Modulation of Protein Phosphorylation, N-Glycosylation and Lys-Acetylation in Grape (Vitis vinifera) Mesocarp and Exocarp Owing to Lobesia botrana Infection

• Published in: Molecular & cellular proteomics Vol. 11; no. 10; pp. 945 - 956
• Main Authors: Melo-Braga, Marcella N., Verano-Braga, Thiago, León, Ileana R., Antonacci, Donato, Nogueira, Fábio C.S., Thelen, Jay J., Larsen, Martin R., Palmisano, Giuseppe
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.10.2012; The American Society for Biochemistry and Molecular Biology
• Subjects: Acetylation; Amino Acid Motifs; Animals; Chromatography, Liquid; Fruit - genetics; Fruit - immunology; Fruit - parasitology; Gene Expression Regulation, Plant; Glycosylation; Host-Parasite Interactions; Molecular Sequence Data; Moths - pathogenicity; Moths - physiology; Phosphopeptides - analysis; Phosphorylation; Plant Diseases; Plant Proteins - genetics; Plant Proteins - metabolism; Protein Processing, Post-Translational; Proteomics; Staining and Labeling; Tandem Mass Spectrometry; Vitis - genetics; Vitis - immunology; Vitis - parasitology
• DOI: 10.1074/mcp.M112.020214
• ISSN: 1535-9476; 1535-9484

Grapevine (Vitis vinifera) is an economically important fruit crop that is subject to many types of insect and pathogen attack. To better elucidate the plant response to Lobesia botrana pathogen infection, we initiated a global comparative proteomic study monitoring steady-state protein expression as well as changes in N-glycosylation, phosphorylation, and Lys-acetylation in control and infected mesocarp and exocarp from V. vinifera cv Italia. A multi-parallel, large-scale proteomic approach employing iTRAQ labeling prior to three peptide enrichment techniques followed by tandem mass spectrometry led to the identification of a total of 3059 proteins, 1135 phosphorylation sites, 323 N-linked glycosylation sites and 138 Lys-acetylation sites. Of these, we could identify changes in abundance of 899 proteins. The occupancy of 110 phosphorylation sites, 10 N-glycosylation sites and 20 Lys-acetylation sites differentially changed during L. botrana infection. Sequence consensus analysis for phosphorylation sites showed eight significant motifs, two of which containing up-regulated phosphopeptides (X-G-S-X and S-X-X-D) and two containing down-regulated phosphopeptides (R-X-X-S and S-D-X-E) in response to pathogen infection. Topographical distribution of phosphorylation sites within primary sequences reveal preferential phosphorylation at both the N- and C termini, and a clear preference for C-terminal phosphorylation in response to pathogen infection suggesting induction of region-specific kinase(s). Lys-acetylation analysis confirmed the consensus X-K-Y-X motif previously detected in mammals and revealed the importance of this modification in plant defense. The importance of N-linked protein glycosylation in plant response to biotic stimulus was evident by an up-regulated glycopeptide belonging to the disease resistance response protein 206. This study represents a substantial step toward the understanding of protein and PTMs-mediated plant-pathogen interaction shedding light on the mechanisms underlying the grape infection.