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猪嵴病毒CH441株VP1基因的克隆与序列分析

祝俊鹏 杨彬 兰喜 柳纪省 马小军

华北农学报Issue(2):72-77,6.
华北农学报Issue(2):72-77,6.DOI:10.7668/hbnxb.2015.02.014

猪嵴病毒CH441株VP1基因的克隆与序列分析

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

祝俊鹏 1杨彬 2兰喜 2柳纪省 2马小军1

作者信息

  • 1. 甘肃农业大学 动物医学院,甘肃 兰州 730070
  • 2. 中国农业科学院 兰州兽医研究所,家畜疫病病原生物学国家重点实验室,草食动物疫病重点开放实验室,甘肃 兰州 730046
  • 折叠

摘要

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%. Evo-lution analysis indicated that the swKoV CH441 strain was closely related to GS-1 strains. The bioinformatics analy-sis 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.

关键词

VP1 基因/克隆/DNA测序/序列分析

Key words

VP1 gene/Cloning/DNA sequencing/Sequence analysis

分类

生物科学

引用本文复制引用

祝俊鹏,杨彬,兰喜,柳纪省,马小军..猪嵴病毒CH441株VP1基因的克隆与序列分析[J].华北农学报,2015,(2):72-77,6.

基金项目

国家国际科技合作专项 ()

华北农学报

OA北大核心CSCDCSTPCD

1000-7091

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