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Publication : Mitochondrial DNA lesions and copy number are strain dependent in endurance-trained mice.

First Author  Vellers HL Year  2020
Journal  Physiol Rep Volume  8
Issue  21 Pages  e14605
PubMed ID  33190396 Mgi Jnum  J:327880
Mgi Id  MGI:6800129 Doi  10.14814/phy2.14605
Citation  Vellers HL, et al. (2020) Mitochondrial DNA lesions and copy number are strain dependent in endurance-trained mice. Physiol Rep 8(21):e14605
abstractText  In this pilot work, we selected two inbred strains that respond well to endurance training (ET) (FVB/NJ, and SJL/J strains), and two strains that respond poorly (BALB/cByJ and NZW/LacJ), to determine the effect of a standardized ET treadmill program on mitochondrial and nuclear DNA (nucDNA) integrity, and mitochondrial DNA (mtDNA) copy number. DNA was isolated from plantaris muscles (n = 37) and a gene-specific quantitative PCR-based assay was used to measure DNA lesions and mtDNA copy number. Mean mtDNA lesions were not different within strains in the sedentary or exercise-trained states. However, mtDNA lesions were significantly higher in trained low-responding NZW/LacJ mice (0.24 +/- 0.06 mtDNA lesions/10 Kb) compared to high-responding strains (mtDNA lesions/10 Kb: FVB/NJ = 0.11 +/- 0.01, p = .049; SJL/J = 0.04 +/- 0.02; p = .003). ET did not alter mean mtDNA copy numbers for any strain, although both sedentary and trained FVB/NJ mice had significantly higher mtDNA copies (99,890 +/- 4,884 mtDNA copies) compared to low-responding strains (mtDNA copies: BALB/cByJ = 69,744 +/- 4,675; NZW/LacJ = 65,687 +/- 5,180; p < .001). ET did not change nucDNA lesions for any strain, however, SJL/J had the lowest mean nucDNA lesions (3.5 +/- 0.14 nucDNA lesions/6.5 Kb) compared to all other strains (nucDNA lesions/6.5 Kb: FVB/NJ = 4.4 +/- 0.11; BALB/cByJ = 4.7 +/- 0.09; NZW/LacJ = 4.4 +/- 0.11; p < .0001). Our results demonstrate strain differences in plantaris muscle mtDNA lesions in ET mice and, independent of condition, differences in mean mtDNA copy and nucDNA lesions between strains.
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