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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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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. |
format | Online Article Text |
id | pubmed-5464964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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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