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Complete genomic sequence of Epstein-Barr virus in nasopharyngeal carcinoma cell line C666-1.
Tso, Ken Kai-Yuen; Yip, Kevin Yuk-Lap; Mak, Cathy Ka-Yan; Chung, Grace Tin-Yun; Lee, Sau-Dan; Cheung, Siu-Tim; To, Ka-Fai; Lo, Kwok-Wai.
Afiliação
  • Tso KK; Department of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Yip KY; Department of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Mak CK; 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 GT; 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.
  • Lee SD; Li Ka Shing Institute of Health Science, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • Cheung ST; Department of Computer Science and Engineering, The Chinese University of Hong Kong, Hong Kong SAR, China.
  • To KF; Department of Surgery, University of Hong Kong, Hong Kong SAR, China.
  • Lo KW; 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.
Infect Agent Cancer ; 8(1): 29, 2013 Aug 02.
Article em En | MEDLINE | ID: mdl-23915735
ABSTRACT

BACKGROUND:

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.

OBJECTIVE:

To determine the complete EBV genome sequence in C666-1 cells.

METHODS:

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.

RESULTS:

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.

CONCLUSION:

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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2013 Tipo de documento: Article