Molecular cloning, characterization and expression of a novel jasmonate-dependent defensin gene from Ginkgo biloba

被引:18
|
作者
Shen, GA
Pang, YZ
Wu, WS
Miao, ZQ
Qian, HM
Zhao, LX
Sun, XF
Tang, KX [1 ]
机构
[1] Shanghai Jiao Tong Univ, Plant Biotechnol Res Ctr, Sch Agr & Biol,SJTU SIBS PSU Joint Ctr Life Sci, Fudan SJTU Nottingham Plant Biotechnol R&D Ctr, Shanghai 200030, Peoples R China
[2] Fudan Univ, Fudan SJTU Nottingham Plant Biotechnol R&D Ctr, State Key Lab Genet Engn, Sch Life Sci,Morgan Tan Int Ctr Life Sci, Shanghai 200433, Peoples R China
关键词
cDNA cloning; defensin; Ginkgo biloba; RACE;
D O I
10.1016/j.jplph.2005.01.019
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
A novel defensin gene was isolated from Ginkgo biloba. The full-Length cDNA of G. biloba defensin (designated as Gbd) was 534 bp. The cDNA contained a 240-bp open reading frame encoding an 80-amino acid protein of 5.68 kDa with a potential 30 aa signal peptide. The putative GbD mature protein showed striking similarity to other plant defensins, representing low molecular size antimicrobial polypeptides. Eight cysteine sites conserved in plant defensins were also found in GbD at similar positions. Three-dimensional structure modeling showed that GbD strongly resembled defensin from tobacco (NaD1) and consisted of an a-helix and a triple-strand antiparallel beta-sheet that were stabilized by four intramolecular disulfide bonds, implying GbD may have functions similar to NaD1. The genomic DNA gel blot indicated that Gbd belonged to a multigene family. Expression analysis revealed that Gbd was up-regulated by wounding and methyl jasmonate treatments, suggesting that Gbd is potentially involved in plant resistance or tolerance to pathogens during wounding. (c) 2005 Elsevier GmbH. All rights reserved.
引用
收藏
页码:1160 / 1168
页数:9
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