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{{Publication | {{Publication | ||
|title=Pichaud N, Chatelain | |title=Pichaud N, Chatelain EH, 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 213:1665-75. | ||
|info=[http://www.ncbi.nlm.nih.gov/pubmed/20435817 PMID:20435817] | |info=[http://www.ncbi.nlm.nih.gov/pubmed/20435817 PMID: 20435817 Open Access] | ||
|authors=Pichaud N, Chatelain | |authors=Pichaud N, Chatelain EH, 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 transfer-pathway]] (ET-pathway) 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 | 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 ET-pathway 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 ยฐC, 24 ยฐC and 28 ยฐC) whereas it is quite high at a lower temperature (12 ยฐC), 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 | |||
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 ( | |||
[http://jeb.biologists.org/cgi/content/full/213/10/1665/DC1 Supplementary material available online] | |||
|keywords=Drosophila simulans, | |keywords=''Drosophila simulans'', Metabolism, Mitochondrial DNA, Mitochondrial respiration, Temperature, Thermal sensitivity | ||
|mipnetlab= | |mipnetlab=CA Rimouski Blier PU, AU Sydney Ballard JW, CA Moncton Pichaud N | ||
}} | }} | ||
{{Labeling | {{Labeling | ||
|area=mtDNA;mt-genetics, Genetic knockout;overexpression | |||
|organism=Drosophila | |||
|tissues=Skeletal muscle | |||
|preparations=Isolated mitochondria | |||
|enzymes=Complex IV;cytochrome c oxidase, Marker enzyme | |||
|couplingstates=OXPHOS, ET | |||
|pathways=N, Gp | |||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
| | |additional=Drosophila | ||
}} | }} |
Latest revision as of 11:05, 23 June 2022
Pichaud N, Chatelain EH, 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 213:1665-75. |
Pichaud N, Chatelain EH, 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 transfer-pathway (ET-pathway) 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 ET-pathway 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 ยฐC, 24 ยฐC and 28 ยฐC) whereas it is quite high at a lower temperature (12 ยฐC), suggesting release of respiration control by COX at low temperature.
Supplementary material available online โข Keywords: Drosophila simulans, Metabolism, Mitochondrial DNA, Mitochondrial respiration, Temperature, Thermal sensitivity
โข O2k-Network Lab: CA Rimouski Blier PU, AU Sydney Ballard JW, CA Moncton Pichaud N
Labels: MiParea: mtDNA;mt-genetics, Genetic knockout;overexpression
Organism: Drosophila
Tissue;cell: Skeletal muscle
Preparation: Isolated mitochondria
Enzyme: Complex IV;cytochrome c oxidase, Marker enzyme
Coupling state: OXPHOS, ET Pathway: N, Gp HRR: Oxygraph-2k
Drosophila