Abstract

BackgroundOomycetes are a large group of economically and ecologically important species. Its most notorious member is Phytophthora infestans, the cause of the devastating potato late blight disease. The life cycle of P. infestans involves hyphae which differentiate into spores used for dispersal and host infection. Protein phosphorylation likely plays crucial roles in these stages, and to help understand this we present here a genome-wide analysis of the protein kinases of P. infestans and several relatives. The study also provides new insight into kinase evolution since oomycetes are taxonomically distant from organisms with well-characterized kinomes.ResultsBioinformatic searches of the genomes of P. infestans, P. ramorum, and P. sojae reveal they have similar kinomes, which for P. infestans contains 354 eukaryotic protein kinases (ePKs) and 18 atypical kinases (aPKs), equaling 2% of total genes. After refining gene models, most were classifiable into families seen in other eukaryotes. Some ePK families are nevertheless unusual, especially the tyrosine kinase-like (TKL) group which includes large oomycete-specific subfamilies. Also identified were two tyrosine kinases, which are rare in non-metazoans. Several ePKs bear accessory domains not identified previously on kinases, such as cyclin-dependent kinases with integral cyclin domains. Most ePKs lack accessory domains, implying that many are regulated transcriptionally. This was confirmed by mRNA expression-profiling studies that showed that two-thirds vary significantly between hyphae, sporangia, and zoospores. Comparisons to neighboring taxa (apicomplexans, ciliates, diatoms) revealed both clade-specific and conserved features, and multiple connections to plant kinases were observed. The kinome of Hyaloperonospora arabidopsidis, an oomycete with a simpler life cycle than P. infestans, was found to be one-third smaller. Some differences may be attributable to gene clustering, which facilitates subfamily expansion (or loss) through unequal crossing-over.ConclusionThe large sizes of the Phytophthora kinomes imply that phosphorylation plays major roles in their life cycles. Their kinomes also include many novel ePKs, some specific to oomycetes or shared with neighboring groups. Little experimentation to date has addressed the biological functions of oomycete kinases, but this should be stimulated by the structural, evolutionary, and expression data presented here. This may lead to targets for disease control.

Highlights

  • Oomycetes are a large group of economically and ecologically important species

  • Protein phosphorylation in eukaryotes is mediated by some proteins not related closely to eukaryotic protein kinases (ePKs), including atypical protein kinases that act on serine or threonine and bacterial-like histidine kinases [2,3]

  • Genes encoding 354 ePKs and 18 atypical protein kinases (aPKs) were identified in P. infestans, and their features are summarized in Additional File 1 Tables S1 and S2

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Summary

Introduction

Oomycetes are a large group of economically and ecologically important species. Its most notorious member is Phytophthora infestans, the cause of the devastating potato late blight disease. Protein kinases regulate numerous cellular processes including mitosis, communication, differentiation, metabolism, and transcription. They constitute the largest protein family in most single-celled and multicellular eukaryotes, underscoring the ubiquitousness of phosphorylation as a control mechanism. Most protein kinases share a common ancestry, belonging to the eukaryotic protein kinase (ePK) superfamily [1] These contain a core domain of about 250 amino acids which catalyzes the phosphorylation of serine, threonine, or tyrosine. The further classification of ePKs into subfamilies is possible using features of the catalytic region as well as non-catalytic accessory domains [5] The latter comprise regulatory modules, affect substrate binding, determine subcellular localization, or allow the kinases to serve as scaffolds for multipeptide complexes. The shuffling of non-catalytic domains is likely a major feature behind the diversification of eukaryotic species

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