Genomic cloning and characterization of a novel lectin gene from Zantedeschia aethiopica

被引:2
作者
Chen, ZH
Sun, XF
Tang, KX [1 ]
机构
[1] Fudan Univ, Fudan SJTU Notitngham Plant Biotechnol R&D Ctr, Morgan Tan Int Ctr Life Sci, Sch Life Sci,State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Agr & Biol, Fudan SJTU Nottingham Plant Biotechnol R&D Ctr, Plant Biotechnol Res Ctr, Shanghai 200030, Peoples R China
关键词
Zantedeschia aethiopica; lectin; genomic cloning; genomic walker technology;
D O I
10.1007/s10540-005-2583-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
A new lectin gene was isolated by using genomic walker technology and revealed to encode a mannose-binding lectin. Analysis of a 2233 bp segment revealed a gene including a 1169 bp 5' flanking region, a 417 bp open reading frame (ORF) and a 649 bp 3' flanking region. There are two putative TATA boxes and eight possible CAAT boxes lie in the 5' flanking region. The ORF encodes a 15.1 kDa precursor, which contains a 24-amino acid signal peptide. One possible polyadenylation signal is found in the 3'-flanking region. No intron was detected within the region of genomic sequence corresponding to zaa (Zantedeschia aethiopica agglutinin) full-length cDNA, which is typical of other mannose-binding lectin gene that have been reported. The deduced amino acid sequence of the lectin gene coding region shares 49-54% homology with other known lectins. The cloning of this new lectin gene will allow us to further study its structure, expression and regulation mechanisms.
引用
收藏
页码:225 / 234
页数:10
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