Abstract :
[en] Sharp eyespot, caused mainly by the necrotrophic fungus Rhizoctonia cerealis, is
a destructive disease in hexaploid wheat (Triticum aestivum L.). In Arabidopsis,
certain cinnamyl alcohol dehydrogenases (CADs) have been implicated in monolignol
biosynthesis and in defense response to bacterial pathogen infection. However, little
is known about CADs in wheat defense responses to necrotrophic or soil-borne
pathogens. In this study, we isolate a wheat CAD gene TaCAD12 in response to
R. cerealis infection through microarray-based comparative transcriptomics, and study
the enzyme activity and defense role of TaCAD12 in wheat. The transcriptional levels
of TaCAD12 in sharp eyespot-resistant wheat lines were significantly higher compared
with those in susceptible wheat lines. The sequence and phylogenetic analyses
revealed that TaCAD12 belongs to IV group in CAD family. The biochemical assay
proved that TaCAD12 protein is an authentic CAD enzyme and possesses catalytic
efficiencies toward both coniferyl aldehyde and sinapyl aldehyde. Knock-down of
TaCAD12 transcript significantly repressed resistance of the gene-silenced wheat plants
to sharp eyespot caused by R. cerealis, whereas TaCAD12 overexpression markedly
enhanced resistance of the transgenic wheat lines to sharp eyespot. Furthermore,
certain defense genes (Defensin, PR10, PR17c, and Chitinase1) and monolignol
biosynthesis-related genes (TaCAD1, TaCCR, and TaCOMT1) were up-regulated in
the TaCAD12-overexpressing wheat plants but down-regulated in TaCAD12-silencing
plants. These results suggest that TaCAD12 positively contributes to resistance against
sharp eyespot through regulation of the expression of certain defense genes and
monolignol biosynthesis-related genes in wheat.
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