Choi Hee Jung, Jin So Dam, Rengaraj Deivendran, Kim Jin Hwa, Pain Bertrand, Han Jae Yong
Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences, Seoul National University, Seoul, 08826, South Korea.
Univ Lyon, Universite ́Lyon 1, INSERM, INRAE, Stem Cell and Brain Research Institute, U1208, USC1361, 69500, Bron, France.
J Anim Sci Biotechnol. 2021 Mar 4;12(1):40. doi: 10.1186/s40104-021-00563-5.
NANOG is a core transcription factor (TF) in embryonic stem cells (ESCs) and primordial germ cells (PGCs). Regulation of the NANOG gene by TFs, epigenetic factors, and autoregulatory factors is well characterized in ESCs, and transcriptional regulation of NANOG is well established in these cells. Although NANOG plays a key role in germ cells, the molecular mechanism underlying its transcriptional regulation in PGCs has not been studied. Therefore, we investigated the mechanism that regulates transcription of the chicken NANOG (cNANOG) gene in PGCs and ESCs.
We first identified the transcription start site of cNANOG by 5'-rapid amplification of cDNA ends PCR analysis. Then, we measured the promoter activity of various 5' flanking regions of cNANOG in chicken PGCs and ESCs using the luciferase reporter assay. cNANOG expression required transcriptional regulatory elements, which were positively regulated by POU5F3 (OCT4) and SOX2 and negatively regulated by TP53 in PGCs. The proximal region of the cNANOG promoter contains a positive transcriptional regulatory element (CCAAT/enhancer-binding protein (CEBP)-binding site) in ESCs. Furthermore, small interfering RNA-mediated knockdown demonstrated that POU5F3, SOX2, and CEBP played a role in cell type-specific transcription of cNANOG.
We show for the first time that different trans-regulatory elements control transcription of cNANOG in a cell type-specific manner. This finding might help to elucidate the mechanism that regulates cNANOG expression in PGCs and ESCs.
NANOG是胚胎干细胞(ESCs)和原始生殖细胞(PGCs)中的一种核心转录因子(TF)。在胚胎干细胞中,转录因子、表观遗传因子和自调控因子对NANOG基因的调控已得到充分表征,并且在这些细胞中NANOG的转录调控也已明确确立。尽管NANOG在生殖细胞中起关键作用,但其在原始生殖细胞中转录调控的分子机制尚未得到研究。因此,我们研究了在原始生殖细胞和胚胎干细胞中调控鸡NANOG(cNANOG)基因转录的机制。
我们首先通过5'-cDNA末端快速扩增PCR分析确定了cNANOG的转录起始位点。然后,我们使用荧光素酶报告基因检测法测量了cNANOG不同5'侧翼区域在鸡原始生殖细胞和胚胎干细胞中的启动子活性。cNANOG的表达需要转录调控元件,在原始生殖细胞中这些元件受到POU5F3(OCT4)和SOX2的正向调控以及TP53的负向调控。在胚胎干细胞中,cNANOG启动子的近端区域包含一个正向转录调控元件(CCAAT/增强子结合蛋白(CEBP)结合位点)。此外,小干扰RNA介导的敲低实验表明,POU5F3、SOX2和CEBP在cNANOG的细胞类型特异性转录中发挥作用。
我们首次表明,不同的反式调控元件以细胞类型特异性方式控制cNANOG的转录。这一发现可能有助于阐明在原始生殖细胞和胚胎干细胞中调控cNANOG表达的机制。