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The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq.
Shi, Yingying; Tu, Huilin; Chen, Xiong; Zhang, Yingying; Chen, Liujun; Liu, Zhongchun; Sheng, Jiqun; Han, Song; Yin, Jun; Peng, Biwen; He, Xiaohua; Liu, Wanhong.
Affiliation
  • Shi Y; Pathogenic Organism and Infectious Diseases Research Institute, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
  • Tu H; Hubei Province Key Laboratory of Allergy and Immunology, Wuhan, 430071, China.
  • Chen X; Pathogenic Organism and Infectious Diseases Research Institute, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
  • Zhang Y; Pathogenic Organism and Infectious Diseases Research Institute, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
  • Chen L; Pathogenic Organism and Infectious Diseases Research Institute, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
  • Liu Z; Pathogenic Organism and Infectious Diseases Research Institute, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
  • Sheng J; Institute of Neuropsychiatry, Renmin Hospital, Wuhan University, Wuhan, 430060, China.
  • Han S; College of Life Science and Technology, Hubei Engineering University, Xiaogan, 432000, China.
  • Yin J; Pathogenic Organism and Infectious Diseases Research Institute, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
  • Peng B; Pathogenic Organism and Infectious Diseases Research Institute, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
  • He X; Pathogenic Organism and Infectious Diseases Research Institute, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
  • Liu W; Hubei Provincial Key Laboratory of Developmentally Originated Disease, School of Basic Medical Sciences, Wuhan University, Wuhan, 430071, China.
Virol Sin ; 31(2): 131-41, 2016 Apr.
Article in En | MEDLINE | ID: mdl-27060091
ABSTRACT
Coxsackievirus A16 (CVA16) is one of major pathogens of hand, foot and mouth disease (HFMD) in children. Long non-coding RNAs (IncRNAs) have been implicated in various biological processes, but they have not been associated with CVA16 infection. In this study, we comprehensively characterized the landscape of IncRNAs of normal and CVA16 infected rhabdomyosarcoma (RD) cells using RNA-Seq to investigate the functional relevance of IncRNAs. We showed that a total of 760 IncRNAs were upregulated and 1210 IncRNAs were downregulated. Out of these dysregulated IncRNAs, 43.64% were intergenic, 22.31% were sense, 15.89% were intronic, 8.67% were bidirectional, 5.59% were antisense, 3.85% were sRNA host IncRNAs and 0.05% were enhancer. Six dysregulated IncRNAs were validated by quantitative PCR assays and the secondary structures of these IncRNAs were projected. Moreover, we conducted a bioinformatics analysis of an IncRNAs (ENST00000602478) to elucidate the diversity of modification and functions of IncRNAs. In summary, the current study compared the dysregulated IncRNAs profile upon CVA16 challenge and illustrated the intricate relationship between coding and IncRNAs transcripts. These results may not only provide a complete picture of transcription in CVA16 infected cells but also provide novel molecular targets for treatments of HFMD.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Enterovirus / Coxsackievirus Infections / RNA, Long Noncoding Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Virol Sin Journal subject: VIROLOGIA Year: 2016 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Enterovirus / Coxsackievirus Infections / RNA, Long Noncoding Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Virol Sin Journal subject: VIROLOGIA Year: 2016 Document type: Article Affiliation country: China