Difference between revisions of "Pichaud 2010 J Exp Biol"
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{{Publication | {{Publication | ||
|title=Pichaud N, Chatelain HE, Ballard JWO, Tanguay R, Morrow G, Blier PU (2010)Thermal sensitivity of mitochondrial metabolism in two distinct mitotypes of Drosophila simulans: evaluation of mitochondrial plasticity. J | |title=Pichaud N, Chatelain HE, Ballard JWO, Tanguay R, Morrow G, Blier PU (2010)Thermal sensitivity of mitochondrial metabolism in two distinct mitotypes of Drosophila simulans: evaluation of mitochondrial plasticity. J Exp Biol 213: 1665-1675. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/20435817 PMID:20435817] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/20435817 PMID:20435817] | ||
|authors=Pichaud N, Chatelain HE, Ballard JWO, Tanguay R, Morrow G, Blier PU | |authors=Pichaud N, Chatelain HE, Ballard JWO, Tanguay R, Morrow G, Blier PU | ||
|year=2010 | |year=2010 | ||
|journal=J | |journal=J Exp Biol | ||
|abstract=The overall aim of this study was to (1) evaluate the adaptive value of mitochondrial DNA by comparing mitochondrial | |abstract=The overall aim of this study was to (1) evaluate the adaptive value of mitochondrial DNA by comparing mitochondrial performance in populations possessing different haplotypes and distribution, and to (2) evaluate the sensitivity of different enzymes of the [[electron transport system]] (ETS) during temperature-induced changes. We measured the impact of temperature of | ||
performance in populations possessing different haplotypes and distribution, and to (2) evaluate the sensitivity of different | mitochondrial respiration and several key enzymes of mitochondrial metabolism in two mitotypes (siII and siIII) of Drosophila simulans. The temperature dependencies of oxygen consumption for mitochondria isolated from flight muscle was assessed with Complex I substrates (pyruvate + malate + proline) and with sn glycerol-3-phosphate (to reduce Complex III via glycerophosphate | ||
enzymes of the electron transport system (ETS) during temperature-induced changes. We measured the impact of temperature of | dehydrogenase) in both coupled and uncoupled states. Activities of citrate synthase, cytochrome c oxidase (COX), catalase and aconitase, and the excess capacity of COX at high convergent pathway flux were also measured as a function of temperature. Overall, our results showed that functional differences between the two mitotypes are few. Results suggest that differences | ||
mitochondrial respiration and several key enzymes of mitochondrial metabolism in two mitotypes (siII and siIII) of Drosophila | between the two mitotypes could hardly explain the temperature-specific differences measured in mitochondria performances. It suggests that some other factor(s) may be driving the maintenance of mitotypes. We also show that the different enzymes of the ETS have different thermal sensitivities. The catalytic capacities of these enzymes vary with temperature changes, and the | ||
simulans. The temperature dependencies of oxygen consumption for mitochondria isolated from flight muscle was assessed with | corresponding involvement of the different steps on mitochondrial regulation probably varies with temperature. For example, the excess COX capacity is low, even non-existent, at high and intermediate temperatures (18 Β°C, 24 Β°C and 28 Β°C) whereas it is quite high at a lower temperature (12 Β°C), suggesting release of respiration control by COX at low temperature. | ||
dehydrogenase) in both coupled and uncoupled states. Activities of citrate synthase, cytochrome c oxidase (COX), catalase and | |||
aconitase, and the excess capacity of COX at high convergent pathway flux were also measured as a function of temperature. | |||
Overall, our results showed that functional differences between the two mitotypes are few. Results suggest that differences | |||
between the two mitotypes could hardly explain the temperature-specific differences measured in mitochondria performances. It | |||
suggests that some other factor(s) may be driving the maintenance of mitotypes. We also show that the different enzymes of the | |||
ETS have different thermal sensitivities. The catalytic capacities of these enzymes vary with temperature changes, and the | |||
corresponding involvement of the different steps on mitochondrial regulation probably varies with temperature. For example, | |||
the excess COX capacity is low, even non-existent, at high and intermediate temperatures ( | |||
quite high at a lower temperature ( | |||
Supplementary material available online at http://jeb.biologists.org/cgi/content/full/213/10/1665/DC1 | Supplementary material available online at http://jeb.biologists.org/cgi/content/full/213/10/1665/DC1 | ||
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{{Labeling | {{Labeling | ||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
|injuries= | |injuries=Genetic Defect; Knockdown; Overexpression | ||
|organism= | |organism=Other Non-Mammal | ||
|tissues=Skeletal Muscle | |||
|preparations=Isolated Mitochondria | |preparations=Isolated Mitochondria | ||
|enzymes=Complex | |enzymes=Complex IV; Cytochrome c Oxidase, Marker Enzyme | ||
|kinetics=Temperature | |kinetics=Temperature | ||
|topics= | |topics=Flux Control; Additivity; Threshold; Excess Capacity | ||
|additional=Drosophila | |||
}} | }} |
Revision as of 19:59, 7 March 2012
Pichaud N, Chatelain HE, Ballard JWO, Tanguay R, Morrow G, Blier PU (2010)Thermal sensitivity of mitochondrial metabolism in two distinct mitotypes of Drosophila simulans: evaluation of mitochondrial plasticity. J Exp Biol 213: 1665-1675. |
Pichaud N, Chatelain HE, Ballard JWO, Tanguay R, Morrow G, Blier PU (2010) J Exp Biol
Abstract: The overall aim of this study was to (1) evaluate the adaptive value of mitochondrial DNA by comparing mitochondrial performance in populations possessing different haplotypes and distribution, and to (2) evaluate the sensitivity of different enzymes of the electron transport system (ETS) during temperature-induced changes. We measured the impact of temperature of mitochondrial respiration and several key enzymes of mitochondrial metabolism in two mitotypes (siII and siIII) of Drosophila simulans. The temperature dependencies of oxygen consumption for mitochondria isolated from flight muscle was assessed with Complex I substrates (pyruvate + malate + proline) and with sn glycerol-3-phosphate (to reduce Complex III via glycerophosphate dehydrogenase) in both coupled and uncoupled states. Activities of citrate synthase, cytochrome c oxidase (COX), catalase and aconitase, and the excess capacity of COX at high convergent pathway flux were also measured as a function of temperature. Overall, our results showed that functional differences between the two mitotypes are few. Results suggest that differences between the two mitotypes could hardly explain the temperature-specific differences measured in mitochondria performances. It suggests that some other factor(s) may be driving the maintenance of mitotypes. We also show that the different enzymes of the ETS have different thermal sensitivities. The catalytic capacities of these enzymes vary with temperature changes, and the corresponding involvement of the different steps on mitochondrial regulation probably varies with temperature. For example, the excess COX capacity is low, even non-existent, at high and intermediate temperatures (18 Β°C, 24 Β°C and 28 Β°C) whereas it is quite high at a lower temperature (12 Β°C), suggesting release of respiration control by COX at low temperature.
Supplementary material available online at http://jeb.biologists.org/cgi/content/full/213/10/1665/DC1 β’ Keywords: Drosophila simulans, metabolism, mitochondrial DNA, mitochondrial respiration, temperature, thermal sensitivity.
β’ O2k-Network Lab: CA_Rimouski_Blier PU, AU Sydney Ballard JWO
Labels:
Stress:Genetic Defect; Knockdown; Overexpression"Genetic Defect; Knockdown; Overexpression" is not in the list (Cell death, Cryopreservation, Ischemia-reperfusion, Permeability transition, Oxidative stress;RONS, Temperature, Hypoxia, Mitochondrial disease) of allowed values for the "Stress" property. Organism: Other Non-Mammal"Other Non-Mammal" is not in the list (Human, Pig, Mouse, Rat, Guinea pig, Bovines, Horse, Dog, Rabbit, Cat, ...) of allowed values for the "Mammal and model" property. Tissue;cell: Skeletal Muscle"Skeletal Muscle" is not in the list (Heart, Skeletal muscle, Nervous system, Liver, Kidney, Lung;gill, Islet cell;pancreas;thymus, Endothelial;epithelial;mesothelial cell, Blood cells, Fat, ...) of allowed values for the "Tissue and cell" property. Preparation: Isolated Mitochondria"Isolated Mitochondria" is not in the list (Intact organism, Intact organ, Permeabilized cells, Permeabilized tissue, Homogenate, Isolated mitochondria, SMP, Chloroplasts, Enzyme, Oxidase;biochemical oxidation, ...) of allowed values for the "Preparation" property. Enzyme: Complex IV; Cytochrome c Oxidase"Complex IV; Cytochrome c Oxidase" is not in the list (Adenine nucleotide translocase, Complex I, Complex II;succinate dehydrogenase, Complex III, Complex IV;cytochrome c oxidase, Complex V;ATP synthase, Inner mt-membrane transporter, Marker enzyme, Supercomplex, TCA cycle and matrix dehydrogenases, ...) of allowed values for the "Enzyme" property., Marker Enzyme"Marker Enzyme" is not in the list (Adenine nucleotide translocase, Complex I, Complex II;succinate dehydrogenase, Complex III, Complex IV;cytochrome c oxidase, Complex V;ATP synthase, Inner mt-membrane transporter, Marker enzyme, Supercomplex, TCA cycle and matrix dehydrogenases, ...) of allowed values for the "Enzyme" property. Regulation: Flux Control; Additivity; Threshold; Excess Capacity"Flux Control; Additivity; Threshold; Excess Capacity" is not in the list (Aerobic glycolysis, ADP, ATP, ATP production, AMP, Calcium, Coupling efficiency;uncoupling, Cyt c, Flux control, Inhibitor, ...) of allowed values for the "Respiration and regulation" property.
HRR: Oxygraph-2k
Drosophila