A Molecular Insight into Algal-Oomycete Warfare cDNA Analysis of Ectocarpus siliculosus Infected with the Basal Oomycete Eurychasma dicksonii 英文参考文献.docVIP
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A Molecular Insight into Algal-Oomycete Warfare cDNA Analysis of Ectocarpus siliculosus Infected with the Basal Oomycete Eurychasma dicksonii 英文参考文献
AMolecularInsightintoAlgal-OomyceteWarfare:cDNA
AnalysisofEctocarpussiliculosusInfectedwiththeBasal
OomyceteEurychasmadicksonii
LauraGrenville-Briggs1.,ClaireM.M.Gachon2.,MartinaStrittmatter1,2,LievenSterck3,4,FrithjofC.
Ku¨pper2,PietervanWest1*
1AberdeenOomyceteLaboratory,UniversityofAberdeen,Aberdeen,UnitedKingdom,2ScottishAssociationforMarineScience,ScottishMarineInstitute,Oban,Argyll,
UnitedKingdom,3DepartmentofPlantSystemsBiology,FlandersInstituteforBiotechnology(VIB),Ghent,Belgium,4DepartmentofPlantBiotechnologyandGenetics,
GhentUniversity,Ghent,Belgium
Abstract
Brown algae are the predominant primary producers in coastal habitats, and like land plants are subject to disease and
parasitism. Eurychasma dicksonii is anabundant,andprobably cosmopolitan,obligate biotrophic oomycete pathogenof
marine brown algae. Oomycetes (or water moulds) are pathogenic or saprophytic non-photosynthetic Stramenopiles,
mostlyknownforcausingdevastatingagriculturalandaquaculturaldiseases.Whilstmolecularknowledgeisrestrictedto
croppathogens,pathogenicoomycetesactuallyinfecthostsfrommosteukaryoticlineages.Molecularevidenceindicates
that Eu. dicksonii belongs to the most early-branching oomycete clade known so far. Therefore Eu. dicksonii is of
considerableinterestduetoitspresumedenvironmentalimpactandphylogeneticposition.Herewereportthefirstlarge
scale functional molecular data acquired on the most basal oomycete to date. 9873 unigenes, totalling over 3.5Mb of
sequencedata,wereproducedfromSanger-sequencedandpyrosequencedESTlibrariesofinfectedEctocarpussiliculosus.
6787unigenes(70%)wereofalgalorigin,and3086(30%)oomyceteorigin.57%ofEu.dicksoniisequenceshadnosimilarity
topublishedsequencedata,indicatingthatthisdatasetislargelyunique.Wewereunabletopositivelyidentifysequences
belongingtotheRXLRandCRNgroupsofoomyceteeffectorsidentifiedinhigheroomycetes,howeverweuncoveredother
unique pathogenicity factors. These included putative algal cell wall degrading enzymes, cell surface proteins, and
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