School of Kinesiology, Auburn University, Auburn, Alabama, United States.
School of Kinesiology, University of Michigan, Ann Arbor, Michigan, United States.
Am J Physiol Regul Integr Comp Physiol. 2024 Sep 1;327(3):R338-R348. doi: 10.1152/ajpregu.00131.2024. Epub 2024 Jul 15.
Ribosomal DNA (rDNA) copies exist across multiple chromosomes, and interindividual variation in copy number is speculated to influence the hypertrophic response to resistance training. Thus, we examined if rDNA copy number was associated with resistance training-induced skeletal muscle hypertrophy. Participants ( = 53 male, 21 ± 1 yr old; = 29 female, 21 ± 2 yr old) performed 10-12 wk of full-body resistance training. Hypertrophy outcomes were determined, as was relative rDNA copy number from preintervention vastus lateralis (VL) biopsies. Pre- and postintervention VL biopsy total RNA was assayed in all participants, and mRNA/rRNA markers of ribosome content and biogenesis were also assayed in the 29 female participants before training, 24 h following , and in the basal state after 10 wk of training. Across all participants, no significant associations were evident between relative rDNA copy number and training-induced changes in whole body lean mass ( = -0.034, = 0.764), vastus lateralis thickness ( = 0.093, = 0.408), mean myofiber cross-sectional area ( = -0.128, = 0.259), or changes in muscle RNA concentrations ( = 0.026, = 0.818), and these trends were similar when examining each gender. However, all Pol-I regulon mRNAs as well as 45S pre-rRNA, 28S rRNA, and 18S rRNA increased 24 h following the first training bout in female participants. Follow-up studies using LHCN-M2 myotubes demonstrated that a reduction in relative rDNA copy number induced by bisphenol A did not significantly affect insulin-like-growth factor-induced myotube hypertrophy. These findings suggest that relative rDNA copy number is not associated with myofiber hypertrophy. We examined ribosomal DNA (rDNA) copy numbers in men and women who resistance trained for 10-12 wk and found no significant associations with skeletal muscle hypertrophy outcomes. These data, along with in vitro data in immortalized human myotubes whereby rDNA copy number was reduced, provide strong evidence that relative rDNA copy number is not associated with anabolism.
核糖体 DNA(rDNA) 拷贝存在于多个染色体中,个体间拷贝数的差异被推测会影响抵抗训练引起的肥大反应。因此,我们研究了 rDNA 拷贝数是否与抵抗训练引起的骨骼肌肥大有关。参与者(男性 53 名,21±1 岁;女性 29 名,21±2 岁)进行了 10-12 周的全身抵抗训练。确定了肥大结果,以及干预前股外侧肌(VL)活检的相对 rDNA 拷贝数。所有参与者均检测了干预前和干预后的 VL 活检总 RNA,并在 29 名女性参与者中检测了核糖体含量和生物发生的 mRNA/rRNA 标记物,这些标记物在训练后 24 小时和 10 周的基础状态下进行了检测。在所有参与者中,相对 rDNA 拷贝数与全身瘦体重的训练诱导变化之间没有明显的相关性(=0.034,=0.764),股外侧肌厚度(=0.093,=0.408),平均肌纤维横截面积(=0.128,=0.259)或肌肉 RNA 浓度的变化(=0.026,=0.818),当分别检查每个性别时,这些趋势也是相似的。然而,在女性参与者中,所有 Pol-I 调控子 mRNAs 以及 45S 前 rRNA、28S rRNA 和 18S rRNA 在第一次训练后 24 小时增加。使用 LHCN-M2 肌管进行的后续研究表明,双酚 A 诱导的相对 rDNA 拷贝数减少不会显著影响胰岛素样生长因子诱导的肌管肥大。这些发现表明,相对 rDNA 拷贝数与肌纤维肥大无关。我们检查了进行 10-12 周抵抗训练的男性和女性的核糖体 DNA(rDNA) 拷贝数,发现与骨骼肌肥大结果没有显著相关性。这些数据,以及体外数据在永生化的人类肌管中,rDNA 拷贝数减少,提供了强有力的证据表明相对 rDNA 拷贝数与合成代谢无关。