A secreted Ustilago maydis effector promotes virulence by targeting anthocyanin biosynthesis in maize

被引:210
作者
Tanaka, Shigeyuki [1 ]
Brefort, Thomas [1 ]
Neidig, Nina [1 ]
Djamei, Armin [1 ]
Kahnt, Joerg [2 ]
Vermerris, Wilfred [3 ,4 ]
Koenig, Stefanie [5 ]
Feussner, Kirstin [5 ]
Feussner, Ivo [5 ]
Kahmann, Regine [1 ]
机构
[1] Max Planck Inst Terr Microbiol, Dept Organism Interact, D-35043 Marburg, Germany
[2] Max Planck Inst Terr Microbiol, Dept Ecophysiol, D-35043 Marburg, Germany
[3] Univ Florida, Dept Microbiol & Cell Sci, Gainesville, FL 32611 USA
[4] Univ Florida, Genet Inst, Gainesville, FL USA
[5] Univ Gottingen, Albrecht von Haller Inst, D-37073 Gottingen, Germany
关键词
BROWN-MIDRIB MUTANTS; LIGNIN BIOSYNTHESIS; ZEA-MAYS; BM3; MUTATION; SMUT FUNGUS; EXPRESSION; GENE; LIGNIFICATION; PROTEIN; RESISTANCE;
D O I
10.7554/eLife.01355
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The biotrophic fungus Ustilago maydis causes smut disease in maize with characteristic tumor formation and anthocyanin induction. Here, we show that anthocyanin biosynthesis is induced by the virulence promoting secreted effector protein Tin2. Tin2 protein functions inside plant cells where it interacts with maize protein kinase ZmTTK1. Tin2 masks a ubiquitin-proteasome degradation motif in ZmTTK1, thus stabilizing the active kinase. Active ZmTTK1 controls activation of genes in the anthocyanin biosynthesis pathway. Without Tin2, enhanced lignin biosynthesis is observed in infected tissue and vascular bundles show strong lignification. This is presumably limiting access of fungal hyphae to nutrients needed for massive proliferation. Consistent with this assertion, we observe that maize brown midrib mutants affected in lignin biosynthesis are hypersensitive to U. maydis infection. We speculate that Tin2 rewires metabolites into the anthocyanin pathway to lower their availability for other defense responses.
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页数:27
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