ACTA AGRICULTURAE BOREALI-SINICA ›› 2015, Vol. 30 ›› Issue (2): 72-77. doi: 10.7668/hbnxb.2015.02.014

Special Issue: Animal husbandry

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Molecular Cloning and Sequence Analysis of the VP1 Gene of Porcine kobuvirus

ZHU Jun-peng1, YANG Bin2, LAN Xi2, LIU Ji-xing2, MA Xiao-jun1   

  1. 1. College of Veterinary Medicine, Gansu Agricultural University, Lanzhou 730070, China;
    2. State Key Laboratory of Veterinary Etiological Biology, Key Laboratory of Grazing Animal Diseases, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China
  • Received:2015-01-24 Published:2015-04-28

Abstract: The aim of the study to investigate the main structural protein of the Kobuvirus VP1 gene.According to the sequences of PKV deposited in GenBank, a pair of special primers was designed for amplifying the VP1 gene of swKoV CH441 strain by RT-PCR.The results of sequence analysis showed that the whole VP1 gene of swKoV CH441 strain consisted of 762 bp.Compared with 15 PKV strains which were deposited in GenBank, the homology of nucleotide sequences was 81.5% ~90.2%, and the homology of deduced amino acids was 86.6% ~96.9%.Evolution analysis indicated that the swKoV CH441 strain was closely related to GS-1 strains.The bioinformatics analysis demonstrated that the isoelectric point and molecular weight of non-structural protein VP1 were 4.40 and 26.978 2 kDa.The protein had no signal peptide and transmembrane domain.There were 18 phosphorylation sites including 7 Sers, 6 Thrs and 5 Tyrs.Protein phosphorylation was concerned with signal transduction, so this protein may be a signaling molecule.The results provided a theoretical foundation for further research on the study of VP1 gene (protein) in the genetic variation.

Key words: VP1 gene, Cloning, DNA sequencing, Sequence analysis

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Cite this article

ZHU Jun-peng, YANG Bin, LAN Xi, LIU Ji-xing, MA Xiao-jun. Molecular Cloning and Sequence Analysis of the VP1 Gene of Porcine kobuvirus[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2015, 30(2): 72-77. doi: 10.7668/hbnxb.2015.02.014.

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