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Arid3a is essential to execution of the first cell fate decision via direct embryonic and extraembryonic transcriptional regulation

  • Catherine Rhee
  • , Bum Kyu Lee
  • , Samuel Beck
  • , Azeen Anjum
  • , Kendra R. Cook
  • , Melissa Popowski
  • , Haley O. Tucker
  • , Jonghwan Kim

Research output: Contribution to journalArticlepeer-review

44 Scopus citations

Abstract

Despite their origin from the inner cell mass, embryonic stem (ES) cells undergo differentiation to the trophectoderm (TE) lineage by repression of the ES cell master regulator Oct4 or activation of the TE master regulator Caudal-type homeobox 2 (Cdx2). In contrast to the in-depth studies of ES cell self-renewal and pluripotency, few TE-specific regulators have been identified, thereby limiting our understanding of mechanisms underlying the first cell fate decision. Here we show that up-regulation and nuclear entry of AT-rich interactive domain 3a (Arid3a) drives TE-like transcriptional programs in ES cells, maintains trophoblast stem (TS) cell selfrenewal, and promotes further trophoblastic differentiation both upstream and independent of Cdx2. Accordingly, Arid3a-/-mouse post-implantation placental development is severely impaired, resulting in early embryonic death. We provide evidence that Arid3a directly activates TE-specific and trophoblast lineage-specific genes while directly repressing pluripotency genes via differential regulation of epigenetic acetylation or deacetylation. Our results identify Arid3a as a critical regulator of TE and placental development through execution of the commitment and differentiation phases of the first cell fate decision.

Original languageEnglish
Pages (from-to)2219-2232
Number of pages14
JournalGenes and Development
Volume28
Issue number20
DOIs
StatePublished - Oct 15 2014

Keywords

  • Arid3a
  • Embryonic stem cells
  • First cell fate decision
  • Transdifferentiation
  • Trophectoderm
  • Trophoblast stem cells

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