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活细胞中转录动力学的定量测量。

Quantitative measurement of transcription dynamics in living cells.

作者信息

Corrigan Adam M, Chubb Jonathan R

机构信息

MRC Laboratory for Molecular Cell Biology, University College London, Gower Street, London, WC1E 6BT, United Kingdom.

出版信息

Methods Cell Biol. 2015;125:29-41. doi: 10.1016/bs.mcb.2014.11.001. Epub 2015 Jan 8.

Abstract

In a wide range of organisms the kinetics of transcription have been found to be noisy, with "bursts" or "pulses" of transcription interspersed with irregular periods of inactivity. The in vivo analysis of transcription dynamics can be most directly monitored using RNA stem loop motifs derived from MS2 and other bacteriophages. Here we describe the implementation of the MS2 RNA detection system and the steps required for precise measurement of transcription dynamics in highly motile cells. Automated image processing techniques are used to track large numbers of cells and measure transcription in a systematic and unbiased manner. We discuss popular methods for automatic image segmentation and frame-to-frame tracking of cells, and the considerations required to make measurements as quantitatively as possible.

摘要

在多种生物体中,转录动力学已被发现具有噪声,转录的“爆发”或“脉冲”穿插着不规则的非活动期。转录动力学的体内分析可以使用源自MS2和其他噬菌体的RNA茎环基序最直接地进行监测。在这里,我们描述了MS2 RNA检测系统的实施以及在高度运动的细胞中精确测量转录动力学所需的步骤。自动化图像处理技术用于跟踪大量细胞,并以系统且无偏差的方式测量转录。我们讨论了用于细胞自动图像分割和逐帧跟踪的常用方法,以及尽可能进行定量测量所需考虑的因素。

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