An Arabidopsis mutant with enhanced resistance to powdery mildew

CA Frye, RW Innes - The Plant Cell, 1998 - academic.oup.com
CA Frye, RW Innes
The Plant Cell, 1998academic.oup.com
We have identified an Arabidopsis mutant that displays enhanced disease resistance to the
fungus Erysiphe cichoracearum, causal agent of powdery mildew. The edr1 mutant does not
constitutively express the pathogenesis-related genes PR-1, BGL2, or PR-5 and thus differs
from previously described disease-resistant mutants of Arabidopsis. E. cichoracearum
conidia (asexual spores) germinated normally and formed extensive hyphae on edr1 plants,
indicating that the initial stages of infection were not inhibited. Production of conidiophores …
Abstract
We have identified an Arabidopsis mutant that displays enhanced disease resistance to the fungus Erysiphe cichoracearum, causal agent of powdery mildew. The edr1 mutant does not constitutively express the pathogenesis-related genes PR-1, BGL2, or PR-5 and thus differs from previously described disease-resistant mutants of Arabidopsis. E. cichoracearum conidia (asexual spores) germinated normally and formed extensive hyphae on edr1 plants, indicating that the initial stages of infection were not inhibited. Production of conidiophores on edr1 plants, however, was <16% of that observed on wild-type Arabidopsis. Reduction in sporulation correlated with a more rapid induction of defense responses. Autofluorescent compounds and callose accumulated in edr1 leaves 3 days after inoculation with E. cichoracearum, and dead mesophyll cells accumulated in edr1 leaves starting 5 days after inoculation. Macroscopic patches of dead cells appeared 6 days after inoculation. This resistance phenotype is similar to that conferred by “late-acting” powdery mildew resistance genes of wheat and barley. The edr1 mutation is recessive and maps to chromosome 1 between molecular markers ATEAT1 and NCC1. We speculate that the edr1 mutation derepresses multiple defense responses, making them more easily induced by virulent pathogens.
Oxford University Press
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