4.7 Article

Resistance training rejuvenates the mitochondrial methylome in aged human skeletal muscle

期刊

FASEB JOURNAL
卷 35, 期 9, 页码 -

出版社

WILEY
DOI: 10.1096/fj.202100873RR

关键词

aging; methylation; mitochondrial DNA; resistance training

资金

  1. Peanut Institute
  2. Research Council of Norway [314157]

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Resistance training (RT) has been shown to impact the mitochondrial DNA (mtDNA) methylome in older males, leading to increased lean tissue mass, muscle thickness, and strength. The study observed reduced methylation and more youthful signatures in mtDNA sites of older males post-RT compared to younger males. These findings suggest that RT may enhance mitochondrial transcription levels and induce mitochondrial methylome profiles resembling those of younger men.
Resistance training (RT) dynamically alters the skeletal muscle nuclear DNA methylome. However, no study has examined if RT affects the mitochondrial DNA (mtDNA) methylome. Herein, ten older, Caucasian untrained males (65 +/- 7 y.o.) performed six weeks of full-body RT (twice weekly). Body composition and knee extensor torque were assessed prior to and 72 h following the last RT session. Vastus lateralis (VL) biopsies were also obtained. VL DNA was subjected to reduced representation bisulfite sequencing providing excellent coverage across the similar to 16-kilobase mtDNA methylome (254 CpG sites). Biochemical assays were also performed, and older male data were compared to younger trained males (22 +/- 2 y.o., n = 7, n = 6 Caucasian & n = 1 African American). RT increased whole-body lean tissue mass (p = .017), VL thickness (p = .012), and knee extensor torque (p = .029) in older males. RT also affected the mtDNA methylome, as 63% (159/254) of the CpG sites demonstrated reduced methylation (p < .05). Several mtDNA sites presented a more youthful signature in older males after RT in comparison to younger males. The 1.12 kilobase mtDNA D-loop/control region, which regulates replication and transcription, possessed enriched hypomethylation in older males following RT. Enhanced expression of mitochondrial H- and L-strand genes and complex III/IV protein levels were also observed (p < .05). While limited to a shorter-term intervention, this is the first evidence showing that RT alters the mtDNA methylome in skeletal muscle. Observed methylome alterations may enhance mitochondrial transcription, and RT evokes mitochondrial methylome profiles to mimic younger men. The significance of these findings relative to broader RT-induced epigenetic changes needs to be elucidated.

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