Abstract

Predominant transcriptional subnetworks called Core, Myc, and PRC modules have been shown to participate in preservation of the pluripotency and self-renewality of embryonic stem cells (ESCs). Epiblast stem cells (EpiSCs) are another cell type that possesses pluripotency and self-renewality. However, the roles of these modules in EpiSCs have not been systematically examined to date. Here, we compared the average expression levels of Core, Myc, and PRC module genes between ESCs and EpiSCs. EpiSCs showed substantially higher and lower expression levels of PRC and Core module genes, respectively, compared with those in ESCs, while Myc module members showed almost equivalent levels of average gene expression. Subsequent analyses revealed that the similarity in gene expression levels of the Myc module between these two cell types was not just overall, but striking similarities were evident even when comparing the expression of individual genes. We also observed equivalent levels of similarity in the expression of individual Myc module genes between induced pluripotent stem cells (iPSCs) and partial iPSCs that are an unwanted byproduct generated during iPSC induction. Moreover, our data demonstrate that partial iPSCs depend on a high level of c-Myc expression for their self-renewal properties.

Highlights

  • Embryonic stem cells (ESCs) derived from blastocysts are able to self-renew indefinitely and bear pluripotency, which is defined as the property enabling differentiation into any cell type of the entire body [1,2,3]

  • The same scatter plot analyses were applied to compare the expression levels of individual Myc module members between ESCs and Epiblast stem cells (EpiSCs) (Figure 1B). These analyses revealed that 92% (392 genes) of Myc module members showed comparable expression between ESCs and EpiSCs

  • We examined the expression of individual Core, Myc, and PRC module genes in ESCs, EpiSCs, epiblast-like cells (EpiLCs), and partial induced pluripotent stem cells (iPSCs)

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Summary

Introduction

Embryonic stem cells (ESCs) derived from blastocysts are able to self-renew indefinitely and bear pluripotency, which is defined as the property enabling differentiation into any cell type of the entire body [1,2,3]. Because of these remarkable biological properties, ESCs are expected to be an unlimited source of functionally mature differentiated cells for therapeutic purposes, such as cardiomyocytes and pancreatic insulinsecreting β cells. In mouse ESCs, most members of Core and Myc modules show high expression levels compared with those in differentiated derivatives, while most PRC module members show a contrasting expression pattern, suggesting that Core and Myc module members, but not PRC module members, actively participate in sustaining the ESC status

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