Department of Synthetic Biology and Immunology, National Institute of Chemistry, Ljubljana, Slovenia.
EN-FIST Centre of Excellence, Ljubljana, Slovenia.
Nat Chem Biol. 2019 Jan;15(1):80-87. doi: 10.1038/s41589-018-0163-8. Epub 2018 Nov 19.
The interplay between DNA-binding proteins plays an important role in transcriptional regulation and could increase the precision and complexity of designed regulatory circuits. Here we show that a transcription activator-like effector (TALE) can displace another TALE protein from DNA in a highly polarized manner, displacing only the 3'- but not 5'-bound overlapping or adjacent TALE. We propose that the polarized displacement by TALEs is based on its multipartite nature of binding to DNA. The polarized TALE displacement provides strategies for the specific regulation of gene expression, for construction of all two-input Boolean genetic logic circuits based on the robust propagation of the displacement across multiple neighboring sites, for displacement of zinc finger-based transcription factors and for suppression of Cas9-gRNA-mediated genome cleavage, enriching the synthetic biology toolbox and contributing to the understanding of the underlying principles of the facilitated displacement.
DNA 结合蛋白的相互作用在转录调控中起着重要作用,并能提高设计的调控回路的精度和复杂性。在这里,我们表明,转录激活子样效应物(TALE)可以高度极化的方式从 DNA 上置换另一个 TALE 蛋白,仅置换 3' 而不是 5' 结合的重叠或相邻 TALE。我们提出,TALEs 的极化置换是基于其与 DNA 的多部分结合性质。极化的 TALE 置换为基因表达的特异性调控提供了策略,为构建所有基于置换在多个相邻位点上稳健传播的双输入布尔遗传逻辑电路提供了策略,为锌指转录因子的置换提供了策略,并为抑制 Cas9-gRNA 介导的基因组切割提供了策略,丰富了合成生物学工具包,并有助于理解促进置换的基本原理。