State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases, Sichuan University, Chengdu, PR China; Department of Orthodontics, West China School & Hospital of Stomatology, Sichuan University, Chengdu, PR China.
State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases, Sichuan University, Chengdu, PR China; Department of Pediatric Dentistry, West China School & Hospital of Stomatology, Sichuan University, Chengdu, PR China.
Genomics. 2021 Jan;113(1 Pt 1):217-228. doi: 10.1016/j.ygeno.2020.12.012. Epub 2020 Dec 10.
The aim of this study was to explore the involvement of long noncoding RNAs (lncRNAs) during intermittent parathyroid hormone (PTH) induced cementogenesis. Expression profiles of lncRNAs and mRNAs were obtained using high-throughput microarray. Gene Ontology enrichment analysis, Kyoto Encyclopedia of Genes and Genomes pathway analysis, and coding-noncoding gene coexpression networks construction were performed. We identified 190 lncRNAs and 135 mRNAs that were differentially expressed during intermittent PTH-induced cementogenesis. In this process, the Wnt signaling pathway was negatively regulated, and eight lncRNAs were identified as possible core regulators of Wnt signaling. Based on the results of microarrray analysis, we further verified the repressed expression of Wnt signaling crucial components β-catenin, APC and Axin2. Above all, we speculated that lncRNAs may play important roles in PTH-induced cementogenesis via the negative regulation of Wnt pathway.
本研究旨在探讨长链非编码 RNA(lncRNAs)在间歇性甲状旁腺激素(PTH)诱导成骨中的作用。采用高通量微阵列技术获取 lncRNAs 和 mRNAs 的表达谱。进行基因本体论富集分析、京都基因与基因组百科全书通路分析以及编码非编码基因共表达网络构建。我们鉴定出 190 个 lncRNAs 和 135 个在间歇性 PTH 诱导成骨过程中差异表达的 mRNAs。在此过程中,Wnt 信号通路受到负调控,有 8 个 lncRNAs 被鉴定为 Wnt 信号的可能核心调控因子。基于微阵列分析的结果,我们进一步验证了 Wnt 信号关键成分β-catenin、APC 和 Axin2 的表达受到抑制。综上所述,我们推测 lncRNAs 可能通过负调控 Wnt 通路在 PTH 诱导成骨中发挥重要作用。