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Multiplexing clonality: combining RGB marking and genetic barcoding

RGB marking and DNA barcoding are two cutting-edge technologies in the field of clonal cell marking. To combine the virtues of both approaches, we equipped LeGO vectors encoding red, green or blue fluorescent proteins with complex DNA barcodes carrying color-specific signatures. For these vectors, w...

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Autores principales: Cornils, Kerstin, Thielecke, Lars, Hüser, Svenja, Forgber, Michael, Thomaschewski, Michael, Kleist, Nadja, Hussein, Kais, Riecken, Kristoffer, Volz, Tassilo, Gerdes, Sebastian, Glauche, Ingmar, Dahl, Andreas, Dandri, Maura, Roeder, Ingo, Fehse, Boris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985654/
https://www.ncbi.nlm.nih.gov/pubmed/24476916
http://dx.doi.org/10.1093/nar/gku081
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author Cornils, Kerstin
Thielecke, Lars
Hüser, Svenja
Forgber, Michael
Thomaschewski, Michael
Kleist, Nadja
Hussein, Kais
Riecken, Kristoffer
Volz, Tassilo
Gerdes, Sebastian
Glauche, Ingmar
Dahl, Andreas
Dandri, Maura
Roeder, Ingo
Fehse, Boris
author_facet Cornils, Kerstin
Thielecke, Lars
Hüser, Svenja
Forgber, Michael
Thomaschewski, Michael
Kleist, Nadja
Hussein, Kais
Riecken, Kristoffer
Volz, Tassilo
Gerdes, Sebastian
Glauche, Ingmar
Dahl, Andreas
Dandri, Maura
Roeder, Ingo
Fehse, Boris
author_sort Cornils, Kerstin
collection PubMed
description RGB marking and DNA barcoding are two cutting-edge technologies in the field of clonal cell marking. To combine the virtues of both approaches, we equipped LeGO vectors encoding red, green or blue fluorescent proteins with complex DNA barcodes carrying color-specific signatures. For these vectors, we generated highly complex plasmid libraries that were used for the production of barcoded lentiviral vector particles. In proof-of-principle experiments, we used barcoded vectors for RGB marking of cell lines and primary murine hepatocytes. We applied single-cell polymerase chain reaction to decipher barcode signatures of individual RGB-marked cells expressing defined color hues. This enabled us to prove clonal identity of cells with one and the same RGB color. Also, we made use of barcoded vectors to investigate clonal development of leukemia induced by ectopic oncogene expression in murine hematopoietic cells. In conclusion, by combining RGB marking and DNA barcoding, we have established a novel technique for the unambiguous genetic marking of individual cells in the context of normal regeneration as well as malignant outgrowth. Moreover, the introduction of color-specific signatures in barcodes will facilitate studies on the impact of different variables (e.g. vector type, transgenes, culture conditions) in the context of competitive repopulation studies.
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spelling pubmed-39856542014-04-18 Multiplexing clonality: combining RGB marking and genetic barcoding Cornils, Kerstin Thielecke, Lars Hüser, Svenja Forgber, Michael Thomaschewski, Michael Kleist, Nadja Hussein, Kais Riecken, Kristoffer Volz, Tassilo Gerdes, Sebastian Glauche, Ingmar Dahl, Andreas Dandri, Maura Roeder, Ingo Fehse, Boris Nucleic Acids Res Methods Online RGB marking and DNA barcoding are two cutting-edge technologies in the field of clonal cell marking. To combine the virtues of both approaches, we equipped LeGO vectors encoding red, green or blue fluorescent proteins with complex DNA barcodes carrying color-specific signatures. For these vectors, we generated highly complex plasmid libraries that were used for the production of barcoded lentiviral vector particles. In proof-of-principle experiments, we used barcoded vectors for RGB marking of cell lines and primary murine hepatocytes. We applied single-cell polymerase chain reaction to decipher barcode signatures of individual RGB-marked cells expressing defined color hues. This enabled us to prove clonal identity of cells with one and the same RGB color. Also, we made use of barcoded vectors to investigate clonal development of leukemia induced by ectopic oncogene expression in murine hematopoietic cells. In conclusion, by combining RGB marking and DNA barcoding, we have established a novel technique for the unambiguous genetic marking of individual cells in the context of normal regeneration as well as malignant outgrowth. Moreover, the introduction of color-specific signatures in barcodes will facilitate studies on the impact of different variables (e.g. vector type, transgenes, culture conditions) in the context of competitive repopulation studies. Oxford University Press 2014-04 2014-01-28 /pmc/articles/PMC3985654/ /pubmed/24476916 http://dx.doi.org/10.1093/nar/gku081 Text en © The Author(s) 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Cornils, Kerstin
Thielecke, Lars
Hüser, Svenja
Forgber, Michael
Thomaschewski, Michael
Kleist, Nadja
Hussein, Kais
Riecken, Kristoffer
Volz, Tassilo
Gerdes, Sebastian
Glauche, Ingmar
Dahl, Andreas
Dandri, Maura
Roeder, Ingo
Fehse, Boris
Multiplexing clonality: combining RGB marking and genetic barcoding
title Multiplexing clonality: combining RGB marking and genetic barcoding
title_full Multiplexing clonality: combining RGB marking and genetic barcoding
title_fullStr Multiplexing clonality: combining RGB marking and genetic barcoding
title_full_unstemmed Multiplexing clonality: combining RGB marking and genetic barcoding
title_short Multiplexing clonality: combining RGB marking and genetic barcoding
title_sort multiplexing clonality: combining rgb marking and genetic barcoding
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985654/
https://www.ncbi.nlm.nih.gov/pubmed/24476916
http://dx.doi.org/10.1093/nar/gku081
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