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基于用于细胞追踪和分类的内源性一体化报告基因的细胞周期定量分析。

Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification.

作者信息

Zerjatke Thomas, Gak Igor A, Kirova Dilyana, Fuhrmann Markus, Daniel Katrin, Gonciarz Magdalena, Müller Doris, Glauche Ingmar, Mansfeld Jörg

机构信息

Institute for Medical Informatics and Biometry, Carl Gustav Carus Faculty of Medicine, Technische Universität Dresden, 01307 Dresden, Germany.

Cell Cycle, Biotechnology Center, Technische Universität Dresden, 01307 Dresden, Germany.

出版信息

Cell Rep. 2017 May 30;19(9):1953-1966. doi: 10.1016/j.celrep.2017.05.022.

Abstract

Cell cycle kinetics are crucial to cell fate decisions. Although live imaging has provided extensive insights into this relationship at the single-cell level, the limited number of fluorescent markers that can be used in a single experiment has hindered efforts to link the dynamics of individual proteins responsible for decision making directly to cell cycle progression. Here, we present fluorescently tagged endogenous proliferating cell nuclear antigen (PCNA) as an all-in-one cell cycle reporter that allows simultaneous analysis of cell cycle progression, including the transition into quiescence, and the dynamics of individual fate determinants. We also provide an image analysis pipeline for automated segmentation, tracking, and classification of all cell cycle phases. Combining the all-in-one reporter with labeled endogenous cyclin D1 and p21 as prime examples of cell-cycle-regulated fate determinants, we show how cell cycle and quantitative protein dynamics can be simultaneously extracted to gain insights into G1 phase regulation and responses to perturbations.

摘要

细胞周期动力学对于细胞命运决定至关重要。尽管实时成像已在单细胞水平上对这种关系提供了广泛的见解,但单个实验中可使用的荧光标记数量有限,阻碍了将负责决策的单个蛋白质的动态变化直接与细胞周期进程联系起来的努力。在此,我们展示了荧光标记的内源性增殖细胞核抗原(PCNA)作为一种一体化细胞周期报告分子,它允许同时分析细胞周期进程,包括进入静止期的转变,以及单个命运决定因素的动态变化。我们还提供了一个图像分析流程,用于对所有细胞周期阶段进行自动分割、跟踪和分类。将这种一体化报告分子与标记的内源性细胞周期蛋白D1和p21相结合,作为细胞周期调控命运决定因素的主要例子,我们展示了如何同时提取细胞周期和定量蛋白质动态变化,以深入了解G1期调控和对扰动的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c88/5464964/ef9e4de2f893/fx1.jpg

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