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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Staufen1 is expressed in preimplantation mouse embryos and is required for embryonic stem cell differentiation.
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Staufen1 is expressed in preimplantation mouse embryos and is required for embryonic stem cell differentiation.

机译:Staufen1在植入前的小鼠胚胎中表达,是胚胎干细胞分化所必需的。

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Pluripotent mouse embryonic stem (mES) cells derived from the blastocyst of the preimplantation embryo can be induced to differentiate in vitro along different cell lineages. However the molecular and cellular factors that signal and/or determine the expression of key genes, and the localisation of the encoded proteins, during the differentiation events are poorly understood. One common mechanism by which proteins can be targeted to specific regions of the cell is through the asymmetric localisation of mRNAs and Staufen, a double-stranded RNA binding protein, is known to play a direct role in mRNA transport and localisation. The aims of the present study were to describe the expression of Staufen in preimplantation embryos and mES cells and to use RNA interference (RNAi) to investigate the roles of Staufen1 in mES cell lineage differentiation. Western blotting and immunocytochemistry demonstrated that Staufen is present in the preimplantation mouse embryo, pluripotent mES cells and mES cells stimulated to differentiate into embryoid bodies, but the Staufen staining patterns did not support asymmetric distribution of the protein. Knockdown of Staufen1 gene expression in differentiating mES cells reduced the synthesis of lineage-specific markers including Brachyury, alpha-fetoprotein (AFP), PAX-6, and Vasa. There was however no significant change in either the gene expression of Nanog and Oct4, or in the synthesis of SSEA-1, all of which are key markers of pluripotency. These data indicate that inhibition of Staufen1 gene expression by RNAi affects an early step in mES cell differentiation and suggest a key role for Staufen in the cell lineage differentiation of mES cells.
机译:可以诱导来自植入前胚胎胚泡的多能小鼠胚胎干(mES)细胞在体外沿不同细胞谱系分化。然而,在分化过程中,信号和/或确定关键基因的表达以及编码蛋白的定位的分子和细胞因素知之甚少。可以将蛋白质靶向细胞特定区域的一种常见机制是通过mRNA的不对称定位,并且已知Staufen(一种双链RNA结合蛋白)在mRNA的运输和定位中起着直接作用。本研究的目的是描述Staufen在植入前胚胎和mES细胞中的表达,并使用RNA干扰(RNAi)研究Staufen1在mES细胞谱系分化中的作用。 Western印迹和免疫细胞化学表明Staufen存在于植入前的小鼠胚胎中,多能mES细胞和受刺激的mES细胞分化成胚状体,但是Staufen染色模式不支持该蛋白的不对称分布。减少分化的mES细胞中Staufen1基因表达的表达减少了谱系特异性标记的合成,包括Brachyury,α-甲胎蛋白(AFP),PAX-6和Vasa。但是,Nanog和Oct4的基因表达或SSEA-1的合成均无显着变化,所有这些都是多能性的关键标志。这些数据表明,RNAi对Staufen1基因表达的抑制影响了mES细胞分化的早期步骤,并暗示了Staufen在mES细胞的细胞谱系分化中的关键作用。

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