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首页> 外文期刊>Molecular and Cellular Biology >Oct-3/4 Maintains the Proliferative Embryonic Stem Cell State via Specific Binding to a Variant Octamer Sequence in the Regulatory Region of the UTF1 Locus
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Oct-3/4 Maintains the Proliferative Embryonic Stem Cell State via Specific Binding to a Variant Octamer Sequence in the Regulatory Region of the UTF1 Locus

机译:Oct-3 / 4通过与UTF1基因座调控区域中的一个变异八面体序列特异性结合来维持增生性胚胎干细胞状态。

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The POU transcription factor Oct-3/4 has been shown to be critical for maintaining embryonic stem (ES) cell character. However, the molecular mechanisms underlying its function remain elusive. We have previously shown that among the POU transcription factor family of proteins, Oct-3/4 alone is able to bind to the regulatory region of the UTF1 gene bearing a variant octamer sequence together with Sox-2. Here, we demonstrate using Oct-3/4-Oct-6 chimeras that there is a precise correlation between the ability of proteins to form a complex on the UTF1 enhancer with Sox-2 and the ability to maintain the stem cell state in ES cells. Different chimeric proteins show differential abilities to form a Sox-2-containing complex on the UTF1 regulatory region, with a decrease in efficiency of the complex formation accompanied by a decrease in the level of UTF1 expression and the rate of cell proliferation. Overexpression of UTF1 in these slow-growing cells was able to restore their proliferation rate to wild-type levels. Moreover, UTF1 was also observed to have an effect on teratoma formation. These results suggest a molecular pathway by which Oct-3/4 induces rapid proliferation and tumorigenic properties of ES cells through activation of the UTF1 gene.
机译:已显示POU转录因子Oct-3 / 4对维持胚胎干(ES)细胞特征至关重要。但是,其功能的分子机制仍然难以捉摸。我们以前已经证明,在POU转录因子家族的蛋白质中,仅Oct-3 / 4就能结合带有变异八聚体序列和Sox-2的 UTF1 基因的调节区。在这里,我们证明了使用Oct-3 / 4-Oct-6嵌合体,蛋白质在具有Sox-2的 UTF1 增强子上形成复合物的能力与维持能力之间存在精确的相关性ES细胞中的干细胞状态。不同的嵌合蛋白显示在 UTF1 调控区形成含Sox-2的复合物的能力不同,复合物形成效率降低,同时UTF1表达水平和速率降低。细胞增殖。在这些缓慢生长的细胞中,UTF1的过度表达能够将其增殖率恢复至野生型水平。此外,还观察到UTF1对畸胎瘤的形成有影响。这些结果表明Oct-3 / 4通过激活 UTF1 基因诱导ES细胞快速增殖和致瘤特性的分子途径。

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