Le Thuc T, Harlepp Sébastien, Guet Calin C, Dittmar Kimberly, Emonet Thierry, Pan Tao, Cluzel Philippe
Institute for Biophysical Dynamics and The James Franck Institute and Department of Biochemistry and Molecular Biology, University of Chicago, 5640 South Ellis Avenue, Chicago, IL 60637, USA.
Proc Natl Acad Sci U S A. 2005 Jun 28;102(26):9160-4. doi: 10.1073/pnas.0503311102. Epub 2005 Jun 20.
Characterizing the dynamics of specific RNA levels requires real-time RNA profiling in a single cell. We show that the combination of a synthetic modular genetic system with fluorescence correlation spectroscopy allows us to directly measure in real time the activity of any specific promoter in prokaryotes. Using a simple inducible gene expression system, we found that induced RNA levels within a single bacterium of Escherichia coli exhibited a pulsating profile in response to a steady input of inducer. The genetic deletion of an efflux pump system, a key determinant of antibiotic resistance, altered the pulsating transcriptional dynamics and caused overexpression of induced RNA. In contrast with population measurements, real-time RNA profiling permits identifying relationships between genotypes and transcriptional dynamics that are accessible only at the level of the single cell.
表征特定RNA水平的动态变化需要在单细胞中进行实时RNA分析。我们表明,合成模块化遗传系统与荧光相关光谱技术的结合使我们能够直接实时测量原核生物中任何特定启动子的活性。使用一个简单的诱导型基因表达系统,我们发现,在稳定输入诱导剂的情况下,单个大肠杆菌细胞内诱导的RNA水平呈现出脉动模式。作为抗生素耐药性关键决定因素的外排泵系统的基因缺失,改变了脉动转录动态,并导致诱导RNA的过表达。与群体测量不同,实时RNA分析能够识别仅在单细胞水平上才会出现的基因型与转录动态之间的关系。