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Cloning and Sequence of Glycoprotein H Gene of Duck Plague Virus
作者姓名:HAN  Xian-jie  WANG  Jun-wei  MA  Bo
作者单位:[1]Faculty of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, P.R. China [2]Faculty of Animal Science and Veterinary Medicine, Laiyang Agricultural College, Qingdao 266109, P.R. China
摘    要:The glycoprotein H (gH) gene homologue of duck plague virus (DPV) was cloned by degenerate polymerase chain reaction (PCR) and sequenced. It was located immediately downstream from the thymidine kinase gene (TK). In addition, the 3'-end of the gene homologue to herpesvirus UL21 was located downstream from the gH gene. DPV gH gene open reading frame (ORF) was 2 505 bp in length and its primary translation product was a polypeptide of 834 amino acids long. It possessed several characteristics of membrane glycoproteins, including an N-terminal hydrophobic signal sequence, an external domain containing eight putative N-linked glycosylation sites, a C-terminal transmembrane domain, and a charged cytoplasmic tail. Comparison with other herpesvirus revealed identities of 20.2, 25.1, 23.0, 23.0, 26.5 and 26.0% with the gH counterparts of the human herpesvirus virus 1 (HSV1), equine herpesvirus 4 (EHV4), bovine herpesvirus 1 (BHV1), pseudorabies virus (PRV), gallid herpesvirus 2 (GHV2) and gallid herpesvirus 3 (GHV3), respectively.

关 键 词:鸭子  瘟疫  糖蛋白类  PCR
收稿时间:2005-10-25
修稿时间:2006-01-25

Cloning and Sequence of Glycoprotein H Gene of Duck Plague Virus
HAN Xian-jie WANG Jun-wei MA Bo.Cloning and Sequence of Glycoprotein H Gene of Duck Plague Virus[J].Agricultural Sciences in China,2006,5(5):397-402.
Authors:HAN Xian-jie  WANG Jun-wei  MA Bo
Institution:1. Faculty of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, P.R. China;Faculty of Animal Science and Veterinary Medicine, Laiyang Agricultural College, Qingdao 266109, P.R. China
2. Faculty of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, P.R. China
Abstract:The glycoprotein H (gH) gene homologue of duck plague virus (DPV) was cloned by degenerate polymerase chain reaction (PCR) and sequenced. It was located immediately downstream from the thymidine kinase gene (TK). In addition, the 3′-end of the gene homologue to herpesvirus UL21 was located downstream from the gH gene. DPV gH gene open reading frame (ORF) was 2505 bp in length and its primary translation product was a polypeptide of 834 amino acids long. It possessed several characteristics of membrane glycoproteins, including an N-terminal hydrophobic signal sequence, an external domain containing eight putative N-linked glycosylation sites, a C-terminal transmembrane domain, and a charged cytoplasmic tail. Comparison with other herpesvirus revealed identities of 20.2, 25.1, 23.0, 23.0, 26.5 and 26.0% with the gH counterparts of the human herpesvirus virus 1 (HSV1), equine herpesvirus 4 (EHV4), bovine herpesvirus 1 (BHV1), pseudorabies virus (PRV), gallid herpesvirus 2 (GHV2) and gallid herpesvirus 3 (GHV3), respectively.
Keywords:duck plague virus  glycoprotein H gene  degenerate PCR
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