GATA6 levels modulate primitive endoderm cell fate choice and timing in the mouse blastocyst.

Journal Article (Journal Article)

Cells of the inner cell mass (ICM) of the mouse blastocyst differentiate into the pluripotent epiblast or the primitive endoderm (PrE), marked by the transcription factors NANOG and GATA6, respectively. To investigate the mechanistic regulation of this process, we applied an unbiased, quantitative, single-cell-resolution image analysis pipeline to analyze embryos lacking or exhibiting reduced levels of GATA6. We find that Gata6 mutants exhibit a complete absence of PrE and demonstrate that GATA6 levels regulate the timing and speed of lineage commitment within the ICM. Furthermore, we show that GATA6 is necessary for PrE specification by FGF signaling and propose a model where interactions between NANOG, GATA6, and the FGF/ERK pathway determine ICM cell fate. This study provides a framework for quantitative analyses of mammalian embryos and establishes GATA6 as a nodal point in the gene regulatory network driving ICM lineage specification.

Full Text

Duke Authors

Cited Authors

  • Schrode, N; Saiz, N; Di Talia, S; Hadjantonakis, A-K

Published Date

  • May 27, 2014

Published In

Volume / Issue

  • 29 / 4

Start / End Page

  • 454 - 467

PubMed ID

  • 24835466

Pubmed Central ID

  • PMC4103658

Electronic International Standard Serial Number (EISSN)

  • 1878-1551

Digital Object Identifier (DOI)

  • 10.1016/j.devcel.2014.04.011


  • eng

Conference Location

  • United States