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首页> 外文期刊>Molecular reproduction and development >Regulation of the Nanog gene by both positive and negative cis-regulatory elements in embryonal carcinoma cells and embryonic stem cells
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Regulation of the Nanog gene by both positive and negative cis-regulatory elements in embryonal carcinoma cells and embryonic stem cells

机译:胚胎癌细胞和胚胎干细胞中正负调控元件对Nanog基因的调控

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摘要

The transcription factor Nanog is essential for mammalian embryogenesis, as well as the pluripotency of embryonic stem (ES) cells. Work with ES cells and embryonal carcinoma (EC) cells previously identified positive and negative cis-regulatory elements that influence the activity of the Nanog promoter, including adjacent cis-regulatory elements that bind Sox2 and Oct-3/4. Given the importance of Nanog during mammalian development, we examined the cis-regulatory elements required for Nanog promoter activity more closely. In this study, we demonstrate that two positive cis-regulatory elements previously shown to be active in F9 EC cells are also active in ES cells. We also identify a novel negative regulatory region that is located in close proximity to two other positive Nanog cis-regulatory elements. Although this negative regulatory region is active in F9 EC cells and ES cells, it is inactive in P19 EC cells. Furthermore, we demonstrate that one of the positive cis-regulatory elements active in F9 EC cells and ES cells is inactive in P19 EC cells. Together, these and other studies suggest that Nanog transcription is regulated by the interplay of positive and negative cis-regulatory elements. Given that P19 appears to be more closely related to a later developmental stage of mammalian development than F9 and ES cells, differential utilization of cis-regulatory elements may reflect mechanisms used during development to achieve the correct level of Nanog expression as embryogenesis unfolds.
机译:转录因子Nanog对于哺乳动物的胚胎发生以及胚胎干(ES)细胞的多能性至关重要。与ES细胞和胚胎癌细胞(EC)的合作先前确定了影响Nanog启动子活性的正和负顺式调控元件,包括与Sox2和Oct-3 / 4结合的相邻顺式调控元件。鉴于Nanog在哺乳动物发育过程中的重要性,我们更加仔细地研究了Nanog启动子活性所需的顺式调控元件。在这项研究中,我们证明了先前显示在F9 EC细胞中有活性的两个顺式正调控元件在ES细胞中也有活性。我们还确定了一个新颖的负调控区域,该区域紧邻其他两个正的Nanog顺式调控元件。尽管此负调控区在F9 EC细胞和ES细胞中有活性,但在P19 EC细胞中无活性。此外,我们证明了在F9 EC细胞和ES细胞中有活性的顺式调控元件之一在P19 EC细胞中是无活性的。总之,这些研究和其他研究表明,Nanog转录受正和负顺式调节元件相互作用的调节。鉴于P19似乎比F9和ES细胞与哺乳动物发育的后期发育阶段更紧密相关,顺式调控元件的差异利用可能反映了胚胎发生过程中发育过程中用于实现正确Nanog表达水平的机制。

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