Home LiteratureArticle Details
PMID: 23550136 Published · epublish English Journal Article Research Support, Non-U.S. Gov't

The genomic and transcriptomic landscape of a HeLa cell line.

G3 (Bethesda, Md.) ·Vol. 3 ·No. 8 ·2013-08-07 ·Pages 1213-24

Landry JJ, Pyl PT, Rausch T, Zichner T, Tekkedil MM, Stütz AM, Jauch A, Aiyar RS, Pau G, Delhomme N, Gagneur J, Korbel JO, Huber W, Steinmetz LM

Abstract

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.

Keywords
HeLa cell line genomics resource transcriptomics variation
MeSH Terms
Alleles DNA Copy Number Variations Databases, Genetic Gene Frequency Genome, Human Genomics HeLa Cells Humans Models, Biological Mutation RNA Interference Sequence Analysis, DNA Sequence Analysis, RNA Transcriptome
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Landry Jonathan J M
European Molecular Biology Laboratory, Genome Biology Unit, 69117 Heidelberg, Germany.
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
References (81)
81 references, click to expand
  1. Post-transcriptional processing generates a diversity of 5'-modified long and short RNAs.
    Nature. 2009 Feb 19;457(7232):1028-32 PMID: 19169241
  2. Phenotypic profiling of the human genome by time-lapse microscopy reveals cell division genes.
    Nature. 2010 Apr 1;464(7289):721-7 PMID: 20360735
  3. Multiplex-fluorescence in situ hybridization for chromosome karyotyping.
    Nat Protoc. 2006;1(3):1172-84 PMID: 17406400
  4. The band patterns of twelve D 98-AH-2 marker chromosomes and their use for identification of intraspecific cell hybrids.
    Chromosoma. 1973;41(1):111-21 PMID: 4120821
  5. Noncanonical transcript forms in yeast and their regulation during environmental stress.
    RNA. 2010 Jun;16(6):1256-67 PMID: 20421314
  6. Histone deacetylase activity modulates alternative splicing.
    PLoS One. 2011 Feb 02;6(2):e16727 PMID: 21311748
  7. Analysis of loss of heterozygosity on chromosome 11 and infrequent inactivation of the MEN1 gene in sporadic pituitary adenomas.
    J Clin Endocrinol Metab. 1998 Aug;83(8):2631-4 PMID: 9709923
  8. Mapping of nasopharyngeal carcinoma tumor-suppressive activity to a 1.8-megabase region of chromosome band 11q13.
    Genes Chromosomes Cancer. 2002 May;34(1):97-103 PMID: 11921287
  9. Multiple genetic alterations cause frequent and heterogeneous human histocompatibility leukocyte antigen class I loss in cervical cancer.
    J Exp Med. 2000 Mar 20;191(6):961-76 PMID: 10727458
  10. Chromothripsis and human disease: piecing together the shattering process.
    Cell. 2012 Jan 20;148(1-2):29-32 PMID: 22265399
  11. DELLY: structural variant discovery by integrated paired-end and split-read analysis.
    Bioinformatics. 2012 Sep 15;28(18):i333-i339 PMID: 22962449
  12. Suppression of tumorigenicity in somatic cell hybrids. III. Cosegregation of human chromosome 11 of a normal cell and suppression of tumorigenicity in intraspecies hybrids of normal diploid x malignant cells.
    Cytogenet Cell Genet. 1986;41(2):65-70 PMID: 3956263
  13. Gene expression profiling of HeLa cells in G1 or G2 phases.
    Oncogene. 2002 Mar 14;21(12):1934-42 PMID: 11896627
  14. Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer.
    Oncogene. 2002 Aug 15;21(36):5631-42 PMID: 12165862
  15. Chromothripsis identifies a rare and aggressive entity among newly diagnosed multiple myeloma patients.
    Blood. 2011 Jul 21;118(3):675-8 PMID: 21628407
  16. Deep proteome and transcriptome mapping of a human cancer cell line.
    Mol Syst Biol. 2011 Nov 08;7:548 PMID: 22068331
  17. Role of viral factor E3L in modified vaccinia virus ankara infection of human HeLa Cells: regulation of the virus life cycle and identification of differentially expressed host genes.
    J Virol. 2005 Feb;79(4):2584-96 PMID: 15681458
  18. Complex landscapes of somatic rearrangement in human breast cancer genomes.
    Nature. 2009 Dec 24;462(7276):1005-10 PMID: 20033038
  19. Normal human chromosome 11 suppresses tumorigenicity of human cervical tumor cell line SiHa.
    Mol Carcinog. 1989;2(1):12-21 PMID: 2730761
  20. Enhancement of cell proliferation in various mammalian cell lines by gene insertion of a cyclin-dependent kinase homolog.
    BMC Biotechnol. 2007 Oct 18;7:71 PMID: 17945021
  21. An integrated map of genetic variation from 1,092 human genomes.
    Nature. 2012 Nov 1;491(7422):56-65 PMID: 23128226
  22. Hallmarks of cancer: the next generation.
    Cell. 2011 Mar 4;144(5):646-74 PMID: 21376230
  23. SIFT: Predicting amino acid changes that affect protein function.
    Nucleic Acids Res. 2003 Jul 1;31(13):3812-4 PMID: 12824425
  24. Aurora B-mediated abscission checkpoint protects against tetraploidization.
    Cell. 2009 Feb 6;136(3):473-84 PMID: 19203582
  25. Chromosomal integration sites of human papillomavirus DNA in three cervical cancer cell lines mapped by in situ hybridization.
    Med Microbiol Immunol. 1987;176(5):245-56 PMID: 2821369
  26. Re-evaluation of HeLa, HeLa S3, and HEp-2 karyotypes.
    Cytogenet Cell Genet. 1988;48(1):19-24 PMID: 3180844
  27. Genomic alterations in cervical carcinoma: losses of chromosome heterozygosity and human papilloma virus tumor status.
    Cancer Res. 1996 Jan 1;56(1):197-205 PMID: 8548763
  28. Diverse and specific gene expression responses to stresses in cultured human cells.
    Mol Biol Cell. 2004 May;15(5):2361-74 PMID: 15004229
  29. Functional analysis of human microtubule-based motor proteins, the kinesins and dyneins, in mitosis/cytokinesis using RNA interference.
    Mol Biol Cell. 2005 Jul;16(7):3187-99 PMID: 15843429
  30. On the nature of heteroploidy.
    Cold Spring Harb Symp Quant Biol. 1974;38:133-44 PMID: 4133981
  31. Specific chromosome loss associated with the expression of tumorigenicity in human cell hybrids.
    Somatic Cell Genet. 1981 Nov;7(6):699-712 PMID: 7323948
  32. Studies on the propagation in vitro of poliomyelitis viruses. IV. Viral multiplication in a stable strain of human malignant epithelial cells (strain HeLa) derived from an epidermoid carcinoma of the cervix.
    J Exp Med. 1953 May;97(5):695-710 PMID: 13052828
  33. dbSNP: the NCBI database of genetic variation.
    Nucleic Acids Res. 2001 Jan 1;29(1):308-11 PMID: 11125122
  34. Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion.
    Nat Genet. 2011 Sep 04;43(10):964-968 PMID: 21892161
  35. Frequent HLA class I loss is an early event in cervical carcinogenesis.
    Hum Immunol. 2005 Nov;66(11):1167-73 PMID: 16571417
  36. Introduction of human chromosome 11 via microcell transfer controls tumorigenic expression of HeLa cells.
    EMBO J. 1986 Dec 20;5(13):3461-6 PMID: 2881780
  37. HeLa D98/aH-2 studied by chromosome painting and conventional cytogenetical techniques.
    Chromosoma. 1993 Jul;102(7):473-7 PMID: 7690695
  38. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
    Genome Res. 2010 Sep;20(9):1297-303 PMID: 20644199
  39. Repbase Update, a database of eukaryotic repetitive elements.
    Cytogenet Genome Res. 2005;110(1-4):462-7 PMID: 16093699
  40. Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer.
    Genome Biol. 2011 Oct 19;12(10):R103 PMID: 22014273
  41. Landscape of transcription in human cells.
    Nature. 2012 Sep 6;489(7414):101-8 PMID: 22955620
  42. Transfer of a normal human chromosome 11 suppresses tumorigenicity of some but not all tumor cell lines.
    J Cell Biochem. 1990 Mar;42(3):135-42 PMID: 2318911
  43. Gene ontology: tool for the unification of biology. The Gene Ontology Consortium.
    Nat Genet. 2000 May;25(1):25-9 PMID: 10802651
  44. Model-based gene set analysis for Bioconductor.
    Bioinformatics. 2011 Jul 1;27(13):1882-3 PMID: 21561920
  45. Poly A- transcripts expressed in HeLa cells.
    PLoS One. 2008 Jul 30;3(7):e2803 PMID: 18665230
  46. Dissecting the genomic complexity underlying medulloblastoma.
    Nature. 2012 Aug 2;488(7409):100-5 PMID: 22832583
  47. National center for biotechnology information viral genomes project.
    J Virol. 2004 Jul;78(14):7291-8 PMID: 15220402
  48. Genome-wide analysis of human kinases in clathrin- and caveolae/raft-mediated endocytosis.
    Nature. 2005 Jul 7;436(7047):78-86 PMID: 15889048
  49. Circos: an information aesthetic for comparative genomics.
    Genome Res. 2009 Sep;19(9):1639-45 PMID: 19541911
  50. Cervical carcinoma-associated fibroblasts are DNA diploid and do not show evidence for somatic genetic alterations.
    Cell Oncol (Dordr). 2011 Dec;34(6):553-63 PMID: 22042555
  51. Massive genomic rearrangement acquired in a single catastrophic event during cancer development.
    Cell. 2011 Jan 7;144(1):27-40 PMID: 21215367
  52. Deletion of chromosome 11 and of 14q sequences in neuroblastoma.
    Genes Chromosomes Cancer. 1993 May;7(1):32-7 PMID: 7688553
  53. Deletion mapping of endocrine tumors localizes a second tumor suppressor gene on chromosome band 11q13.
    Genes Chromosomes Cancer. 1998 Jun;22(2):130-7 PMID: 9598800
  54. Differential expression analysis for sequence count data.
    Genome Biol. 2010;11(10):R106 PMID: 20979621
  55. Fast and SNP-tolerant detection of complex variants and splicing in short reads.
    Bioinformatics. 2010 Apr 1;26(7):873-81 PMID: 20147302
  56. Identification of genes periodically expressed in the human cell cycle and their expression in tumors.
    Mol Biol Cell. 2002 Jun;13(6):1977-2000 PMID: 12058064
  57. The genomic complexity of primary human prostate cancer.
    Nature. 2011 Feb 10;470(7333):214-20 PMID: 21307934
  58. Allelotype analysis of cervical carcinoma.
    Cancer Res. 1994 Aug 15;54(16):4481-7 PMID: 8044799
  59. Accurate whole human genome sequencing using reversible terminator chemistry.
    Nature. 2008 Nov 6;456(7218):53-9 PMID: 18987734
  60. Ubiquitin-binding protein RAP80 mediates BRCA1-dependent DNA damage response.
    Science. 2007 May 25;316(5828):1202-5 PMID: 17525342
  61. Preferential sites for viral integration on mammalian genome.
    Cancer Genet Cytogenet. 1989 Oct 15;42(2):157-71 PMID: 2551486
  62. Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping.
    Cancer Res. 1999 Jan 1;59(1):141-50 PMID: 9892199
  63. An endoribonuclease-prepared siRNA screen in human cells identifies genes essential for cell division.
    Nature. 2004 Dec 23;432(7020):1036-40 PMID: 15616564
  64. Identical allelic loss on chromosome 11q13 in microdissected in situ and invasive human breast cancer.
    Cancer Res. 1995 Feb 1;55(3):467-71 PMID: 7834608
  65. Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads.
    Bioinformatics. 2009 Nov 1;25(21):2865-71 PMID: 19561018
  66. Relating CNVs to transcriptome data at fine resolution: assessment of the effect of variant size, type, and overlap with functional regions.
    Genome Res. 2011 Dec;21(12):2004-13 PMID: 21862627
  67. Loss of heterozygosity in squamous cell carcinomas of the head and neck defines a tumor suppressor gene region on 11q13.
    Cancer Genet Cytogenet. 1998 Jul 15;104(2):124-32 PMID: 9666806
  68. RNAiAtlas: a database for RNAi (siRNA) libraries and their specificity.
    Database (Oxford). 2012 Jun 14;2012:bas027 PMID: 22700939
  69. Characteristics of HeLa strains: permanent vs. variable features.
    Cytogenet Cell Genet. 1980;27(4):216-31 PMID: 7002488
  70. Paired-end mapping reveals extensive structural variation in the human genome.
    Science. 2007 Oct 19;318(5849):420-6 PMID: 17901297
  71. Analysis of gene expression profiles in HeLa cells in response to overexpression or siRNA-mediated depletion of NASP.
    Reprod Biol Endocrinol. 2009 May 13;7:45 PMID: 19439102
  72. Classification of human chromosome 21 gene-expression variations in Down syndrome: impact on disease phenotypes.
    Am J Hum Genet. 2007 Sep;81(3):475-91 PMID: 17701894
  73. HeLa cells and their possible contamination of other cell lines: karyotype studies.
    Hereditas. 1976 Jun 14;82(2):217-48 PMID: 985810
  74. Implication of chromosome 11 in the suppression of neoplastic expression in human cell hybrids.
    Cancer Res. 1986 Dec;46(12 Pt 1):6174-9 PMID: 2877730
  75. Clustering phenotype populations by genome-wide RNAi and multiparametric imaging.
    Mol Syst Biol. 2010 Jun 8;6:370 PMID: 20531400
  76. The International HapMap Project.
    Nature. 2003 Dec 18;426(6968):789-96 PMID: 14685227
  77. Transcriptome analysis by strand-specific sequencing of complementary DNA.
    Nucleic Acids Res. 2009 Oct;37(18):e123 PMID: 19620212
  78. Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.
    Cell. 2012 Jan 20;148(1-2):59-71 PMID: 22265402
  79. Cervical intraepithelial neoplasia III shows frequent allelic loss in 3p and 6p.
    Genes Chromosomes Cancer. 1998 May;22(1):57-65 PMID: 9591635
  80. Genomic responses to abnormal gene dosage: the X chromosome improved on a common strategy.
    PLoS Biol. 2010 Feb 23;8(2):e1000318 PMID: 20186268
  81. A faster circular binary segmentation algorithm for the analysis of array CGH data.
    Bioinformatics. 2007 Mar 15;23(6):657-63 PMID: 17234643
Article Info
Journal
G3 (Bethesda, Md.)
Abbr.
G3 (Bethesda)
ISSN
2160-1836
Published
2013-08-07
Epub
2013-00-07
Pages
1213-24
Language
English
Region
England
NLM ID
101566598
PMCID
PMC3737162
Subset
IM
Corrections
CommentIn
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com