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GASA基因超家族新成员——烟草抗菌肽基因的克隆及序列分析
引用本文:林世锋,任学良,王东茂,张拓,王仁刚. GASA基因超家族新成员——烟草抗菌肽基因的克隆及序列分析[J]. 中国烟草学报, 2012, 18(3): 97-102
作者姓名:林世锋  任学良  王东茂  张拓  王仁刚
作者单位:1. 贵州省烟草科学研究所,贵阳,550081
2. 北京蛋白质组研究中心/蛋白质组学国家重点实验室,北京,102206
基金项目:贵州省烟草专卖局(公司)科技专项(200911);中国烟草总公司重点项目(2010-221);贵州省科学技术基金项目(黔科合J字[2012]2256号)
摘    要:抗菌肽可以增强植物对病原微生物的抵抗能力,本研究利用生物信息学方法,获得了烟草品种K326的3种抗菌肽cDNA序列(NtSN1a、NtSN16和NtSN2a),并对其进行了序列分析.结果表明,3种抗茵肽cDNA序列均具有完整的开放读码框,NtSNIa和NtSNIb均编码88个氨基酸,NtSN2a编码104个氨基酸.对推导的氨基酸序列分析发现,它们都具有典型的GASA基因超家族保守结构域,属于GASA基因超家族成员.系统进化分析表明,NtSN1a和NtSN16与马铃薯抗菌肽snaking-1聚为一类,NtSN2a与马铃薯抗菌肽snaking-2聚为一类.这些结果为进一步研究抗菌肽基因的抑菌效应,比较其在烟草抗病防御反应中的作用奠定了基础.

关 键 词:烟草  GASA基因超家族  抗菌肽  克隆  序列分析

Cloning and sequence analysis of tobacco antimicrobial peptide genes,novel members of GASA gene superfamily
LIN Shi-feng , REN Xue-liang , WANG Dong-mao , ZHANG Tuo , WANG Ren-gang. Cloning and sequence analysis of tobacco antimicrobial peptide genes,novel members of GASA gene superfamily[J]. Acta Tabacaria Sinica, 2012, 18(3): 97-102
Authors:LIN Shi-feng    REN Xue-liang    WANG Dong-mao    ZHANG Tuo    WANG Ren-gang
Affiliation:1 Guizhou Tobacco Research Institute,Guiyang 550081,China; 2 Beijing Proteomics Research Center/State Key Laboratory of Proteomics,Beijing 102206,China
Abstract:Antimicrobial peptides(AMPs) have been considered to play a key role in plant defense.Three distinct AMP cDNAs(NtSN1a,NtSN1b and NtSN2a) were cloned from tobacco cultivar K326 using in silicon cloning technique,and were analyzed by bioinformatics method.Sequence analysis revealed that both NtSN1a and NtSN1b encoded an open-reading frame of 88 amino acids,and NtSN2a encoded an open-reading frame of 104 amino acids.,all of them shared the conserved domain of the GASA superfamily.Phylogenetic analysis showed that NtSN1a and NtSN1b cluster with potato snaking-1,and NtSN2a clusters with potato snaking-2.These results lay the foundation for clarifying the inhibitory effect of AMPs,discovering their functional differences and understanding the molecular mechanisms underlying tobacco defense responses.
Keywords:Nicotiana tabacum  GASA gene superfamily  antibacterial peptide  cloning  sequence analysis
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