Stem Cell Reports (Dec 2017)

Small RNA Sequencing Reveals Dlk1-Dio3 Locus-Embedded MicroRNAs as Major Drivers of Ground-State Pluripotency

  • Sharif Moradi,
  • Ali Sharifi-Zarchi,
  • Amirhossein Ahmadi,
  • Sepideh Mollamohammadi,
  • Alexander Stubenvoll,
  • Stefan Günther,
  • Ghasem Hosseini Salekdeh,
  • Sassan Asgari,
  • Thomas Braun,
  • Hossein Baharvand

Journal volume & issue
Vol. 9, no. 6
pp. 2081 – 2096

Abstract

Read online

Summary: Ground-state pluripotency is a cell state in which pluripotency is established and maintained through efficient repression of endogenous differentiation pathways. Self-renewal and pluripotency of embryonic stem cells (ESCs) are influenced by ESC-associated microRNAs (miRNAs). Here, we provide a comprehensive assessment of the “miRNome” of ESCs cultured under conditions favoring ground-state pluripotency. We found that ground-state ESCs express a distinct set of miRNAs compared with ESCs grown in serum. Interestingly, most “ground-state miRNAs” are encoded by an imprinted region on chromosome 12 within the Dlk1-Dio3 locus. Functional analysis revealed that ground-state miRNAs embedded in the Dlk1-Dio3 locus (miR-541-5p, miR-410-3p, and miR-381-3p) promoted pluripotency via inhibition of multi-lineage differentiation and stimulation of self-renewal. Overall, our results demonstrate that ground-state pluripotency is associated with a unique miRNA signature, which supports ground-state self-renewal by suppressing differentiation. : Ground-state pluripotency is a cell state in which pluripotency is maintained through inhibition of differentiation. In this paper, Baharvand and colleagues report that ground-state pluripotency is associated with a unique microRNA signature. They find that ground-state microRNAs, which are mostly encoded by the Dlk1-Dio3 locus, contribute to the maintenance of ESCs through stimulating self-renewal and inhibiting differentiation. Keywords: Dlk1-Dio3 locus, ground-state pluripotency, microRNA, small RNA sequencing, differentiation, self-renewal, Sfmbt2 locus