Luoyang Orthopedic-Traumatological Hospital of Henan Province (Henan Provincial Orthopedic Hospital), Orthopedic Institute of Henan Province, Luoyang, 471002, Henan Province, People's Republic of China.
Department of Orthopedics, Minhang Hospital, Fudan University, 170 Xin Song Road, Shanghai, 201199, People's Republic of China.
Sci Rep. 2020 Jul 2;10(1):10896. doi: 10.1038/s41598-020-67750-8.
Circular RNAs (circRNAs) serve as competing endogenous RNAs (ceRNAs) and indirectly regulate gene expression through shared microRNAs (miRNAs). However, the potential circRNAs functioning as ceRNAs in osteoporosis remain unclear. The bone marrow mesenchymal stem cells (BMSCs) were isolated from ovariectomy (OVX) mice and controls. We systematically analyzed RNA-seq and miRNA-microarray data, miRNA-target interactions, and prominently coexpressed gene pairs to identify aberrantly expressed circRNAs, miRNAs, and messenger RNAs (mRNAs) between the OVX mice and controls. A total of 45 circRNAs, 22 miRNAs, and 548 mRNAs were significantly dysregulated (fold change > 1.5; p < 0.05). Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses were conducted for differentially expressed mRNAs, and subsequently a circRNA-associated ceRNA network involved in osteoporosis was constructed. We identified two ceRNA regulatory pathways in this osteoporosis mouse model-novel circRNA 0020/miR-206-3p/Nnmt and circRNA 3832/miR-3473e/Runx3, which were validated by real-time PCR. This is the first study to elucidate the circRNA-associated ceRNA network in OVX and control mice using deep RNA-seq and RNA-microarray analysis. The data further expanded the understanding of circRNA-associated ceRNA networks, and the regulatory functions of circRNAs, miRNAs and mRNAs in the pathogenesis and pathology of osteoporosis.
环状 RNA(circRNAs)作为竞争性内源性 RNA(ceRNAs),通过共享 microRNA(miRNA)间接调节基因表达。然而,作为骨质疏松症 ceRNA 的潜在 circRNAs 尚不清楚。本研究从去卵巢(OVX)小鼠和对照组中分离骨髓间充质干细胞(BMSCs)。我们系统地分析了 RNA-seq 和 miRNA 微阵列数据、miRNA 靶标相互作用以及显著共表达基因对,以鉴定 OVX 小鼠和对照组之间差异表达的 circRNAs、miRNAs 和信使 RNA(mRNA)。共有 45 个 circRNAs、22 个 miRNAs 和 548 个 mRNAs 显著失调(倍数变化>1.5;p<0.05)。对差异表达的 mRNAs 进行了基因本体论和京都基因与基因组百科全书通路分析,随后构建了一个涉及骨质疏松症的 circRNA 相关 ceRNA 网络。在该骨质疏松症小鼠模型中,我们鉴定了两个 ceRNA 调控通路——新型 circRNA 0020/miR-206-3p/Nnmt 和 circRNA 3832/miR-3473e/Runx3,通过实时 PCR 进行了验证。这是首次使用深度 RNA-seq 和 RNA 微阵列分析阐明 OVX 和对照组小鼠中 circRNA 相关 ceRNA 网络的研究。该数据进一步扩展了对 circRNA 相关 ceRNA 网络以及 circRNAs、miRNAs 和 mRNAs 在骨质疏松症发病机制和病理学中的调控功能的理解。