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Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations

The HEK293 human cell lineage is widely used in cell biology and biotechnology. Here we use whole-genome resequencing of six 293 cell lines to study the dynamics of this aneuploid genome in response to the manipulations used to generate common 293 cell derivatives, such as transformation and stable...

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Autores principales: Lin, Yao-Cheng, Boone, Morgane, Meuris, Leander, Lemmens, Irma, Van Roy, Nadine, Soete, Arne, Reumers, Joke, Moisse, Matthieu, Plaisance, Stéphane, Drmanac, Radoje, Chen, Jason, Speleman, Frank, Lambrechts, Diether, Van de Peer, Yves, Tavernier, Jan, Callewaert, Nico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166678/
https://www.ncbi.nlm.nih.gov/pubmed/25182477
http://dx.doi.org/10.1038/ncomms5767
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author Lin, Yao-Cheng
Boone, Morgane
Meuris, Leander
Lemmens, Irma
Van Roy, Nadine
Soete, Arne
Reumers, Joke
Moisse, Matthieu
Plaisance, Stéphane
Drmanac, Radoje
Chen, Jason
Speleman, Frank
Lambrechts, Diether
Van de Peer, Yves
Tavernier, Jan
Callewaert, Nico
author_facet Lin, Yao-Cheng
Boone, Morgane
Meuris, Leander
Lemmens, Irma
Van Roy, Nadine
Soete, Arne
Reumers, Joke
Moisse, Matthieu
Plaisance, Stéphane
Drmanac, Radoje
Chen, Jason
Speleman, Frank
Lambrechts, Diether
Van de Peer, Yves
Tavernier, Jan
Callewaert, Nico
author_sort Lin, Yao-Cheng
collection PubMed
description The HEK293 human cell lineage is widely used in cell biology and biotechnology. Here we use whole-genome resequencing of six 293 cell lines to study the dynamics of this aneuploid genome in response to the manipulations used to generate common 293 cell derivatives, such as transformation and stable clone generation (293T); suspension growth adaptation (293S); and cytotoxic lectin selection (293SG). Remarkably, we observe that copy number alteration detection could identify the genomic region that enabled cell survival under selective conditions (i.c. ricin selection). Furthermore, we present methods to detect human/vector genome breakpoints and a user-friendly visualization tool for the 293 genome data. We also establish that the genome structure composition is in steady state for most of these cell lines when standard cell culturing conditions are used. This resource enables novel and more informed studies with 293 cells, and we will distribute the sequenced cell lines to this effect.
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spelling pubmed-41666782014-09-22 Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations Lin, Yao-Cheng Boone, Morgane Meuris, Leander Lemmens, Irma Van Roy, Nadine Soete, Arne Reumers, Joke Moisse, Matthieu Plaisance, Stéphane Drmanac, Radoje Chen, Jason Speleman, Frank Lambrechts, Diether Van de Peer, Yves Tavernier, Jan Callewaert, Nico Nat Commun Article The HEK293 human cell lineage is widely used in cell biology and biotechnology. Here we use whole-genome resequencing of six 293 cell lines to study the dynamics of this aneuploid genome in response to the manipulations used to generate common 293 cell derivatives, such as transformation and stable clone generation (293T); suspension growth adaptation (293S); and cytotoxic lectin selection (293SG). Remarkably, we observe that copy number alteration detection could identify the genomic region that enabled cell survival under selective conditions (i.c. ricin selection). Furthermore, we present methods to detect human/vector genome breakpoints and a user-friendly visualization tool for the 293 genome data. We also establish that the genome structure composition is in steady state for most of these cell lines when standard cell culturing conditions are used. This resource enables novel and more informed studies with 293 cells, and we will distribute the sequenced cell lines to this effect. Nature Publishing Group 2014-09-03 /pmc/articles/PMC4166678/ /pubmed/25182477 http://dx.doi.org/10.1038/ncomms5767 Text en Copyright © 2014, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Article
Lin, Yao-Cheng
Boone, Morgane
Meuris, Leander
Lemmens, Irma
Van Roy, Nadine
Soete, Arne
Reumers, Joke
Moisse, Matthieu
Plaisance, Stéphane
Drmanac, Radoje
Chen, Jason
Speleman, Frank
Lambrechts, Diether
Van de Peer, Yves
Tavernier, Jan
Callewaert, Nico
Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
title Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
title_full Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
title_fullStr Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
title_full_unstemmed Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
title_short Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
title_sort genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166678/
https://www.ncbi.nlm.nih.gov/pubmed/25182477
http://dx.doi.org/10.1038/ncomms5767
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