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Book of Abstracts <strong>First</strong> <strong>Legume</strong> <strong>Society</strong> <strong>Conference</strong> 2013: A <strong>Legume</strong> Odyssey Novi Sad, Serbia, 9-11 May 2013<br />

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Identification of genes involved in resistance to Didymella pinodes in pea by<br />

deepSuperSAGE genome-wide transcriptome profiling<br />

Sara Fondevilla 1,2 , Björn Rotter 3 , Nicolas Krezdorn 3 , Ruth Jüngling 3 , Peter Winter 3 , Diego<br />

Rubiales 1<br />

1 Institute for Sustainable Agriculture, CSIC, Córdoba, Spain<br />

2 University of Frankfurt, Biocenter, Frankfurt, Germany<br />

3 GenXPro GmbH, Frankfurt am Main, Germany<br />

Didymella pinodes, causing ascochyta blight, is one of the most important pea pathogens. Despite<br />

the devastating consequences of this disease, very little is known about the mechanisms of<br />

resistance in the host. We employed the open-architecture transcriptome profiling technique<br />

deepSuperSAGE, coupled with next-generation sequencing, to identify pea-specific genes<br />

involved in the resistance to this important disease in the resistant Pisum sativum ssp. syriacum<br />

accession P665.Two deepSuperSAGE libraries were constructed from leaf RNA of infected and<br />

control plants, yielding a total of 17,561 different UniTags. 70% of them could be assigned to<br />

known sequences from pea or other plants. 509 UniTags were significantly differentially<br />

expressed (p < 0.05; fold change ≥ 2, ≤ 2) in inoculated versus control plants. This study<br />

provides a detailed picture of all expressed genes and metabolic pathways differentially regulated<br />

during D. pinodes-Pisum sativum interaction and contribute to the identification of candidate<br />

resistance genes. Protease inhibitors, antifungal compounds, strengthening of host cell walls,<br />

detoxification of D. pinodes toxins and repair of cell walls could contribute to resistance. Ethylene,<br />

ABA and indole-3-acetic acid pathways were up-, while the GA pathway was down-regulated.<br />

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