天冬酰胺合成酶调节鸡骨骼肌卫星细胞的增殖和分化

IF 2.4 2区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Animal Bioscience Pub Date : 2024-11-01 Epub Date: 2024-08-26 DOI:10.5713/ab.24.0271
Hangfeng Jin, Han Wang, Jianqing Wu, Moran Hu, Xiaolong Zhou, Songbai Yang, Ayong Zhao, Ke He
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引用次数: 0

摘要

目的:天冬酰胺合成酶(ASNS)是一种氨基转移酶,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 在快速生长肉鸡中高表达,但很少有研究报道 ASNS 在肌肉发育中的调控作用:为了探索 ASNS 在鸡肌肉发育中的功能,首先通过实时定量反转录聚合酶链反应(RT-PCR)检测 ASNS 在不同鸡种和组织中的表达。然后,利用实时定量 RT-PCR、Western 印迹、EdU 检测、细胞周期检测和免疫荧光等方法,研究了 ASNS 对鸡骨骼肌卫星细胞(SMSC)增殖和分化的影响。最后,通过RNA-Seq鉴定了ASNS影响鸡肌纤维分化的潜在机制:结果:ASNS在肌肉中的mRNA表达模式反映了不同品种鸡的肌纤维横截面积、平均日增重和肌肉重量的变化趋势。ASNS 基因敲除会抑制 SMSC 的增殖,而过表达则相反。此外,ASNS还通过激活5'-单磷酸腺苷(AMP)激活的蛋白激酶(AMPK)通路来抑制SMSC的分化。此外,5-氨基咪唑-4-甲酰胺1-β-D-呋喃核苷(AICAR)处理抑制了siRNA-ASNS诱导的细胞分化。RNA-Seq鉴定了过表达ASNS时鸡SMSC分化过程中的1968个差异表达基因(DEGs)。基因本体(GO)富集分析显示,这些DEGs主要参与了8个生物过程、8个细胞组分和4个分子功能。京都基因和基因组百科全书(KEGG)通路分析发现了几条显著富集的信号通路,如JAK-STAT信号通路、TNF信号通路、Toll样受体信号通路和PI3K-Akt信号通路:结论:ASNS 可促进鸡骨骼肌卫星细胞的增殖,同时抑制其分化。本研究为研究 ASNS 在肌肉发育中的作用提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Asparagine synthetase regulates the proliferation and differentiation of chicken skeletal muscle satellite cells.

Objective: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

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来源期刊
Animal Bioscience
Animal Bioscience AGRICULTURE, DAIRY & ANIMAL SCIENCE-
CiteScore
5.00
自引率
0.00%
发文量
223
审稿时长
3 months
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