Coleman Robert A, Liu Zhe, Darzacq Xavier, Tjian Robert, Singer Robert H, Lionnet Timothée
Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, New York 10461.
HHMI Janelia Research Campus, Ashburn, Virginia 20147.
Cold Spring Harb Symp Quant Biol. 2015;80:1-8. doi: 10.1101/sqb.2015.80.027201. Epub 2016 Jan 13.
Transcription, the first step of gene expression, is exquisitely regulated in higher eukaryotes to ensure correct development and homeostasis. Traditional biochemical, genetic, and genomic approaches have proved successful at identifying factors, regulatory sequences, and potential pathways that modulate transcription. However, they typically only provide snapshots or population averages of the highly dynamic, stochastic biochemical processes involved in transcriptional regulation. Single-molecule live-cell imaging has, therefore, emerged as a complementary approach capable of circumventing these limitations. By observing sequences of molecular events in real time as they occur in their native context, imaging has the power to derive cause-and-effect relationships and quantitative kinetics to build predictive models of transcription. Ongoing progress in fluorescence imaging technology has brought new microscopes and labeling technologies that now make it possible to visualize and quantify the transcription process with single-molecule resolution in living cells and animals. Here we provide an overview of the evolution and current state of transcription imaging technologies. We discuss some of the important concepts they uncovered and present possible future developments that might solve long-standing questions in transcriptional regulation.
转录作为基因表达的第一步,在高等真核生物中受到精确调控,以确保正确的发育和体内平衡。传统的生化、遗传和基因组方法已成功识别出调控转录的因子、调控序列和潜在途径。然而,它们通常只能提供转录调控中高度动态、随机生化过程的快照或群体平均值。因此,单分子活细胞成像已成为一种能够克服这些局限性的补充方法。通过在分子事件于其天然环境中发生时实时观察其序列,成像能够得出因果关系和定量动力学,从而构建转录预测模型。荧光成像技术的不断进步带来了新的显微镜和标记技术,现在已经能够在活细胞和动物中以单分子分辨率可视化和量化转录过程。在这里,我们概述转录成像技术的发展历程和现状。我们讨论了它们揭示的一些重要概念,并介绍了可能解决转录调控中长期存在问题的未来发展方向。