Liu Na, Feng Xiaoming, Fang Zhihong, Ma Fengxia, Lu Shihong, Lu Min, Han Zhongchao
State Key Laboratory of Experimental Hematology, National Research Center for Stem Cell Engineering and Technology, Institute of Hematology, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
J Cell Biochem. 2008 Aug 15;104(6):2348-62. doi: 10.1002/jcb.21795.
Nanog plays an important role in embryonic stem (ES) cells pluripotency and self-renewal, yet the precise mechanism through which Nanog accomplishes this important function remains unclear. To understand comprehensive molecular mechanism by which Nanog mediates, we identified genome-wide molecular changes upon silencing Nanog in ES cells by using microarray technology. In order to downregulate Nanog expression efficiently, four siRNAs were designed on the basis of the conserved Nanog sequence and their effects on the Nanog expression were tested. Among these four siRNAs, Nanog-siRNA-P1 was found to be most effective. Once Nanog was downregulated, ES cells underwent differentiation by showing morphological change and decreased proliferation rate. Microarray analysis was then used to identify the altered gene expression after Nanog was silenced. A series of differentially expressed genes due to reduced expression of Nanog was identified as Nanog-related genes. These genes identified here could provide insights into the roles of Nanog in ES cells self-renewal and early differentiation.
Nanog在胚胎干细胞(ES细胞)的多能性和自我更新中发挥着重要作用,然而Nanog实现这一重要功能的确切机制仍不清楚。为了全面了解Nanog介导的分子机制,我们利用微阵列技术鉴定了ES细胞中沉默Nanog后全基因组范围内的分子变化。为了有效下调Nanog的表达,根据保守的Nanog序列设计了四种小干扰RNA(siRNA),并测试了它们对Nanog表达的影响。在这四种siRNA中,发现Nanog-siRNA-P1最有效。一旦Nanog被下调,ES细胞就会通过形态变化和增殖速率降低而发生分化。然后利用微阵列分析来鉴定Nanog沉默后基因表达的改变。一系列由于Nanog表达降低而差异表达的基因被鉴定为Nanog相关基因。这里鉴定出的这些基因可以为Nanog在ES细胞自我更新和早期分化中的作用提供见解。