNA (mtDNA) (Chan, 2006; Hoppins et al , 2007).”
- Transcriptional control of mitochondrial biogenesis: the central role of PGC-1alpha. (2008, background): “The processes of fission/fusion are controlled by GTPases, most of which were identified in genetic screens in yeast (for recent reviews see reference 4,5 ).”
- Mitochondrial dynamics and apoptosis. (2008, background): “Dynamin-related protein 1 (Drp1), a large GTPase, mediates mitochondrial fission in mammalian cells (for reviews, see Okamoto and Shaw 2005; Hoppins et al. 2007).”
- Mitochondria: In Sickness and in Health (2012, background): “Mitochondrial division and fusion aremediated by the action of large multidomain dynamin-related GTPases that function via self-assembly to remodel diverse membranes in cells (Hoppins et al., 2007).”
- Mff is an essential factor for mitochondrial recruitment of Drp1 during mitochondrial fission in mammalian cells (2010, background): “mitochondrial networks, and this dynamic morphology is essential for normal mitochondrial and cellular functions (Karbowski and Youle, 2003; Okamoto and Shaw, 2005; Chan, 2006; McBride et al., 2006; Cerveny et al., 2007b; Hoppins et al., 2007; Benard and Karbowski, 2009).”
- The dynamin-related GTPase Drp1 is required for embryonic and brain development in mice (2009, background): “…are highly dynamic organelles that continuously fuse and divide within cells (Karbowski and Youle, 2003; Osteryoung and Nunnari, 2003; Rube and van der Bliek, 2004; Okamoto and Shaw, 2005; Anesti and Scorrano, 2006; Chan, 2006; McBride et al., 2006; Cerveny et al., 2007a; Hoppins et al., 2007).”
- Mitochondrial dynamics in mammalian health and disease. (2009, background): “strict the mitochondrial tubule by DRP1 oligomers, which surround it, thereby forming a spiral ring around the scission site (133, 143, 273, 327).”
- Mitochondrial fusion and fission in cell life and death (2010, background): “Although most of the evolutionarily conserved core components of the mitochondrial fusion and fission machineries have been described in the past 15 years ( Table 1 ), more recent work revealed mechanistic insights into their molecular functio”
- Mechanisms of mesenchymal stem/stromal cell function (2016, background): “, fusion, fission, tethering, and trafficking) [127, 128] may also promote or inhibit intercellular mitochondria transfer.”
- Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations (2010, positive): “INTRODUCTION Mitochondrial fusion and fission have emerged as important processes that govern mitochondrial function from yeast to mammals (Detmer and Chan, 2007a; Suen et al., 2008; Okamoto and Shaw, 2005; Hoppins et al., 2007).”
- Mitochondrial Dysfunction in Parkinson's Disease (2011, background): “Several independent groups reported a role of PINK1 in mitochondrial integrity by regulating the mitochondrial fission machinery [95], which might have an impact on dopaminergic synapses and contribute to DA neuron degeneration [96–98].”