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Species-specific developmental timing is maintained by pluripotent stem cells ex utero

  • Christopher Barry
  • , Matthew T. Schmitz
  • , P. Jiang
  • , Michael P. Schwartz
  • , Bret M. Duffin
  • , Scott Swanson
  • , Rhonda Bacher
  • , Jennifer M. Bolin
  • , Angela L. Elwell
  • , Brian E. McIntosh
  • , Ron Stewart
  • , James A. Thomson
  • Morgridge Institute for Research
  • University of Wisconsin-Madison
  • University of Wisconsin – Madison
  • University of Wisconsin School of Medicine and Public Health
  • University of California Santa Barbara

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

How species-specific developmental timing is controlled is largely unknown. By following human embryonic stem (ES) cell and mouse epiblast stem (EpiS) cell differentiation through detailed RNA-sequencing time courses, here we show that pluripotent stem cells closely retain in vivo species-specific developmental timing in vitro. In identical neural differentiation conditions in vitro, gene expression profiles are accelerated in mouse EpiS cells compared to human ES cells with relative rates of differentiation closely reflecting the rates of progression through the Carnegie stages in utero. Dynamic Time Warping analysis identified 3389 genes that were regulated more quickly in mouse EpiS cells and identified none that were regulated more quickly in human ES cells. Interestingly, we also find that human ES cells differentiated in teratomas maintain the same rate of differentiation observed in vitro in spite of being grown in a mouse host. These results suggest the existence of a cell autonomous, species-specific developmental clock that pluripotent stem cells maintain even out of context of an intact embryo.
Original languageEnglish
Pages (from-to)101-110
Number of pages10
JournalDevelopmental Biology
Volume423
Issue number2
DOIs
StatePublished - Mar 15 2017

Keywords

  • Brain development
  • Developmental time
  • Differentiation
  • Embryonic stem cells

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