4.6 Review

Building Pluripotency Identity in the Early Embryo and Derived Stem Cells

Journal

CELLS
Volume 10, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/cells10082049

Keywords

peri-implantation embryo; EGA; lineage specification; pluripotent stem cells; pluripotency transcriptional networks; epigenetic; DNA methylation and histone modification; X chromosome inactivation; non-coding RNAs

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Funding

  1. Italian Ministry of Education, University and Research (MIUR): Dipartimenti di Eccellenza Program (2018-2022)-Department of Biology and Biotechnology L. Spallanzani, University of Pavia
  2. University of Pavia FRG

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The fusion of differentiated cells forms a totipotent zygote capable of developing into a complete organism; as development progresses, cells acquire their own identities through programmed cell divisions until pluripotency is achieved; transcriptome modulation and remodeling of chromatin epigenetics play roles in the path to pluripotency.
The fusion of two highly differentiated cells, an oocyte with a spermatozoon, gives rise to the zygote, a single totipotent cell, which has the capability to develop into a complete, fully functional organism. Then, as development proceeds, a series of programmed cell divisions occur whereby the arising cells progressively acquire their own cellular and molecular identity, and totipotency narrows until when pluripotency is achieved. The path towards pluripotency involves transcriptome modulation, remodeling of the chromatin epigenetic landscape to which external modulators contribute. Both human and mouse embryos are a source of different types of pluripotent stem cells whose characteristics can be captured and maintained in vitro. The main aim of this review is to address the cellular properties and the molecular signature of the emerging cells during mouse and human early development, highlighting similarities and differences between the two species and between the embryos and their cognate stem cells.

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