lncRNA LINC00941 modulates MTA2/NuRD occupancy to suppress premature human epidermal differentiation.
Eva MorgensternCarolin MolthofUwe SchwartzJohannes GrafAstrid BruckmannSonja HombachMarkus KretzPublished in: Life science alliance (2024)
Numerous long non-coding RNAs (lncRNAs) were shown to have a functional impact on cellular processes such as human epidermal homeostasis. However, the mechanism of action for many lncRNAs remains unclear to date. Here, we report that lncRNA LINC00941 regulates keratinocyte differentiation on an epigenetic level through association with the NuRD complex, one of the major chromatin remodelers in cells. We find that LINC00941 interacts with NuRD-associated MTA2 and CHD4 in human primary keratinocytes. LINC00941 perturbation changes MTA2/NuRD occupancy at bivalent chromatin domains in close proximity to transcriptional regulator genes, including the EGR3 gene coding for a transcription factor regulating epidermal differentiation. Notably, LINC00941 depletion resulted in reduced NuRD occupancy at the EGR3 gene locus, increased EGR3 expression in human primary keratinocytes, and increased abundance of EGR3-regulated epidermal differentiation genes in cells and human organotypic epidermal tissues. Our results therefore indicate a role of LINC00941/NuRD in repressing EGR3 expression in non-differentiated keratinocytes, consequentially preventing premature differentiation of human epidermal tissues.
Keyphrases
- long non coding rna
- endothelial cells
- transcription factor
- poor prognosis
- long noncoding rna
- genome wide
- gene expression
- cell proliferation
- induced pluripotent stem cells
- pluripotent stem cells
- wound healing
- genome wide identification
- induced apoptosis
- dna methylation
- cell death
- binding protein
- cell cycle arrest
- dna binding
- pi k akt