Merkin Institute for Transformative Technologies in Healthcare, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA, and Department of Chemistry and Chemical Biology and Howard Hughes Medical Institute, Harvard University, Cambridge, MA 02138, USA.
Science. 2018 Apr 13;360(6385). doi: 10.1126/science.aap8992. Epub 2018 Feb 15.
We present two CRISPR-mediated analog multi-event recording apparatus (CAMERA) systems that use base editors and Cas9 nucleases to record cellular events in bacteria and mammalian cells. The devices record signal amplitude or duration as changes in the ratio of mutually exclusive DNA sequences (CAMERA 1) or as single-base modifications (CAMERA 2). We achieved recording of multiple stimuli in bacteria or mammalian cells, including exposure to antibiotics, nutrients, viruses, light, and changes in Wnt signaling. When recording to multicopy plasmids, reliable readout requires as few as 10 to 100 cells. The order of stimuli can be recorded through an overlapping guide RNA design, and memories can be erased and re-recorded over multiple cycles. CAMERA systems serve as "cell data recorders" that write a history of endogenous or exogenous signaling events into permanent DNA sequence modifications in living cells.
我们提出了两种基于 CRISPR 的模拟多事件记录装置(CAMERA)系统,它们使用碱基编辑器和 Cas9 核酸酶来记录细菌和哺乳动物细胞中的细胞事件。这些设备记录信号幅度或持续时间的变化,作为互斥 DNA 序列的比率变化(CAMERA1)或作为单碱基修饰(CAMERA2)。我们实现了对细菌或哺乳动物细胞中的多个刺激的记录,包括暴露于抗生素、营养物质、病毒、光和 Wnt 信号的变化。当记录在多拷贝质粒上时,可靠的读出需要少至 10 到 100 个细胞。通过重叠的指导 RNA 设计,可以记录刺激的顺序,并且可以通过多个循环擦除和重新记录记忆。CAMERA 系统充当“细胞数据记录器”,将内源性或外源性信号事件的历史记录写入活细胞的永久 DNA 序列修饰中。