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

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 pro...

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Autores principales: Zerjatke, Thomas, Gak, Igor A., Kirova, Dilyana, Fuhrmann, Markus, Daniel, Katrin, Gonciarz, Magdalena, Müller, Doris, Glauche, Ingmar, Mansfeld, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5464964/
https://www.ncbi.nlm.nih.gov/pubmed/28564611
http://dx.doi.org/10.1016/j.celrep.2017.05.022
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author Zerjatke, Thomas
Gak, Igor A.
Kirova, Dilyana
Fuhrmann, Markus
Daniel, Katrin
Gonciarz, Magdalena
Müller, Doris
Glauche, Ingmar
Mansfeld, Jörg
author_facet Zerjatke, Thomas
Gak, Igor A.
Kirova, Dilyana
Fuhrmann, Markus
Daniel, Katrin
Gonciarz, Magdalena
Müller, Doris
Glauche, Ingmar
Mansfeld, Jörg
author_sort Zerjatke, Thomas
collection PubMed
description 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.
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spelling pubmed-54649642017-06-16 Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification Zerjatke, Thomas Gak, Igor A. Kirova, Dilyana Fuhrmann, Markus Daniel, Katrin Gonciarz, Magdalena Müller, Doris Glauche, Ingmar Mansfeld, Jörg Cell Rep Resource 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. Cell Press 2017-05-30 /pmc/articles/PMC5464964/ /pubmed/28564611 http://dx.doi.org/10.1016/j.celrep.2017.05.022 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Resource
Zerjatke, Thomas
Gak, Igor A.
Kirova, Dilyana
Fuhrmann, Markus
Daniel, Katrin
Gonciarz, Magdalena
Müller, Doris
Glauche, Ingmar
Mansfeld, Jörg
Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification
title Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification
title_full Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification
title_fullStr Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification
title_full_unstemmed Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification
title_short Quantitative Cell Cycle Analysis Based on an Endogenous All-in-One Reporter for Cell Tracking and Classification
title_sort quantitative cell cycle analysis based on an endogenous all-in-one reporter for cell tracking and classification
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5464964/
https://www.ncbi.nlm.nih.gov/pubmed/28564611
http://dx.doi.org/10.1016/j.celrep.2017.05.022
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