Department of Animal Molecular Biology, Laboratory of Genomics, National Research Institute of Animal Production, Krakowska 1, 32-083 Balice, Poland.
Department of Cattle Breeding, National Research Institute of Animal Production, Krakowska 1, 32-083 Balice, Poland.
Int J Mol Sci. 2018 Apr 16;19(4):1208. doi: 10.3390/ijms19041208.
Recently, selection in pigs has been focused on improving the lean meat content in carcasses; this focus has been most evident in breeds constituting a paternal component in breeding. Such sire-breeds are used to improve the meat quantity of cross-breed pig lines. However, even in one breed, a significant variation in the meatiness level can be observed. In the present study, the comprehensive analysis of genes and microRNA expression profiles in porcine muscle tissue was applied to identify the genetic background of meat content. The comparison was performed between whole gene expression and miRNA profiles of muscle tissue collected from two sire-line pig breeds (Pietrain, Hampshire). The RNA-seq approach allowed the identification of 627 and 416 differentially expressed genes (DEGs) between pig groups differing in terms of loin weight between Pietrain and Hampshire breeds, respectively. The comparison of miRNA profiles showed differential expression of 57 microRNAs for Hampshire and 34 miRNAs for Pietrain pigs. Next, 43 genes and 18 miRNAs were selected as differentially expressed in both breeds and potentially related to muscle development. According to Gene Ontology analysis, identified DEGs and microRNAs were involved in the regulation of the cell cycle, fatty acid biosynthesis and regulation of the actin cytoskeleton. The most deregulated pathways dependent on muscle mass were the Hippo signalling pathway connected with the TGF-β signalling pathway and controlling organ size via the regulation of ubiquitin-mediated proteolysis, cell proliferation and apoptosis. The identified target genes were also involved in pathways such as the FoxO signalling pathway, signalling pathways regulating pluripotency of stem cells and the PI3K-Akt signalling pathway. The obtained results indicate molecular mechanisms controlling porcine muscle growth and development. Identified genes (, , , and genes belonging to the transforming growth factor beta superfamily) could be considered candidate genes for determining muscle mass in pigs.
最近,猪的选育重点一直放在提高胴体瘦肉含量上;在构成选育父本成分的品种中,这一重点最为明显。这些父本品种用于提高杂交猪系的肉质数量。然而,即使在一个品种中,也可以观察到肉质水平的显著差异。在本研究中,综合分析了猪肌肉组织中的基因和 microRNA 表达谱,以确定肉质的遗传背景。比较了来自两个父本品种(皮特兰、汉普夏)的肌肉组织的全基因表达和 microRNA 图谱。RNA-seq 方法允许鉴定出 627 个和 416 个差异表达基因(DEGs),分别是皮特兰和汉普夏品种之间腰肉重量不同的两组之间的差异表达基因。microRNA 图谱的比较显示,汉普夏猪的 57 个 microRNAs 和皮特兰猪的 34 个 microRNAs 表达差异。接下来,选择 43 个基因和 18 个 microRNAs 作为两个品种中差异表达的基因和 microRNAs,它们可能与肌肉发育有关。根据基因本体论分析,鉴定出的 DEGs 和 microRNAs 参与了细胞周期、脂肪酸生物合成和肌动蛋白细胞骨架调节的调控。依赖于肌肉质量的最失调途径是 Hippo 信号通路,该通路与 TGF-β 信号通路相连,通过调节泛素介导的蛋白水解、细胞增殖和细胞凋亡来控制器官大小。鉴定出的靶基因还参与了 FoxO 信号通路、调节干细胞多能性的信号通路和 PI3K-Akt 信号通路等途径。研究结果表明,控制猪肌肉生长和发育的分子机制。鉴定出的基因(、、、和属于转化生长因子β超家族的基因)可以被认为是决定猪肌肉量的候选基因。