lncRNA LINC00941 modulates MTA2/NuRD occupancy to suppress premature human epidermal differentiation

Author:

Morgenstern Eva1ORCID,Molthof Carolin1,Schwartz Uwe2ORCID,Graf Johannes1,Bruckmann Astrid1ORCID,Hombach Sonja13,Kretz Markus13ORCID

Affiliation:

1. Regensburg Center for Biochemistry (RCB), University of Regensburg

2. NGS Analysis Center Biology and Pre-Clinical Medicine, University of Regensburg

3. Institute for Molecular Medicine, MSH Medical School Hamburg

Abstract

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 theEGR3gene coding for a transcription factor regulating epidermal differentiation. Notably, LINC00941 depletion resulted in reduced NuRD occupancy at theEGR3gene 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.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Life Science Alliance, LLC

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