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

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dc.contributor.author Lin, Yao-Cheng
dc.contributor.author Boone, Morgane
dc.contributor.author Meuris, Leander
dc.contributor.author Lemmens, Irma
dc.contributor.author Van Roy, Nadine
dc.contributor.author Soete, Arne
dc.contributor.author Reumers, Joke
dc.contributor.author Moisse, Matthieu
dc.contributor.author Plaisance, Stéphane
dc.contributor.author Drmanac, Radoje
dc.contributor.author Chen, Jason
dc.contributor.author Speleman, Frank
dc.contributor.author Lambrechts, Diether
dc.contributor.author Van de Peer, Yves
dc.contributor.author Tavernier, Jan
dc.contributor.author Callewaert, Nico
dc.date.accessioned 2014-11-04T08:57:52Z
dc.date.available 2014-11-04T08:57:52Z
dc.date.issued 2014-09
dc.description.abstract The HEK293 human cell lineage is widely used in cell biology and biotechnology. We here 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. en_US
dc.description.librarian hb2014 en_US
dc.description.uri http://www.nature.com/naturecommunications en_US
dc.identifier.citation Lin, Y-C, Boone, M, Meuris, L, Lemmens, I, Van Roy, N, Soete, A, Reumers, J, Moisse, M, Plaisance, S, Drmanac, R, Chen, J, Speleman, F, Lambrechts, D, Van De Peer, Y, Tavernier, J & Callewaert, N 2014, 'Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations', Nature Communications, vol. 5, art. #4767, pp. 1-12. en_US
dc.identifier.issn 1934-578X (print)
dc.identifier.issn 1555-9475 (online)
dc.identifier.other 10.1038/ncomms5767
dc.identifier.uri http://hdl.handle.net/2263/42484
dc.language.iso en en_US
dc.publisher Natural Product en_US
dc.rights © 2014 Macmillan Publishers Limited. All rights reserved. This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. en_US
dc.subject Genome dynamics en_US
dc.subject Cell biology manipulations en_US
dc.subject Human embryonic kidney (HEK) 293 en_US
dc.title Genome dynamics of the human embryonic kidney 293 lineage in response to cell biology manipulations en_US
dc.type Article en_US


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