| Literature DB >> 27989715 |
Sanjeet Patel1, Giancarlo Bonora1, Anna Sahakyan1, Rachel Kim1, Constantinos Chronis1, Justin Langerman1, Sorel Fitz-Gibbon2, Liudmilla Rubbi2, Rhys J P Skelton3, Reza Ardehali3, Matteo Pellegrini2, William E Lowry2, Amander T Clark2, Kathrin Plath4.
Abstract
Applications of embryonic stem cells (ESCs) require faithful chromatin changes during differentiation, but the fate of the X chromosome state in differentiating ESCs is unclear. Female human ESC lines either carry two active X chromosomes (XaXa), an Xa and inactive X chromosome with or without XIST RNA coating (XiXIST+Xa;XiXa), or an Xa and an eroded Xi (XeXa) where the Xi no longer expresses XIST RNA and has partially reactivated. Here, we established XiXa, XeXa, and XaXa ESC lines and followed their X chromosome state during differentiation. Surprisingly, we found that the X state pre-existing in primed ESCs is maintained in differentiated cells. Consequently, differentiated XeXa and XaXa cells lacked XIST, did not induce X inactivation, and displayed higher X-linked gene expression than XiXa cells. These results demonstrate that X chromosome dosage compensation is not required for ESC differentiation. Our data imply that XiXIST+Xa ESCs are most suited for downstream applications and show that all other X states are abnormal byproducts of our ESC derivation and propagation method.Entities:
Keywords: DNA methylation; X-chromosome dosage compensation; X-inactivation; Xi-erosion; Xist; human embryonic stem cells; human induced pluripotent stem cells; inactive X chromosome
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Year: 2016 PMID: 27989715 PMCID: PMC5214931 DOI: 10.1016/j.celrep.2016.11.054
Source DB: PubMed Journal: Cell Rep Impact factor: 9.995