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

Yao‐Cheng Lin(VIB-UGent Center for Plant Systems Biology), Morgane Boone(VIB-UGent Center for Inflammation Research), Leander Meuris(VIB-UGent Center for Inflammation Research), Irma Lemmens(VIB-UGent Center for Medical Biotechnology), Nadine Van Roy(Ghent University Hospital), Arne Soete(VIB-UGent Center for Inflammation Research), Joke Reumers(KU Leuven), Matthieu Moisse(KU Leuven), Stéphane Plaisance, Radoje Drmanac(Complete Genomics (United States)), Jason Chen(Complete Genomics (United States)), Frank Speleman(Ghent University Hospital), Diether Lambrechts(KU Leuven), Yves Van de Peer(Ghent University), Jan Tavernier(Ghent University), Nico Callewaert(Ghent University)
Nature Communications
September 3, 2014
Cited by 588Open Access
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Abstract

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. The human embryonic kidney 293 (HEK293) cell lineage is widely used in cell biology and biotechnology. Here, the authors apply whole genome resequencing methods to characterise genomic variation in six HEK293 cell lines and suggest that this variation could affect experiments using these cell lines.


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