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
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