Gu Shuang, Huang Qiang, Jie Yuchen, Sun Congjiao, Wen Chaoliang, Yang Ning
State Key Laboratory of Animal Biotech Breeding and Frontier Science Center for Molecular Design Breeding, China Agricultural University, Beijing, 100193, China.
National Engineering Laboratory for Animal Breeding and Key Laboratory of Animal Genetics, Breeding and Reproduction, Ministry of Agriculture and Rural Affairs, Department of Animal Genetics and Breeding, College of Animal Science and Technology China Agricultural University, Beijing, 100193, China.
J Anim Sci Biotechnol. 2024 Jul 4;15(1):91. doi: 10.1186/s40104-024-01049-w.
Broilers stand out as one of the fastest-growing livestock globally, making a substantial contribution to animal meat production. However, the molecular and epigenetic mechanisms underlying the rapid growth and development of broiler chickens are still unclear. This study aims to explore muscle development patterns and regulatory networks during the postnatal rapid growth phase of fast-growing broilers. We measured the growth performance of Cornish (CC) and White Plymouth Rock (RR) over a 42-d period. Pectoral muscle samples from both CC and RR were randomly collected at day 21 after hatching (D21) and D42 for RNA-seq and ATAC-seq library construction.
The consistent increase in body weight and pectoral muscle weight across both breeds was observed as they matured, with CC outpacing RR in terms of weight at each stage of development. Differential expression analysis identified 398 and 1,129 genes in the two dimensions of breeds and ages, respectively. A total of 75,149 ATAC-seq peaks were annotated in promoter, exon, intron and intergenic regions, with a higher number of peaks in the promoter and intronic regions. The age-biased genes and breed-biased genes of RNA-seq were combined with the ATAC-seq data for subsequent analysis. The results spotlighted the upregulation of ACTC1 and FDPS at D21, which were primarily associated with muscle structure development by gene cluster enrichment. Additionally, a noteworthy upregulation of MUSTN1, FOS and TGFB3 was spotted in broiler chickens at D42, which were involved in cell differentiation and muscle regeneration after injury, suggesting a regulatory role of muscle growth and repair.
This work provided a regulatory network of postnatal broiler chickens and revealed ACTC1 and MUSTN1 as the key responsible for muscle development and regeneration. Our findings highlight that rapid growth in broiler chickens triggers ongoing muscle damage and subsequent regeneration. These findings provide a foundation for future research to investigate the functional aspects of muscle development.
肉鸡是全球生长速度最快的家畜之一,对动物肉类生产做出了重大贡献。然而,肉鸡快速生长发育的分子和表观遗传机制仍不清楚。本研究旨在探索快速生长肉鸡出生后快速生长阶段的肌肉发育模式和调控网络。我们在42天的时间里测量了科尼什鸡(CC)和白普利茅斯洛克鸡(RR)的生长性能。在孵化后第21天(D21)和第42天(D42),从CC和RR中随机采集胸肌样本,用于RNA测序和ATAC测序文库构建。
随着两个品种的成熟,观察到体重和胸肌重量持续增加,在发育的每个阶段,CC的体重均超过RR。差异表达分析在品种和年龄两个维度上分别鉴定出398个和1129个基因。在启动子、外显子、内含子和基因间区域共注释了75149个ATAC测序峰,启动子和内含子区域的峰数较多。将RNA测序的年龄偏向基因和品种偏向基因与ATAC测序数据结合进行后续分析。结果显示,ACTC1和FDPS在D21上调,主要通过基因簇富集与肌肉结构发育相关。此外,在D42的肉鸡中发现MUSTN1、FOS和TGFB3显著上调,它们参与细胞分化和损伤后的肌肉再生,表明对肌肉生长和修复具有调控作用。
本研究提供了肉鸡出生后发育的调控网络,并揭示ACTC1和MUSTN1是肌肉发育和再生的关键因子。我们的研究结果表明,肉鸡的快速生长引发了持续的肌肉损伤和随后的再生。这些发现为未来研究肌肉发育的功能方面奠定了基础。