4.7 Article

Quantitative Label-Free Phosphoproteomics of Six Different Life Stages of the Late Blight Pathogen Phytophthora infestans Reveals Abundant Phosphorylation of Members of the CRN Effector Family

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 13, Issue 4, Pages 1848-1859

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/pr4009095

Keywords

Phytophthora infestans; late blight; potato; protein phosphorylation; proteomics; phosphoproteomics; effectors; Crinklers; CRN proteins; tyrosine phosphorylation; phosphorylation motifs; appressorium

Funding

  1. Swedish Foundation for Strategic Research
  2. Crafoord Foundation
  3. Royal Physiographical Society of Lund
  4. Swedish Research Council for Environment, Agricultural Sciences and Spatial Planning
  5. Technology Foundation of The Netherlands Organization for Scientific Research (STW-NWO) [10281]
  6. Centre for BioSystems Genomics (CBSG), part of The Netherlands Genomics Initiative/Netherlands Organization for Scientific Research

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The oomycete Phytophthora infestans is the causal agent of late blight in potato and tomato. Since the underlying processes that govern pathogenicity and development in P. infestans are largely unknown, we have performed a large-scale phosphoproteomics study of six different P. infestans life stages. We have obtained quantitative data for 2922 phosphopeptides and compared their abundance. Life-stages-pecific phosphopeptides include ATP-binding cassette transporters and a kinase that only occurs in appressoria. In an extended data set, we identified 2179 phosphorylation sites and deduced 22 phosphomotifs. Several of the phosphomotifs matched consensus sequences of kinases that occur in P. infestans but not Arabidopsis. In addition, we detected tyrosine phosphopeptides that are potential targets of kinases resembling mammalian tyrosine kinases. Among the phosphorylated proteins are members of the RXLR and Crinkler effector families. The latter are phosphorylated in several life stages and at multiple positions, in sites that are conserved between different members of the Crinkler family. This indicates that proteins in the Crinkler family have functions beyond their putative role as (necrosis-inducing) effectors. This phosphoproteomics data will be instrumental for studies on oomycetes and host oomycete interactions. The data sets have been deposited to ProteomeXchange (identifier PXD000433).

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