Wada Takeo, Wallerich Sandrine, Becskei Attila
Biozentrum , University of Basel , Klingelbergstrasse 50/70 , 4056 Basel , Switzerland.
ACS Synth Biol. 2019 Feb 15;8(2):223-231. doi: 10.1021/acssynbio.8b00369. Epub 2019 Jan 17.
Genes, including promoters and enhancers, are regulated by short- and long-range interactions in higher eukaryotes. It is unclear how mammalian gene expression subject to such a combinatorial regulation can be controlled by synthetic transcription factors (TF). Here, we studied how synthetic TALE transcriptional activators and repressors affect the expression of genes in a gene array during cellular differentiation. The protocadherin gene array is silent in mouse embryonic stem (ES) and neuronal progenitor cells. The TALE transcriptional activator recruited to a promoter activates specifically the target gene in ES cells. Upon differentiation into neuronal progenitors, the transcriptional regulatory logic changes: the same activator behaves like an enhancer, activating distant genes in a correlated, stochastic fashion. The long-range effect is reflected by the alterations in CpG methylation. Our findings reveal the limits of precision and the opportunities in the control of gene expression for TF-based therapies in cells of various differentiation stages.
包括启动子和增强子在内的基因,在高等真核生物中受到短程和长程相互作用的调控。目前尚不清楚受这种组合调控的哺乳动物基因表达如何由合成转录因子(TF)来控制。在此,我们研究了合成的TALE转录激活因子和抑制因子如何在细胞分化过程中影响基因阵列中基因的表达。原钙黏蛋白基因阵列在小鼠胚胎干细胞(ES)和神经祖细胞中是沉默的。招募到启动子上的TALE转录激活因子在ES细胞中特异性地激活靶基因。在分化为神经祖细胞后,转录调控逻辑发生变化:相同的激活因子表现得像一个增强子,以相关的、随机的方式激活远处的基因。这种长程效应通过CpG甲基化的改变得以体现。我们的研究结果揭示了基于TF的疗法在不同分化阶段细胞中控制基因表达时的精确性局限和机遇。