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首页> 外文期刊>DNA and Cell Biology >RNA-seq Used to Explore circRNA Expression and Identify Key circRNAs During the DNA Synthesis Phase of Mice Liver Regeneration
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RNA-seq Used to Explore circRNA Expression and Identify Key circRNAs During the DNA Synthesis Phase of Mice Liver Regeneration

机译:RNA-SEQ用于探索CircRNA表达并在小鼠肝再生的DNA合成阶段鉴定关键CircrNA

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摘要

The liver has an excellent capacity for regeneration when faced with external injury and the damage differs from that of other organs in the body. Our aim was to identify the role of circular RNA (circRNA) during the DNA synthesis phase (36 h) of mice liver regeneration. High-throughput RNA sequencing was conducted to explore circRNA and messenger RNA (mRNA) expression in three pairs of mice liver tissue at 0 and 36 h after 2/3 partial hepatectomy. One hundred differentially expressed circRNAs were detected, including 66 upregulated and 34 downregulated circRNAs. We also explored 2483 differentially expressed mRNAs, including 1422 upregulated and 1061 downregulated mRNAs. Gene ontology and Kyoto Encyclopedia of Genes and Genomes indicated that cell cycle regulation, material metabolism, and multiple classical pathways were involved in the DNA synthesis process. A competing endogenous RNA (ceRNA) network containing 5 circRNAs, 28 target genes, and 533 microRNAs (miRNAs) was constructed, and we selected the top 5 miRNAs to map it. Potential key circRNAs were validated with the quantitative real-time PCR technique and their regeneration curves, including consecutive time points, were produced. Finally, a cell counting kit-8 assay on key circRNAs of ceRNA network was performed to further confirm their roles in the DNA synthesis phase of liver regeneration. This study provides a circRNA expression profile for liver regeneration and contributes valuable information for future research.
机译:当面对外部损伤时,肝脏具有优异的再生能力,并且损坏与身体中其他器官的损坏不同。我们的目的是在小鼠肝再生的DNA合成相(36小时)期间识别圆形RNA(CircrNA)的作用。进行高通量RNA测序以在2/3部分肝切除术后在0和36小时的三对小鼠肝组织中探索CircrNA和信使RNA(mRNA)表达。检测到一百个差异表达的CircrNA,包括66个上调和34个下调的Circrnas。我们还探讨了2483个差异表达的MRNA,包括1422个上调和1061个下调MRNA。基因本体和基因组的京都百科全书表明,细胞周期调节,材料代谢和多种经典途径涉及DNA合成方法。构建了含有5个CircrNA,28个靶基因和533 microRNA(MiRNA)的竞争内源性RNA(Cerna)网络,并选择了前5名MiRNA来映射它。通过定量实时PCR技术验证潜在的键CircRNA,并产生它们的再生曲线,包括连续时间点。最后,进行了Cerna网络关键CircRNA的细胞计数试剂盒测定,以进一步证实它们在肝再生的DNA合成阶段中的作用。本研究为肝脏再生提供了Circrna表达谱,并为未来的研究提供了有价值的信息。

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