期刊文献+

广西巴马小型猪β-干扰素基因的克隆、序列分析和蛋白结构预测 被引量:5

Cloning and Sequence Analysis of Interferon β Gene and Its Predicted Protein Structure in Bama Mini Pig
在线阅读 下载PDF
导出
摘要 从刀豆素A刺激12 h和15 h的巴马小型猪外周血淋巴细胞中提取总RNA,用RT-PCR方法扩增出β-干扰素(IFN-β)基因,将其克隆到PMD18-T载体上,进行序列分析和蛋白结构预测。结果表明,克隆的巴马猪IFN-β基因氨基酸序列与GenBank上登录的梅山猪和长白猪的IFN-β基因氨基酸同源性为98.4%和98.9%,与人、牛、马的IFN-β氨基酸同源性分别为65.1%,65.1%,66.1%。人和猪IFN-β基因在5个螺旋结构序列上同源性很高,而且在维持蛋白结构和生物学活性上的氨基酸位点也非常保守。 The lymphocytes of Bama mini pig were separated from peripheral blood and the total RNA was extracted from the peripheral blood lymphocytes after 12 hours and 15 hours of stimulation with ConA, respectively. The interferon β (IFN--v) gene was amplified by reverse transcription polymerase chain reaction (RT--PCR) and cloned into PMD18-T vector, and then sequenced. The deduced amino acid sequence analysis of IFN-β gene of Bama mini pig showed that it shared 98. 4%- 98. 9% homology with corresponding pig genes registered in GenBank, and 65.1% ,65.1% and 66.1% similarity with those of human,bovine and horse,respectively. The identity of five helix structure sequences of IFN-β were similar between human and pig. The amino acid loci that maintain protein structure and biological activity were also conservative.
出处 《河南农业科学》 CSCD 北大核心 2007年第5期105-108,共4页 Journal of Henan Agricultural Sciences
关键词 巴马小型猪 β-干扰素基因 克隆 序列分析 结构预测 Bama mini pig Interferon β gene Cloning Sequence analysis Predicted protein structure
  • 相关文献

参考文献7

二级参考文献49

  • 1曹瑞兵,包晶晶,周海霞,郑其升,周斌,陈溥言.猪β-干扰素的原核表达及其对猪流行性腹泻病毒的抑制作用研究[J].中国病毒学,2004,19(4):364-368. 被引量:16
  • 2黄海,谢蓓,于瑞嵩,刘惠莉,张德福,曹祥荣,李震.猪IFNα基因在毕赤酵母中的高效分泌表达[J].遗传,2005,27(2):215-220. 被引量:12
  • 3Chinsangaram J ,Koster M ,Grubman M J. Inhibition of L-deleted foot-and-mouth disease virus replication by alpha/beta interferon involves double-stranded RNA-dependent protein kinase [J]. J Virol,2001,75(12) :5 498-5 503.
  • 4Derbyshire J B. The interferon sensitivity of selected porcine viruses[J]. Can J Vet Res, 1989,53( 1 ) :52-55.
  • 5Piccone M E,Riedere E, Mason P W,et al. The foot-and-mouth disease virus leader proteinase gene is not required for viral replieation[J]. J Virol,1995,69:5 376-5 382.
  • 6Chinsangaram J, Piccone M E,Grubman M J. Ability of footand-mouth disease virus to form plaques in cell culture is associated with suppression of alpha/beta interferon [J]. J Virol,1999,73(12):9 891-9 898.
  • 7Qin X Q,Tao N,r)ergary A,et al. Interferon-beta gene therpy inhibits tumor formation and causes regression of establi shed tumors in immune-deficient mice[J]. Proc Natl Acad Sei USA,1998,95:14 411-14 416.
  • 8Chinsangaram J, Mauro P M, Maria K ,et al. Novel viral disease control strategy:adenovirus expressiong alpha interferon rapidly protects swine from foot-and-mouth disease [J]. J Virol, 2003,77(2):1 621-1 625.
  • 9Shekhter Ⅱ, Beiko VP, Bulenkov MT, et al. Obtaining human recombinant (serine-17) beta-interferon by the method of oligonucleotide-directed mutagenesis and its expression in Escherichia coli [J].Antibiot Khimioter, 1991, 36(8): 25-8.
  • 10Lefevre F, L`haridon R, Borras-Cuesta R et al. Production, purification and biological propertities of an Escherichia coli-derived recombinant porcine alpha interferon [J]. J Gen Virol, 1990, 71:1057-1063.

共引文献39

同被引文献51

引证文献5

二级引证文献11

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部