Table 1.
Epigenomic Feature | Intestinal Epithelial Process | References |
---|---|---|
3D chromatin looping | TADs are thought to be stable across cell types | |
Genome-wide 3D chromatin interactions have not been mapped in the intestine | ||
Chromatin accessiblity | Generally similar across intestinal epithelial cell populations | 37, 40 |
Secretory cells have specific accessible regions bound to secretory cell-specific TFs | 32, 49 | |
These regions lose chromatin accessiblity when secretory cells dedifferentiate into ISCs | 32 | |
Histone Modifications | ||
H3K4me1/2, H3K27ac | Overall similar across intestinal cell lineages | 37, 40 |
Differences correlate with dynamic gene expression | 69 | |
H3K27me3 | Associated with promoters of silent genes and largely stable across cell types. About 200 ISC-specific genes show increases H3K27me3 levels in differentiated cells | 31 |
Loss of H3K27 methyltransferase activity permits reexpression of developmentally silenced genes, but ISC-specific genes are not reactivated in mature cells. | 31 | |
DNA methylation | Majority of enhancers have similar methylation profiles across intestinal epithelial cell types | 30, 35 |
Small differences occur at a subset of cell type-specific genes | 58 |
ISC, intestinal stem cells; TADS, topological associating domains; TFs, transcription factors; 3D, three-dimensional.