| Literature DB >> 26224411 |
M Águila Ruiz-Sola1, Diana Coman2, Gilles Beck2, M Victoria Barja1, Maite Colinas2, Alexander Graf2, Ralf Welsch3, Philipp Rütimann4, Peter Bühlmann4, Laurent Bigler5, Wilhelm Gruissem2, Manuel Rodríguez-Concepción1, Eva Vranová2.
Abstract
Most plastid isoprenoids, including photosynthesis-related metabolites such as carotenoids and the side chain of chlorophylls, tocopherols (vitamin E), phylloquinones (vitamin K), and plastoquinones, derive from geranylgeranyl diphosphate (GGPP) synthesized by GGPP synthase (GGPPS) enzymes. Seven out of 10 functional GGPPS isozymes in Arabidopsis thaliana reside in plastids. We aimed to address the function of different GGPPS paralogues for plastid isoprenoid biosynthesis. We constructed a gene co-expression network (GCN) using GGPPS paralogues as guide genes and genes from the upstream and downstream pathways as query genes. Furthermore, knock-out and/or knock-down ggpps mutants were generated and their growth and metabolic phenotypes were analyzed. Also, interacting protein partners of GGPPS11 were searched for. Our data showed that GGPPS11, encoding the only plastid isozyme essential for plant development, functions as a hub gene among GGPPS paralogues and is required for the production of all major groups of plastid isoprenoids. Furthermore, we showed that the GGPPS11 protein physically interacts with enzymes that use GGPP for the production of carotenoids, chlorophylls, tocopherols, phylloquinone, and plastoquinone. GGPPS11 is a hub isozyme required for the production of most photosynthesis-related isoprenoids. Both gene co-expression and protein-protein interaction likely contribute to the channeling of GGPP by GGPPS11.Entities:
Keywords: Arabidopsis thaliana; GGPPS11; gene paralogues; geranylgeranyl diphosphate synthase
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Year: 2015 PMID: 26224411 DOI: 10.1111/nph.13580
Source DB: PubMed Journal: New Phytol ISSN: 0028-646X Impact factor: 10.151