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用于时间转录控制的CRISPR/dCas9开关系统

CRISPR/dCas9 Switch Systems for Temporal Transcriptional Control.

作者信息

Gjaltema Rutger A F, Schulz Edda G

机构信息

Otto-Warburg-Laboratory, Max Planck Institute for Molecular Genetics, Berlin, Germany.

出版信息

Methods Mol Biol. 2018;1767:167-185. doi: 10.1007/978-1-4939-7774-1_8.

Abstract

In a swift revolution, CRISPR/Cas9 has reshaped the means and ease of interrogating biological questions. Particularly, mutants that result in a nuclease-deactivated Cas9 (dCas9) provide scientists with tools to modulate transcription of genomic loci at will by targeting transcriptional effector domains. To interrogate the temporal order of events during transcriptional regulation, rapidly inducible CRISPR/dCas9 systems provide previously unmet molecular tools. In only a few years of time, numerous light and chemical-inducible switches have been applied to CRISPR/dCas9 to generate dCas9 switches. As these inducible switch systems are able to modulate dCas9 directly at the protein level, they rapidly affect dCas9 stability, activity, or target binding and subsequently rapidly influence downstream transcriptional events. Here we review the current state of such biotechnological CRISPR/dCas9 enhancements. Specifically we provide details on their flaws and strengths and on the differences in molecular design between the switch systems. With this we aim to provide a selection guide for researchers with keen interest in rapid temporal control over transcriptional modulation through the CRISPR/dCas9 system.

摘要

在一场迅速的变革中,CRISPR/Cas9重塑了探究生物学问题的方式并使其变得更加简便。特别是那些产生核酸酶失活型Cas9(dCas9)的突变体,为科学家们提供了通过靶向转录效应结构域来随意调控基因组位点转录的工具。为了探究转录调控过程中事件的时间顺序,快速诱导型CRISPR/dCas9系统提供了前所未有的分子工具。在短短几年时间里,众多光诱导和化学诱导开关已被应用于CRISPR/dCas9以生成dCas9开关。由于这些诱导型开关系统能够在蛋白质水平直接调控dCas9,它们能迅速影响dCas9的稳定性、活性或与靶点的结合,进而迅速影响下游转录事件。在此,我们综述此类生物技术对CRISPR/dCas9的改进现状。具体而言,我们详细介绍了它们的缺点和优点,以及各开关系统在分子设计上的差异。以此,我们旨在为那些热衷于通过CRISPR/dCas9系统对转录调控进行快速时间控制的研究人员提供一份选择指南。

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