CircRNA profiling of skeletal muscle satellite cells in goats reveals circTGFβ2 promotes myoblast differentiation.

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Siyuan Zhan, Rui Jiang, Zongqi An, Yang Zhang, Tao Zhong, Linjie Wang, Jiazhong Guo, Jiaxue Cao, Li Li, Hongping Zhang
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Abstract

Background: Circular RNAs (circRNAs) function as essential regulatory elements with pivotal roles in various biological processes. However, their expression profiles and functional regulation during the differentiation of goat myoblasts have not been thoroughly explored. This study conducts an analysis of circRNA expression profiles during the proliferation phase (cultured in growth medium, GM) and differentiation phase (cultured in differentiation medium, DM1/DM5) of skeletal muscle satellite cells (MuSCs) in goats.

Results: A total of 2,094 circRNAs were identified, among which 84 were differentially expressed as determined by pairwise comparisons across three distinct groups. Validation of the expression levels of six randomly selected circRNAs was performed using reverse transcription PCR (RT-PCR) and quantitative RT-PCR (qRT-PCR), with confirmation of their back-splicing junction sites. Enrichment analysis of the host genes associated with differentially expressed circRNAs (DEcircRNAs) indicated significant involvement in biological processes such as muscle contraction, muscle hypertrophy, and muscle tissue development. Additionally, these host genes were implicated in key signaling pathways, including Hippo, TGF-beta, and MAPK pathways. Subsequently, employing Cytoscape, we developed a circRNA-miRNA interaction network to elucidate the complex regulatory mechanisms underlying goat muscle development, encompassing 21 circRNAs and 47 miRNAs. Functional assays demonstrated that circTGFβ2 enhances myogenic differentiation in goats, potentially through a miRNA sponge mechanism.

Conclusion: In conclusion, we identified the genome-wide expression profiles of circRNAs in goat MuSCs during both proliferation and differentiation phases, and established that circTGFβ2 plays a role in the regulation of myogenesis. This study offers a significant resource for the advanced exploration of the biological functions and mechanisms of circRNAs in the myogenesis of goats.

山羊骨骼肌卫星细胞的 CircRNA 分析显示,circTGFβ2 能促进肌母细胞分化。
背景:环状 RNA(circRNA)是在各种生物过程中起关键作用的重要调控元件。然而,它们在山羊成肌细胞分化过程中的表达谱和功能调控尚未得到深入探讨。本研究对山羊骨骼肌卫星细胞(MuSCs)增殖期(在生长培养基 GM 中培养)和分化期(在分化培养基 DM1/DM5 中培养)的 circRNA 表达谱进行了分析:结果:共鉴定出 2,094 个 circRNA,其中 84 个在三个不同组别中通过配对比较确定为差异表达。利用反转录 PCR(RT-PCR)和定量 RT-PCR(qRT-PCR)对随机选择的六个 circRNA 的表达水平进行了验证,并确认了它们的反向剪接连接点。对与差异表达的 circRNAs(DEcircRNAs)相关的宿主基因进行的富集分析表明,这些基因在肌肉收缩、肌肉肥大和肌肉组织发育等生物过程中有重要参与。此外,这些宿主基因还与关键信号通路有关,包括 Hippo、TGF-beta 和 MAPK 通路。随后,我们利用Cytoscape开发了一个circRNA-miRNA相互作用网络,以阐明山羊肌肉发育的复杂调控机制,其中包括21个circRNA和47个miRNA。功能测试表明,circTGFβ2可通过miRNA海绵机制增强山羊肌肉分化:总之,我们鉴定了山羊MuSCs在增殖和分化阶段的全基因组circRNA表达谱,并确定了circTGFβ2在调控成肌过程中的作用。这项研究为进一步探索circRNA在山羊肌生成过程中的生物学功能和机制提供了重要资源。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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