Lie Shervi, Morrison Janna L, Williams-Wyss Olivia, Suter Catherine M, Humphreys David T, Ozanne Susan E, Zhang Song, MacLaughlin Severence M, Kleemann David O, Walker Simon K, Roberts Claire T, McMillen I Caroline
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, South Australia, Australia.
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, South Australia, Australia Discipline of Physiology, School of Medical Sciences, University of Adelaide, Adelaide, South Australia, Australia.
Physiol Rep. 2015 Aug;3(8). doi: 10.14814/phy2.12495.
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.
在本研究中,我们确定了孕期前(PCUN:受孕前约80天至受孕后6天)和植入前(PIUN:受孕后0 - 6天)母体营养不足对调节肌生成和蛋白质合成的关键因子的mRNA和蛋白质丰度的影响,以及这些因子的丰度与妊娠135 - 138天时单胎和双胎绵羊胎儿股四头肌中特定微小RNA表达之间的关系。PCUN和PIUN导致单胎和双胎中决定肌源性谱系的因子MYF5的蛋白质丰度降低。有趣的是,在单胎和双胎的PCUN和PIUN组中,胰岛素样生长因子-1 mRNA表达同时增加,肌生成抑制剂肌肉生长抑制素(MSTN)的蛋白质丰度降低,而MSTN抑制剂卵泡抑素(FST)的mRNA和蛋白质丰度增加。这些促肌生成变化可能补偿早期胚胎营养不足引起的MYF5蛋白质丰度降低。PCUN和PIUN还增加了单胎和双胎胎儿肌肉中磷酸化真核翻译起始因子结合蛋白1(EIF4EBP1;T70和S65)的蛋白质丰度。在单胎或双胎中,miR - 30a - 5p、miR - 30d - 5p、miR - 27b - 3p、miR106b - 5p和miR - 376b的表达与雷帕霉素靶蛋白(MTOR)、FST或MYF5的蛋白质丰度之间存在显著的负相关关系。特别是,在PCUN和PIUN双胎中,miR - 30a - 5p的表达增加而MYF5蛋白质丰度降低,支持了PCUN和PIUN的影响主要作用于胚胎的结论。