Single-Molecule Nanoscopy Elucidates RNA Polymerase II Transcription at Single Genes in Live Cells

被引:95
作者
Li, Jieru [1 ]
Dong, Ankun [1 ,2 ]
Saydaminova, Kamola [1 ]
Chang, Hill [1 ,3 ]
Wang, Guanshi [1 ]
Ochiai, Hiroshi [4 ]
Yamamoto, Takashi [4 ]
Pertsinidis, Alexandros [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Struct Biol Program, New York, NY 10065 USA
[2] Brown Univ, Dept Phys, Providence, RI 02912 USA
[3] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08854 USA
[4] Hiroshima Univ, Grad Sch Integrated Sci Life, Program Math & Life Sci, Higashihiroshima 7398526, Japan
基金
美国国家卫生研究院;
关键词
P-TEFB; FACTOR-BINDING; ELONGATION; DYNAMICS; TARGET; CYCLE; VISUALIZATION; LOCALIZATION; ORGANIZATION; ACETYLATION;
D O I
10.1016/j.cell.2019.05.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transforming the vast knowledge from genetics, biochemistry, and structural biology into detailed molecular descriptions of biological processes inside cells remains a major challenge-one in sore need of better imaging technologies. For example, transcription involves the complex interplay between RNA polymerase II (Pol II), regulatory factors (RFs), and chromatin, but visualizing these dynamic molecular transactions in their native intracellular milieu remains elusive. Here, we zoom into single tagged genes using nanoscopy techniques, including an active target-locking, ultra-sensitive system that enables single-molecule detection in addressable sub-diffraction volumes, within crowded intracellular environments. We image, track, and quantify Pol II with single-molecule resolution, unveiling its dynamics during the transcription cycle. Further probing multiple functionally linked events-RF-chromatin interactions, Pol II dynamics, and nascent transcription kinetics-reveals detailed operational parameters of gene-regulatory mechanisms hither-to-unseen in vivo. Our approach sets the stage for single-molecule studies of complex molecular processes in live cells.
引用
收藏
页码:491 / +
页数:44
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