Lu Cindy C, Robertson Elizabeth J
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Dev Biol. 2004 Sep 1;273(1):149-59. doi: 10.1016/j.ydbio.2004.06.004.
The TGFbeta family member Nodal has been shown to be involved in a variety of processes in development, including early axis formation. Here, we use a conditional gene inactivation strategy to show a specific requirement for Nodal in the epiblast. Complete inactivation of the Nodal locus in the epiblast using the Sox2-Cre deleter strain results in a failure to establish global anterior-posterior patterning, a phenotype that resembles the Nodal null phenotype. By contrast, mosaic inactivation of Nodal in the epiblast using the Mox2-Cre (MORE) deleter strain affects formation of the anterior mesendoderm and subsequent anterior neurectoderm patterning. Furthermore, ES cell chimera experiments indicate that Nodal-deficient ES cells preferentially populate the anterior compartment of the epiblast, suggesting that cell mixing in the epiblast is not random and that Nodal signaling mediates a novel anterior-posterior cell-sorting process within the epiblast before gastrulation.
转化生长因子β(TGFβ)家族成员Nodal已被证明参与发育过程中的多种进程,包括早期轴的形成。在此,我们采用条件性基因失活策略来显示上胚层中对Nodal的特定需求。使用Sox2-Cre删除菌株完全失活上胚层中的Nodal基因座会导致无法建立整体的前后模式,这种表型类似于Nodal基因敲除表型。相比之下,使用Mox2-Cre(MORE)删除菌株对上胚层中的Nodal进行镶嵌失活会影响前内胚层的形成以及随后的前神经外胚层模式。此外,胚胎干细胞嵌合体实验表明,缺乏Nodal的胚胎干细胞优先定位于上胚层的前部区域,这表明上胚层中的细胞混合并非随机的,并且Nodal信号传导在原肠胚形成之前介导了上胚层内一种新的前后细胞分选过程。