Department of Genetics, Stanford University, Stanford, CA 94305, USA.
Department of Genetics, Stanford University, Stanford, CA 94305, USA; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
Cell. 2020 Dec 23;183(7):2003-2019.e16. doi: 10.1016/j.cell.2020.11.015. Epub 2020 Dec 11.
The ability to record transient cellular events in the DNA or RNA of cells would enable precise, large-scale analysis, selection, and reprogramming of heterogeneous cell populations. Here, we report a molecular technology for stable genetic tagging of cells that exhibit activity-related increases in intracellular calcium concentration (FLiCRE). We used FLiCRE to transcriptionally label activated neural ensembles in the nucleus accumbens of the mouse brain during brief stimulation of aversive inputs. Using single-cell RNA sequencing, we detected FLiCRE transcripts among the endogenous transcriptome, providing simultaneous readout of both cell-type and calcium activation history. We identified a cell type in the nucleus accumbens activated downstream of long-range excitatory projections. Taking advantage of FLiCRE's modular design, we expressed an optogenetic channel selectively in this cell type and showed that direct recruitment of this otherwise genetically inaccessible population elicits behavioral aversion. The specificity and minute resolution of FLiCRE enables molecularly informed characterization, manipulation, and reprogramming of activated cellular ensembles.
能够在细胞的 DNA 或 RNA 中记录瞬时细胞事件,将使对异质细胞群体进行精确的、大规模的分析、选择和重编程成为可能。在这里,我们报告了一种用于稳定遗传标记细胞的分子技术,这些细胞表现出与细胞内钙浓度增加相关的活性(FLiCRE)。我们使用 FLiCRE 在对厌恶输入进行短暂刺激期间,对小鼠大脑伏隔核中的激活神经簇进行转录标记。使用单细胞 RNA 测序,我们在内源性转录组中检测到了 FLiCRE 转录本,同时提供了细胞类型和钙激活历史的直接读出。我们在伏隔核中鉴定出一种细胞类型,该细胞类型被长程兴奋性投射激活。利用 FLiCRE 的模块化设计,我们在这种细胞类型中选择性地表达了一种光遗传学通道,并表明直接招募这种在遗传上无法接近的群体可引起行为厌恶。FLiCRE 的特异性和微小分辨率使激活细胞群的分子信息特征分析、操作和重编程成为可能。