Molecular genetics of nucleotide sugar interconversion pathways in plants

被引:182
作者
Reiter, WD [1 ]
Vanzin, GF [1 ]
机构
[1] Univ Connecticut, Dept Mol & Cell Biol, Storrs, CT 06269 USA
关键词
Arabidopsis thaliana; cell wall; genomics; monosaccharide; mutant;
D O I
10.1023/A:1010671129803
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nucleotide sugar interconversion pathways represent a series of enzymatic reactions by which plants synthesize activated monosaccharides for the incorporation into cell wall material. Although biochemical aspects of these metabolic pathways are reasonably well understood, the identification and characterization of genes encoding nucleotide sugar interconversion enzymes is still in its infancy. Arabidopsis mutants defective in the activation and interconversion of specific monosaccharides have recently become available, and several genes in these pathways have been cloned and characterized. The sequence determination of the entire Arabidopsis genome offers a unique opportunity to identify candidate genes encoding nucleotide sugar interconversion enzymes via sequence comparisons to bacterial homologues. An evaluation of the Arabidopsis databases suggests that the majority of these enzymes are encoded by small gene families, and that most of these coding regions are transcribed. Although most of the putative proteins are predicted to be soluble, others contain N-terminal extensions encompassing a transmembrane domain. This suggests that some nucleotide sugar interconversion enzymes are targeted to an endomembrane system, such as the Golgi apparatus, where they may co-localize with glycosyltransferases in cell wall synthesis. The functions of the predicted coding regions can most likely be established via reverse genetic approaches and the expression of proteins in heterologous systems. The genetic characterization of nucleotide sugar interconversion enzymes has the potential to understand the regulation of these complex metabolic pathways and to permit the modification of cell wall material by changing the availability of monosaccharide precursors.
引用
收藏
页码:95 / 113
页数:19
相关论文
共 72 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   A MEMBRANE-ASSOCIATED FORM OF SUCROSE SYNTHASE AND ITS POTENTIAL ROLE IN SYNTHESIS OF CELLULOSE AND CALLOSE IN PLANTS [J].
AMOR, Y ;
HAIGLER, CH ;
JOHNSON, S ;
WAINSCOTT, M ;
DELMER, DP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9353-9357
[3]  
[Anonymous], 1980, CARBOHYDRATES STRUCT, DOI DOI 10.1016/B978-0-12-675403-2.50010-7
[4]  
BARBER GA, 1979, J BIOL CHEM, V254, P7600
[5]   ROOT MORPHOLOGY MUTANTS IN ARABIDOPSIS-THALIANA [J].
BASKIN, TI ;
BETZNER, AS ;
HOGGART, R ;
CORK, A ;
WILLIAMSON, RE .
AUSTRALIAN JOURNAL OF PLANT PHYSIOLOGY, 1992, 19 (04) :427-437
[6]   SEQUENCE AND ANALYSIS OF THE O-ANTIGEN GENE (RFB) CLUSTER OF ESCHERICHIA-COLI-O111 [J].
BASTIN, DA ;
REEVES, PR .
GENE, 1995, 164 (01) :17-23
[7]   A bifunctional epimerase-reductase acts downstream of the MUR1 gene product and completes the de novo synthesis of GDP-L-fucose in Arabidopsis [J].
Bonin, CP ;
Reiter, WD .
PLANT JOURNAL, 2000, 21 (05) :445-454
[8]   The MUR1 gene of Arabidopsis thaliana encodes an isoform of GDP-D-mannose-4,6-dehydratase, catalyzing the first step in the de novo synthesis of GDP-L-fucose [J].
Bonin, CP ;
Potter, I ;
Vanzin, GF ;
Reiter, WD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :2085-2090
[9]   The mur4 mutant of arabidopsis is partially defective in the de novo synthesis of uridine diphospho L-arabinose [J].
Burget, EG ;
Reiter, WD .
PLANT PHYSIOLOGY, 1999, 121 (02) :383-389
[10]   STRUCTURAL MODELS OF PRIMARY-CELL WALLS IN FLOWERING PLANTS - CONSISTENCY OF MOLECULAR-STRUCTURE WITH THE PHYSICAL-PROPERTIES OF THE WALLS DURING GROWTH [J].
CARPITA, NC ;
GIBEAUT, DM .
PLANT JOURNAL, 1993, 3 (01) :1-30