Ouyang Hongjia, Wang Zhijun, Chen Xiaolan, Yu Jiao, Li Zhenhui, Nie Qinghua
Department of Animal Genetics, Breeding and Reproduction, College of Animal Science, South China Agricultural UniversityGuangzhou, China.
Guangdong Provincial Key Lab of Agro-Animal Genomics and Molecular Breeding, and Key Lab of Chicken Genetics, Breeding and Reproduction, Ministry of AgricultureGuangzhou, China.
Front Physiol. 2017 May 8;8:281. doi: 10.3389/fphys.2017.00281. eCollection 2017.
Embryonic growth and development of skeletal muscle is a major determinant of muscle mass, and has a significant effect on meat production in chicken. To assess the protein expression profiles during embryonic skeletal muscle development, we performed a proteomics analysis using isobaric tags for relative and absolute quantification (iTRAQ) in leg muscle tissues of female Xinghua chicken at embryonic age (E) 11, E16, and 1-day post hatch (D1). We identified 3,240 proteins in chicken embryonic muscle and 491 of them were differentially expressed (fold change ≥ 1.5 or ≤ 0.666 and < 0.05). There were 19 up- and 32 down-regulated proteins in E11 vs. E16 group, 238 up- and 227 down-regulated proteins in E11 vs. D1 group, and 13 up- and 5 down-regulated proteins in E16 vs. D1 group. Protein interaction network analyses indicated that these differentially expressed proteins were mainly involved in the pathway of protein synthesis, muscle contraction, and oxidative phosphorylation. Integrative analysis of proteome and our previous transcriptome data found 189 differentially expressed proteins that correlated with their mRNA level. The interactions between these proteins were also involved in muscle contraction and oxidative phosphorylation pathways. The lncRNA-protein interaction network found four proteins DMD, MYL3, TNNI2, and TNNT3 that are all involved in muscle contraction and may be lncRNA regulated. These results provide several candidate genes for further investigation into the molecular mechanisms of chicken embryonic muscle development, and enable us to better understanding their regulation networks and biochemical pathways.
骨骼肌的胚胎生长和发育是肌肉量的主要决定因素,对鸡的肉类生产有显著影响。为了评估胚胎骨骼肌发育过程中的蛋白质表达谱,我们使用相对和绝对定量的等压标签(iTRAQ)对雌性杏花鸡胚胎期(E)11、E16和出壳后1天(D1)的腿部肌肉组织进行了蛋白质组学分析。我们在鸡胚胎肌肉中鉴定出3240种蛋白质,其中491种差异表达(倍数变化≥1.5或≤0.666且P<0.05)。E11与E16组中有19种上调和32种下调蛋白质,E11与D1组中有238种上调和227种下调蛋白质,E16与D1组中有13种上调和5种下调蛋白质。蛋白质相互作用网络分析表明,这些差异表达的蛋白质主要参与蛋白质合成、肌肉收缩和氧化磷酸化途径。蛋白质组与我们之前的转录组数据的综合分析发现189种差异表达的蛋白质与其mRNA水平相关。这些蛋白质之间的相互作用也参与肌肉收缩和氧化磷酸化途径。lncRNA-蛋白质相互作用网络发现四种蛋白质DMD、MYL3、TNNI2和TNNT3都参与肌肉收缩,可能受lncRNA调控。这些结果为进一步研究鸡胚胎肌肉发育的分子机制提供了几个候选基因,并使我们能够更好地理解其调控网络和生化途径。