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Difference between revisions of "Towheed 2012 Abstract IOC72"

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{{Abstract
{{Abstract
|title=Towheed MA (2012) Elucidating pathogenesis of ATP synthase dysfunction in a Drosophila model of mitochondrial encephalomyopathy. Mitochondr Physiol Network 17.13.
|title=Towheed A (2012) Elucidating pathogenesis of ATP synthase dysfunction in a ''Drosophila'' model of mitochondrial encephalomyopathy. Mitochondr Physiol Network 17.13.
|info=[http://www.oroboros.at/?IOC-dec_schroecken IOC72 Open Access]
|info=[http://www.oroboros.at/?IOC-dec_schroecken IOC72 Open Access]
|authors=Towheed MA, Celotto AM, Palladino MJ
|authors=Towheed A, Celotto AM, Palladino MJ
|year=2012
|year=2012
|event=[[IOC72]]
|event=[[IOC72]]
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References:  
References:  


[1] Celotto, A.M., et al., Mitochondrial encephalomyopathy in Drosophila. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2006. 26(3): p. 810-20.
[1] [http://www.ncbi.nlm.nih.gov/pubmed/16421301 Celotto AM, Frank AC, McGrath SW, Fergestad T, Van Voorhies WA, Buttle KF, Mannella CA, Palladino MJ (2006) Mitochondrial encephalomyopathy in Drosophila. J Neurosci 26: 810-820 Open Access]


[2] Dudkina, N.V., et al., Structure of dimeric ATP synthase from mitochondria: an angular association of monomers induces the strong curvature of the inner membrane. FEBS letters, 2005. 579(25): p. 5769-72.
[2] [http://www.ncbi.nlm.nih.gov/pubmed?term=Structure%20of%20dimeric%20ATP%20synthase%20from%20mitochondria%3A%20an%20angular%20association%20of%20monomers%20induces%20the%20strong%20curvature%20of%20the%20inner%20membrane Dudkina NV, Heinemeyer J, Keegstra W, Boekema EJ, Braun HP (2005) Structure of dimeric ATP synthase from mitochondria: an angular association of monomers induces the strong curvature of the inner membrane. FEBS Lett 579: 5769-5772]


[3] Strauss, M., et al., Dimer ribbons of ATP synthase shape the inner mitochondrial membrane. The EMBO journal, 2008. 27(7): p. 1154-60.
[3] [http://www.ncbi.nlm.nih.gov/pubmed?term=Dimer%20ribbons%20of%20ATP%20synthase%20shape%20the%20inner%20mitochondrial%20membrane Strauss M, Hofhaus G, Schroeder RR, Kühlbrandt W (2008) Dimer ribbons of ATP synthase shape the inner mitochondrial membrane. EMBO J 27: 1154-1160 Open Access]
 
[4] Wagner, K., et al., Stepwise assembly of dimeric F(1)F(o)-ATP synthase in mitochondria involves the small F(o)-subunits k and i. Molecular biology of the cell, 2010. 21(9): p. 1494-504.
 
[5] Rabl, R., et al., Formation of cristae and crista junctions in mitochondria depends on antagonism between Fcj1 and Su e/g. Journal of Cell Biology, 2009. 185(6): p. 1047-1063.
|keywords=Mitochondrial missense mutations, ''Drosophila'', Complex V
|keywords=Mitochondrial missense mutations, ''Drosophila'', Complex V
|mipnetlab=US PA Pittsburgh Palladino MJ
|mipnetlab=US PA Pittsburgh Palladino MJ
}}
}}
{{Labeling
{{Labeling
|area=Respiration, Genetic knockout;overexpression, mt-Medicine
|diseases=Neurodegenerative
|organism=Drosophila, Hexapods
|preparations=Intact organism, Permeabilized tissue
|enzymes=Complex V;ATP synthase
|topics=Substrate
|couplingstates=LEAK, ROUTINE, OXPHOS, ET
|pathways=N, S, NS
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|injuries=Mitochondrial Disease; Degenerative Disease and Defect
|organism=Other Non-Mammal
|preparations=Intact Organism, Permeabilized tissue, Homogenate, Isolated Mitochondria
|substratestates=CI, CII, CI+II
|enzymes=Complex II; Succinate Dehydrogenase, Complex V; ATP Synthase
|kinetics=ADP; Pi, Oxygen, Reduced Substrate; Cytochrome c, Inhibitor; Uncoupler, Temperature, pH
|topics=Respiration; OXPHOS; ETS Capacity, Flux Control; Threshold; Excess Capacity
}}
}}
__NOTOC__
__NOTOC__
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(2) Pittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, 15261
(2) Pittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, 15261
== Supplementary references ==
[4] [http://www.ncbi.nlm.nih.gov/pubmed?term=Stepwise%20assembly%20of%20dimeric%20F(1)F(o)-ATP%20synthase%20in%20mitochondria%20involves%20the%20small%20F(o)-subunits%20k%20and%20i Wagner K, Perschil I, Fichter CD, van der Laan M (2010 Stepwise assembly of dimeric F(1)F(o)-ATP synthase in mitochondria involves the small F(o)-subunits k and i. Mol Biol Cell 21: 1494-1504 Open Access]
[5] [http://www.ncbi.nlm.nih.gov/pubmed?term=Formation%20of%20cristae%20and%20crista%20junctions%20in%20mitochondria%20depends%20on%20antagonism%20between%20Fcj1 Rabl R, Soubannier V, Scholz R, Vogel F, Mendl N, Vasiljev-Neumeyer A, Körner C, Jagasia R, Keil T, Baumeister W, Cyrklaff M, Neupert W, Reichert AS  (2009) Formation of cristae and crista junctions in mitochondria depends on antagonism between Fcj1 and Su e/g. J Cell Biol 185: 1047-1063 Open Access]


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Latest revision as of 15:18, 13 November 2017

Towheed A (2012) Elucidating pathogenesis of ATP synthase dysfunction in a Drosophila model of mitochondrial encephalomyopathy. Mitochondr Physiol Network 17.13.

Link: IOC72 Open Access

Towheed A, Celotto AM, Palladino MJ (2012)

Event: IOC72

Mohammad Atif Towheed

Mitochondrial missense mutations lead to devastating disorders in humans known as mitochondrial encephalomyopathies. Our lab has previously identified a pathogenic mutation (G116E) in Drosophila ATP6, which is a subunit of Complex V of the mitochondrial electron transport chain. This mutation causes progressive neuromuscular dysfunction and myodegeneration, and is a model for human mitochondrial disorders such as NARP (neuropathy, ataxia, and retinitis pigmentosa), MILS (maternally inherited Leigh's syndrome), and FBSN (familial bilateral striatal necrosis). The underlying pathophysiology of these mutant flies is not clearly understood. In addition to shortened lifespan, myopathy and neural dysfunction, these flies also exhibit abnormal mitochondrial morphology in ~60% of its mitochondria. The mitochondrial cristae are dilated as opposed to flat cristae in wild-type flies. Complex V is unable to efficiently dimerize and ATP synthase activity is severely diminished in ATP6 [1] flies [1]. However, complex V ATPase activity is detectable and the membrane potential is not affected. These mutant flies also show an increase in ROS as a function of age. Earlier studies suggest that the complexes of the electron transport chain play a role in maintaining normal mitochondrial cristae morphology [2,3]. We hypothesize that this missense mutation affects Complex V dimerization as it lies at the dimer interface and contributes significantly to the pathogenesis. To test our hypothesis, we use RNAi to knock down subunits ATPe and ATPg that are known to assist in ATP synthase dimerization [4,5]. Since, mitochondrial disorders have a tissue specific pattern of presentation, we examine which tissue contributes to the pathophysiology most by using specific GAL4 fly lines. ATPe and/or ATPg are knocked down in either muscle or neuronal tissues and their motor function and life spans are tested. In addition, we are investigating the altered physiology of the mitochondria in these mutants. To determine how the ATP6 [1] flies use their mitochondrial electron transport chain, we will investigate the mitochondrial oxidative phosphorylation using high-resolution respirometry. Respirometry and measures of biochemical activities of mitochondrial specific enzymes will help to elucidate the pathophysiology of mitochondrial diseases in vivo.

References:

[1] Celotto AM, Frank AC, McGrath SW, Fergestad T, Van Voorhies WA, Buttle KF, Mannella CA, Palladino MJ (2006) Mitochondrial encephalomyopathy in Drosophila. J Neurosci 26: 810-820 Open Access

[2] Dudkina NV, Heinemeyer J, Keegstra W, Boekema EJ, Braun HP (2005) Structure of dimeric ATP synthase from mitochondria: an angular association of monomers induces the strong curvature of the inner membrane. FEBS Lett 579: 5769-5772

[3] Strauss M, Hofhaus G, Schroeder RR, Kühlbrandt W (2008) Dimer ribbons of ATP synthase shape the inner mitochondrial membrane. EMBO J 27: 1154-1160 Open Access

Keywords: Mitochondrial missense mutations, Drosophila, Complex V

O2k-Network Lab: US PA Pittsburgh Palladino MJ


Labels: MiParea: Respiration, Genetic knockout;overexpression, mt-Medicine  Pathology: Neurodegenerative 

Organism: Drosophila, Hexapods 

Preparation: Intact organism, Permeabilized tissue  Enzyme: Complex V;ATP synthase  Regulation: Substrate  Coupling state: LEAK, ROUTINE, OXPHOS, ET  Pathway: N, S, NS  HRR: Oxygraph-2k 




Affiliations and author contributions

Towheed MA (1,2), Celotto AM (1,2), Palladino MJ (1,2)

(1) Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, 15261

(2) Pittsburgh Institute for Neurodegenerative Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, 15261

Supplementary references

[4] Wagner K, Perschil I, Fichter CD, van der Laan M (2010 Stepwise assembly of dimeric F(1)F(o)-ATP synthase in mitochondria involves the small F(o)-subunits k and i. Mol Biol Cell 21: 1494-1504 Open Access

[5] Rabl R, Soubannier V, Scholz R, Vogel F, Mendl N, Vasiljev-Neumeyer A, Körner C, Jagasia R, Keil T, Baumeister W, Cyrklaff M, Neupert W, Reichert AS (2009) Formation of cristae and crista junctions in mitochondria depends on antagonism between Fcj1 and Su e/g. J Cell Biol 185: 1047-1063 Open Access

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