Single molecule tracking of quantum dot-labeled mRNAs in a cell nucleus

被引:37
|
作者
Ishihama, Yo [1 ,2 ]
Funatsu, Takashi [1 ,2 ,3 ]
机构
[1] Univ Tokyo, Lab Bioanalyt Chem, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Ctr NanoBio Integrat, Bunkyo Ku, Tokyo 1138656, Japan
[3] Japan Sci & Technol Agcy, CREST, Chiyoda Ku, Tokyo 1020075, Japan
基金
日本学术振兴会;
关键词
Single particle tracking; mRNA; Anomalous diffusion; Quantum dots; LIVING MAMMALIAN-CELLS; ANOMALOUS DIFFUSION; PARTICLE TRACKING; MONTE-CARLO; POLY(A) RNA; IN-VIVO; DYNAMICS; CHROMATIN; MOVEMENT; SPECTROSCOPY;
D O I
10.1016/j.bbrc.2009.02.001
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
Single particle tracking (SPT) is a powerful technique for studying mRNA dynamics in cells. Although SPT of mRNA has been performed by labeling mRNA with fluorescent dyes or proteins, observation of mRNA for long durations with high temporal resolution has been difficult due to weak fluorescence and rapid photobleaching. Using quantum dots (QDs), we succeeded in observing the movement of individual mRNAs for more than 60 s, with a temporal resolution of 30 ms. Intronless and truncated ftz mRNA, synthesized in vitro and labeled with QDs, was microinjected into the nuclei of Cos7 cells. Almost all mRNAs were in motion, and statistical analyses revealed anomalous diffusion between barriers, with a microscopic diffusion coefficient of 0.12 mu m(2)/s and a macroscopic diffusion coefficient of 0.025 mu m(2)/s. Diffusion of mRNA was observed in interchromatin regions but not in histone2B-GFP-labeled chromatin regions. These results provide direct evidence of channeled mRNA diffusion in interchromatin regions. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:33 / 38
页数:6
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