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

被引:0
|
作者
He, Yanhong [1 ,2 ,3 ]
Li, Jianshuang [1 ,2 ,3 ,4 ]
Chen, Yun [1 ,2 ,3 ]
Ren, Bingxuan [1 ,2 ,3 ]
Zhou, Zheng [1 ,2 ,3 ]
Liu, Jinjin [1 ,2 ,3 ]
Gao, Haiyan [1 ,2 ,3 ]
Li, Fan [1 ,2 ,3 ]
Li, Baoxiang [1 ,2 ,3 ]
Liu, Lixiang [1 ,2 ,3 ]
Shen, Hongmei [1 ,2 ,3 ]
机构
[1] Harbin Med Univ, Chinese Ctr Dis Control & Prevent, Ctr Endem Dis Control, Harbin City 15008, Heilongjiang, Peoples R China
[2] Harbin Medical Univ, Commiss Educ Bur Heilongjiang Prov, Key Lab Etiol & Epidemiol Natl Hlth, Harbin City 15008, Heilongjiang, Peoples R China
[3] Harbin Med Univ, Heilongjiang Prov Key Lab Trace Elements & Human, Heilongjiang Prov, Harbin 150081, Heilongjiang, Peoples R China
[4] Harbin Med Univ, Coll Med Lab Sci & Technol, Daqing, Heilongjiang 16331, Peoples R China
基金
中国国家自然科学基金;
关键词
Iodine deficiency; Endemic cretinism; IDO1; RNA-seq; IODINE-DEFICIENCY; INDOLEAMINE 2,3-DIOXYGENASE; BRAIN-DEVELOPMENT; HYPOTHYROIDISM; RAT; PLASTICITY; MIGRATION; PACKAGE; AREA;
D O I
10.1007/s12035-024-04358-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
引用
收藏
页码:1770 / 1787
页数:18
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