Epigenetic Insights Into Necrotizing Enterocolitis: Unraveling Methylation-Regulated Biomarkers

被引:0
作者
Tian, Bowen [1 ]
Xu, Xiaogang [1 ,2 ]
Li, Lin [2 ]
Tian, Yan [3 ]
Liu, Yanqing [2 ]
Mu, Yide [2 ]
Lu, Jieting [1 ]
Song, Kai [2 ]
Lv, Junjian [2 ]
He, Qiuming [2 ]
Zhong, Wei [2 ]
Xia, Huimin [1 ,2 ]
Lan, Chaoting [2 ]
机构
[1] Southern Med Univ, Sch Clin Med 1, Guangzhou, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Guangdong Prov Key Lab Res Struct Birth Defect Dis, Guangzhou Women & Childrens Med Ctr, Guangdong Prov Clin Res Ctr Child Hlth,Dept Pediat, 9 Jinsui Rd, Guangzhou 510623, Guangdong, Peoples R China
[3] Jiangxi Prov Childrens Hosp, Dept Anesthesiol, Nanchang, Jiangxi, Peoples R China
关键词
DNA methylation; single-cell transcriptomics; necrotizing enterocolitis; multiomics network; methylation-regulated genes; DNA METHYLATION; MODEL;
D O I
10.1007/s10753-024-02054-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Necrotizing enterocolitis (NEC) is a multifactorial gastrointestinal disease with high morbidity and mortality among premature infants. This study aimed to identify novel methylation-regulated biomarkers in NEC intestinal tissue through multiomics analysis. We analyzed DNA methylation and transcriptome datasets from ileum and colon tissues of patients with NEC. We identify methylation-related differential genes (MrDEGs) based on the rule that the degree of methylation in the promoter region is inversely proportional to RNA transcription. These MrDEGs included ADAP1, GUCA2A, BCL2L14, FUT3, MISP, USH1C, ITGA3, UNC93A and IL22RA1. Single-cell data revealed that MrDEGs were mainly located in the intestinal epithelial part of intestinal tissue. These MrDEGs were verified through Target gene bisulfite sequencing and RT-qPCR. We successfully identified and verified the ADAP1, GUCA2A, IL22RA1 and MISP, primarily expressed in intestinal epithelial villus cells through single-cell data. Through single-gene gene set enrichment analysis, we found that these genes participate mainly in the pathological process of T-cell differentiation and the suppression of intestinal inflammation in NEC. This study enhances our understanding of the pathogenesis of NEC and may promote the development of new precision medicine methods for NEC prediction and diagnosis.
引用
收藏
页码:236 / 253
页数:18
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