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利用靶向增强子的设计型 TALE 转录因子重编程为多能性。

Reprogramming to pluripotency using designer TALE transcription factors targeting enhancers.

机构信息

Wellcome Trust Sanger Institute, Hinxton, Cambridge CB10 1HH, UK.

出版信息

Stem Cell Reports. 2013 Jul 11;1(2):183-97. doi: 10.1016/j.stemcr.2013.06.002. eCollection 2013.

Abstract

The modular DNA recognition code of the transcription-activator-like effectors (TALEs) from plant pathogenic bacterial genus Xanthomonas provides a powerful genetic tool to create designer transcription factors (dTFs) targeting specific DNA sequences for manipulating gene expression. Previous studies have suggested critical roles of enhancers in gene regulation and reprogramming. Here, we report dTF activator targeting the distal enhancer of the Pou5f1 (Oct4) locus induces epigenetic changes, reactivates its expression, and substitutes exogenous OCT4 in reprogramming mouse embryonic fibroblast cells (MEFs) to induced pluripotent stem cells (iPSCs). Similarly, dTF activator targeting a Nanog enhancer activates Nanog expression and reprograms epiblast stem cells (EpiSCs) to iPSCs. Conversely, dTF repressors targeting the same genetic elements inhibit expression of these loci, and effectively block reprogramming. This study indicates that dTFs targeting specific enhancers can be used to study other biological processes such as transdifferentiation or directed differentiation of stem cells.

摘要

来自植物病原性黄单胞菌属的转录激活子样效应物(TALEs)的模块化 DNA 识别密码为创建针对特定 DNA 序列的设计转录因子(dTFs)以操纵基因表达提供了强大的遗传工具。先前的研究表明,增强子在基因调控和重编程中起关键作用。在这里,我们报告了靶向 Pou5f1(Oct4)基因座远端增强子的 dTF 激活剂诱导表观遗传变化,重新激活其表达,并在外源 OCT4 取代下将小鼠胚胎成纤维细胞(MEFs)重编程为诱导多能干细胞(iPSCs)。类似地,靶向 Nanog 增强子的 dTF 激活剂激活 Nanog 表达并将胚胎外胚层干细胞(EpiSCs)重编程为 iPSCs。相反,靶向相同遗传元件的 dTF 抑制剂抑制这些基因座的表达,并有效阻断重编程。本研究表明,靶向特定增强子的 dTFs 可用于研究其他生物学过程,如干细胞的转分化或定向分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7790/3757749/29aca93048e1/fx1.jpg

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