Department of Cellular and Molecular Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Ontario, Canada.
Dev Biol. 2012 Jan 1;361(1):1-11. doi: 10.1016/j.ydbio.2011.09.034. Epub 2011 Oct 8.
Vertebrate Cdx genes encode homeodomain transcription factors related to caudal in Drosophila. The murine Cdx homologues Cdx1, Cdx2 and Cdx4 play important roles in anterior-posterior patterning of the embryonic axis and the intestine, as well as axial elongation. While our understanding of the ontogenic programs requiring Cdx function has advanced considerably, the molecular bases underlying these functions are less well understood. In this regard, Cdx1-Cdx2 conditional mutants exhibit abnormal somite formation, while loss of Cdx1-Cdx2 in the intestinal epithelium results in a shift in differentiation toward the Goblet cell lineage. The aim of the present study was to identify the Cdx-dependent mechanisms impacting on these events. Consistent with prior work implicating Notch signaling in these pathways, we found that expression of the Notch ligand Dll1 was reduced in Cdx mutants in both the intestinal epithelium and paraxial mesoderm. Cdx members occupied the Dll1 promoter both in vivo and in vitro, while genetic analysis indicated interaction between Cdx and Dll1 pathways in both somitogenesis and Goblet cell differentiation. These findings suggest that Cdx members operate upstream of Dll1 to convey different functions in two distinct lineages.
脊椎动物 Cdx 基因编码与果蝇尾部相关的同源域转录因子。鼠类 Cdx 同源物 Cdx1、Cdx2 和 Cdx4 在胚胎轴和肠道的前后模式以及轴向伸长中发挥重要作用。虽然我们对需要 Cdx 功能的个体发生程序的理解已经有了很大的进展,但这些功能的分子基础还不太清楚。在这方面,Cdx1-Cdx2 条件性突变体表现出异常的体节形成,而肠道上皮细胞中 Cdx1-Cdx2 的缺失导致向杯状细胞谱系的分化转变。本研究的目的是确定影响这些事件的 Cdx 依赖性机制。与先前的工作表明 Notch 信号通路在这些途径中起作用一致,我们发现,在肠道上皮细胞和轴旁中胚层中,Notch 配体 Dll1 的表达在 Cdx 突变体中均减少。Cdx 成员在体内和体外都占据 Dll1 启动子,而遗传分析表明,在体节发生和杯状细胞分化中,Cdx 和 Dll1 途径之间存在相互作用。这些发现表明,Cdx 成员在两个不同谱系中在上游作用于 Dll1 以传递不同的功能。