Effects of Transcription Factor AP2γ on Gene Expression of Desmosome Components in Mouse Embryos

Hak-Jae Chung, Jiyeon Jeong, Yelin Jeong, I. Choi
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Abstract

Transcription factor called activating enhancer binding protein 2C (AP2-gamma) is found in a variety of species and expressed from oocyte stage onwards, particularly restricted to the trophectoderm. Recent studies demonstrated that ablation of Tfap2c led to failure of tight junction biogenesis, particularly the knock-down embryos of Tfap2c did not form cavity from morula to blastocyst in mouse and pig. We speculated that the Tfa2pc may also be involved in desmosome biogenesis because blastocoel formation is coincident with the establishment of desmosome. To determine this, we depleted Tfap2c injecting siRNA into one-cell zygote and analysed the expression levels of genes that are required for desmosome complex such as PkP2, Pkp3, Dsc2, and Dsg2. We found only Pkp3 was up-regulated in the knockdowned morula embryos. Interestingly, upstream region of Pkp3 had putative Tfap2c binding sites. In conclusion, our results suggest that Tfap2c is not a crucial factor but somehow it might be involved in desmosome biogenesis directly or indirectly via Pkp3. (
转录因子AP2γ对小鼠胚胎桥粒组分基因表达的影响
被称为活化增强子结合蛋白2C (ap2 - γ)的转录因子存在于多种物种中,并从卵母细胞阶段开始表达,特别是局限于滋养外胚层。最近的研究表明,Tfap2c基因的敲除导致紧密连接生物发生的失败,特别是在小鼠和猪的胚胎中,敲除Tfap2c基因的胚胎不能形成从桑葚胚到囊胚的腔体。我们推测Tfa2pc也可能参与桥粒的生物发生,因为囊胚的形成与桥粒的建立是一致的。为了确定这一点,我们将siRNA注射到单细胞受精卵中去除了Tfap2c,并分析了桥粒复合物(如PkP2、Pkp3、Dsc2和Dsg2)所需基因的表达水平。我们发现只有Pkp3在敲除的桑葚胚中表达上调。有趣的是,Pkp3的上游区域有推测的Tfap2c结合位点。总之,我们的结果表明Tfap2c不是一个关键因素,但它可能直接或间接地通过Pkp3参与桥粒的生物发生。(
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