پديدآورندگان :
Moradi Sharif Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran. , Sharifi-Zarchi Ali Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran , Mollamohammadi Sepideh Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran , Asgari Sassan Australian Infectious Disease Research Centre, School of Biological Sciences, The University of Queensland, Brisbane, Queensland, Australia , Braun Thomas Max-Planck Institute for Heart and Lung Research, Department of Cardiac Development and Remodelling, Bad Nauheim, Germany , Baharvand Hossein Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran
كليدواژه :
Dlk1 , Dio3 locus , ground state pluripotency , microRNA , small RNA sequencing , differentiation
چكيده فارسي :
Embryonic stem cells (ESCs) are characterized by unlimited self-renewal and multi-lineage
differentiation. They have numerous applications in studying embryonic development, drug
screening, disease modeling, and cell therapy. Self-renewal and multi-lineage differentiation
potential of ESCs are orchestrated by an integrated network of biomolecules including
transcription factors and non-coding RNAs such as microRNAs. Here, we show that
microRNAs are differentially expressed in ground state ESCs compared to serum cells. We
find that the imprinted Dlk1-Dio3 locus expresses the majority of ground state-specific
microRNAs. Computational analysis predicts that ground state microRNAs repress numerous
differentiation pathways. Functional analysis reveals that ground state microRNAs embedded
in the Dlk1-Dio3 locus promote pluripotency via inhibition of multi-lineage differentiation and
stimulation of self-renewal. Taken together, we demonstrate that microRNAs are differentially
expressed in different pluripotency contexts and that ground state microRNAs promote
pluripotency by stimulating diverse aspects of self-renewal and inhibiting differentiation.