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The Genomic and Transcriptomic Landscape of a HeLa Cell Line

HeLa is the most widely used model cell line for studying human cellular and molecular biology. To date, no genomic reference for this cell line has been released, and experiments have relied on the human reference genome. Effective design and interpretation of molecular genetic studies performed us...

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Autores principales: Landry, Jonathan J. M., Pyl, Paul Theodor, Rausch, Tobias, Zichner, Thomas, Tekkedil, Manu M., Stütz, Adrian M., Jauch, Anna, Aiyar, Raeka S., Pau, Gregoire, Delhomme, Nicolas, Gagneur, Julien, Korbel, Jan O., Huber, Wolfgang, Steinmetz, Lars M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737162/
https://www.ncbi.nlm.nih.gov/pubmed/23550136
http://dx.doi.org/10.1534/g3.113.005777
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author Landry, Jonathan J. M.
Pyl, Paul Theodor
Rausch, Tobias
Zichner, Thomas
Tekkedil, Manu M.
Stütz, Adrian M.
Jauch, Anna
Aiyar, Raeka S.
Pau, Gregoire
Delhomme, Nicolas
Gagneur, Julien
Korbel, Jan O.
Huber, Wolfgang
Steinmetz, Lars M.
author_facet Landry, Jonathan J. M.
Pyl, Paul Theodor
Rausch, Tobias
Zichner, Thomas
Tekkedil, Manu M.
Stütz, Adrian M.
Jauch, Anna
Aiyar, Raeka S.
Pau, Gregoire
Delhomme, Nicolas
Gagneur, Julien
Korbel, Jan O.
Huber, Wolfgang
Steinmetz, Lars M.
author_sort Landry, Jonathan J. M.
collection PubMed
description HeLa is the most widely used model cell line for studying human cellular and molecular biology. To date, no genomic reference for this cell line has been released, and experiments have relied on the human reference genome. Effective design and interpretation of molecular genetic studies performed using HeLa cells require accurate genomic information. Here we present a detailed genomic and transcriptomic characterization of a HeLa cell line. We performed DNA and RNA sequencing of a HeLa Kyoto cell line and analyzed its mutational portfolio and gene expression profile. Segmentation of the genome according to copy number revealed a remarkably high level of aneuploidy and numerous large structural variants at unprecedented resolution. Some of the extensive genomic rearrangements are indicative of catastrophic chromosome shattering, known as chromothripsis. Our analysis of the HeLa gene expression profile revealed that several pathways, including cell cycle and DNA repair, exhibit significantly different expression patterns from those in normal human tissues. Our results provide the first detailed account of genomic variants in the HeLa genome, yielding insight into their impact on gene expression and cellular function as well as their origins. This study underscores the importance of accounting for the strikingly aberrant characteristics of HeLa cells when designing and interpreting experiments, and has implications for the use of HeLa as a model of human biology.
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spelling pubmed-37371622013-08-08 The Genomic and Transcriptomic Landscape of a HeLa Cell Line Landry, Jonathan J. M. Pyl, Paul Theodor Rausch, Tobias Zichner, Thomas Tekkedil, Manu M. Stütz, Adrian M. Jauch, Anna Aiyar, Raeka S. Pau, Gregoire Delhomme, Nicolas Gagneur, Julien Korbel, Jan O. Huber, Wolfgang Steinmetz, Lars M. G3 (Bethesda) Investigations HeLa is the most widely used model cell line for studying human cellular and molecular biology. To date, no genomic reference for this cell line has been released, and experiments have relied on the human reference genome. Effective design and interpretation of molecular genetic studies performed using HeLa cells require accurate genomic information. Here we present a detailed genomic and transcriptomic characterization of a HeLa cell line. We performed DNA and RNA sequencing of a HeLa Kyoto cell line and analyzed its mutational portfolio and gene expression profile. Segmentation of the genome according to copy number revealed a remarkably high level of aneuploidy and numerous large structural variants at unprecedented resolution. Some of the extensive genomic rearrangements are indicative of catastrophic chromosome shattering, known as chromothripsis. Our analysis of the HeLa gene expression profile revealed that several pathways, including cell cycle and DNA repair, exhibit significantly different expression patterns from those in normal human tissues. Our results provide the first detailed account of genomic variants in the HeLa genome, yielding insight into their impact on gene expression and cellular function as well as their origins. This study underscores the importance of accounting for the strikingly aberrant characteristics of HeLa cells when designing and interpreting experiments, and has implications for the use of HeLa as a model of human biology. Genetics Society of America 2013-03-11 /pmc/articles/PMC3737162/ /pubmed/23550136 http://dx.doi.org/10.1534/g3.113.005777 Text en Copyright © 2013 Landry et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Landry, Jonathan J. M.
Pyl, Paul Theodor
Rausch, Tobias
Zichner, Thomas
Tekkedil, Manu M.
Stütz, Adrian M.
Jauch, Anna
Aiyar, Raeka S.
Pau, Gregoire
Delhomme, Nicolas
Gagneur, Julien
Korbel, Jan O.
Huber, Wolfgang
Steinmetz, Lars M.
The Genomic and Transcriptomic Landscape of a HeLa Cell Line
title The Genomic and Transcriptomic Landscape of a HeLa Cell Line
title_full The Genomic and Transcriptomic Landscape of a HeLa Cell Line
title_fullStr The Genomic and Transcriptomic Landscape of a HeLa Cell Line
title_full_unstemmed The Genomic and Transcriptomic Landscape of a HeLa Cell Line
title_short The Genomic and Transcriptomic Landscape of a HeLa Cell Line
title_sort genomic and transcriptomic landscape of a hela cell line
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737162/
https://www.ncbi.nlm.nih.gov/pubmed/23550136
http://dx.doi.org/10.1534/g3.113.005777
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