Evidence for a role of AtCAD 1 in lignification of elongating stems of Arabidopsis thaliana
Crop and Pasture Production
0301 basic medicine
570
Plant Biology & Botany
Agricultural biotechnology
Blotting, Western
Arabidopsis
Plant Biology
lignin
Genetically Modified
GENE FAMILY
Flowers
Lignin
Promoter Regions
[SDV.GEN.GPL]Life Sciences [q-bio]/Genetics/Plants genetics
03 medical and health sciences
Genetic
Gene Expression Regulation, Plant
Xylem
LIGNIFICATION
Genetics
stem
Promoter Regions, Genetic
Phylogeny
Glucuronidase
580
Plant biology
Phenylpropionates
Plant Stems
Blotting
Arabidopsis Proteins
Reverse Transcriptase Polymerase Chain Reaction
cinnamyl alcohol dehydrogenase
Genetic Complementation Test
Plant
Biological Sciences
Plants
STEM
Plants, Genetically Modified
Isoenzymes
Alcohol Oxidoreductases
Gene Expression Regulation
Multigene Family
Mutation
gene family
Western
CINNAMYL ALCOHOL DEHYDROGENASE
LIGNIN
DOI:
10.1007/s00425-006-0326-9
Publication Date:
2006-07-10T18:07:58Z
AUTHORS (7)
ABSTRACT
The cinnamyl alcohol dehydrogenase (AtCAD) multigene family in Arabidopsis is composed of nine genes. Our previous studies focused on the two isoforms AtCAD C and AtCAD D which show a high homology to those related to lignification in other plants. This study focuses on the seven other Arabidopsis CAD for which functions are not yet elucidated. Their expression patterns were determined in different parts of Arabidopsis. Only CAD 1 protein can be detected in elongating stems, flowers, and siliques using Western-blot analysis. Tissue specific expression of CAD 1, B1, and G genes was determined using their promoters fused to the GUS reporter gene. CAD 1 expression was observed in primary xylem in accordance with a potential role in lignification. Arabidopsis T-DNA mutants knockout for the different genes CAD genes were characterized. Their stems displayed no substantial reduction of CAD activities for coniferyl and sinapyl alcohols as well as no modifications of lignin quantity and structure in mature inflorescence stems. Only a small reduction of lignin content could be observed in elongating stems of Atcad 1 mutant. These CAD genes in combination with the CAD D promoter were used to complement a CAD double mutant severely altered in lignification (cad c cad d). The expression of AtCAD A, B1, B2, F, and G had no effect on restoring a normal lignin profile of this mutant. In contrast, CAD 1 complemented partly this mutant as revealed by the partial restoration of conventional lignin units and by the decrease in the frequency of beta-O-4 linked p-OH cinnamaldehydes.
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