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首页> 外文期刊>Mechanisms of Development >Identification of presomitic mesoderm (PSM)-specific Mesp1 enhancer and generation of a PSM-specific Mesp1/Mesp2-null mouse using BAC-based rescue technology.
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Identification of presomitic mesoderm (PSM)-specific Mesp1 enhancer and generation of a PSM-specific Mesp1/Mesp2-null mouse using BAC-based rescue technology.

机译:使用基于BAC的营救技术,鉴定早熟中胚层(PSM)特定的Mesp1增强子并生成PSM特定的Mesp1 / Mesp2空小鼠。

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摘要

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.
机译:细菌人工染色体(BAC)修饰技术是鉴定增强子序列和遗传修饰的有力方法。使用这种方法,我们已经分析了Mesp1和/或Mesp2增强子,并鉴定了P1-PSME,Mesp1的PSM特异性增强子,它包含一个T-box结合位点,类似于先前鉴定的P2-PSME。因此,Mesp1和Mesp2为它们的PSM特定表达使用不同的增强子。此外,我们发现这两个基因还为早期中胚层表达使用了不同的增强子。基于这些结果,我们通过将BAC克隆引入到Mesp1 / Mesp2双敲除(dKO)遗传背景中,从而产生了PSM特异性的Mesp1 / Mesp2-null小鼠,该克隆只能从中胚层Mesp1早期表达。这成功地挽救了由于dKO小鼠缺乏早期中胚层而导致的胃排毒缺陷,因此我们获得了PSM特异性的Mesp1 / Mesp2-null小鼠,其缺乏节段的节节。

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