| Literature DB >> 27989770 |
Anna Sahakyan1, Rachel Kim2, Constantinos Chronis3, Shan Sabri4, Giancarlo Bonora5, Thorold W Theunissen6, Edward Kuoy3, Justin Langerman3, Amander T Clark7, Rudolf Jaenisch8, Kathrin Plath9.
Abstract
Naive human embryonic stem cells (hESCs) can be derived from primed hESCs or directly from blastocysts, but their X chromosome state has remained unresolved. Here, we show that the inactive X chromosome (Xi) of primed hESCs was reactivated in naive culture conditions. Like cells of the blastocyst, the resulting naive cells contained two active X chromosomes with XIST expression and chromosome-wide transcriptional dampening and initiated XIST-mediated X inactivation upon differentiation. Both establishment of and exit from the naive state (differentiation) happened via an XIST-negative XaXa intermediate. Together, these findings identify a cell culture system for functionally exploring the two X chromosome dosage compensation processes in early human development: X dampening and X inactivation. However, remaining differences between naive hESCs and embryonic cells related to mono-allelic XIST expression and non-random X inactivation highlight the need for further culture improvement. As the naive state resets Xi abnormalities seen in primed hESCs, it may provide cells better suited for downstream applications. Published by Elsevier Inc.Entities:
Keywords: X chromosome; X chromosome dampening; X chromosome inactivation; XIST; embryonic stem cells; human development; human stem cells; lncRNA; naive pluripotency; pluripotent stem cells
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Year: 2016 PMID: 27989770 PMCID: PMC5218861 DOI: 10.1016/j.stem.2016.10.006
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 25.269