Yamada Kayo, Kanda Hiromi, Tanaka Satoshi, Takamatsu Nobuhiko, Shiba Tadayoshi, Ito Michihiko
Department of Biosciences, School of Science, Kitasato University, 1-15-1 Kitasato, Sagamihara, Kanagawa 228-8555, Japan.
Differentiation. 2006 Jun;74(5):212-21. doi: 10.1111/j.1432-0436.2006.00070.x.
Some members of the Sry-type HMG box (Sox) protein family play important roles in embryogenesis as transcription factors. Here, we report that Sox15 transcripts were much more abundant in mouse placenta than in the fetus, the yolk sac, or several adult tissues. In situ hybridization analysis of the mouse E8.0 conceptus indicated that Sox15 mRNA was predominantly expressed in the trophoblast giant cells of the placenta. We also observed that the amount of Sox15 mRNA dramatically increased during the differentiation of mouse trophoblast stem cells. Ectopic expression of Sox15 in Rat choriocarcinoma cells enhanced the giant cell differentiation induced by a bHLH transcription factor, Hand1. Binding experiments in cotransfected 293 T cells and in vitro revealed that Sox15 interacted with Hand1. We next examined the effects of this interaction on the transcriptional activity of Hand1 and Sox15 using the luciferase reporter assay. Overexpression of Hand1 repressed the Sox15-driven reporter expression, but Sox15 enhanced the Hand1-driven transcription. This enhancement required both the Hand1-binding region and the transactivation domain of Sox15. These results may suggest that the increased transcriptional activity of Hand1 caused by Sox15 might promote the transcription of the target gene resulting in the trophoblast giant cell differentiation in the mouse placenta.
Sry 型 HMG 盒(Sox)蛋白家族的一些成员作为转录因子在胚胎发生中发挥重要作用。在此,我们报告 Sox15 转录本在小鼠胎盘中的丰度远高于胎儿、卵黄囊或几种成年组织。对小鼠 E8.0 胚胎的原位杂交分析表明,Sox15 mRNA 主要在胎盘的滋养层巨细胞中表达。我们还观察到,在小鼠滋养层干细胞分化过程中,Sox15 mRNA 的量显著增加。Sox15 在大鼠绒毛膜癌细胞中的异位表达增强了由 bHLH 转录因子 Hand1 诱导的巨细胞分化。在共转染的 293T 细胞中的结合实验和体外实验表明,Sox15 与 Hand1 相互作用。接下来,我们使用荧光素酶报告基因测定法研究了这种相互作用对 Hand1 和 Sox15 转录活性的影响。Hand1 的过表达抑制了 Sox15 驱动的报告基因表达,但 Sox15 增强了 Hand1 驱动的转录。这种增强需要 Sox15 的 Hand1 结合区域和反式激活结构域。这些结果可能表明,Sox15 引起的 Hand1 转录活性增加可能促进靶基因的转录,从而导致小鼠胎盘中滋养层巨细胞的分化。