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Comprehensive Analysis of Differentially Expressed lncRNA, circRNA and mRNA and Their ceRNA Networks in Mice With Severe Acute Pancreatitis

机译:具有严重急性胰腺炎的小鼠差异表达的LNCRNA,CircRNA和mRNA及其Cerna网络的综合分析

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Severe acute pancreatitis (SAP) is an acute digestive system disease with high morbidity mortality and hospitalization rate worldwide, due to various causes and unknown pathogenesis. In recent years, a large number of studies have confirmed that non-coding RNAs (ncRNAs) play an important role in many cellular processes and disease occurrence. However, the underlying mechanisms based on the function of ncRNAs, including long noncoding RNA (lncRNA) and circular RNA (circRNA), in SAP remain unclear. In this study, we performed high-throughput sequencing on the pancreatic tissues of three normal mice and three SAP mice for the first time to describe and analyze the expression profiles of ncRNAs, including lncRNA and circRNA. Our results identified that 49 lncRNAs, 56 circRNAs and 1,194 mRNAs were differentially expressed in the SAP group, compared with the control group. Furthermore, we performed Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis of differentially expressed lncRNAs and circRNAs, and found that the functions of the parental genes are enriched in the calcium-regulated signaling pathway, NF-κB signaling pathway, autophagy and protein digestion and absorption processes, which are closely related to the central events in pathogenesis of SAP. We also constructed lncRNA/circRNA-miRNA-mRNA networks to further explore their underlying mechanism and possible relationships in SAP. We found that in the competitive endogenous RNA (ceRNA) networks, differentially expressed lncRNAs and circRNAs are mainly involved in the apoptosis pathway and calcium signal transduction pathway. In conclusion, we found that lncRNAs and circRNAs play an important role in the pathogenesis of SAP, which may provide new insights in further exploring the pathogenesis of SAP and seek new targets for SAP.
机译:严重的急性胰腺炎(SAP)是一种急性消化系统疾病,具有良好的发病性死亡率和全球住院率,由于各种原因和未知的发病机制。近年来,大量研究证实,非编码RNA(NCRNA)在许多细胞过程和疾病发生中起着重要作用。然而,基于NCRNA的功能的潜在机制,包括在SAP中的长度非编码RNA(LNCRNA)和圆形RNA(CircrNA)仍然尚不清楚。在这项研究中,我们首次对三个正常小鼠的胰腺组织和三个SAP小鼠进行高通量测序,以描述和分析NCRNA的表达谱,包括LNCRNA和CircrNA。与对照组相比,我们的结果发现49℃,56个CircrNA和1,194 mRNA在SAP组中差异表达。此外,我们进行了基因本体(GO)和京都基因组(KEGG)(KEGG)分析差异表达的LNCRNA和CircrNA,发现富含钙调节信号通路,NF-κB信号传导的核生物基因的功能途径,自噬和蛋白质消化和吸收过程,与SAP发病机制中的中央事件密切相关。我们还构建了LNCRNA / Circrna-miRNA-mRNA网络,以进一步探索其潜在的机制和SAP中可能的关系。我们发现,在竞争性内源性RNA(CERNA)网络中,差异表达的LNCRNA和CircrNA主要参与凋亡途径和钙信号转导途径。总之,我们发现LNCRNA和Circrnas在SAP的发病机制中发挥着重要作用,这可能在进一步探索SAP的发病机制并寻求SAP的新目标方面发挥着新的见解。

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