• DocumentCode
    619341
  • Title

    Identifying hsa-miR-122 target sites in HCV isolate JFH-1

  • Author

    Sim-Hui Tee ; Quek, Albert

  • Author_Institution
    Multimedia Univ., Cyberjaya, Malaysia
  • fYear
    2013
  • fDate
    7-9 April 2013
  • Firstpage
    863
  • Lastpage
    868
  • Abstract
    MicroRNAs are short regulatory genes that regulate the gene expression in various cellular activities and pathways. Identification of microRNA target site is important for the understanding of pathogenesis and cellular functions. This study applies a computational approach to identify hsa-miR-122 target sites in hepatitis C virus isolate JFH-1. The minimum free energy, seed region complementarity, and 3´ region complementarity were taken as the determining factors for the binding affinity. We have identified a total of four hsa-miR-122 target sites. The identified target sites can be used in therapy strategies and drug designs for hepatocellular carcinoma and hepatitis C.
  • Keywords
    RNA; cellular biophysics; free energy; genetics; microorganisms; molecular biophysics; 3´ region complementarity; HCV iusolate; JFH-1; binding affinity; cellular activities; cellular functions; computational approach; drug designs; gene expression; hepatitis C virus; hepatocellular carcinoma; hsa-miR-122 target site identification; microRNAs; minimum free energy; pathogenesis; pathways; seed region complementarity; short regulatory genes; therapy strategies; Bioinformatics; Cancer; DNA; Immune system; Lungs; RNA; Viruses (medical); bioinformatics; hepatitic C virus; microRNA;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Business Engineering and Industrial Applications Colloquium (BEIAC), 2013 IEEE
  • Conference_Location
    Langkawi
  • Print_ISBN
    978-1-4673-5967-2
  • Type

    conf

  • DOI
    10.1109/BEIAC.2013.6560259
  • Filename
    6560259