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http://purl.uniprot.org/citations/25794895http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/25794895http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/25794895http://www.w3.org/2000/01/rdf-schema#comment"Although sphingolipids are essential for male gametophytic development in Arabidopsis thaliana, sphingolipid composition and biosynthetic gene expression have not been previously examined in pollen. In this report, electrospray ionization (ESI)-MS/MS was applied to characterization of sphingolipid compositional profiles in pollen isolated from wild type Arabidopsis Col-0 and a long-chain base (LCB) Δ4 desaturase mutant. Pollen fractions were highly enriched in glucosylceramides (GlcCer) relative to levels previously reported in leaves. Accompanying the loss of the Δ4 unsaturated LCB sphingadiene (d18:2) in the Δ4 desaturase mutant was a 50% reduction in GlcCer concentrations. In addition, pollen glycosylinositolphosphoceramides (GIPCs) were found to have a complex array of N-acetyl-glycosylated GIPCs, including species with up to three pentose units that were absent from leaf GIPCs. Underlying the distinct sphingolipid composition of pollen, genes for key biosynthetic enzymes for GlcCer and d18:2 synthesis and metabolism were more highly expressed in pollen than in leaves or seedlings, including genes for GlcCer synthase (GCS), sphingoid base C-4 hydroxylase 2 (SBH2), LCB Δ8 desaturases (SLD1 and SLD2), and LOH2 ceramide synthase (LOH2). Overall, these findings indicate strikingly divergent sphingolipid metabolism between pollen and leaves in Arabidopsis, the significance of which remains to be determined."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.org/dc/terms/identifier"doi:10.1016/j.phytochem.2015.02.019"xsd:string
http://purl.uniprot.org/citations/25794895http://purl.org/dc/terms/identifier"doi:10.1016/j.phytochem.2015.02.019"xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Cahoon E.B."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Cahoon E.B."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Cahoon R.E."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Cahoon R.E."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Markham J.E."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Markham J.E."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Napier J.A."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Napier J.A."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Cerny R.L."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Cerny R.L."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Kimberlin A.N."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Kimberlin A.N."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Luttgeharm K.D."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/author"Luttgeharm K.D."xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/name"Phytochemistry"xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/name"Phytochemistry"xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/pages"121-129"xsd:string
http://purl.uniprot.org/citations/25794895http://purl.uniprot.org/core/pages"121-129"xsd:string