Home LiteratureArticle Details
PMID: 23915735 Published · epublish English Journal Article

Complete genomic sequence of Epstein-Barr virus in nasopharyngeal carcinoma cell line C666-1.

Infectious agents and cancer ·Vol. 8 ·No. 1 ·2013-08-02 ·Pages 29

Tso KK, Yip KY, Mak CK, Chung GT, Lee SD, Cheung ST, To KF, Lo KW

Abstract

Nasopharyngeal carcinoma is a distinct type of head and neck cancer which is consistently associated with Epstein-Barr virus (EBV). The C666-1 cell line is the only in vitro native EBV-infected NPC cell model commonly used for study of the viral-host interaction. Nevertheless, the complete EBV genome sequence in this in vitro EBV-infected NPC model has not been characterized. To determine the complete EBV genome sequence in C666-1 cells. The C666-1 genome was sequenced by 100-bases pair-end massive parallel sequencing. Bioinformatics analysis was performed to extract the EBV sequences and construct an EBV consensus sequence map. PCR amplification and Sanger DNA sequencing were used for sequence validation and gap filling. A phylogenetic analysis of EBV strain in C666-1 cells and other reported EBV strains was performed. A 171,317 bp complete EBV genome of C666-1 was successfully constructed (GenBank accession number: KC617875). Phylogenetic analysis of EBV genome in C666-1 revealed that the C666-1 EBV strain is closely related to the reported strains in NPC primary tumors. C666-1 contains a representative NPC-associated EBV genome and might serve as an important model for studying the roles or function of viral proteins in NPC tumorigenesis.

Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Tso Ken Kai-Yuen
Department of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.
Yip Kevin Yuk-Lap
Department of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.
Mak Cathy Ka-Yan
Department of Anatomical and Cellular Pathology, State Key Laboratory in Oncology in South China, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China.
Chung Grace Tin-Yun
Department of Anatomical and Cellular Pathology, State Key Laboratory in Oncology in South China, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China. | Li Ka Shing Institute of Health Science, The Chinese University of Hong Kong, Hong Kong SAR, China.
Lee Sau-Dan
Department of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.
Cheung Siu-Tim
Department of Surgery, University of Hong Kong, Hong Kong SAR, China.
To Ka-Fai
Department of Anatomical and Cellular Pathology, State Key Laboratory in Oncology in South China, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China. | Li Ka Shing Institute of Health Science, The Chinese University of Hong Kong, Hong Kong SAR, China.
Lo Kwok-Wai
Department of Anatomical and Cellular Pathology, State Key Laboratory in Oncology in South China, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong SAR, China. | Li Ka Shing Institute of Health Science, The Chinese University of Hong Kong, Hong Kong SAR, China.
References (12)
12 references, click to expand
  1. Nasopharyngeal carcinoma cell line (C666-1) consistently harbouring Epstein-Barr virus.
    Int J Cancer. 1999 Sep 24;83(1):121-6 PMID: 10449618
  2. A transforming KIF5B and RET gene fusion in lung adenocarcinoma revealed from whole-genome and transcriptome sequencing.
    Genome Res. 2012 Mar;22(3):436-45 PMID: 22194472
  3. Potential selection of LMP1 variants in nasopharyngeal carcinoma.
    J Virol. 2004 Jan;78(2):868-81 PMID: 14694118
  4. Genomic sequencing and comparative analysis of Epstein-Barr virus genome isolated from primary nasopharyngeal carcinoma biopsy.
    PLoS One. 2012;7(5):e36939 PMID: 22590638
  5. Specific latent membrane protein 1 gene sequences in type 1 and type 2 Epstein-Barr virus from nasopharyngeal carcinoma in Hong Kong.
    Int J Cancer. 1998 May 4;76(3):399-406 PMID: 9579578
  6. Epstein-Barr virus BNRF1 protein allows efficient transfer from the endosomal compartment to the nucleus of primary B lymphocytes.
    J Virol. 2006 Oct;80(19):9435-43 PMID: 16973549
  7. Modulation of LMP2A expression by a newly identified Epstein-Barr virus-encoded microRNA miR-BART22.
    Neoplasia. 2009 Nov;11(11):1174-84 PMID: 19881953
  8. EBV tegument protein BNRF1 disrupts DAXX-ATRX to activate viral early gene transcription.
    PLoS Pathog. 2011 Nov;7(11):e1002376 PMID: 22102817
  9. Direct sequencing and characterization of a clinical isolate of Epstein-Barr virus from nasopharyngeal carcinoma tissue by using next-generation sequencing technology.
    J Virol. 2011 Nov;85(21):11291-9 PMID: 21880770
  10. Re: Discrete alterations in the BZLF1 promoter in tumor and non-tumor-associated Epstein-Barr virus.
    J Natl Cancer Inst. 2003 Jul 2;95(13):1008-9; author reply 1009 PMID: 12837838
  11. Modulation of LMP1 protein expression by EBV-encoded microRNAs.
    Proc Natl Acad Sci U S A. 2007 Oct 9;104(41):16164-9 PMID: 17911266
  12. Deciphering the molecular genetic basis of NPC through molecular, cytogenetic, and epigenetic approaches.
    Semin Cancer Biol. 2012 Apr;22(2):79-86 PMID: 22245473
Article Info
Journal
Infectious agents and cancer
Abbr.
Infect Agent Cancer
ISSN
1750-9378
Published
2013-08-02
Epub
2013-00-02
Pages
29
Language
English
Region
England
NLM ID
101276559
PMCID
PMC3734220
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