p300 is not required for metabolic adaptation to endurance exercise training

骨骼肌 耐力训练 新陈代谢 体内 内分泌学 化学 内科学 生物化学 生物 细胞生物学 医学 遗传学
作者
Samuel LaBarge,Christopher Migdal,Elisa H. Buckner,Hiroshi Okuno,Ilya Gertsman,Ben Stocks,Bruce A. Barshop,Sarah Nalbandian,Andrew Philp,Carrie E. McCurdy,Simon Schenk
出处
期刊:The FASEB Journal [Wiley]
卷期号:30 (4): 1623-1633 被引量:22
标识
DOI:10.1096/fj.15-281741
摘要

The acetyltransferase, E1a-binding protein (p300), is proposed to regulate various aspects of skeletal muscle development, metabolism, and mitochondrial function,viaits interaction with numerous transcriptional regulators and other proteins. Remarkably, however, the contribution of p300 to skeletal muscle function and metabolism,in vivo, is poorly understood. To address this, we used Cre-LoxP methodology to generate mice with skeletal muscle-specific knockout of E1a-binding protein (mKO). mKO mice were indistinguishable from their wild-type/floxed littermates, with no differences in lean mass, skeletal muscle structure, fiber type, respirometry flux, or metabolites of fatty acid and amino acid metabolism.Ex vivomuscle function in extensor digitorum longus and soleus muscles, including peak stress and time to fatigue, as well asin vivorunning capacity were also comparable. Moreover, expected adaptations to a 20 d voluntary wheel running regime were not compromised in mKO mice. Taken together, these findings demonstrate that p300 is not required for the normal development or functioning of adult skeletal muscle, nor is it required for endurance exercise-mediated mitochondrial adaptations.-LaBarge, S. A., Migdal, C. W., Buckner, E. H., Okuno, H., Gertsman, I., Stocks, B., Barshop, B. A., Nalbandian, S. R., Philp, A., McCurdy, C. E., Schenk, S. p300 is not required for metabolic adaptation to endurance exercise training.
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