Effects of MFN2 mutation (Homo sapiens)

From WikiPathways

Revision as of 00:29, 23 April 2024 by Eweitz (Talk | contribs)
Jump to: navigation, search
ArcPathVisio Brace Ellipse EndoplasmicReticulum GolgiApparatus HexagonPathVisio MimDegradation Mitochondria Octagon PentagonPathVisio Rectangle RoundedRectangle SarcoplasmicReticulum TriangleEquilateralEast TrianglePathVisio none Retrogate transportKinesinAccumulationER-mitochondria tetheringDecreased energy metabolismBindsAxon degenerationLinkSynaptic vesicleLow negative resting membrane potentialLate endosome / lysosomePhospholipase DATPNa+KIF1BCa2+SNCAATAT1Defect(s) in mitochondrial axonal transportAutophagyCardiolipinsSYPL1SynaptogenesisPhosphatidic acidsMFN2ApoptosisTUBB3MAP2RABAC1RAB7ATRAK1RHOT1DYNC1H1DYNC1I1DYNC1LI2DYNC2H1DYNC2I1DYNC2I2DCTN1BAXCASP8CASP3TP53RAB3BRAB3AMutatedName: MFN2 draftOrganism: Homo sapiens


Description

Mutation in Mitofusin2 and all the proteins that are changed because of the mutation

Try the New WikiPathways

View approved pathways at the new wikipathways.org.

Quality Tags

Image:Curated.pngReview changes for Approved

Ontology Terms

No Tags!
 

Bibliography

View all...
  1. Fang D, Yan S, Yu Q, Chen D, Yan SS; ''Mfn2 is Required for Mitochondrial Development and Synapse Formation in Human Induced Pluripotent Stem Cells/hiPSC Derived Cortical Neurons.''; Sci Rep, 2016 PubMed Europe PMC Scholia
  2. Larrea D, Pera M, Gonnelli A, Quintana-Cabrera R, Akman HO, Guardia-Laguarta C, Velasco KR, Area-Gomez E, Dal Bello F, De Stefani D, Horvath R, Shy ME, Schon EA, Giacomello M; ''MFN2 mutations in Charcot-Marie-Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics.''; Hum Mol Genet, 2019 PubMed Europe PMC Scholia
  3. Zanfardino P, Amati A, Petracca EA, Santorelli FM, Petruzzella V; ''Torin1 restores proliferation rate in Charcot-Marie-Tooth disease type 2A cells harbouring MFN2 (mitofusin 2) mutation.''; Acta Myol, 2022 PubMed Europe PMC Scholia
  4. Misko A, Jiang S, Wegorzewska I, Milbrandt J, Baloh RH; ''Mitofusin 2 is necessary for transport of axonal mitochondria and interacts with the Miro/Milton complex.''; J Neurosci, 2010 PubMed Europe PMC Scholia
  5. Rizzo F, Ronchi D, Salani S, Nizzardo M, Fortunato F, Bordoni A, Stuppia G, Del Bo R, Piga D, Fato R, Bresolin N, Comi GP, Corti S; ''Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neurons.''; Hum Mol Genet, 2016 PubMed Europe PMC Scholia
  6. Wang JT, Medress ZA, Barres BA; ''Axon degeneration: molecular mechanisms of a self-destruction pathway.''; J Cell Biol, 2012 PubMed Europe PMC Scholia
  7. Misko AL, Sasaki Y, Tuck E, Milbrandt J, Baloh RH; ''Mitofusin2 mutations disrupt axonal mitochondrial positioning and promote axon degeneration.''; J Neurosci, 2012 PubMed Europe PMC Scholia
  8. Kumar A, Larrea D, Pero ME, Infante P, Conenna M, Shin GJ, Grueber WB, Di Marcotullio L, Area-Gomez E, Bartolini F; ''MFN2-dependent recruitment of ATAT1 coordinates mitochondria motility with alpha-tubulin acetylation and is disrupted in CMT2A.''; bioRxiv, 2023 PubMed Europe PMC Scholia
  9. Mou Y, Dein J, Chen Z, Jagdale M, Li XJ; ''MFN2 Deficiency Impairs Mitochondrial Transport and Downregulates Motor Protein Expression in Human Spinal Motor Neurons.''; Front Mol Neurosci, 2021 PubMed Europe PMC Scholia
  10. Chandhok G, Lazarou M, Neumann B; ''Structure, function, and regulation of mitofusin-2 in health and disease.''; Biol Rev Camb Philos Soc, 2018 PubMed Europe PMC Scholia
  11. Baloh RH, Schmidt RE, Pestronk A, Milbrandt J; ''Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations.''; J Neurosci, 2007 PubMed Europe PMC Scholia
  12. Lee S, Min KT; ''The Interface Between ER and Mitochondria: Molecular Compositions and Functions.''; Mol Cells, 2018 PubMed Europe PMC Scholia

History

View all...
CompareRevisionActionTimeUserComment
129470
Approved
view02:26, 23 April 2024EweitzEconomize layout
129465view01:56, 23 April 2024EweitzImprove interaction alignment
129464view01:55, 23 April 2024EweitzDisambiguate interaction source, economize layout
129463view01:52, 23 April 2024EweitzRemove superfluous descriptor
129462view01:50, 23 April 2024EweitzUse standard pathway color
129461view01:43, 23 April 2024EweitzOntology Term : 'altered transport pathway' added !
129460view01:42, 23 April 2024EweitzEconomize layout, improve alignment
129457view00:58, 23 April 2024EweitzOntology Term : 'altered cellular autophagy' added !
129456view00:58, 23 April 2024EweitzOntology Term : 'apoptotic cell death pathway' added !
129455view00:57, 23 April 2024EweitzModified title
129454view00:55, 23 April 2024EweitzModified description
129453view00:53, 23 April 2024EweitzEconomize layout
129452view00:47, 23 April 2024EweitzEconomize layout
129451view00:29, 23 April 2024EweitzEconomize layout, standardize shapes
129014view10:48, 6 March 2024JordyG02Improved arrows
129000view18:15, 28 February 2024JordyG02removed opa1 and mtor
128999view15:39, 28 February 2024JordyG02New pathway

External references

DataNodes

View all...
Name  ↓Type  ↓Database reference  ↓Comment  ↓
ATAT1GeneProductENSG00000137343 (Ensembl)
ATPMetaboliteCHEBI:30616 (ChEBI)
ApoptosisPathwayWP254 (WikiPathways)
AutophagyPathwayWP4923 (WikiPathways)
BAXGeneProductENSG00000087088 (Ensembl)
CASP3GeneProductENSG00000164305 (Ensembl)
CASP8GeneProductENSG00000064012 (Ensembl)
Ca2+MetaboliteCHEBI:29108 (ChEBI)
CardiolipinsMetaboliteCHEBI:28494 (ChEBI)
DCTN1GeneProductENSG00000204843 (Ensembl)
DYNC1H1GeneProductENSG00000197102 (Ensembl)
DYNC1I1GeneProductENSG00000158560 (Ensembl)
DYNC1LI2GeneProductENSG00000135720 (Ensembl)
DYNC2H1GeneProductENSG00000187240 (Ensembl)
DYNC2I1GeneProductENSG00000126870 (Ensembl)
DYNC2I2GeneProductENSG00000119333 (Ensembl)
Defect(s) in mitochondrial axonal transportPathwayWP4856 (WikiPathways)
KIF1BGeneProductENSG00000054523 (Ensembl)
MAP2GeneProductENSG00000078018 (Ensembl)
MFN2GeneProductENSG00000116688 (Ensembl)
Na+MetaboliteCHEBI:29101 (ChEBI)
Phosphatidic acidsMetaboliteCHEBI:16337 (ChEBI)
Phospholipase DMetaboliteQ700007 (Wikidata)
RAB3AGeneProductENSG00000105649 (Ensembl)
RAB3BGeneProductENSG00000169213 (Ensembl)
RAB7AGeneProductENSG00000075785 (Ensembl)
RABAC1GeneProductENSG00000105404 (Ensembl)
RHOT1GeneProductENSG00000126858 (Ensembl)
SNCAGeneProductENSG00000145335 (Ensembl)
SYPL1GeneProductENSG00000008282 (Ensembl)
SynaptogenesisPathwayWP5231 (WikiPathways)
TP53GeneProductENSG00000141510 (Ensembl)
TRAK1GeneProductENSG00000182606 (Ensembl)
TUBB3GeneProductENSG00000258947 (Ensembl)

Annotated Interactions

No annotated interactions

Retrieved from "https://classic.wikipathways.org/index.php/Pathway:WP5443"
Personal tools