| Abstract: |
FGF/ERK signaling is crucial for the patterning and proliferation of cell lineages that comprise the mouse blastocyst. However, ERK signaling dynamics have never been directly visualized in live embryos. To address whether differential signaling is associated with particular cell fates and states, we generated a targeted mouse line expressing an ERK-kinase translocation reporter (KTR) that enables live quantification of ERK activity at single-cell resolution. 3D time-lapse imaging of this biosensor in embryos revealed spatially graded ERK activity in the trophectoderm prior to overt polar versus mural differentiation. Within the inner cell mass (ICM), all cells relayed FGF/ERK signals with varying durations and magnitude. Primitive endoderm cells displayed higher overall levels of ERK activity, while pluripotent epiblast cells exhibited lower basal activity with sporadic pulses. These results constitute a direct visualization of signaling events during mammalian pre-implantation development and reveal the existence of spatial and temporal lineage-specific dynamics. © 2020 Elsevier Inc. FGF/ERK signaling is crucial for the patterning and proliferation of cell lineages that comprise the mouse blastocyst. Using an ERK-kinase translocation biosensor, Simon et al. show that the trophectoderm is patterned by spatially graded ERK activity and that primitive endoderm and epiblast cells have distinct ERK dynamics. © 2020 Elsevier Inc. |
