Long range inter-chromosomal interaction of Oct4 distal enhancer loci regulates ESCs pluripotency.
Byoung-San MoonDavid HuangFan GaoMingyang CaiGuochang LyuLei ZhangJun ChenWange LuPublished in: Cell death discovery (2023)
Nuclear architecture underlies the transcriptional programs within the cell to establish cell identity. As previously demonstrated, long-range chromatin interactions of the Oct4 distal enhancer (DE) are correlated with active transcription in naïve state embryonic stem cells. Here, we identify and characterize extreme long-range interactions of the Oct4 DE through a novel CRISPR labeling technique we developed and chromosome conformation capture to identify lethal giant larvae 2 (Llgl2) and growth factor receptor-bound protein 7 (Grb7) as putative functional interacting target genes in different chromosomes. We show that the Oct4 DE directly regulates expression of Llgl2 and Grb7 in addition to Oct4. Expression of Llgl2 and Grb7 closely correlates with the pluripotent state, where knock down of either result in loss of pluripotency, and overexpression enhances somatic cell reprogramming. We demonstrated that biologically important interactions of the Oct4 DE can occur at extreme distances that are necessary for the maintenance of the pluripotent state.
Keyphrases
- optical coherence tomography
- embryonic stem cells
- transcription factor
- diabetic retinopathy
- growth factor
- binding protein
- genome wide
- single cell
- cell therapy
- optic nerve
- gene expression
- copy number
- climate change
- minimally invasive
- public health
- dna damage
- stem cells
- cell proliferation
- crispr cas
- oxidative stress
- genome editing
- long non coding rna
- genome wide association study