Lr34-Mediated Leaf Rust Resistance in Wheat: Transcript Profiling Reveals a High Energetic Demand Supported by Transient Recruitment of Multiple Metabolic Pathways
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Bolton, Melvin D.
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Univ Minnesota, USDA ARS, Plant Sci Res Unit, St Paul, MN 55108 USAUniv Minnesota, USDA ARS, Plant Sci Res Unit, St Paul, MN 55108 USA
Bolton, Melvin D.
[1
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Kolmer, James A.
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Univ Minnesota, USDA ARS, Cereal Dis Lab, St Paul, MN 55108 USAUniv Minnesota, USDA ARS, Plant Sci Res Unit, St Paul, MN 55108 USA
Kolmer, James A.
[2
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Xu, Wayne W.
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Univ Minnesota, Inst Supercomp, Minneapolis, MN 55455 USAUniv Minnesota, USDA ARS, Plant Sci Res Unit, St Paul, MN 55108 USA
Xu, Wayne W.
[3
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Garvin, David F.
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Univ Minnesota, USDA ARS, Plant Sci Res Unit, St Paul, MN 55108 USAUniv Minnesota, USDA ARS, Plant Sci Res Unit, St Paul, MN 55108 USA
Garvin, David F.
[1
]
机构:
[1] Univ Minnesota, USDA ARS, Plant Sci Res Unit, St Paul, MN 55108 USA
[2] Univ Minnesota, USDA ARS, Cereal Dis Lab, St Paul, MN 55108 USA
[3] Univ Minnesota, Inst Supercomp, Minneapolis, MN 55455 USA
The wheat gene Lr34 confers partial resistance to all races of Puccinia triticina, the causal agent of wheat leaf rust. However, the biological basis for the exceptional durability of Lr34 is unclear. We used the Affymetrix GeneChip Wheat Genome Array to compare transcriptional changes of near-isogenic lines of Thatcher wheat in a compatible interaction, an incompatible interaction conferred by the resistance gene Lr1, and the race-nonspecific response conditioned by Lr34 3 and 7 days postinoculation (dpi) with P. triticina. No differentially expressed genes were detected in Lr1 plants at either timepoint whereas, in the compatible Thatcher interaction, differentially expressed genes were detected only at 7 dpi. In contrast, differentially expressed genes were identified at both timepoints in P. triticina-inoculated Lr34 plants. At 3 dpi, upregulated genes associated with Lr34-mediated resistance encoded various defense and stress-related proteins, secondary metabolism enzymes, and transcriptional regulation and cellular-signaling proteins. Further, coordinated upregulation of key genes in several metabolic pathways that can contribute to increased carbon flux through the tricarboxylic cycle was detected. This indicates that Lr34-mediated resistance imposes a high energetic demand that leads to the induction of multiple metabolic responses to support cellular energy requirements. These metabolic responses were not sustained through 7 dpi, and may explain why Lr34 fails to inhibit the pathogen fully but does increase the latent period.
机构:Iowa State Univ, Dept Plant Pathol, USDA, ARS,Corn Insects & Crop Genet Unit, Ames, IA 50011 USA
Caldo, Rico A.
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Nettleton, Dan
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Peng, Jiqing
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机构:Iowa State Univ, Dept Plant Pathol, USDA, ARS,Corn Insects & Crop Genet Unit, Ames, IA 50011 USA
Peng, Jiqing
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Wise, Roger P.
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Iowa State Univ, Dept Plant Pathol, USDA, ARS,Corn Insects & Crop Genet Unit, Ames, IA 50011 USAIowa State Univ, Dept Plant Pathol, USDA, ARS,Corn Insects & Crop Genet Unit, Ames, IA 50011 USA
机构:Iowa State Univ, Dept Plant Pathol, USDA, ARS,Corn Insects & Crop Genet Unit, Ames, IA 50011 USA
Caldo, Rico A.
;
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机构:
Nettleton, Dan
;
Peng, Jiqing
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机构:Iowa State Univ, Dept Plant Pathol, USDA, ARS,Corn Insects & Crop Genet Unit, Ames, IA 50011 USA
Peng, Jiqing
;
Wise, Roger P.
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h-index: 0
机构:
Iowa State Univ, Dept Plant Pathol, USDA, ARS,Corn Insects & Crop Genet Unit, Ames, IA 50011 USAIowa State Univ, Dept Plant Pathol, USDA, ARS,Corn Insects & Crop Genet Unit, Ames, IA 50011 USA