He Yanhong, Li Jianshuang, Chen Yun, Ren Bingxuan, Zhou Zheng, Liu Jinjin, Gao Haiyan, Li Fan, Li Baoxiang, Liu Lixiang, Shen Hongmei
Chinese Centre for Disease Control and Prevention, Centre for Endemic Disease Control, Harbin Medical University, Heilongjiang Province 150081, Harbin City, People's Republic of China.
Commission & Education Bureau of Heilongjiang Province, Key Laboratory of Etiology and Epidemiology, National Health, Harbin Medical University, Heilongjiang Province 150081, Harbin City, People's Republic of China.
Mol Neurobiol. 2025 Feb;62(2):1770-1787. doi: 10.1007/s12035-024-04358-3. Epub 2024 Jul 20.
Endemic cretinism (EC) is one of the most severe iodine deficiency disorders, leading to typical symptoms such as neurodevelopmental impairments or mental deficits. In addition to environmental factors, the pathogenesis of its genetic contribution remains unclear. The study revealed the differential expression profiles of long non-coding RNA(lncRNA) and messenger RNA(mRNA) based on high-throughput RNA-seq. GO and KEGG analyses were used to annotate the function and pathway of differentially expressed (DE) mRNA and co-expressed mRNA. The protein-protein interaction(PPI) network was established. The expression levels of three lncRNAs and six mRNAs were validated by quantitative real-time PCR analysis (qRT-PCR) and subjected to correlation analysis. Compared to controls, a total of 864 lncRNAs and 393 mRNAs were differentially expressed. The PPI network had 149 nodes and 238 edges, and three key protein-coding genes were observed. Levels of LINC01220 and target mRNA IDO1 were statistically elevated in EC patients. Differentially expressed lncRNA may be a new potential player in EC. LINC01220 and IDO1 might interact with each other to participate in EC. The biological process of regulation of postsynaptic membrane potential and the Rap1 signaling pathway might exert a regulating role in the pathophysiological process of EC. Our findings could provide more theoretical and experimental evidence for investigating the pathophysiological mechanisms of EC.
地方性克汀病(EC)是最严重的碘缺乏病之一,会导致典型症状,如神经发育障碍或智力缺陷。除环境因素外,其遗传因素的发病机制仍不清楚。该研究基于高通量RNA测序揭示了长链非编码RNA(lncRNA)和信使RNA(mRNA)的差异表达谱。使用基因本体论(GO)和京都基因与基因组百科全书(KEGG)分析对差异表达(DE)mRNA和共表达mRNA的功能及通路进行注释。建立了蛋白质-蛋白质相互作用(PPI)网络。通过定量实时PCR分析(qRT-PCR)验证了3种lncRNA和6种mRNA的表达水平,并进行了相关性分析。与对照组相比,共有864种lncRNA和393种mRNA差异表达。PPI网络有149个节点和238条边,观察到3个关键蛋白质编码基因。EC患者中LINC01220和靶标mRNA IDO1的水平在统计学上有所升高。差异表达的lncRNA可能是EC中的一个新的潜在因素。LINC01220和IDO1可能相互作用参与EC。突触后膜电位调节的生物学过程和Rap1信号通路可能在EC的病理生理过程中发挥调节作用。我们的研究结果可为探究EC的病理生理机制提供更多的理论和实验依据。