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1.
Biocell ; 29(2): 187-193, ago. 2005. ilus
Artigo em Inglês | LILACS | ID: lil-429674

RESUMO

Using RNA extracted from Zantedeschia aethiopica young leaves and primers designed according to the conservative regions of Araceae lectins, the full-length cDNA of Z. aethiopica agglutinin (ZAA) was cloned by rapid amplification of cDNA ends (RACE). The full-length cDNA of zaa was 871 bp and contained a 417 bp open reading frame (ORF) encoding a lectin precursor of 138 amino acids. Through comparative analysis of zaa gene and its deduced amino acid sequence with those of other Araceae species, it was found that zaa encoded a precursor lectin with signal peptide. Secondary and three-dimensional structure analyses showed that ZAA had many common characters of mannose-binding lectin superfamily and ZAA was a mannose-binding lectin with three mannose-binding sites. Southern blot analysis of the genomic DNA revealed that zaa belonged to a multi-copy gene family


Assuntos
Lectina de Ligação a Manose/fisiologia , Lectina de Ligação a Manose/genética , Lectina de Ligação a Manose/química , Lectina de Ligação a Manose , Proteínas de Plantas/fisiologia , Proteínas de Plantas/genética , Proteínas de Plantas/química , Genes de Plantas/fisiologia , Genes de Plantas/genética , Plantas Geneticamente Modificadas/fisiologia , Plantas Geneticamente Modificadas/genética , Plantas Geneticamente Modificadas/química , Regulação da Expressão Gênica de Plantas/fisiologia , Regulação da Expressão Gênica de Plantas/genética
2.
J Biosci ; 2005 Mar; 30(2): 213-20
Artigo em Inglês | IMSEAR | ID: sea-111342

RESUMO

Using RNA extracted from Zingiber officinale rhizomes and primers designed according to the conservative regions of monocot mannose-binding lectins, the full-length cDNA of Z. officinale agglutinin (ZOA) was cloned by rapid amplification of cDNA ends (RACE). The full-length cDNA of zoa was 746 bp and contained a 510 bp open reading frame (ORF) encoding a lectin precursor of 169 amino acids with a signal peptide. ZOA was a mannose-binding lectin with three typical mannose-binding sites (QDNY). Semi-quantitative RT-PCR analysis revealed that zoa expressed in all the tested tissues of Z. officinale including leaf, root and rhizome, suggesting it to be a constitutively expressing form. ZOA protein was successfully expressed in Escherichia coli with the molecular weight expected. To our knowledge, this is the first mannose-binding lectin cDNA cloned from the family Zingiberaceae. Our results demonstrate that monocot mannose-binding lectins also occur within the family Zingiberaceae.


Assuntos
Sequência de Aminoácidos , Sequência de Bases , Sítios de Ligação , Clonagem Molecular , Análise por Conglomerados , Biologia Computacional , Primers do DNA , DNA Complementar/genética , Expressão Gênica , Zingiber officinale/genética , Hemaglutinação , Lectina de Ligação a Manose/genética , Dados de Sequência Molecular , Filogenia , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Rizoma/química , Análise de Sequência de DNA
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