Department of Biomedical Science, College of Life Science, CHA University, Gyeonggi-Do, South Korea.
FEBS Lett. 2012 Sep 21;586(19):3529-35. doi: 10.1016/j.febslet.2012.08.013. Epub 2012 Aug 19.
We investigated transactivation by NANOG in regulating growth and differentiation factor 3 (GDF3) expression in NCCIT cells. GDF3 expression was affected by shRNA-mediated downregulation and by exogenous overexpression of NANOG specifically, as well as by retinoic acid-mediated differentiation. GDF3 transcription was activated by NANOG, and the upstream region (-183 to -1) was sufficient to induce minimal transcriptional activity. Moreover, NANOG binds to the GDF3 minimal promoter in vivo and the transcriptional activity is mediated by NANOG transactivation domain. This study provides the first evidence that NANOG is a transcriptional activator of the expression of the oncogenic growth factor GDF3 in embryonic carcinoma cells.
我们研究了 NANOG 的反式激活作用在调节 NCCIT 细胞中生长分化因子 3(GDF3)表达中的作用。GDF3 的表达受到 shRNA 介导的下调以及 NANOG 的外源过表达的影响,同时也受到维甲酸介导的分化的影响。NANOG 激活了 GDF3 的转录,上游区域(-183 到-1)足以诱导最小的转录活性。此外,NANOG 在体内与 GDF3 的最小启动子结合,转录活性由 NANOG 反式激活结构域介导。这项研究首次提供了证据,表明 NANOG 是胚胎癌细胞中致癌生长因子 GDF3 表达的转录激活因子。