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Altered expression of circular RNA in human dental pulp cells during odontogenic differentiation

机译:牙科分化过程中人牙髓细胞中圆弧菌的表达改变

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The alterations in expression and function of circular RNA (circRNA) in human dental pulp cells (hDPCs) during odontogenic differentiation were investigated. To induce odontogenic differentiation, hDPCs (passage 3) were cultured for 14 days in odontogenic induction medium. circRNA high-throughput sequencing was performed using Illumina HiSeqseq (TM) 2000. Subsequently, Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses were used to evaluate the bio-functions of the identified circRNAs. To validate the results of circRNA sequencing, reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was performed for two selected differentially expressed circRNAs. The RNA sequencing results revealed that 1,314 and 1,780 circRNAs were upregulated and downregulated, respectively, during odontogenic induction. Their predicted target miRNAs and genes are involved in several biological functions and signaling pathways, including the mitogen-associated protein kinase signaling pathway. The RT-qPCR results of the two selected circRNAs (hsa_circ_0015260 and hsa_circ_0006984) were consistent with the expression trend obtained using high-throughput sequencing. The results of the present study add to the current understanding of the regulatory mechanisms underlying hDPCs differentiation.
机译:研究了人牙髓细胞(HDPC)在非肠癌分化过程中圆形RNA(CircrNA)的表达和功能的改变。为了诱导偶联分化,HDPC(通过3)在牙肠诱导培养基中培养14天。使用Illumina Hiseqseq(TM)2000进行Circrna高通量测序。随后,使用基因和基因组的基因本体和京都植物分析来评估所鉴定的Circrnas的生物功能。为了验证Circrna测序的结果,对两个选定的差异表达的Circrna进行逆转录定量聚合酶链反应(RT-QPCR)。 RNA测序结果表明,在牙核诱导期间,分别上调和下调1,314和1,780个CircrNA。它们预测的目标miRNA和基因涉及若干生物学功能和信号通路,包括丝分裂相关蛋白激酶信号传导途径。两个所选Circrnas(HSA_CIRC_0015260和HSA_CIRC_0006984)的RT-QPCR结果与使用高吞吐量排序获得的表达趋势一致。本研究结果增加了目前对HDPCS分化的监管机制的理解。

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