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编辑表观基因组:用于可编程转录和表观遗传调控的技术

Editing the epigenome: technologies for programmable transcription and epigenetic modulation.

作者信息

Thakore Pratiksha I, Black Joshua B, Hilton Isaac B, Gersbach Charles A

机构信息

Department of Biomedical Engineering, Duke University, Durham, North Carolina, USA.

Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, USA.

出版信息

Nat Methods. 2016 Feb;13(2):127-37. doi: 10.1038/nmeth.3733.

Abstract

Gene regulation is a complex and tightly controlled process that defines cell identity, health and disease, and response to pharmacologic and environmental signals. Recently developed DNA-targeting platforms, including zinc finger proteins, transcription activator-like effectors (TALEs) and the clustered, regularly interspaced, short palindromic repeats (CRISPR)-Cas9 system, have enabled the recruitment of transcriptional modulators and epigenome-modifying factors to any genomic site, leading to new insights into the function of epigenetic marks in gene expression. Additionally, custom transcriptional and epigenetic regulation is facilitating refined control over cell function and decision making. The unique properties of the CRISPR-Cas9 system have created new opportunities for high-throughput genetic screens and multiplexing targets to manipulate complex gene expression patterns. This Review summarizes recent technological developments in this area and their application to biomedical challenges. We also discuss remaining limitations and necessary future directions for this field.

摘要

基因调控是一个复杂且受到严格控制的过程,它决定了细胞的特性、健康与疾病,以及对药物和环境信号的反应。最近开发的DNA靶向平台,包括锌指蛋白、转录激活样效应因子(TALEs)和成簇规律间隔短回文重复序列(CRISPR)-Cas9系统,能够将转录调节因子和表观基因组修饰因子招募到任何基因组位点,从而为基因表达中表观遗传标记的功能带来了新的见解。此外,定制的转录和表观遗传调控有助于对细胞功能和决策进行更精细的控制。CRISPR-Cas9系统的独特特性为高通量基因筛选和多重靶向以操纵复杂基因表达模式创造了新机会。本综述总结了该领域最近的技术发展及其在生物医学挑战中的应用。我们还讨论了该领域仍然存在的局限性以及必要的未来发展方向。

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