• DocumentCode
    3128149
  • Title

    Molecular Cloning and Nucleotide Sequence Analysis of the Newly Identified UL53 Gene of Duck Enteritis Virus

  • Author

    Shunchuan Zhang ; Anchun Cheng ; Mingshu Wang ; Jun Xiang

  • Author_Institution
    Avian Disease Res. Center, Sichuan Agric. Univ., Ya´an, China
  • fYear
    2010
  • fDate
    18-20 June 2010
  • Firstpage
    1
  • Lastpage
    6
  • Abstract
    Duck enteritis virus (DEV) is an alphaherpesvirinae that causes an acute, contagious, and fatal disease. In this study, the DEV-ULS3 gene from Key Laboratory of Animal Disease and Human Health of Sichuan Province was cloned and sequenced. Nucleotide sequence analysis revealed a 1032 bp open reading frame (ORF) theoretically encoding a 343-amino acid polypeptide was homologous to UL53 gene of alphaherpesvirinaes but there was just a predicted 226aa peptide , which could be expressed facilely, by using GENSCAN. The DEV-ULS3 gene had a base composition of 270 adenine (26.2%), 206cytosine (20.0%), 232 guanine (22.5%) and 324 thymine (31.4%). Compared with the ULS3 gene of other alphaherpesvirinaes, the DEV-ULS3 gene had a close evolutionary relationship with members of the Mardivirus genus. Therefore, the phylogenetic tree of ULS3 might be used as a basis for DEV classification. In conclusion, all data will provide a basis for further functional analysis of the DEV-ULS3 gene.
  • Keywords
    agriculture; bioinformatics; biological techniques; diseases; evolution (biological); evolutionary computation; genetics; microorganisms; molecular biophysics; DEV-ULS3 gene; GENSCAN; Mardivirus genus; UL53 gene; duck enteritis virus; molecular cloning; nucleotide sequence analysis; open reading frame; phylogenetic tree; polypeptide; Animals; Classification tree analysis; Cloning; Diseases; Encoding; Humans; Laboratories; Peptides; Phylogeny; Sequences;
  • 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.2010.5516769
  • Filename
    5516769