Department of Haematology, University of Cambridge, CB2 0AW Cambridge, UK; Wellcome-Medical Research Council Cambridge Stem Cell Institute, University of Cambridge, CB2 0AW Cambridge, UK; Sahlgrenska Center for Cancer Research, Department of Microbiology and Immunology, University of Gothenburg, 413 90 Gothenburg, Sweden.
Cancer Research UK Cambridge Institute, University of Cambridge, CB2 0RE Cambridge, UK.
Dev Cell. 2021 Jan 11;56(1):141-153.e6. doi: 10.1016/j.devcel.2020.11.013. Epub 2020 Dec 11.
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.
体节形成是构建脊椎动物节段体计划的基础。在这里,我们描述了早期小鼠胚胎中朝向体节形成的三个转录轨迹。最前面的体节前体在 E7 之前通过原始条纹进入,并在 E7.5 之前向前迁移,而第二波更后面的体节在条纹附近发育。最后,神经中胚层祖细胞(NMP)被预留用于随后的躯干体节发生。T 嵌合胚胎的单细胞分析表明,前体节在没有 T 的情况下发育,并表明 T 作为轴旁中胚层产生和 NMP 池构建之间的门控的自主功能。此外,我们鉴定了早期 T 独立体节的潜在调节因子,并在早期 NMP 中挑战 T-Sox2 交叉拮抗模型。我们的研究强调了早期细胞类型特化过程中分子灵活性的概念,这对多能干细胞分化和疾病建模具有广泛的意义。