| 论文作者 |
Jacques, M; Landen, S; Sharples, AP; Garnham, A; Schittenhelm, R; Steele, J; Jones-Freeman, B; Eynon, N; Heikkinen, A; Sillanp??, E; Ollikainen, M; Broatch, J; Zarekookandeh, N; Hanson, O; Ekstr?m, O; Asplund, O; Lamon, S; Alexander, SE; Smith, C; Bauer, C; Woessner, MN; Levinger, I; Teschendorff, AE; Gillberg, L; Blom, I; Helge, JW; Harvey, NR; Haupt, LM; Griffiths, LR; Deshmukh, AS; Pietil?inen, KH; Piiril?, P; Seaborne, RAE; Klevjer, M; Bye, A; Wisloff, U; Eynon, N |
| 摘要 |
We investigated the molecular mechanisms of exercise adaptations in human muscle by integrating genome, methylome, transcriptome, and proteome data from over 1,000 participants (2,340 muscle samples). We identified distinctive signatures associated with maximal oxygen consumption (VO2max), and multi-omics integration uncovered five key genes as robust exercise markers across layers, with transcription factors functioning as activators, synergizing with DNA methylation to regulate gene expression. Minimal sex differences were observed, while modality-specific analysis highlighted distinct pathways for aerobic and resistance exercise, contrasting with muscle disuse patterns. Finally, we created a webtool, OMAx, featuring our individual omics and integration analysis. These findings provide a comprehensive multi-omics framework for understanding exercise-induced molecular adaptations, offering insights into muscle health, cardiorespiratory fitness, and their roles in aging and disease prevention. |
官方微信
