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胡椒 PnNPR2 基因的克隆
引用本文:范 睿,胡丽松,伍宝朵,郝朝运.胡椒 PnNPR2 基因的克隆[J].热带作物学报,2018,39(10):1983-1989.
作者姓名:范 睿  胡丽松  伍宝朵  郝朝运
作者单位:1. 中国热带农业科学院香料饮料研究所,海南万宁 571533; 2. 农业部香辛饮料作物遗传资源利用重点实验室, 海南 万宁 571533; 3. 海南省热带香辛饮料作物遗传改良与品质调控重点实验室,海南万宁 571533
摘    要:基于胡椒转录组数据库,筛选胡椒病程相关基因非表达子基因的 EST 序列,设计引物,运用 RACE 法克隆得 到 1 个 NPR 基因,命名为 PnNPR2;该基因全长 2 260 bp,开放阅读框 1 722 bp,编码 573 个氨基酸;开放读码框含有 BTB/POT 结构域、ANK 锚蛋白重复序列、DUF 和 NPR1-like C 4 个结构域,具有植物 NPR1 所共有的保守结构域,并 将 PnNPR2 基因插入 pCAMBIA1300-35S-sGFP 超表达载体中。本研究结果为 PnNPR2 的功能研究奠定基础。

关 键 词:胡椒  NPR2  克隆  抗病  

Cloning of PnNPR2 from Piper nigrum
FAN Rui,HU Lisong WU Baoduo,HAO Chaoyun.Cloning of PnNPR2 from Piper nigrum[J].Chinese Journal of Tropical Crops,2018,39(10):1983-1989.
Authors:FAN Rui  HU Lisong WU Baoduo  HAO Chaoyun
Institution:1. Spice and Beverage Research Institute, Chinese Academy of Tropical Agricultural Sciences, Wanning, Hainan 571533, China;  2. Key Laboratory of Genetic Resources Utilization of Spice and Beverage Crops, Ministry of Agriculture, Wanning, Hainan 571533, China;  3. Hainan Provincial Key Laboratory of Genetic Improvement and Quality Regulation for Tropical Spice and Beverage Crops, Wanning, Hainan 571533, China
Abstract:The full-length cDNA encoding nonexpressor of pathogenesis-related genes (NPR), designated PnNPR2, was isolated from black pepper by using RACE. The sequence of PnNPR2 was 2 260 bp in length, containing a 1 722 bp open reading frame, and encoding a polypeptide of 573 amino acids. The protein had conserved domains of BTB/POT, ANK anchored protein repeat sequences, DUF and NPR1-like C. The recombinant plasmid pCAMBIA1300-PnNPR2 was obtained by inserting the PnNPR2 gene into the pCAMBIA1300 vector. The results showed that the recombinant plasmid pCAMBIA1300-PnNPR2 which contained the target gene was constructed successfully. The result would generate an important theoretical and practical significance for black pepper genetic improvements.
Keywords:black pepper  nonexpressor of pathogenesis-related genes 2 (NPR2)  cloning  disease resistance  
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