The Medical School of Jiaxing University, Jiaxing, China.
Department of Health Toxicology, College of Public Health, Xinjiang Medical University, Urumqi, China.
Biomed Res Int. 2021 Oct 8;2021:7162270. doi: 10.1155/2021/7162270. eCollection 2021.
Screening and preliminary identification of high DNMT1 expression-related lncRNA, which is involved in various interrelated signaling pathways, has led to the development of a theoretical basis for various types of disease mechanisms. Differential expression profiles of lncRNA and mRNA were identified in a microarray. Ten lncRNAs with high levels of variation were identified by qRT-PCR. KEGG and GO analyses were used to identify differentially expressed mRNAs. Six signaling pathways were selected based on the KEGG results of the lncRNA-mRNA expression network analysis. From the microarrays in the experimental and control groups, we found a total of 6987 differentially expressed lncRNAs, and 7421 differentially expressed mRNAs were obtained ( < 0.05; fold change > 2.0x). GO analysis and KEGG pathway analysis showed high expression of DNMT1 in esophageal epithelial cells. Nine pathways were involved in mRNA upregulation, including natural killer cell-mediated cytotoxicity and many other prominent biochemical pathways. Forty-six pathways were associated with downregulated mRNAs and ribosomes involving multiple biological pathways. Coexpression network analysis showed that 8 mRNAs and 16 lncRNAs were linked to the p53 signaling pathway. In Helicobacter pylori infections, interactions occurred between 22 lncRNAs and 11 mRNAs in the ErbB signaling pathway and between 19 lncRNAs and 8 mRNAs in epithelial cell signal transduction. Interactions were present between 19 lncRNAs and 5 mRNAs in the sphingolipid signaling pathway, along with interactions between 21 lncRNAs and 12 mRNAs in the PI3K-Akt signaling pathway. Cytotoxicity interactions occurred between 22 lncRNAs and 9 mRNAs in natural killer cells.
筛选和初步鉴定高表达的 DNMT1 相关 lncRNA,这些 lncRNA 涉及各种相互关联的信号通路,为各种类型的疾病机制的发展提供了理论基础。通过微阵列鉴定 lncRNA 和 mRNA 的差异表达谱。通过 qRT-PCR 鉴定了 10 个高水平变化的 lncRNA。KEGG 和 GO 分析用于鉴定差异表达的 mRNAs。基于 lncRNA-mRNA 表达网络分析的 KEGG 结果,选择了 6 个信号通路。从实验组和对照组的微阵列中,我们总共发现了 6987 个差异表达的 lncRNA,以及 7421 个差异表达的 mRNA(<0.05;倍数变化>2.0x)。GO 分析和 KEGG 通路分析显示 DNMT1 在食管上皮细胞中高表达。有 9 个通路涉及 mRNA 的上调,包括自然杀伤细胞介导的细胞毒性和许多其他重要的生化通路。46 个通路与下调的 mRNAs 相关,涉及核糖体和多个生物学通路。共表达网络分析显示,8 个 mRNA 和 16 个 lncRNA 与 p53 信号通路相关。在幽门螺杆菌感染中,22 个 lncRNA 和 11 个 mRNA 在 ErbB 信号通路中相互作用,19 个 lncRNA 和 8 个 mRNA 在上皮细胞信号转导中相互作用。19 个 lncRNA 和 5 个 mRNA 在鞘脂信号通路中相互作用,同时 21 个 lncRNA 和 12 个 mRNA 在 PI3K-Akt 信号通路中相互作用。在自然杀伤细胞中,22 个 lncRNA 和 9 个 mRNA 之间存在细胞毒性相互作用。