A Lethal de Novo Mutation in the Middle Domain of the Dynamin-related GTPase Drp1 Impairs Higher Order Assembly and Mitochondrial Division*
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Summary
TheDrp1 A395D lethal defect likely resulted in impaired higher order assembly of Drp1 at mitochondria, leading to decreased fission, elongated mitochondria), and altered cellular distribution of mitochondria.
- Type
- article
- Published
- 2010-08-09
- Cited by
- 186
- References
- 47
- Access
- Open access
- OpenAlex
- https://openalex.org/W1963940229
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:31489811
Keywords
Mitochondrial fission, GTPase, Mitochondrion, Biology, Cell biology
References
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- Structure of human guanylate-binding protein 1 representing a unique class of GTP-binding proteins
- Simultaneous determination of protein aggregation, degradation, and absolute molecular weight by size exclusion chromatography-multiangle laser light scattering.
- Mitochondrial Fission and Fusion Mediators, hFis1 and OPA1, Modulate Cellular Senescence*
Cited by
- Mitochondrial Membrane Dynamics and Inherited Optic Neuropathies.
- Peroxisome interactions and cross-talk with other subcellular compartments in animal cells.
- Dynamin-Related Protein 1 as a therapeutic target in cardiac arrest
- The Roles of SUMO in Metabolic Regulation
- Posttranslational regulation of protein function and stability at the mitochondria and beyond
- Mitochondrien als Kraftwerk der β-Zelle
- How the Wnt signaling pathway protects from neurodegeneration: the mitochondrial scenario
- Peroxisome morphology in pathology.
- Metabolic Stress and Disorders Related to Alterations in Mitochondrial Fission or Fusion
- Heterogeneous nuclear ribonucleoprotein A1 post-transcriptionally regulates Drp1 expression in neuroblastoma cells
- Parkinson-causing α-synuclein missense mutations shift native tetramers to monomers as a mechanism for disease initiation
- Proliferation and fission of peroxisomes - An update.
- The mitochondrial fission receptor Mff selectively recruits oligomerized Drp1
- Mécanodétection des forces hémodynamiques lors du développement endocardique chez l'espèce Danio rerio
- Mitochondrial Genetics and Optic Neuropathy.
- Human MIEF1 recruits Drp1 to mitochondrial outer membranes and promotes mitochondrial fusion rather than fission
- Purification, crystallization and X-ray diffraction analysis of human dynamin-related protein 1 GTPase-GED fusion protein.
- In vivo functions of Drp1: Lessons learned from yeast genetics and mouse knockouts
- The power of yeast to model diseases of the powerhouse of the cell
- A designed point mutant in Fis1 disrupts dimerization and mitochondrial fission
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