Nanomaterials and Nanotechnology Research Center (CINN-CSIC), Health Research Institute of Asturias (ISPA), Institute of Oncology of Asturias (IUOPA), Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), 33011 Oviedo, Asturias, Spain.
Departamento de Biología Funcional, Fisiología, Universidad de Oviedo, Oviedo 33006, Spain; Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo 33011, Spain.
Mol Metab. 2021 Dec;54:101398. doi: 10.1016/j.molmet.2021.101398. Epub 2021 Nov 18.
To analyze the genome-wide epigenomic and transcriptomic changes induced by long term resistance or endurance training in the hippocampus of wild-type mice.
We performed whole-genome bisulfite sequencing (WGBS) and RNA sequencing (RNA-seq) of mice hippocampus after 4 weeks of specific training. In addition, we used a novel object recognition test before and after the intervention to determine whether the exercise led to an improvement in cognitive function.
Although the majority of DNA methylation changes identified in this study were training-model specific, most were associated with hypomethylation and were enriched in similar histone marks, chromatin states, and transcription factor biding sites. It is worth highlighting the significant association found between the loss of DNA methylation in Tet1 binding sites and gene expression changes, indicating the importance of these epigenomic changes in transcriptional regulation. However, endurance and resistance training activate different gene pathways, those being associated with neuroplasticity in the case of endurance exercise, and interferon response pathways in the case of resistance exercise, which also appears to be associated with improved learning and memory functions.
Our results help both understand the molecular mechanisms by which different exercise models exert beneficial effects for brain health and provide new potential therapeutic targets for future research.
分析野生型小鼠海马体中由长期抗阻训练或耐力训练引起的全基因组表观基因组和转录组变化。
我们对经过 4 周特定训练的小鼠海马体进行了全基因组亚硫酸氢盐测序(WGBS)和 RNA 测序(RNA-seq)。此外,我们在干预前后使用新物体识别测试来确定运动是否导致认知功能的改善。
尽管本研究中鉴定的大多数 DNA 甲基化变化是特定于训练模型的,但大多数与低甲基化相关,并富集在相似的组蛋白标记、染色质状态和转录因子结合位点上。值得强调的是,在 Tet1 结合位点的 DNA 去甲基化与基因表达变化之间发现了显著关联,这表明这些表观遗传变化在转录调控中的重要性。然而,抗阻训练和耐力训练激活了不同的基因途径,耐力运动与神经可塑性相关,而抗阻运动与干扰素反应途径相关,这似乎也与学习和记忆功能的改善有关。
我们的研究结果有助于了解不同运动模型对大脑健康产生有益影响的分子机制,并为未来的研究提供新的潜在治疗靶点。