Jin Hangfeng, Wang Han, Wu Jianqing, Hu Moran, Zhou Xiaolong, Yang Songbai, Zhao Ayong, He Ke
Key Laboratory of Applied Technology on Green-Eco-Healthy Animal Husbandry of Zhejiang Province, Zhejiang Provincial Engineering Laboratory for Animal Health Inspection & Internet Technology, Zhejiang International Science and Technology Cooperation Base for Veterinary Medicine and Health Management, China-Australia Joint Laboratory for Animal Health Big Data Analytics, College of Animal Science and Technology & College of Veterinary Medicine of Zhejiang A&F University, Hangzhou, Zhejiang, 311300, China.
Anim Biosci. 2024 Nov;37(11):1848-1862. doi: 10.5713/ab.24.0271. Epub 2024 Aug 26.
Asparagine synthetase (ASNS) is an aminotransferase responsible for the biosynthesis of aspartate by using aspartic acid and glutamine. ASNS is highly expressed in fast-growing broilers, but few studies have reported the regulatory role of ASNS in muscle development.
To explore the function of ASNS in chicken muscle development, the expression of ASNS in different chicken breeds and tissues were first performed by real-time quantitative reverse transcription polymerase chain reaction (RT-PCR). Then, using real-time quantitative RT-PCR, western blot, EdU assay, cell cycle assay and immunofluorescence, the effects of ASNS on the proliferation and differentiation of chicken skeletal muscle satellite cell (SMSC) were investigated. Finally, potential mechanisms by which ASNS influences chicken muscle fiber differentiation were identified through RNA-Seq.
The mRNA expression pattern of ASNS in muscles mirrors trends in muscle fiber cross-sectional area, average daily weight gain, and muscle weight across different breeds. ASNS knockdown inhibited SMSC proliferation, while overexpression showed the opposite. Moreover, ASNS attenuated SMSC differentiation by activating the adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK) pathway. Additionally, 5-aminoimidazole4-carboxamide1-β-D-ribofuranoside (AICAR) treatment suppressed the cell differentiation induced by siRNA-ASNS. RNA-Seq identified 1,968 differentially expressed genes (DEGs) during chicken SMSC differentiation when overexpression ASNS. Gene ontology (GO) enrichment analysis revealed that these DEGs primarily participated in 8 biological processes, 8 cellular components, and 4 molecular functions. Kyoto encyclopedia of genes and genomes (KEGG) pathway analysis identified several significantly enriched signaling pathways, such as the JAK-STAT signaling pathway, tumor necrosis factor signaling pathway, toll-like receptor signaling pathway, and PI3K-Akt signaling pathway.
ASNS promotes proliferation while inhibits the differentiation of chicken SMSCs. This study provides a theoretical basis for studying the role of ASNS in muscle development.
天冬酰胺合成酶(ASNS)是一种转氨酶,负责利用天冬氨酸和谷氨酰胺进行天冬氨酸的生物合成。ASNS在快速生长的肉鸡中高度表达,但鲜有研究报道ASNS在肌肉发育中的调控作用。
为探究ASNS在鸡肌肉发育中的功能,首先通过实时定量逆转录聚合酶链反应(RT-PCR)检测ASNS在不同鸡品种和组织中的表达。然后,运用实时定量RT-PCR、蛋白质免疫印迹法、EdU检测、细胞周期检测和免疫荧光技术,研究ASNS对鸡骨骼肌卫星细胞(SMSC)增殖和分化的影响。最后,通过RNA测序确定ASNS影响鸡肌纤维分化的潜在机制。
ASNS在肌肉中的mRNA表达模式反映了不同品种间肌纤维横截面积、平均日增重和肌肉重量的变化趋势。敲低ASNS抑制SMSC增殖,而过表达则产生相反效果。此外,ASNS通过激活5'-单磷酸腺苷(AMP)激活的蛋白激酶(AMPK)途径减弱SMSC分化。另外,5-氨基咪唑-4-甲酰胺-1-β-D-呋喃核糖苷(AICAR)处理可抑制siRNA-ASNS诱导的细胞分化。RNA测序确定过表达ASNS时鸡SMSC分化过程中有1968个差异表达基因(DEG)。基因本体(GO)富集分析表明,这些DEG主要参与8个生物学过程、8个细胞成分和4个分子功能。京都基因与基因组百科全书(KEGG)通路分析确定了几个显著富集的信号通路,如JAK-STAT信号通路、肿瘤坏死因子信号通路、Toll样受体信号通路和PI3K-Akt信号通路。
ASNS促进鸡SMSC增殖,同时抑制其分化。本研究为探究ASNS在肌肉发育中的作用提供了理论依据。