Black Adam J, Ravi Suhana, Jefferson Leonard S, Kimball Scot R, Schilder Rudolf J
Intercollege Graduate Degree Program in Physiology and.
Department of Cellular and Molecular Physiology, Penn State College of Medicine, Hershey, PA; and.
J Nutr. 2017 Sep;147(9):1648-1657. doi: 10.3945/jn.117.254482. Epub 2017 Aug 2.
Fat-enriched diets produce metabolic changes in skeletal muscle, which in turn can mediate changes in gene regulation. We examined the high-fat-diet-induced changes in skeletal muscle gene expression by characterizing variations in pre-mRNA alternative splicing. Affymetrix Exon Array analysis was performed on the transcriptome of the gastrocnemius/plantaris complex of male obesity-prone Sprague-Dawley rats fed a 10% or 60% fat (lard) diet for 2 or 8 wk. The validation of exon array results was focused on troponin T (). splice form analyses were extended in studies of rats fed 10% or 30% fat diets across 1- to 8-wk treatment periods and rats fed 10% or 45% fat diets with fat sources from lard or mono- or polyunsaturated fats for 2 wk. Nuclear magnetic resonance (NMR) was used to measure body composition. Consumption of a 60% fat diet for 2 or 8 wk resulted in alternative splicing of 668 and 726 pre-mRNAs, respectively, compared with rats fed a 10% fat diet. transcripts were alternatively spliced in rats fed a 60% fat diet for either 2 or 8 wk. The high-fat-diet-induced changes in alternative splicing were observed in rats fed a 30% fat diet across 1- to 8-wk treatment periods. Moreover, this effect depended on fat type, because alternative splicing occurred in response to 45% fat diets enriched with lard but not in response to diets enriched with mono- or polyunsaturated fatty acids. Fat mass (a proxy for obesity as measured by NMR) did not differ between groups in any study. Rat skeletal muscle responds to overconsumption of dietary fat by modifying gene expression through pre-mRNA alternative splicing. Variations in alternative splicing occur independently of obesity and are dependent on dietary fat quantity and suggest a role for saturated fatty acids in the high-fat-diet-induced modifications in alternative splicing.
富含脂肪的饮食会引起骨骼肌的代谢变化,进而可能介导基因调控的改变。我们通过表征前体信使核糖核酸(pre-mRNA)可变剪接的变化,研究了高脂饮食诱导的骨骼肌基因表达变化。对易肥胖的雄性斯普拉格-道利大鼠的腓肠肌/跖肌复合体的转录组进行了Affymetrix外显子阵列分析,这些大鼠分别喂食10%或60%脂肪(猪油)的饮食2周或8周。外显子阵列结果的验证集中在肌钙蛋白T()上。在对喂食10%或30%脂肪饮食长达1至8周治疗期的大鼠以及喂食10%或45%脂肪饮食(脂肪来源为猪油或单不饱和或多不饱和脂肪)2周的大鼠的研究中,扩展了剪接形式分析。使用核磁共振(NMR)测量身体成分。与喂食10%脂肪饮食的大鼠相比,喂食60%脂肪饮食2周或8周分别导致668个和726个前体信使核糖核酸发生可变剪接。在喂食60%脂肪饮食2周或8周的大鼠中,转录本发生了可变剪接。在喂食30%脂肪饮食长达1至8周治疗期的大鼠中,观察到了高脂饮食诱导的可变剪接变化。此外,这种效应取决于脂肪类型,因为可变剪接发生在富含猪油的45%脂肪饮食中,而不是富含单不饱和或多不饱和脂肪酸的饮食中。在任何研究中,各组之间的脂肪量(通过NMR测量的肥胖指标)没有差异。大鼠骨骼肌通过前体信使核糖核酸可变剪接来修饰基因表达,从而对饮食脂肪的过量摄入做出反应。可变剪接的变化独立于肥胖发生,并且取决于饮食脂肪的量,这表明饱和脂肪酸在高脂饮食诱导的可变剪接修饰中起作用。