Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Department of Pathology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
Nat Commun. 2019 Mar 12;10(1):1185. doi: 10.1038/s41467-019-09128-7.
Cellular products derived from the activity of DNA, RNA, and protein synthesis collectively control cell identity and function. Yet there is little information on how these three biosynthesis activities are coordinated during transient and sparse cellular processes, such as activation and differentiation. Here, we describe Simultaneous Overview of tri-Molecule Biosynthesis (SOMB), a molecular labeling and simultaneous detection strategy to quantify DNA, RNA, and protein synthesis in individual cells. Comprehensive interrogation of biosynthesis activities during transient cell states, such as progression through cell cycle or cellular differentiation, is achieved by partnering SOMB with parallel quantification of select biomolecules with conjugated antibody reagents. Here, we investigate differential de novo DNA, RNA, and protein synthesis dynamics in transformed human cell lines, primary activated human immune cells, and across the healthy human hematopoietic continuum, all at a single-cell resolution.
细胞产物源自 DNA、RNA 和蛋白质合成的活动,共同控制着细胞的特性和功能。然而,关于这三种生物合成活动在短暂而稀疏的细胞过程(如激活和分化)中是如何协调的,信息却很少。在这里,我们描述了三分子生物合成的同时概述(SOMB),这是一种分子标记和同时检测策略,用于定量单个细胞中的 DNA、RNA 和蛋白质合成。通过将 SOMB 与共轭抗体试剂对选定生物分子的并行定量相结合,实现了对细胞周期进程或细胞分化等短暂细胞状态下生物合成活性的全面研究。在这里,我们在单细胞分辨率下研究了转化的人类细胞系、原代激活的人类免疫细胞以及整个健康人类造血系统中不同的从头 DNA、RNA 和蛋白质合成动力学。