Li Zijian, Feng Juan, Yuan Zhengwei
Department of Neurology, Shengjing Hospital of China Medical University, Shenyang, China.
Key Laboratory of Health Ministry for Congenital Malformation, Shengjing Hospital of China Medical University, Shenyang, China.
Front Genet. 2020 Dec 2;11:583316. doi: 10.3389/fgene.2020.583316. eCollection 2020.
Spina bifida is a common neural tube defect (NTD) accounting for 5-10% of perinatal mortalities. As a polygenic disease, spina bifida is caused by a combination of genetic and environmental factors, for which the precise molecular pathogenesis is still not systemically understood. In the present study, we aimed to identify the related gene module that might play a vital role in the occurrence and development of spina bifida by using weighted gene co-expression network analysis (WGCNA). Transcription profiling according to an array of human amniocytes from patients with spina bifida and healthy controls was downloaded from the Gene Expression Omnibus database. First, outliers were identified and removed by principal component analysis (PCA) and sample clustering. Then, genes in the top 25% of variance in the GSE4182 dataset were then determined in order to explore candidate genes in potential hub modules using WGCNA. After data preprocessing, 5407 genes were obtained for further WGCNA. Highly correlated genes were divided into nineteen modules. Combined with a co-expression network and significant differentially expressed genes, 967 candidate genes were identified that may be involved in the pathological processes of spina bifida. Combined with our previous microRNA (miRNA) microarray results, we constructed an miRNA-mRNA network including four miRNAs and 39 mRNA among which three key genes were, respectively, linked to two miRNA-associated gene networks. Following the verification of qRT-PCR and KCND3 was upregulated in the spina bifida. KCND3 and its related miR-765 and miR-142-3p are worthy of further study. These findings may be conducive for early detection and intervention in spina bifida, as well as be of great significance to pregnant women and clinical staff.
脊柱裂是一种常见的神经管缺陷(NTD),占围产期死亡率的5%-10%。作为一种多基因疾病,脊柱裂由遗传和环境因素共同引起,其确切的分子发病机制仍未得到系统的理解。在本研究中,我们旨在通过加权基因共表达网络分析(WGCNA)来识别可能在脊柱裂的发生和发展中起关键作用的相关基因模块。从基因表达综合数据库下载了根据脊柱裂患者和健康对照的一系列人羊膜细胞进行的转录谱分析。首先,通过主成分分析(PCA)和样本聚类识别并去除异常值。然后,确定GSE4182数据集中方差前25%的基因,以便使用WGCNA探索潜在枢纽模块中的候选基因。经过数据预处理,获得了5407个基因用于进一步的WGCNA。高度相关的基因被分为19个模块。结合共表达网络和显著差异表达基因,鉴定出967个可能参与脊柱裂病理过程的候选基因。结合我们之前的微小RNA(miRNA)微阵列结果,我们构建了一个miRNA-mRNA网络,其中包括四个miRNA和39个mRNA,其中三个关键基因分别与两个miRNA相关基因网络相连。经过qRT-PCR验证,KCND3在脊柱裂中上调。KCND3及其相关的miR-765和miR-142-3p值得进一步研究。这些发现可能有助于脊柱裂的早期检测和干预,对孕妇和临床工作人员也具有重要意义。