Comprehensive 3D epigenomic maps define limbal stem/progenitor cell function and identity.
Mingsen LiHuaxing HuangBofeng WangShaoshuai JiangHuizhen GuoLiqiong ZhuSiqi WuJiafeng LiuLi WangXihong LanWang ZhangJin ZhuFuxi LiJieying TanZhen MaoChunqiao LiuJianping JiJunjun DingKang ZhangJin YuanYizhi LiuHong OuyangPublished in: Nature communications (2022)
The insights into how genome topology couples with epigenetic states to govern the function and identity of the corneal epithelium are poorly understood. Here, we generate a high-resolution Hi-C interaction map of human limbal stem/progenitor cells (LSCs) and show that chromatin multi-hierarchical organisation is coupled to gene expression. By integrating Hi-C, epigenome and transcriptome data, we characterize the comprehensive 3D epigenomic landscapes of LSCs. We find that super-silencers mediate gene repression associated with corneal development, differentiation and disease via chromatin looping and/or proximity. Super-enhancer (SE) interaction analysis identified a set of SE interactive hubs that contribute to LSC-specific gene activation. These active and inactive element-anchored loop networks occur within the cohesin-occupied CTCF-CTCF loops. We further reveal a coordinated regulatory network of core transcription factors based on SE-promoter interactions. Our results provide detailed insights into the genome organization principle for epigenetic regulation of gene expression in stratified epithelia.
Keyphrases
- genome wide
- dna methylation
- gene expression
- transcription factor
- copy number
- high resolution
- genome wide identification
- endothelial cells
- optical coherence tomography
- dna binding
- wound healing
- mass spectrometry
- induced pluripotent stem cells
- electronic health record
- machine learning
- rna seq
- single cell
- liquid chromatography
- artificial intelligence