Oginuma Masayuki, Hirata Tatsumi, Saga Yumiko
Department of Genetics, SOKENDAI, Yata 1111, Mishima, Shizuoka 411-8540, Japan.
Mech Dev. 2008 May-Jun;125(5-6):432-40. doi: 10.1016/j.mod.2008.01.010. Epub 2008 Feb 5.
Bacterial artificial chromosome (BAC) modification technology is a powerful method for the identification of enhancer sequences and genetic modifications. Using this method, we have analyzed the Mesp1 and/or Mesp2 enhancers and identified P1-PSME, a PSM-specific enhancer of Mesp1, which contains a T-box binding site similar to the previously identified P2-PSME. Hence, Mesp1 and Mesp2 use different enhancers for their PSM-specific expression. In addition, we find that these two genes also use distinct enhancers for their early mesodermal expression. Based on these results, we generated a PSM-specific Mesp1/Mesp2-null mouse by introducing a BAC clone, from which only early mesodermal Mesp1 expression is possible, into the Mesp1/Mesp2 double knockout (dKO) genetic background. This successfully rescued gastrulation defects due to the lack of the early mesoderm in the dKO mouse and we thereby obtained a PSM-specific Mesp1/Mesp2-null mouse showing a lack of segmented somites.
细菌人工染色体(BAC)修饰技术是鉴定增强子序列和基因修饰的一种强大方法。利用这种方法,我们分析了Mesp1和/或Mesp2增强子,并鉴定出P1-PSME,它是Mesp1的PSM特异性增强子,含有一个与先前鉴定的P2-PSME相似的T-box结合位点。因此,Mesp1和Mesp2在其PSM特异性表达中使用不同的增强子。此外,我们发现这两个基因在其早期中胚层表达中也使用不同的增强子。基于这些结果,我们通过将一个BAC克隆引入Mesp1/Mesp2双敲除(dKO)基因背景中,构建了一只PSM特异性Mesp1/Mesp2基因敲除小鼠,该BAC克隆仅能实现早期中胚层Mesp1的表达。这成功挽救了dKO小鼠因早期中胚层缺失而导致的原肠胚形成缺陷,从而我们获得了一只PSM特异性Mesp1/Mesp2基因敲除小鼠,其表现出缺乏分节的体节。