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Comprehensive analysis of circular RNA profiles in skeletal muscles of aging mice and after aerobic exercise intervention

机译:综合分析衰老小鼠骨骼肌和有氧运动干预后的环状RNA谱

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摘要

Aging induces gradual accumulation of damages in cells and tissues, which leads to physiological dysfunctions. Aging-associated muscle dysfunction is commonly seen in aged population and severely affects their physical activity and life quality, against which aerobic training has been shown to exert antagonizing or alleviating effects. Circular RNAs (circRNAs) play important roles in various physiological processes, yet their involvement in aging-associated muscle dysfunction is not well understood. In this study, we performed comprehensive analysis of circRNAs profiles in quadriceps muscles in sedentary young and aging mice, as well as aging mice with aerobic exercise using RNA sequencing. Our results identified circRNAs altered by factors of aging and aerobic exercise. Their host genes were then predicted and analyzed by gene ontology enrichment analysis. Importantly, we found that circBBS9 featured decreased levels in aging compared to young mice and elevated expression in exercise versus sedentary aging mice. Besides, we performed GO and KEGG analysis on circBBS9 target genes, as well as established the circBBS9-miRNA-mRNAs interaction network. Our results indicate that circBBS9 may play active roles in muscle aging by mediating the benefits of aerobic training intervention, thus may serve as a novel therapeutic target combating aging-associated muscle dysfunction.
机译:衰老引起细胞和组织损伤的逐渐积累,从而导致生理功能障碍。与衰老相关的肌肉功能障碍常见于老年人群中,并严重影响其身体活动和生活质量,有氧训练已被证明具有拮抗或缓解作用。环状RNA(circRNA)在各种生理过程中都起着重要作用,但是人们对它们与衰老相关的肌肉功能障碍的参与尚不清楚。在这项研究中,我们对久坐的年轻和衰老小鼠以及有氧运动衰老小鼠的四头肌肌肉中circRNA进行了综合分析,使用RNA测序。我们的结果确定了circRNA受衰老和有氧运动因素的影响。然后通过基因本体富集分析对它们的宿主基因进行预测和分析。重要的是,我们发现circBBS9的特征是与年轻小鼠相比,衰老水平降低,而与久坐的小鼠相比,运动表达升高。此外,我们对circBBS9靶基因进行了GO和KEGG分析,并建立了circBBS9-miRNA-mRNAs相互作用网络。我们的结果表明,circBBS9可能通过介导有氧训练干预的益处而在肌肉衰老中发挥积极作用,因此可以作为对抗衰老相关的肌肉功能障碍的新型治疗靶标。

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