Lee Han B, Sundberg Brynn N, Sigafoos Ashley N, Clark Karl J
Neurobiology of Disease Graduate Program, Mayo Graduate School Rochester, MN, USA.
Department of Biochemistry and Molecular Biology, Mayo Clinic Rochester, MN, USA.
Front Genet. 2016 Apr 6;7:47. doi: 10.3389/fgene.2016.00047. eCollection 2016.
Recent advancement in genome engineering technology is changing the landscape of biological research and providing neuroscientists with an opportunity to develop new methodologies to ask critical research questions. This advancement is highlighted by the increased use of programmable DNA-binding agents (PDBAs) such as transcription activator-like effector (TALE) and RNA-guided clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR associated (Cas) systems. These PDBAs fused or co-expressed with various effector domains allow precise modification of genomic sequences and gene expression levels. These technologies mirror and extend beyond classic gene targeting methods contributing to the development of novel tools for basic and clinical neuroscience. In this Review, we discuss the recent development in genome engineering and potential applications of this technology in the field of neuroscience.
基因组工程技术的最新进展正在改变生物学研究的格局,并为神经科学家提供了开发新方法来解答关键研究问题的机会。可编程DNA结合剂(PDBA)如转录激活样效应因子(TALE)和RNA引导的成簇规律间隔短回文重复序列(CRISPR)/CRISPR相关(Cas)系统的使用增加,凸显了这一进展。这些与各种效应域融合或共表达的PDBA能够精确修饰基因组序列和基因表达水平。这些技术反映并超越了经典的基因靶向方法,有助于开发用于基础和临床神经科学的新型工具。在本综述中,我们讨论了基因组工程的最新进展以及该技术在神经科学领域的潜在应用。