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STAT3-dependent long non-coding RNA Lncenc1 contributes to mouse ES cells pluripotency via stabilizing Klf4 mRNA.

Authors :
Monteleone E
Corrieri P
Provero P
Viavattene D
Pulvirenti L
Raggi L
Carbognin E
Bianchi ME
Martello G
Oliviero S
Pandolfi PP
Poli V
Source :
Briefings in functional genomics [Brief Funct Genomics] 2024 Sep 27; Vol. 23 (5), pp. 651-662.
Publication Year :
2024

Abstract

Embryonic stem cells (ESCs) preserve the unique ability to differentiate into any somatic cell lineage while maintaining their self-renewal potential, relying on a complex interplay of extracellular signals regulating the expression/activity of pluripotency transcription factors and their targets. Leukemia inhibitory factor (LIF)-activated STAT3 drives ESCs' stemness by a number of mechanisms, including the transcriptional induction of pluripotency factors such as Klf4 and the maintenance of a stem-like epigenetic landscape. However, it is unknown if STAT3 directly controls stem-cell specific non-coding RNAs, crucial to balance pluripotency and differentiation. Applying a bioinformatic pipeline, here we identify Lncenc1 in mouse ESCs as an STAT3-dependent long non-coding RNA that supports pluripotency. Lncenc1 acts in the cytoplasm as a positive feedback regulator of the LIF-STAT3 axis by competing for the binding of microRNA-128 to the 3'UTR of the Klf4 core pluripotency factor mRNA, enhancing its expression. Our results unveil a novel non-coding RNA-based mechanism for LIF-STAT3-mediated pluripotency.<br /> (© The Author(s) 2023. Published by Oxford University Press.)

Details

Language :
English
ISSN :
2041-2657
Volume :
23
Issue :
5
Database :
MEDLINE
Journal :
Briefings in functional genomics
Publication Type :
Academic Journal
Accession number :
37801430
Full Text :
https://doi.org/10.1093/bfgp/elad045