Fenno Lief E, Mattis Joanna, Ramakrishnan Charu, Deisseroth Karl
Department of Bioengineering, Stanford University, Stanford, California.
Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, California.
Curr Protoc Neurosci. 2017 Jul 5;80:4.39.1-4.39.24. doi: 10.1002/cpns.30.
As the power of genetically encoded interventional and observational tools for neuroscience expands, the boundaries of experimental design are increasingly defined by limits in selectively expressing these tools in relevant cell types. Single-recombinase-dependent expression systems have been widely used as a means to restrict gene expression based on single features by combining recombinase-dependent viruses with recombinase-expressing transgenic animals. This protocol details how to create INTRSECT constructs and use multiple recombinases to achieve targeting of a desired gene to subsets of neurons that are defined by multiple genetic and/or topological features. This method includes the design and utilization of both viruses and transgenic animals: these tools are inherently flexible and modular and may be used in different combinations to achieve the desired gene expression pattern. © 2017 by John Wiley & Sons, Inc.
随着用于神经科学的基因编码干预和观察工具的能力不断扩展,实验设计的边界越来越多地由在相关细胞类型中选择性表达这些工具的限制来界定。单重组酶依赖性表达系统已被广泛用作通过将重组酶依赖性病毒与表达重组酶的转基因动物相结合,基于单一特征来限制基因表达的一种手段。本方案详细介绍了如何构建INTRSECT构建体,并使用多种重组酶将所需基因靶向到由多种遗传和/或拓扑特征定义的神经元亚群。该方法包括病毒和转基因动物的设计与利用:这些工具本质上具有灵活性和模块化,可以以不同组合使用以实现所需的基因表达模式。© 2017约翰威立父子公司版权所有