• DocumentCode
    3115612
  • Title

    Molecular Cloning and Sequence Analysis of the Duck Plague Virus gI Gene

  • Author

    Li, Lijuan ; Cheng, Anchun ; Wang, Mingshu ; Zhu, Dekang ; Jia, Renyong ; Luo, Qihui ; Cui, Hengmin ; Zhou, Yi ; Wang, Yin ; Xu, Zhiwen ; Chen, Zhengli ; Chen, Xiaoyue ; Wang, Xiaoyu

  • Author_Institution
    Avian Diseases Res. Center, Sichuan Agric. Univ., Yaan, China
  • fYear
    2010
  • fDate
    18-20 June 2010
  • Firstpage
    1
  • Lastpage
    6
  • Abstract
    The glycoprotein I (gI) gene homologue of duck plague virus (DPV) was cloned by degenerate polymerase chain reaction (PCR) and sequenced. DPV gI gene open reading frame (ORF) was 1116 bp in length and its primary translation product was a polypeptide of 371 amino acids long. Comparison with other herpesvirus revealed higher similarity, had a close evolution relationship with members of the genus Mardivirus which consisted of MeHV-1, GaHV-2 and GaHV-3, but itself branched and was independent to others. It possessed several characteristics of membrane glycoproteins, including an N-terminal hydrophobic signal peptide, an external domain containing 3 putative N-linked glycosylation sites, a C-terminal transmembrane domain, and a charged cytoplasmic tail. Moreover, gI protein of DPV contained 19 potention phosphorylation sites, 13 epitopes, a YY-motif, principally located in endoplasmic reticulum (55.6%). We inffered that DPV gI protein had good immunogenicity and probably linked to virion sorting and promoting direct cell-to-cell spread in polarized cells .
  • Keywords
    biochemistry; biological techniques; cellular biophysics; genetics; microorganisms; molecular biophysics; proteins; C-terminal transmembrane; DPV gI gene; Mardivirus; amino acids; cytoplasmic tail; degenerate polymerase chain reaction; duck plague virus; endoplasmic reticulum; glycoprotein I; glycosylation; hydrophobic signal peptide; immunogenicity; molecular cloning; open reading frame; phosphorylation; sequence analysis; Amino acids; Biomembranes; Cloning; Immune system; Peptides; Polymers; Proteins; Sequences; Sorting; Tail;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
  • Conference_Location
    Chengdu
  • ISSN
    2151-7614
  • Print_ISBN
    978-1-4244-4712-1
  • Electronic_ISBN
    2151-7614
  • Type

    conf

  • DOI
    10.1109/ICBBE.2010.5516186
  • Filename
    5516186