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Genomic Cloning and Characterization of a Novel Lectin Gene from Zantedeschia aethiopica

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Bioscience Reports

Abstract

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.

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Correspondence to Kexuan Tang.

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Chen, Z., Sun, X. & Tang, K. Genomic Cloning and Characterization of a Novel Lectin Gene from Zantedeschia aethiopica. Biosci Rep 24, 225–234 (2004). https://doi.org/10.1007/s10540-005-2583-4

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