Max Planck Institute for Molecular Genetics, Department of Developmental Genetics, Ihnestr. 63-73, 14195 Berlin, Germany.
Institute of Biology, Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Königin-Luise-Str. 1-3, 14195 Berlin, Germany.
Development. 2021 Dec 1;148(23). doi: 10.1242/dev.200059. Epub 2021 Dec 15.
The node-streak border region comprising notochord progenitor cells (NPCs) at the posterior node and neuro-mesodermal progenitor cells (NMPs) in the adjacent epiblast is the prime organizing center for axial elongation in mouse embryos. The T-box transcription factor brachyury (T) is essential for both formation of the notochord and maintenance of NMPs, and thus is a key regulator of trunk and tail development. The T promoter controlling T expression in NMPs and nascent mesoderm has been characterized in detail; however, control elements for T expression in the notochord have not been identified yet. We have generated a series of deletion alleles by CRISPR/Cas9 genome editing in mESCs, and analyzed their effects in mutant mouse embryos. We identified a 37 kb region upstream of T that is essential for notochord function and tailbud outgrowth. Within that region, we discovered a T-binding enhancer required for notochord cell specification and differentiation. Our data reveal a complex regulatory landscape controlling cell type-specific expression and function of T in NMP/nascent mesoderm and node/notochord, allowing proper trunk and tail development.
由后部节结 streak 边界区域的脊索祖细胞(NPCs)和相邻的上胚层神经中胚层祖细胞(NMPs)组成的轴延长的主要组织中心,是小鼠胚胎中轴向伸长的主要组织中心。T 框转录因子 brachyury(T)对于脊索的形成和 NMPs 的维持都是必不可少的,因此是躯干和尾巴发育的关键调节因子。已经详细描述了控制 NMPs 和新生中胚层中 T 表达的 T 启动子;然而,脊索中 T 表达的控制元件尚未被鉴定。我们通过 CRISPR/Cas9 基因组编辑在 mESCs 中生成了一系列缺失等位基因,并分析了它们在突变体小鼠胚胎中的作用。我们鉴定了 T 上游的一个 37kb 区域,该区域对于脊索功能和尾芽的延伸是必需的。在该区域内,我们发现了一个 T 结合增强子,对于脊索细胞的特化和分化是必需的。我们的数据揭示了一个复杂的调控景观,控制 T 在 NMP/新生中胚层和节点/脊索中的细胞类型特异性表达和功能,从而允许适当的躯干和尾巴发育。