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Impact of periconceptional and preimplantation undernutrition on factors regulating myogenesis and protein synthesis in muscle of singleton and twin fetal sheep

机译:围孕期和植入前营养不足对单胎和双胎绵羊肌肉中肌生成和蛋白质合成调节因子的影响

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摘要

In this study, we determined the effect of maternal undernutrition in the periconceptional (PCUN: ∼80 days before to 6 days after conception) and preimplantation (PIUN: 0–6 days after conception) periods on the mRNA and protein abundance of key factors regulating myogenesis and protein synthesis, and on the relationship between the abundance of these factors and specific microRNA expression in the quadriceps muscle of singleton and twin fetal sheep at 135–138 days of gestation. PCUN and PIUN resulted in a decrease in the protein abundance of MYF5, a factor which determines the myogenic lineage, in singletons and twins. Interestingly, there was a concomitant increase in insulin-like growth factor-1 mRNA expression, a decrease in the protein abundance of the myogenic inhibitor, myostatin (MSTN), and an increase in the mRNA and protein abundance of the MSTN inhibitor, follistatin (FST), in the PCUN and PIUN groups in both singletons and twins. These promyogenic changes may compensate for the decrease in MYF5 protein abundance evoked by early embryonic undernutrition. PCUN and PIUN also increased the protein abundance of phosphorylated eukaryotic translation initiation factor binding protein 1 (EIF4EBP1; T70 and S65) in fetal muscle in singletons and twins. There was a significant inverse relationship between the expression of miR-30a-5p, miR-30d-5p, miR-27b-3p, miR106b-5p, and miR-376b and the protein abundance of mechanistic target of rapamycin (MTOR), FST, or MYF5 in singletons or twins. In particular, the expression of miR-30a-5p was increased and MYF5 protein abundance was decreased, in PCUN and PIUN twins supporting the conclusion that the impact of PCUN and PIUN is predominantly on the embryo.
机译:在这项研究中,我们确定了母体营养不足在围孕期(PCUN:受孕前〜80天至受孕后6天)和植入前(PIUN:受孕后0–6天)对调节关键因子的mRNA和蛋白质丰度的影响妊娠135-138天时单胎和双胎羊的股四头肌中这些因子的丰度和这些因子的丰度与特定microRNA表达之间的关系。 PCUN和PIUN导致单胎和双胎MYF5蛋白质丰度降低,MYF5是决定肌原性谱系的因素。有趣的是,胰岛素样生长因子-1 mRNA表达随之增加,肌源性抑制剂myostatin(MSTN)的蛋白质丰度降低,而MSTN抑制剂卵泡抑素(mollistatin)的mRNA和蛋白质丰度增加( FST),在PCUN和PIUN组中都是单身和双胞胎。这些早生的变化可能弥补了早期胚胎营养不良引起的MYF5蛋白丰度的下降。 PCUN和PIUN还增加了单胎和双胎胎儿肌肉中磷酸化的真核翻译起始因子结合蛋白1(EIF4EBP1; T70和S65)的蛋白丰度。 miR-30a-5p,miR-30d-5p,miR-27b-3p,miR106b-5p和miR-376b的表达与雷帕霉素(MTOR),FST机制靶蛋白的丰度之间存在显着的负相关关系,或单身或双胞胎MYF5。特别是,在PCUN和PIUN双胞胎中,miR-30a-5p的表达增加,MYF5蛋白丰度降低,这支持了PCUN和PIUN的影响主要是对胚胎的影响这一结论。

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