首页> 外文OA文献 >Regulation of Stem Cell Pluripotency and Differentiation Involves a Mutual Regulatory Circuit of the Nanog, OCT4, and SOX2 Pluripotency Transcription Factors With Polycomb Repressive Complexes and Stem Cell microRNAs
【2h】

Regulation of Stem Cell Pluripotency and Differentiation Involves a Mutual Regulatory Circuit of the Nanog, OCT4, and SOX2 Pluripotency Transcription Factors With Polycomb Repressive Complexes and Stem Cell microRNAs

机译:干细胞多能性和分化的调节涉及具有多梳抑制复合物和干细胞微小RNa的Nanog,OCT4和sOX2多能性转录因子的相互调节电路。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Coordinated transcription factor networks have emerged as the master regulatory mechanisms of stem cell pluripotency and differentiation. Many stem cell-specific transcription factors, including the pluripotency transcription factors, OCT4, NANOG, and SOX2 function in combinatorial complexes to regulate the expression of loci, which are involved in embryonic stem (ES) cell pluripotency and cellular differentiation. This review will address how these pathways form a reciprocal regulatory circuit whereby the equilibrium between stem cell self-renewal, proliferation, and differentiation is in perpetual balance. We will discuss how distinct epigenetic repressive pathways involving polycomb complexes, DNA methylation, and microRNAs cooperate to reduce transcriptional noise and to prevent stochastic and aberrant induction of differentiation. We will provide a brief overview of how these networks cooperate to modulate differentiation along hematopoietic and neuronal lineages. Finally, we will describe how aberrant functioning of components of the stem cell regulatory network may contribute to malignant transformation of adult stem cells and the establishment of a "cancer stem cell" phenotype and thereby underlie multiple types of human malignancies.
机译:协调转录因子网络已成为干细胞多能性和分化的主要调控机制。许多干细胞特异性转录因子,包括多能性转录因子,OCT4,NANOG和SOX2在组合复合物中发挥功能来调节基因座的表达,这些基因参与胚胎干(ES)细胞多能性和细胞分化。这篇综述将探讨这些途径如何形成相互调节回路,从而使干细胞自我更新,增殖和分化之间的平衡处于永久平衡。我们将讨论涉及多梳复合物,DNA甲基化和microRNA的独特表观遗传抑制途径如何协作以减少转录噪声并防止随机和异常诱导分化。我们将简要概述这些网络如何协同调节沿造血和神经元谱系的分化。最后,我们将描述干细胞调节网络的异常功能如何导致成年干细胞的恶性转化和“癌症干细胞”表型的建立,从而成为多种人类恶性肿瘤的基础。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号