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Comparative Analyses between Skeletal Muscle miRNAomes from Large White and Min Pigs Revealed MicroRNAs Associated with Postnatal Muscle Hypertrophy

机译:大型白猪和小猪的骨骼肌miRNAome之间的比较分析揭示了与产后肌肉肥大相关的microRNA

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摘要

The molecular mechanism regulated by microRNAs (miRNAs) that underlies postnatal hypertrophy of skeletal muscle is complex and remains unclear. Here, the miRNAomes of longissimus dorsi muscle collected at five postnatal stages (60, 120, 150, 180, and 210 days after birth) from Large White (commercial breed) and Min pigs (indigenous breed of China) were analyzed by Illumina sequencing. We identified 734 miRNAs comprising 308 annotated miRNAs and 426 novel miRNAs, of which 307 could be considered pig-specific. Comparative analysis between two breeds suggested that 60 and 120 days after birth were important stages for skeletal muscle hypertrophy and intramuscular fat accumulation. A total of 263 miRNAs were significantly differentially expressed between two breeds at one or more developmental stages. In addition, the differentially expressed miRNAs between every two adjacent developmental stages in each breed were determined. Notably, ssc-miR-204 was significantly more highly expressed in Min pig skeletal muscle at all postnatal stages compared with its expression in Large White pig skeletal muscle. Based on gene ontology and KEGG pathway analyses of its predicted target genes, we concluded that ssc-miR-204 may exert an impact on postnatal hypertrophy of skeletal muscle by regulating myoblast proliferation. The results of this study will help in elucidating the mechanism underlying postnatal hypertrophy of skeletal muscle modulated by miRNAs, which could provide valuable information for improvement of pork quality and human myopathy.
机译:由产后骨骼肌肥大的microRNA(miRNA)调控的分子机制是复杂的,目前仍不清楚。在这里,通过Illumina测序分析了从大白种(商业品种)和小猪(中国本土品种)出生后五个阶段(出生后60、120、150、180和210天)收集的背最长肌的miRNAome。我们鉴定了734个miRNA,其中包括308个带注释的miRNA和426个新颖的miRNA,其中307个可以被认为是猪特异性的。两个品种之间的比较分析表明,出生后60天和120天是骨骼肌肥大和肌肉内脂肪积累的重要阶段。在一个或多个发育阶段,两个品种之间共有263个miRNA显着差异表达。此外,确定了每个品种中每两个相邻发育阶段之间差异表达的miRNA。值得注意的是,与大白猪骨骼肌中的表达相比,ssc-miR-204在产后所有阶段的小猪骨骼肌中的表达明显更高。基于基因本体论和预测目标基因的KEGG通路分析,我们得出结论,ssc-miR-204可能通过调节成肌细胞增殖对骨骼肌产后肥大产生影响。这项研究的结果将有助于阐明由miRNA调节的骨骼肌产后肥大的潜在机制,这可能为改善猪肉质量和人类肌病提供有价值的信息。

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