Diverse Routes toward Early Somites in the Mouse Embryo

Dev Cell. 2021 Jan 11;56(1):141-153.e6. doi: 10.1016/j.devcel.2020.11.013. Epub 2020 Dec 11.

Abstract

Somite formation is foundational to creating the vertebrate segmental body plan. Here, we describe three transcriptional trajectories toward somite formation in the early mouse embryo. Precursors of the anterior-most somites ingress through the primitive streak before E7 and migrate anteriorly by E7.5, while a second wave of more posterior somites develops in the vicinity of the streak. Finally, neuromesodermal progenitors (NMPs) are set aside for subsequent trunk somitogenesis. Single-cell profiling of T-/- chimeric embryos shows that the anterior somites develop in the absence of T and suggests a cell-autonomous function of T as a gatekeeper between paraxial mesoderm production and the building of the NMP pool. Moreover, we identify putative regulators of early T-independent somites and challenge the T-Sox2 cross-antagonism model in early NMPs. Our study highlights the concept of molecular flexibility during early cell-type specification, with broad relevance for pluripotent stem cell differentiation and disease modeling.

Keywords: Brachyury; cell fate regulation; developmental trajectories; neuromesodermal progenitors; somites.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Patterning / genetics*
  • Cell Differentiation / genetics
  • Cell Differentiation / physiology
  • Cell Line
  • Chimera / embryology
  • Chimera / genetics
  • Chimera / metabolism*
  • Embryo, Mammalian
  • Female
  • Fetal Proteins / genetics
  • Fetal Proteins / metabolism*
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental / genetics*
  • Germ Cells / cytology
  • Germ Cells / metabolism
  • Heterozygote
  • Male
  • Mesoderm / cytology*
  • Mesoderm / metabolism
  • Mice
  • Mice, Inbred C57BL
  • SOXB1 Transcription Factors / metabolism*
  • Single-Cell Analysis
  • Somites / cytology*
  • Somites / metabolism
  • T-Box Domain Proteins / genetics
  • T-Box Domain Proteins / metabolism*
  • Transcriptome / genetics

Substances

  • Fetal Proteins
  • SOXB1 Transcription Factors
  • Sox2 protein, mouse
  • T-Box Domain Proteins
  • Brachyury protein