Chalamalasetty Ravindra B, Tran Haley, Kelly Ryan, Kuo Samuel, Kennedy Mark W, Lee Moonsup, Thomas Sara, Mandalos Nikolaos, Koparde Vishal, Lobo Francisco Pereira, Yamaguchi Terry P
Cancer and Developmental Biology Laboratory, Center for Cancer Research, NCI-Frederick, NIH, Frederick, MD, 21702, USA.
Thermofisher Scientific, Frederick, MD, USA.
bioRxiv. 2025 Jun 4:2025.06.03.657492. doi: 10.1101/2025.06.03.657492.
Neuromesodermal competent progenitors (NMCs) are located in the caudal epiblast near the node and primitive streak and give rise to spinal cord and somitic mesoderm during trunk and tail elongation. Their self-renewal depends on an autoregulatory loop involving Wnt3a and Fgf signaling, and the Tbxt and Cdx transcription factors, but the mechanisms underlying loop formation and the establishment of the niche are poorly understood. Here, we identify the zinc-finger transcription factors and () as essential regulators of NMC maintenance. expression is controlled by Wnt, Fgf and retinoic acid signaling, and they cooperate with Tbxt, Tcf7 and Cdx2 to sustain a robust autoregulatory network that promotes high Wnt/Fgf and low retinoic acid activity in the niche. These factors bind a novel enhancer essential for expression and feedback-loop integrity. Mechanistically, Sp5/8 regulate the dynamic exchange of activating and repressive Tcf complexes at Wnt-responsive enhancers. Our findings define a transcriptional module centered on Sp5/8 that stabilizes niche signaling and transcriptional circuitry essential for NMC fate decisions and trunk development.
神经中胚层能干祖细胞(NMCs)位于节点和原条附近的尾侧上胚层,在躯干和尾部延伸过程中产生脊髓和体节中胚层。它们的自我更新依赖于一个涉及Wnt3a和Fgf信号以及Tbxt和Cdx转录因子的自动调节环,但对于环形成和生态位建立的潜在机制了解甚少。在这里,我们确定锌指转录因子Sp5和Sp8是NMC维持的关键调节因子。Sp5/8的表达受Wnt、Fgf和视黄酸信号控制,它们与Tbxt、Tcf7和Cdx2协同作用,维持一个强大的自动调节网络,该网络促进生态位中高Wnt/Fgf和低视黄酸活性。这些因子结合一个对Sp5/8表达和反馈环完整性至关重要的新型增强子。从机制上讲,Sp5/8调节Wnt反应性增强子上激活和抑制性Tcf复合物的动态交换。我们的研究结果定义了一个以Sp5/8为中心的转录模块,该模块稳定了对NMC命运决定和躯干发育至关重要的生态位信号和转录回路。