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急性运动重塑人类骨骼肌启动子甲基化。

Acute exercise remodels promoter methylation in human skeletal muscle.

机构信息

Department of Molecular Medicine and Surgery, Karolinska University Hospital, Karolinska Institutet, SE-171 77 Stockholm, Sweden.

出版信息

Cell Metab. 2012 Mar 7;15(3):405-11. doi: 10.1016/j.cmet.2012.01.001.

Abstract

DNA methylation is a covalent biochemical modification controlling chromatin structure and gene expression. Exercise elicits gene expression changes that trigger structural and metabolic adaptations in skeletal muscle. We determined whether DNA methylation plays a role in exercise-induced gene expression. Whole genome methylation was decreased in skeletal muscle biopsies obtained from healthy sedentary men and women after acute exercise. Exercise induced a dose-dependent expression of PGC-1α, PDK4, and PPAR-δ, together with a marked hypomethylation on each respective promoter. Similarly, promoter methylation of PGC-1α, PDK4, and PPAR-δ was markedly decreased in mouse soleus muscles 45 min after ex vivo contraction. In L6 myotubes, caffeine exposure induced gene hypomethylation in parallel with an increase in the respective mRNA content. Collectively, our results provide evidence that acute gene activation is associated with a dynamic change in DNA methylation in skeletal muscle and suggest that DNA hypomethylation is an early event in contraction-induced gene activation.

摘要

DNA 甲基化是一种共价生化修饰,可控制染色质结构和基因表达。运动可引发基因表达的变化,从而触发骨骼肌的结构和代谢适应。我们确定 DNA 甲基化是否在运动引起的基因表达中起作用。在急性运动后,从健康的久坐男性和女性获得的骨骼肌活检中,全基因组甲基化水平降低。运动诱导了 PGC-1α、PDK4 和 PPAR-δ 的剂量依赖性表达,以及每个启动子上明显的低甲基化。同样,在离体收缩后 45 分钟,小鼠比目鱼肌中 PGC-1α、PDK4 和 PPAR-δ 的启动子甲基化明显降低。在 L6 肌管中,咖啡因暴露会导致基因低甲基化,同时相应的 mRNA 含量增加。总之,我们的研究结果提供了证据,表明急性基因激活与骨骼肌中 DNA 甲基化的动态变化有关,并表明 DNA 低甲基化是收缩诱导基因激活的早期事件。

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