Arabidopsis Cell Death in Compatible and Incompatible Interactions with Alternaria brassicicolaopen access
- Authors
- Su'udi, Mukhamad; Kim, Min Gab; Park, Sang-Ryeol; Hwang, Duk-Ju; Bae, Shin-Chul; Ahn, Il-Pyung
- Issue Date
- Jun-2011
- Publisher
- KOREAN SOC MOLECULAR & CELLULAR BIOLOGY
- Keywords
- necrotroph; programmed cell death
- Citation
- MOLECULES AND CELLS, v.31, no.6, pp 593 - 601
- Pages
- 9
- Indexed
- SCI
SCIE
SCOPUS
KCI
- Journal Title
- MOLECULES AND CELLS
- Volume
- 31
- Number
- 6
- Start Page
- 593
- End Page
- 601
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/23720
- DOI
- 10.1007/s10059-011-2203-z
- ISSN
- 1016-8478
0219-1032
- Abstract
- Two strains of necrotrophic Alternaria brassicicola, Ab40857 and Ab42464, are virulent on Korean cabbage and several wild types of Arabidopsis thaliana. Interaction between Ab42464 and Col-0 was compatible, whereas interaction between Ab40857 and Col-0 was incompatible. The loss of defense, no death (dnd) 1 function abrogated the compatibility between Ab42464 and Col-0, and the accelerated cell death (acd) 2 mutation attenuated the Col-0' s resistance against Ab40857. These two fungal strains induced PR1 transcription in Col-0. Ab40857 accelerated transcription of PDF1.2, THI2.1, CAT, and POX by 12 h compared to those challenged with Ab42464. More abundant cell death was observed in Col-0 infected with Ab42464, however, callose deposition was evident in the incompatible interaction. Remarkably, Ab40857-infected areas of acd2-2 underwent rampant cell death and Ab42464 triggered callose production in dnd1-1. Furthermore, the incompatibility between Ab40857 and Col-0 was nullified by the coronatine-insensitive 1 (coi1) and phytoalexin-deficient 3 (pad3) mutations but not by nonexpresser of PR genes (npr1) and pad4. Ab40857 induced abundant cell death in pad3. Taken together, cell death during the early infection stage is a key determinant that discriminates between a compatible interaction and an incompatible one, and the resistance within Col-0 against Ab40857 is dependent on a defensesignaling pathway mediated by jasmonic acid and PAD3.
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