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山羊骨骼肌分化过程中mRNA的分析及功能研究

Profiling and Functional Analysis of mRNAs during Skeletal Muscle Differentiation in Goats.

作者信息

Zhan Siyuan, Zhai Hongfan, Tang Min, Xue Yanan, Li Dandan, Wang Linjie, Zhong Tao, Dai Dinghui, Cao Jiaxue, Guo Jiazhong, Li Li, Zhang Hongping

机构信息

Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, College of Animal Science and Technology, Sichuan Agricultural University, Chengdu 611130, China.

出版信息

Animals (Basel). 2022 Apr 18;12(8):1048. doi: 10.3390/ani12081048.

Abstract

Skeletal myogenesis is a complicated biological event that involves a succession of tightly controlled gene expressions. In order to identify novel regulators of this process, we performed mRNA-Seq studies of goat skeletal muscle satellite cells (MuSCs) cultured under proliferation (GM) and differentiation (DM1/DM5) conditions. A total of 19,871 goat genes were expressed during these stages, 198 of which represented novel transcripts. Notably, in pairwise comparisons at the different stages, 2551 differentially expressed genes (DEGs) were identified (p < 0.05), including 1560 in GM vs. DM1, 1597 in GM vs. DM5, and 959 in DM1 vs. DM5 DEGs. The time-series expression profile analysis clustered the DEGs into eight gene groups, three of which had significantly upregulated and downregulated patterns (p < 0.05). Functional enrichment analysis showed that DEGs were enriched for essential biological processes such as muscle structure development, muscle contraction, muscle cell development, striated muscle cell differentiation, and myofibril assembly, and were involved in pathways such as the MAPK, Wnt and PPAR signaling pathways. Moreover, the expression of eight DEGs (MYL2, DES, MYOG, FAP, PLK2, ADAM, WWC1, and PRDX1) was validated. These findings offer novel insights into the transcriptional regulation of skeletal myogenesis in goats.

摘要

骨骼肌生成是一个复杂的生物学过程,涉及一系列严格控制的基因表达。为了鉴定该过程的新调节因子,我们对在增殖(GM)和分化(DM1/DM5)条件下培养的山羊骨骼肌卫星细胞(MuSCs)进行了mRNA测序研究。在这些阶段共表达了19,871个山羊基因,其中198个代表新转录本。值得注意的是,在不同阶段的成对比较中,鉴定出2551个差异表达基因(DEGs)(p < 0.05),包括GM与DM1比较中有1560个,GM与DM5比较中有1597个,DM1与DM5比较中有959个DEGs。时间序列表达谱分析将DEGs聚类为八个基因组,其中三个具有显著上调和下调模式(p < 0.05)。功能富集分析表明,DEGs富集于肌肉结构发育、肌肉收缩、肌肉细胞发育、横纹肌细胞分化和肌原纤维组装等重要生物学过程,并参与MAPK、Wnt和PPAR信号通路等途径。此外,验证了八个DEGs(MYL2、DES、MYOG、FAP、PLK2、ADAM、WWC1和PRDX1)的表达。这些发现为山羊骨骼肌生成的转录调控提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/690b/9024908/3f9a4fd59fd7/animals-12-01048-g001.jpg

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