Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8318872 | Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology | 2016 | 8 Pages |
Abstract
In response to changes in energy demand and nutrient supply, the organism regulates mitochondrial metabolic status to coordinate ATP production. To survey mitochondrial metabolic adaptation in response to dietary lipid concentration, citrate synthase (EC 2.3.3.1, CS) activity, the expression of several mitochondrial transcription factors, mitochondrial DNA (mtDNA) copy number, mitochondrial gene expression, mtDNA methylation, and oxidative stress parameters were analyzed in the liver of large yellow croaker fed one of three diets with a low (6%), moderate (12%, the control diet) or high (18%) crude lipid content for 70Â d. MtDNA copy number was significantly increased in the low- and high-lipid groups compared to the control. The transcription of cytochrome c oxidase 1 (COX1), COX2, COX3, ATP synthase 6 (ATPase 6), 12S rRNA and 16S rRNA was also significantly increased in the low-lipid group compared with the control, while the transcription of these genes in the high-lipid group was unchanged. Moreover, D-loop (displacement loop) methylation in the high-lipid group was significantly higher than the control. The increase in mtDNA copy number and mitochondrial transcription might be a compensatory mechanism that matches ATP supply to demand under a low-lipid diet, while the increase of mtDNA copy number with unchanged mitochondrial transcription in the high-lipid group probably came from the increase of D-loop methylation.
Keywords
8-OHdGNRF1ND6NADH dehydrogenase subunit 6cytBPGC1αHIF1αATP synthase 6PPARND2Mitochondrial DNA copy numberMDANADH dehydrogenase subunit 2ND4LrRNAATPase 6COX5mC5-Methylcytosine8-hydroxydeoxyguanosineMitochondrial DNARibosomal RNAMitochondrial gene expressionD-loopdisplacement loopmtDNASODCitrate synthaseCytochrome bcytochrome c oxidasehypoxia-inducible factor 1αNuclear respiratory factor 1Superoxide dismutase activitymalondialdehydeLarge yellow croakerperoxisome proliferator-activated receptor
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Authors
Kai Liao, Jing Yan, Kangsen Mai, Qinghui Ai,