Serveur d'exploration sur le peuplier

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Molecular characterization of PoGT8D and PoGT43B, two secondary wall-associated glycosyltransferases in poplar.

Identifieur interne : 003B19 ( Main/Exploration ); précédent : 003B18; suivant : 003B20

Molecular characterization of PoGT8D and PoGT43B, two secondary wall-associated glycosyltransferases in poplar.

Auteurs : Gong-Ke Zhou [États-Unis] ; Ruiqin Zhong ; David S. Himmelsbach ; Brooks T. Mcphail ; Zheng-Hua Ye

Source :

RBID : pubmed:17379696

Descripteurs français

English descriptors

Abstract

Dicot wood is mainly composed of cellulose, lignin and glucuronoxylan (GX). Although the biosynthetic genes for cellulose and lignin have been studied intensively, little is known about the genes involved in the biosynthesis of GX during wood formation. Here, we report the molecular characterization of two genes, PoGT8D and PoGT43B, which encode putative glycosyltransferases, in the hybrid poplar Populus alba x tremula. The predicted amino acid sequences of PoGT8D and PoGT43B exhibit 89 and 75% similarity to the Arabidopsis thaliana IRREGULAR XYLEM8 (IRX8) and IRX9, respectively, both of which have been shown to be required for GX biosynthesis. The PoGT8D and PoGT43B genes were found to be expressed in cells undergoing secondary wall thickening, including the primary xylem, secondary xylem and phloem fibers in stems, and the secondary xylem in roots. Both PoGT8D and PoGT43B are predicted to be type II membrane proteins and shown to be targeted to Golgi. Overexpression of PoGT43B in the irx9 mutant was able to rescue the defects in plant size and secondary wall thickness and partially restore the xylose content. Taken together, our results demonstrate that PoGT8D and PoGT43B are Golgi-localized, secondary wall-associated proteins, and PoGT43B is a functional ortholog of IRX9 involved in GX biosynthesis during wood formation.

DOI: 10.1093/pcp/pcm037
PubMed: 17379696


Affiliations:


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<term>Gene Expression Regulation, Enzymologic (MeSH)</term>
<term>Gene Expression Regulation, Plant (MeSH)</term>
<term>Genetic Complementation Test (MeSH)</term>
<term>Glycosyltransferases (genetics)</term>
<term>Glycosyltransferases (metabolism)</term>
<term>In Situ Hybridization (MeSH)</term>
<term>Isoenzymes (genetics)</term>
<term>Isoenzymes (metabolism)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Mutation (MeSH)</term>
<term>Phloem (enzymology)</term>
<term>Phloem (genetics)</term>
<term>Phloem (metabolism)</term>
<term>Phylogeny (MeSH)</term>
<term>Plant Proteins (genetics)</term>
<term>Plant Proteins (metabolism)</term>
<term>Populus (enzymology)</term>
<term>Populus (genetics)</term>
<term>Populus (metabolism)</term>
<term>Reverse Transcriptase Polymerase Chain Reaction (MeSH)</term>
<term>Sequence Homology, Amino Acid (MeSH)</term>
<term>Xylans (metabolism)</term>
<term>Xylem (enzymology)</term>
<term>Xylem (genetics)</term>
<term>Xylem (metabolism)</term>
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<term>Données de séquences moléculaires (MeSH)</term>
<term>Glycosyltransferase (génétique)</term>
<term>Glycosyltransferase (métabolisme)</term>
<term>Hybridation in situ (MeSH)</term>
<term>Isoenzymes (génétique)</term>
<term>Isoenzymes (métabolisme)</term>
<term>Mutation (MeSH)</term>
<term>Paroi cellulaire (métabolisme)</term>
<term>Phloème (enzymologie)</term>
<term>Phloème (génétique)</term>
<term>Phloème (métabolisme)</term>
<term>Phylogenèse (MeSH)</term>
<term>Populus (enzymologie)</term>
<term>Populus (génétique)</term>
<term>Populus (métabolisme)</term>
<term>Protéines végétales (génétique)</term>
<term>Protéines végétales (métabolisme)</term>
<term>RT-PCR (MeSH)</term>
<term>Régulation de l'expression des gènes codant pour des enzymes (MeSH)</term>
<term>Régulation de l'expression des gènes végétaux (MeSH)</term>
<term>Similitude de séquences d'acides aminés (MeSH)</term>
<term>Séquence d'acides aminés (MeSH)</term>
<term>Test de complémentation (MeSH)</term>
<term>Xylanes (métabolisme)</term>
<term>Xylème (enzymologie)</term>
<term>Xylème (génétique)</term>
<term>Xylème (métabolisme)</term>
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<term>Isoenzymes</term>
<term>Plant Proteins</term>
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<term>Populus</term>
<term>Xylème</term>
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<term>Phloem</term>
<term>Populus</term>
<term>Xylem</term>
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<term>Phloem</term>
<term>Populus</term>
<term>Xylem</term>
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<term>Glycosyltransferase</term>
<term>Isoenzymes</term>
<term>Phloème</term>
<term>Populus</term>
<term>Protéines végétales</term>
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<term>Cell Wall</term>
<term>Glycosyltransferases</term>
<term>Isoenzymes</term>
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<term>Plant Proteins</term>
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<term>Isoenzymes</term>
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<term>Reverse Transcriptase Polymerase Chain Reaction</term>
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<term>Données de séquences moléculaires</term>
<term>Hybridation in situ</term>
<term>Mutation</term>
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<term>RT-PCR</term>
<term>Régulation de l'expression des gènes codant pour des enzymes</term>
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<div type="abstract" xml:lang="en">Dicot wood is mainly composed of cellulose, lignin and glucuronoxylan (GX). Although the biosynthetic genes for cellulose and lignin have been studied intensively, little is known about the genes involved in the biosynthesis of GX during wood formation. Here, we report the molecular characterization of two genes, PoGT8D and PoGT43B, which encode putative glycosyltransferases, in the hybrid poplar Populus alba x tremula. The predicted amino acid sequences of PoGT8D and PoGT43B exhibit 89 and 75% similarity to the Arabidopsis thaliana IRREGULAR XYLEM8 (IRX8) and IRX9, respectively, both of which have been shown to be required for GX biosynthesis. The PoGT8D and PoGT43B genes were found to be expressed in cells undergoing secondary wall thickening, including the primary xylem, secondary xylem and phloem fibers in stems, and the secondary xylem in roots. Both PoGT8D and PoGT43B are predicted to be type II membrane proteins and shown to be targeted to Golgi. Overexpression of PoGT43B in the irx9 mutant was able to rescue the defects in plant size and secondary wall thickness and partially restore the xylose content. Taken together, our results demonstrate that PoGT8D and PoGT43B are Golgi-localized, secondary wall-associated proteins, and PoGT43B is a functional ortholog of IRX9 involved in GX biosynthesis during wood formation.</div>
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<AbstractText>Dicot wood is mainly composed of cellulose, lignin and glucuronoxylan (GX). Although the biosynthetic genes for cellulose and lignin have been studied intensively, little is known about the genes involved in the biosynthesis of GX during wood formation. Here, we report the molecular characterization of two genes, PoGT8D and PoGT43B, which encode putative glycosyltransferases, in the hybrid poplar Populus alba x tremula. The predicted amino acid sequences of PoGT8D and PoGT43B exhibit 89 and 75% similarity to the Arabidopsis thaliana IRREGULAR XYLEM8 (IRX8) and IRX9, respectively, both of which have been shown to be required for GX biosynthesis. The PoGT8D and PoGT43B genes were found to be expressed in cells undergoing secondary wall thickening, including the primary xylem, secondary xylem and phloem fibers in stems, and the secondary xylem in roots. Both PoGT8D and PoGT43B are predicted to be type II membrane proteins and shown to be targeted to Golgi. Overexpression of PoGT43B in the irx9 mutant was able to rescue the defects in plant size and secondary wall thickness and partially restore the xylose content. Taken together, our results demonstrate that PoGT8D and PoGT43B are Golgi-localized, secondary wall-associated proteins, and PoGT43B is a functional ortholog of IRX9 involved in GX biosynthesis during wood formation.</AbstractText>
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