Expression and Function of Long Non-coding RNA in Endemic Cretinism.

IF 4.6 2区 医学 Q1 NEUROSCIENCES Molecular Neurobiology Pub Date : 2025-02-01 Epub Date: 2024-07-20 DOI:10.1007/s12035-024-04358-3
Yanhong He, Jianshuang Li, Yun Chen, Bingxuan Ren, Zheng Zhou, Jinjin Liu, Haiyan Gao, Fan Li, Baoxiang Li, Lixiang Liu, Hongmei Shen
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Abstract

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.

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地方性克汀病中长非编码 RNA 的表达和功能
地方性克汀病(EC)是最严重的缺碘疾病之一,会导致神经发育障碍或智力缺陷等典型症状。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-seq,揭示了长非编码RNA(lncRNA)和信使RNA(mRNA)的差异表达谱。通过GO和KEGG分析,对差异表达(DE)mRNA和共表达mRNA的功能和通路进行了注释。建立了蛋白质-蛋白质相互作用(PPI)网络。通过实时定量 PCR 分析(qRT-PCR)验证了三个 lncRNA 和六个 mRNA 的表达水平,并进行了相关性分析。与对照组相比,共有864个lncRNA和393个mRNA存在差异表达。PPI网络有149个节点和238条边,并观察到三个关键蛋白编码基因。据统计,EC患者中LINC01220和靶mRNA IDO1的水平升高。差异表达的lncRNA可能是心肌梗死的一个新的潜在参与者。LINC01220和IDO1可能相互影响,共同参与心肌梗死的发生。突触后膜电位调控的生物学过程和Rap1信号通路可能在EC的病理生理过程中发挥调控作用。我们的发现可为研究EC的病理生理机制提供更多的理论和实验证据。
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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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