Piestun Dan, Kochupurakkal Bose S, Jacob-Hirsch Jasmine, Zeligson Sharon, Koudritsky Mark, Domany Eytan, Amariglio Ninette, Rechavi Gideon, Givol David
Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 76100, Israel.
Biochem Biophys Res Commun. 2006 Apr 28;343(1):279-85. doi: 10.1016/j.bbrc.2006.02.152. Epub 2006 Mar 6.
The transcription factor Nanog is uniquely expressed in embryonic stem (ES) cells and in germ cell tumors and is important for self-renewal. To understand the relation between this and cell transformation, we expressed Nanog in NIH3T3 cells, and these cells showed an increased growth rate and a transformed phenotype as demonstrated by foci formation and colony growth in soft agar. This suggests that Nanog possesses an oncogenic potential that may be related to the role it plays in germ cell tumors and to its function in self renewal of ES cells. We studied the transcription targets of Nanog using microarrays to identify Nanog regulated genes. The list of genes regulated by Nanog was unique for each cell type and more than 10% of the Nanog regulated genes, including transcription factors, are primary Nanog targets since their promoters bind Nanog in ES cells. Some of these target genes can explain the transformation of NIH3T3.
转录因子Nanog在胚胎干细胞和生殖细胞肿瘤中独特表达,对自我更新很重要。为了解其与细胞转化的关系,我们在NIH3T3细胞中表达Nanog,这些细胞显示出生长速率增加和转化表型,如在软琼脂中形成集落和克隆生长所证明的。这表明Nanog具有致癌潜力,这可能与其在生殖细胞肿瘤中的作用及其在胚胎干细胞自我更新中的功能有关。我们使用微阵列研究了Nanog的转录靶点,以鉴定受Nanog调控的基因。受Nanog调控的基因列表在每种细胞类型中都是独特的,超过10%的受Nanog调控的基因,包括转录因子,是主要的Nanog靶点,因为它们的启动子在胚胎干细胞中与Nanog结合。其中一些靶基因可以解释NIH3T3细胞的转化。