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Arabidopsis MAP kinase 4 regulates salicylic acid- and jasmonic acid/ethylene-dependent responses via EDS1 and PAD4
被引:291
作者:

Brodersen, Peter
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机构: Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen K, Denmark

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Nielsen, Henrik Bjorn
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机构: Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen K, Denmark

Zhu, Shijiang
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机构: Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen K, Denmark

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Shokat, Kevan M.
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机构: Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen K, Denmark

Rietz, Steffen
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机构: Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen K, Denmark

Parker, Jane
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机构: Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen K, Denmark

Mundy, John
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机构: Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen K, Denmark
机构:
[1] Univ Copenhagen, Inst Mol Biol, DK-1353 Copenhagen K, Denmark
[2] Tech Univ Denmark, BioCentrum, Ctr Biol Sequence Anal, DK-2800 Lyngby, Denmark
[3] Royal Vet & Agr Univ, Inst Plant Biol, DK-1871 Frederiksberg, Denmark
[4] Univ Calif San Francisco, Dept Cell & Mol Pharmacol, San Francisco, CA 94143 USA
[5] Max Planck Inst Plant Breeding Res, Dept Plant Microbe Interact, D-50829 Cologne, Germany
关键词:
hormone interactions;
MAP kinase;
pathogen responses;
D O I:
10.1111/j.1365-313X.2006.02806.x
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
Arabidopsis MPK4 has been implicated in plant defense regulation because mpk4 knockout plants exhibit constitutive activation of salicylic acid (SA)-dependent defenses, but fail to induce jasmonic acid (JA) defense marker genes in response to JA. We show here that mpk4 mutants are also defective in defense gene induction in response to ethylene (ET), and that they are more susceptible than wild-type (WT) to Alternaria brassicicola that induces the ET/JA defense pathway(s). Both SA-repressing and ET/JA-(co)activating functions depend on MPK4 kinase activity and involve the defense regulators EDS1 and PAD4, as mutations in these genes suppress de-repression of the SA pathway and suppress the block of the ET/JA pathway in mpk4. EDS1/PAD4 thus affect SA-ET/JA signal antagonism as activators of SA but as repressors of ET/JA defenses, and MPK4 negatively regulates both of these functions. We also show that the MPK4-EDS1/PAD4 branch of ET defense signaling is independent of the ERF1 transcription factor, and use comparative microarray analysis of ctr1, ctr1/mpk4, mpk4 and WT to show that MPK4 is required for induction of a small subset of ET-regulated genes. The regulation of some, but not all, of these genes involves EDS1 and PAD4.
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页码:532 / 546
页数:15
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