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Identification and integrated analysis of differentially expressed lncRNAs and circRNAs reveal the potential ceRNA networks during PDLSC osteogenic differentiation

机译:差异表达的lncRNA和circRNA的鉴定和整合分析揭示了在PDLSC成骨分化过程中潜在的ceRNA网络

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Researchers have been exploring the molecular mechanisms underlying the control of periodontal ligament stem cell (PDLSC) osteogenic differentiation. Recently, long noncoding RNAs (lncRNAs) and circular RNAs (circRNAs) were shown to function as competitive endogenous RNAs (ceRNAs) to regulate the effect of microRNAs (miRNAs) on their target genes during cell differentiation. However, comprehensive identification and integrated analysis of lncRNAs and circRNAs acting as ceRNAs during PDLSC osteogenic differentiation have not been performed. PDLSCs were derived from healthy human periodontal ligament and cultured separately with osteogenic induction and normal media for 7 days. Cultured PDLSCs were positive for STRO-1 and CD146 and negative for CD31 and CD45. Osteo-induced PDLSCs showed increased ALP (alkaline phosphatase) activity and up-regulated expression levels of the osteogenesis-related markers ALP, Runt-related transcription factor 2 and osteocalcin. Then, a total of 960 lncRNAs and 1456 circRNAs were found to be differentially expressed by RNA sequencing. The expression profiles of eight lncRNAs and eight circRNAs were measured with quantitative real-time polymerase chain reaction and were shown to agree with the RNA-seq results. Furthermore, the potential functions of lncRNAs and circRNAs as ceRNAs were predicted based on miRanda and were investigated using Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analysis. In total, 147 lncRNAs and 1382 circRNAs were predicted to combine with 148 common miRNAs and compete for miRNA binding sites with 744 messenger RNAs. These mRNAs were predicted to significantly participate in osteoblast differentiation, the MAPK pathway, the Wnt pathway and the signaling pathways regulating pluripotency of stem cells. Among them, lncRNAs coded as TCONS_00212979 and TCONS_00212984, as well as circRNA BANP and circRNA ITCH, might interact with miRNA34a and miRNA146a to regulate PDLSC osteogenic differentiation via the MAPK pathway. This study comprehensively identified lncRNAs/circRNAs and first integrated their potential ceRNA function during PDLSC osteogenic differentiation. These findings suggest that specific lncRNAs and circRNAs might function as ceRNAs to promote PDLSC osteogenic differentiation and periodontal regeneration.
机译:研究人员一直在探索控制牙周膜干细胞(PDLSC)成骨分化的分子机制。近来,长的非编码RNA(lncRNA)和环状RNA(circRNA)被显示为竞争性内源RNA(ceRNA),可在细胞分化过程中调节微小RNA(miRNA)对其靶基因的作用。但是,尚未进行PDLSC成骨分化过程中作为ceRNA的lncRNA和circRNA的全面鉴定和综合分析。 PDLSCs来自健康的人牙周膜,并分别用成骨诱导和正常培养基培养7天。培养的PDLSC对STRO-1和CD146呈阳性,而对CD31和CD45呈阴性。骨诱导的PDLSCs表现出增加的ALP(碱性磷酸酶)活性,并与成骨相关标志物ALP,Runt相关转录因子2和骨钙素表达水平上调。然后,通过RNA测序发现总共960个lncRNA和1456个circRNA差异表达。用定量实时聚合酶链反应测量了八个lncRNA和八个circRNA的表达谱,显示与RNA-seq结果一致。此外,基于miRanda预测了lncRNA和circRNA作为ceRNA的潜在功能,并使用“基因本体论”和“京都基因与基因组百科全书”进行了研究。预计总共有147个lncRNA和1382个circRNA与148个常见miRNA结合,并与744个Messenger RNA竞争miRNA结合位点。预测这些mRNA将显着参与成骨细胞分化,MAPK途径,Wnt途径和调节干细胞多能性的信号传导途径。其中,编码为TCONS_00212979和TCONS_00212984的lncRNA,以及circRNA BANP和circRNA ITCH,可能与miRNA34a和miRNA146a相互作用,通过MAPK途径调节PDLSC成骨分化。这项研究全面鉴定了lncRNA / circRNA,并在PDLSC成骨分化过程中首先整合了其潜在的ceRNA功能。这些发现表明特定的lncRNA和circRNA可能作为ceRNA来促进PDLSC成骨分化和牙周再生。

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