Weng Wendong, Liu Xiuxiu, Lui Kathy O, Zhou Bin
State Key Laboratory of Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Shanghai 200031, China.
Department of Chemical Pathology, Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong, SAR 999077, China.
Trends Cell Biol. 2022 Apr;32(4):324-337. doi: 10.1016/j.tcb.2021.09.007. Epub 2021 Oct 15.
Precisely deciphering the cellular plasticity in vivo is essential in understanding many key biological processes. Site-specific recombinases are genetic tools used for in vivo lineage tracing and gene manipulation. Conventional Cre-loxP, Dre-rox, and Flp-frt technologies form the orthogonal recombination systems that can also be used in combination to increase the precision. As such, more than one marker gene can be targeted for lineage tracing, studying cellular heterogeneity, recording cellular activities, or even genome editing. Their combinatory use has recently resolved some controversies in defining cellular fate plasticity. Focusing on cell fate studies, we introduce the design principles of orthogonal recombinases-based strategies, describe some working examples in resolving cell fate-related controversies, and discuss some of their technical strengths and limits.
精确解析体内细胞可塑性对于理解许多关键生物学过程至关重要。位点特异性重组酶是用于体内谱系追踪和基因操作的遗传工具。传统的Cre-loxP、Dre-rox和Flp-frt技术构成了正交重组系统,这些系统也可以组合使用以提高精度。因此,可以针对一个以上的标记基因进行谱系追踪、研究细胞异质性、记录细胞活动,甚至进行基因组编辑。它们的组合使用最近解决了一些在定义细胞命运可塑性方面的争议。本文聚焦于细胞命运研究,介绍基于正交重组酶策略的设计原则,描述一些在解决细胞命运相关争议方面的实际例子,并讨论它们的一些技术优势和局限性。