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

S. Resjö, A. Ali, H.J.G. Meijer, M.F. Seidl, B. Snel, M. Sandin, F. Levander, F. Govers, E. Andreasson

Research output: Contribution to journalArticleAcademicpeer-review

18 Citations (Scopus)

Abstract

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-stage-specific 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).
Original languageEnglish
Pages (from-to)1848-1859
JournalJournal of Proteome Research
Volume13
Issue number4
DOIs
Publication statusPublished - 2014

Keywords

  • tandem mass-spectrometry
  • protein-kinases
  • arabidopsis-thaliana
  • in-vitro
  • proteomics
  • identification
  • expression
  • potato
  • organization
  • specificity

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