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Identification of noncoding RNA expression profiles and regulatory interaction networks following traumatic spinal cord injury by sequence analysis

机译:通过序列分析鉴定创伤性脊髓损伤后非编码RNA表达谱和调控相互作用网络

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摘要

Aim: To systematically profile and characterize the noncoding RNA (ncRNA) expression pattern in the lesion epicenter of spinal tissues after traumatic spinal cord injury (TSCI) and predicted the structure and potential functions of the regulatory networks associated with these differentially expressed ncRNAs and mRNAs.Results: A total of 498 circRNAs, 458 lncRNAs, 155 miRNAs and 1203 mRNAs were identified in TSCI mice models to be differentially expressed. The regulatory networks associated with these differentially expressed ncRNAs and mRNAs were constructed.Materials and methods: We used RNA-Seq, Gene ontology (GO), KEGG pathway analysis and co-expression network analyses to profle the expression and regulation patterns of noncoding RNAs and mRNAs of mice models after TSCI. The findings were validated by quantitative real-time PCR (qRT-PCR) and Luciferase assay.Conclusion: noncoding RNAs might play important roles via the competing endogenous RNA regulation pattern after TSCI, further findings arising from this study will not only expand the understanding of potential ncRNA biomarkers but also help guide therapeutic strategies for TSCI.
机译:目的:系统地描述和表征创伤性脊髓损伤(TSCI)后脊髓组织病变中心的非编码RNA(ncRNA)表达模式,并预测与这些差异表达的ncRNA和mRNA相关的调控网络的结构和潜在功能。结果:在TSCI小鼠模型中共鉴定出498个circRNA,458个lncRNA,155个miRNA和1203个mRNA差异表达。构建了与这些差异表达的ncRNA和mRNA相关的调控网络。材料和方法:我们使用RNA-Seq,基因本体论(GO),KEGG通路分析和共表达网络分析来分析非编码RNA和蛋白的表达和调控模式。 TSCI后小鼠模型的mRNA。结论:非编码RNA可能通过TSCI后的竞争性内源RNA调控模式发挥重要作用,本研究产生的更多发现不仅会扩大人们对TSCI的认识。潜在的ncRNA生物标志物,但也有助于指导TSCI的治疗策略。

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