Iyer Pranav, Asante Diana M, Vyavahare Sagar, Jin Lee Tae, Ahluwalia Pankaj, Kolhe Ravindra, Kashyap Hari, Isales Carlos, Fulzele Sadanand
Department of Medicine, Augusta University, Augusta, GA 30909, USA.
Department of Cell Biology and Anatomy, Augusta University, Augusta, GA 30909, USA.
J Funct Morphol Kinesiol. 2025 Jul 19;10(3):281. doi: 10.3390/jfmk10030281.
: Aerobic exercise induces a range of complex molecular adaptations in skeletal muscle. However, a complete understanding of the specific transcriptional changes following exercise warrants further research. : This study aimed to identify gene expression patterns following acute aerobic exercise by analyzing Gene Expression Omnibus (GEO) datasets. We performed a comparative analysis of transcriptional profiles of related genes in two independent studies, focusing on both established and novel genes involved in muscle physiology. : Our analysis revealed ten consistently upregulated and eight downregulated genes across both datasets. The upregulated genes were predominantly associated with mitochondrial function and cellular respiration, including MDH1, ATP5MC1, ATP5IB, and ATP5F1A. Conversely, downregulated genes such as YTHDC1, CDK5RAP2, and PALS2 were implicated in vascular structure and cellular organization. Importantly, our findings also revealed novel exercise-responsive genes not previously characterized in this context. Among these, MRPL41 and VEGF were significantly upregulated and are associated with p53-mediated apoptotic signaling and fatty acid metabolism, respectively. Novel downregulated genes included LIMCH1, CMYA5, and FOXJ3, which are putatively involved in cytoskeletal dynamics and muscle fiber type specification. : These findings enhance our understanding of the transcriptional landscape of skeletal muscle following acute aerobic exercise and identify novel molecular targets for further investigation in the fields of exercise physiology and metabolic health.
有氧运动可诱导骨骼肌发生一系列复杂的分子适应性变化。然而,要全面了解运动后特定的转录变化,仍需进一步研究。本研究旨在通过分析基因表达综合数据库(GEO)数据集,确定急性有氧运动后的基因表达模式。我们在两项独立研究中对相关基因的转录谱进行了比较分析,重点关注参与肌肉生理学的已知基因和新基因。我们的分析揭示了两个数据集中一致上调的10个基因和下调的8个基因。上调的基因主要与线粒体功能和细胞呼吸相关,包括MDH1、ATP5MC1、ATP5IB和ATP5F1A。相反,下调的基因如YTHDC1、CDK5RAP2和PALS2与血管结构和细胞组织有关。重要的是,我们的研究结果还揭示了此前在此背景下未被表征的新的运动反应基因。其中,MRPL41和VEGF显著上调,分别与p53介导的凋亡信号和脂肪酸代谢相关。新的下调基因包括LIMCH1、CMYA5和FOXJ3,它们可能参与细胞骨架动力学和肌纤维类型的确定。这些发现增进了我们对急性有氧运动后骨骼肌转录图谱的理解,并确定了运动生理学和代谢健康领域进一步研究的新分子靶点。