Regulation of MicroRNAs After Spinal Cord Injury in Adult Zebrafish.

IF 2.8 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Neuroscience Pub Date : 2024-07-11 DOI:10.1007/s12031-024-02242-2
Wenyuan Shen, Jun Cai, Jinze Li, Wenchang Li, Pengcheng Shi, Xiumei Zhao, Shiqing Feng
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Abstract

Spinal cord injury (SCI) is a central nerve injury that often leads to loss of motor and sensory functions at or below the level of the injury. Zebrafish have a strong ability to repair after SCI, but the role of microRNAs (miRNAs) after SCI remains unclear. Locomotor behavior analysis showed that adult zebrafish recovered about 30% of their motor ability at 2 weeks and 55% at 3 weeks after SCI, reflecting their strong ability to repair SCI. Through miRNA sequencing, mRNA sequencing, RT-qPCR experiment verification, and bioinformatics predictive analysis, the key miRNAs and related genes in the repair of SCI were screened. A total of 38 miRNAs were significantly different, the top ten miRNAs were verified by RT-qPCR. The prediction target genes were verified by the mRNAs sequencing results at the same time point. Finally, 182 target genes were identified as likely to be networked regulated by the 38 different miRNAs. GO and KEGG enrichment analysis found that miRNAs targeted gene regulation of many key pathways, such as membrane tissue transport, ribosome function, lipid binding, and peroxidase activity. The PPI network analysis showed that miRNAs were involved in SCI repair through complex network regulation, among which dre-miR-21 may enhance cell reversibility through nop56, and that dre-miR-125c regulates axon growth through kpnb1 to repair SCI.

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成年斑马鱼脊髓损伤后的微RNA调控
脊髓损伤(SCI)是一种中枢神经损伤,通常会导致损伤部位或损伤部位以下的运动和感觉功能丧失。斑马鱼在脊髓损伤后有很强的修复能力,但微小RNA(miRNA)在脊髓损伤后的作用仍不清楚。运动行为分析表明,成年斑马鱼在损伤后2周和3周分别恢复了约30%和55%的运动能力,这反映了斑马鱼具有很强的损伤修复能力。通过miRNA测序、mRNA测序、RT-qPCR实验验证和生物信息学预测分析,筛选出修复SCI的关键miRNA和相关基因。共有 38 个 miRNA 存在显著差异,前 10 个 miRNA 已通过 RT-qPCR 验证。预测的靶基因由同一时间点的 mRNAs 测序结果验证。最后,确定了 182 个可能受 38 种不同 miRNA 网络调控的靶基因。GO和KEGG富集分析发现,miRNAs靶向调控了许多关键通路的基因,如膜组织转运、核糖体功能、脂质结合和过氧化物酶活性等。PPI网络分析显示,miRNA通过复杂的网络调控参与SCI修复,其中dre-miR-21可通过nop56增强细胞可逆性,dre-miR-125c可通过kpnb1调控轴突生长以修复SCI。
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来源期刊
Journal of Molecular Neuroscience
Journal of Molecular Neuroscience 医学-神经科学
CiteScore
6.60
自引率
3.20%
发文量
142
审稿时长
1 months
期刊介绍: The Journal of Molecular Neuroscience is committed to the rapid publication of original findings that increase our understanding of the molecular structure, function, and development of the nervous system. The criteria for acceptance of manuscripts will be scientific excellence, originality, and relevance to the field of molecular neuroscience. Manuscripts with clinical relevance are especially encouraged since the journal seeks to provide a means for accelerating the progression of basic research findings toward clinical utilization. All experiments described in the Journal of Molecular Neuroscience that involve the use of animal or human subjects must have been approved by the appropriate institutional review committee and conform to accepted ethical standards.
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