Molecular cloning and characterization of a novel lectin gene from Lycoris radiata

被引:9
|
作者
Zhao, XY
Yao, JH
Sun, XF
Tang, KX
机构
[1] Fudan Univ, Sch Life Sci,State Key Lab Gent Engn, Funda SJTU Nottingham Plant Biotechnol R&D Ctr, Morgan Tan Int Ctr Life Sci, Shanghai 200433, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Agr & Biol, Fudan SJTU Nottingham Plant Biotechnol R&D Ctr, Ctr Plant Biotechnol, Shanghai 200030, Peoples R China
来源
DNA SEQUENCE | 2003年 / 14卷 / 03期
关键词
Amaryllidaceae; cDNA; lectin; RACE-PCR; Lycoris radiata;
D O I
10.1080/1042517031000101716
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
By the use of RACE-PCR with RNA extracted from Lycoris radiata young leaves, the full-length cDNA of L. radiata agglutinin (LRA) was cloned. The full-length cDNA of LRA was 669 bp and contained a 477 bp open reading frame encoding a 158 amino acid protein. Through comparative analysis of lra gene and its deduced amino acid sequence with those of other Amaryllidaceae species, it was found that lra encoded a precursor lectin with signal peptide. LRA was a mannose-binding lectin with three mannose-binding boxes like lectins from other Amaryllidaceae species. Southern blot analysis of genomic DNA revealed that lra belonged to a low copy gene family. Northern blot analysis demonstrated that lra constitutively expressed in various plant tissues including leaf, root, stem and inflorescence, and highly expressed in the inflorescence.
引用
收藏
页码:223 / 226
页数:4
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