首页|梅山猪氨肽酶基因N(pAPN) cDNA克隆、序列分析及重要变异位点的筛选

梅山猪氨肽酶基因N(pAPN) cDNA克隆、序列分析及重要变异位点的筛选

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氨肽酶N(aminopeptidase N,APN)蛋白是猪(Sus scrofa)传染性胃肠炎病毒(Transmissible gastroenteritis virus,TGEV)和猪的流行性腹泻病毒(Porcine epidemic diarrhea virus,PEDV)等一系列冠状病毒的受体蛋白.为探讨梅山猪APN基因的分子结构特征以及重要的变异位点,本研究通过PCR扩增和测序技术,结合生物信息学分析梅山猪APN基因功能区域和重要变异位点,对其蛋白质结构进行预测和分析.结果表明,梅山猪APN基因cDNA全长2 886 bp (GenBank登录号:KF280271),含有20个外显子,编码961个氨基酸.与GenBank数据库公布的标准序列(登录号:NM_214277.1)相比,梅山猪APN基因编码区变异共引起10处氨基酸突变与2处氨基酸缺失,其中Phe82Asn、Leu107Phe、Leu108 Ile、Ser330Pro、Trp399Arg和Glu465 Gly等6处突变位于APN酶催化活性区域,Gln747His突变、748Tyr和749Ser缺失突变位于APN病毒结合区域.蛋白结构和编码产物功能分析发现,pAPN为不稳定的亲水性蛋白,无信号肽,具有1个跨膜螺旋(跨膜区位于12~34氨基酸,二级结构元件以α螺旋和β折叠为主,编码产物主要参与细胞被膜(cell envelope)、中央中间代谢(central intermediary metabolism)、辅酶因子生物合成(biosynthesisof cofactors)等功能.Gln747His、748Tyr和749Ser缺失突变可能与氨肽酶N结合病毒能力有关.本研究对梅山猪APN基因功能的分析及变异位点的筛选,为今后筛选猪抗病毒性腹泻的有效遗传标记提供理论基础.
Cloning and Screening of Important Mutation Loci of Aminopeptidase N Gene (pAPN) in Meishan Pigs (Sus scrofa)
Porcine aminopeptidase N (pAPN) was the receptor protein of a series of virus,such as Transmissible gastroenteritis virus (TGEV) and Porcine epidemic diarrhea virus (PEDV).So this study aimed to probe into the structures and important mutation loci of pAPN gene and provide basis for screening out effective genetic markers of the resistance to viral diarrhea in Meishan pigs (Sus scrofa).The functional regions and important mutation loci were screened out by bioinformatics analysis of the protein structure through PCR,cloning,sequencing and bioinformatics tools.The results showed that the cDNA sequence of pAPN gene (GenBank accession No.KF280271) of Meishan pigs was 2 886 bp in length,including 20 exons,which encoded 961 amino acids.Compared with standard pAPN gene (Accession No.NM_214277.1) sequence in the Genbank database,there were 10-amino acid mutations and 2-amino acid deletions.Six mutations of Phe82Asn,Leu107Phe,Leu108Ile,Ser330Pro,Trp399Arg,and Glu465Gly occurred in the catalytic activity area of APN enzyme.One mutation of Gln747His and 2 deletions of 748Tyr and 749Ser occurred in APN virus combined area.Prediction of protein structure and functional analysis of encoding product showed that pAPN protein was unstable and hydrophilic,without signal peptide,including 1 transmembrane helice (transmembrane region between 12th and 34th amino acid).Secondary structure of pAPN protein mainly contained alpha helix and beta folding.Encoded product was mainly responsible for cell envelope,central intermediary metabolism and biosynthesis of cofactors.One mutation of Gln747His and 2 deletions of 748Tyr and 749Ser might associate with the combination ability of aminopeptidase N and virus.This study analyzed the function and screened out the mutations of pAPN gene,which provides theoretical basis for selecting effective genetic marker of the resistance to viral diarrhea in future.

PigsEpidemic diarrheaAminopeptidase N gene(APN)Mutation loci

刘颖、董文华、孙寿永、吴正常、夏芃芃、朱国强、包文斌、吴圣龙

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扬州大学动物科学与技术学院/江苏省动物遗传繁育与分子设计重点实验室,扬州225009

扬州大学兽医学院,扬州225009

流行性腹泻 氨肽酶N基因(APN) 变异位点

国家转基因生物新品种培育科技重大专项江苏省科技支撑计划(农业)江苏省产学研前瞻性联合研究项目

2014ZX08006-001BBE2012330 和BE2013345BY2012157

2014

农业生物技术学报
中国农业大学 中国农业生物技术学会

农业生物技术学报

CSTPCDCSCD北大核心
影响因子:0.801
ISSN:1674-7968
年,卷(期):2014.22(9)
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