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首页> 外文期刊>Development Growth and Differentiation >Pou5f3.2-induced proliferative state of embryonic cells during gastrulation of Xenopus laevis embryo
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Pou5f3.2-induced proliferative state of embryonic cells during gastrulation of Xenopus laevis embryo

机译:Pou5f3.2诱导非洲爪蟾胚胎胃形成过程中胚胎细胞的增殖状态

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摘要

POU class V (POU-V) transcription factors play the important role in maintenance of pluripotency and cell differentiation. Pou5f3.2 (Oct25), one of Xenopus POU-V transcription factors, shows the zygotic expression prior to gastrulation. In order to know the molecular mechanism of pou5f3.2 expression at gastrula stage, we examined a responsiveness of pou5f3.2 to Nodal signaling. Animal cap assay demonstrated that Xnr2 activates the gene expression of pou5f3.2. In comparative analysis of the 5'-flanking region of pou5f3.2 between Xenopus laevis and X. tropicalis, two conserved regions were detected within the flanking region. Reporter analyses showed that one of the conserved regions contained an enhancer region, which had several Smad2/3 and FoxH1 binding motifs. ChIP assay demonstrated that Smad2 binds to the enhancer region. These results suggest that Nodal signaling induces zygotic expression of pou5f3.2 at gastrula stage. To understand a role of pou5f3.2 in gastrula embryos, morpholino oligo DNA of pou5f3.2 was injected into the lateral side of one blastomere at the 2-cell stage. The morphant embryos showed diminution of Xbra1 expression and gastrulation defect in the injection side, suggesting the essential role of pou5f3.2 at the gastrula stage. Xbra1 expression and gastrulation were also inhibited by injecting with the synthesized RNAs of pou5f3.2. Furthermore, in the pou5f3.2-injected embryo, gene expression of p27Xic1 was drastically suppressed, and the number of dividing cells increased in the injection side. These results suggest that one role of pou5f3.2 is to keep the embryonic cells in undifferentiated and proliferative state during gastrulation.
机译:POU V类(POU-V)转录因子在维持多能性和细胞分化中起重要作用。 Xoupus POU-V转录因子之一Pou5f3.2(Oct25)显示了在促胃动之前的合子表达。为了了解在胃胚期pou5f3.2表达的分子机制,我们检查了pou5f3.2对Nodal信号的响应。动物帽分析表明,Xnr2激活了pou5f3.2的基因表达。在对非洲爪蟾和热带假单胞菌之间的pou5f3.2的5'侧翼区域的比较分析中,在侧翼区域内检测到两个保守区域。记者分析表明,其中一个保守区含有一个增强子区,该增强子区具有几个Smad2 / 3和FoxH1结合基序。 ChIP检测证明Smad2结合增强子区域。这些结果表明,节点信号在胃胚期诱导pou5f3.2的合子表达。为了了解pou5f3.2在腹胚胚胎中的作用,在2细胞阶段将pou5f3.2的吗啉代寡核苷酸DNA注入一个卵裂球的侧面。 morph虫胚在注射侧表现出Xbra1表达减少和胃形成缺陷,提示pou5f3.2在胃胚期中起着重要作用。注射pou5f3.2的合成RNA也会抑制Xbra1的表达和胃排毒。此外,在注射了pou5f3.2的胚胎中,p27Xic1的基因表达被显着抑制,并且注射侧的分裂细胞数量增加。这些结果表明,pou5f3.2的作用之一是在胚芽形成过程中将胚胎细胞保持在未分化和增殖状态。

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