Keller Janine, Ringseis Robert, Eder Klaus
Institute of Animal Nutrition and Nutritional Physiology, Justus-Liebig-University, Heinrich-Buff-Ring 26-32, Giessen 35392, Germany.
BMC Genomics. 2014 Jun 21;15(1):512. doi: 10.1186/1471-2164-15-512.
In the past, numerous studies revealed that supplementation with carnitine has multiple effects on performance characteristics and gene expression in livestock and model animals. The molecular mechanisms underlying these observations are still largely unknown. Increasing evidence suggests that microRNAs (miRNAs), a class of small non-coding RNA molecules, play an important role in post-transcriptional regulation of gene expression and thereby influencing several physiological and pathological processes. Based on these findings, the aim of the present study was to investigate the influence of carnitine supplementation on the miRNA expression profile in skeletal muscle of obese Zucker rats using miRNA microarray analysis.
Obese Zucker rats supplemented with carnitine had higher concentrations of total carnitine in plasma and muscle than obese control rats (P < 0.05). miRNA expression profiling in skeletal muscle revealed a subset of 152 miRNAs out of the total number of miRNAs analysed (259) were identified to be differentially regulated (adjusted P-value < 0.05) by carnitine supplementation. Compared to the obese control group, 111 miRNAs were up-regulated and 41 down-regulated by carnitine supplementation (adjusted P-value < 0.05). 14 of these miRNAs showed a log2 ratio ≥ 0.5 and 7 miRNAs showed a log2 ratio ≤ -0.5 (adjusted P-value < 0.05). After confirmation by qRT-PCR, 11 miRNAs were found to be up-regulated and 6 miRNAs were down-regulated by carnitine supplementation (P < 0.05). Furthermore, a total of 1,446 target genes within the validated miRNAs were revealed using combined three bioinformatic algorithms. Analysis of Gene Ontology (GO) categories and KEGG pathways of the predicted targets revealed that carnitine supplementation regulates miRNAs that target a large set of genes involved in protein-localization and -transport, regulation of transcription and RNA metabolic processes, as well as genes involved in several signal transduction pathways, like ubiquitin-mediated proteolysis and longterm depression, are targeted by the miRNAs regulated by carnitine supplementation.
The present study shows for the first time that supplementation of carnitine affects a large set of miRNAs in skeletal muscle of obese Zucker rats suggesting a novel mechanism through which carnitine exerts its multiple effects on gene expression, which were observed during the past.
过去,众多研究表明,补充肉碱对家畜和模式动物的性能特征及基因表达有多种影响。这些观察结果背后的分子机制仍大多未知。越来越多的证据表明,微小RNA(miRNA),一类小的非编码RNA分子,在基因表达的转录后调控中起重要作用,从而影响多个生理和病理过程。基于这些发现,本研究的目的是使用miRNA微阵列分析研究补充肉碱对肥胖Zucker大鼠骨骼肌中miRNA表达谱的影响。
补充肉碱的肥胖Zucker大鼠血浆和肌肉中的总肉碱浓度高于肥胖对照大鼠(P < 0.05)。骨骼肌中的miRNA表达谱分析显示,在所分析的miRNA总数(259个)中,有152个miRNA被鉴定为受补充肉碱的差异调节(校正P值< 0.05)。与肥胖对照组相比,补充肉碱使111个miRNA上调,41个miRNA下调(校正P值< 0.05)。其中14个miRNA的log2比值≥ 0.5,7个miRNA的log2比值≤ -0.5(校正P值< 0.05)。经qRT-PCR验证后,发现补充肉碱使11个miRNA上调,6个miRNA下调(P < 0.05)。此外,使用三种生物信息学算法联合揭示了经过验证的miRNA中的总共1446个靶基因。对预测靶标的基因本体论(GO)类别和KEGG途径的分析表明,补充肉碱调节的miRNA靶向大量参与蛋白质定位和转运、转录调控和RNA代谢过程的基因,以及参与多种信号转导途径的基因,如泛素介导的蛋白水解和长时程抑制,这些基因被补充肉碱调节的miRNA靶向。
本研究首次表明,补充肉碱会影响肥胖Zucker大鼠骨骼肌中的大量miRNA,提示肉碱对基因表达发挥多种作用的一种新机制,这在过去已被观察到。