53 research outputs found

    Host origin of plastid solute transporters in the first photosynthetic eukaryotes

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    Analysis of plastid transporter proteins in Arabidopsis suggests a host origin and provides new insights into plastid evolution

    Eukaryote-to-eukaryote gene transfer gives rise to genome mosaicism in euglenids

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    <p>Abstract</p> <p>Background</p> <p>Euglenophytes are a group of photosynthetic flagellates possessing a plastid derived from a green algal endosymbiont, which was incorporated into an ancestral host cell via secondary endosymbiosis. However, the impact of endosymbiosis on the euglenophyte nuclear genome is not fully understood due to its complex nature as a 'hybrid' of a non-photosynthetic host cell and a secondary endosymbiont.</p> <p>Results</p> <p>We analyzed an EST dataset of the model euglenophyte <it>Euglena gracilis </it>using a gene mining program designed to detect laterally transferred genes. We found <it>E. gracilis </it>genes showing affinity not only with green algae, from which the secondary plastid in euglenophytes evolved, but also red algae and/or secondary algae containing red algal-derived plastids. Phylogenetic analyses of these 'red lineage' genes suggest that <it>E. gracilis </it>acquired at least 14 genes via eukaryote-to-eukaryote lateral gene transfer from algal sources other than the green algal endosymbiont that gave rise to its current plastid. We constructed an EST library of the aplastidic euglenid <it>Peranema trichophorum</it>, which is a eukaryovorous relative of euglenophytes, and also identified 'red lineage' genes in its genome.</p> <p>Conclusions</p> <p>Our data show genome mosaicism in <it>E. gracilis </it>and <it>P. trichophorum</it>. One possible explanation for the presence of these genes in these organisms is that some or all of them were independently acquired by lateral gene transfer and contributed to the successful integration and functioning of the green algal endosymbiont as a secondary plastid. Alternative hypotheses include the presence of a phagocytosed alga as the single source of those genes, or a cryptic tertiary endosymbiont harboring secondary plastid of red algal origin, which the eukaryovorous ancestor of euglenophytes had acquired prior to the secondary endosymbiosis of a green alga.</p

    Photosynthesis in C3-C4 intermediate Moricandia species.

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    Evolution of C4 photosynthesis is not distributed evenly in the plant kingdom. Particularly interesting is the situation in the Brassicaceae, because the family contains no C4 species, but several C3-C4 intermediates, mainly in the genus Moricandia Investigation of leaf anatomy, gas exchange parameters, the metabolome, and the transcriptome of two C3-C4 intermediate Moricandia species, M. arvensis and M. suffruticosa, and their close C3 relative M. moricandioides enabled us to unravel the specific C3-C4 characteristics in these Moricandia lines. Reduced CO2 compensation points in these lines were accompanied by anatomical adjustments, such as centripetal concentration of organelles in the bundle sheath, and metabolic adjustments, such as the balancing of C and N metabolism between mesophyll and bundle sheath cells by multiple pathways. Evolution from C3 to C3-C4 intermediacy was probably facilitated first by loss of one copy of the glycine decarboxylase P-protein, followed by dominant activity of a bundle sheath-specific element in its promoter. In contrast to recent models, installation of the C3-C4 pathway was not accompanied by enhanced activity of the C4 cycle. Our results indicate that metabolic limitations connected to N metabolism or anatomical limitations connected to vein density could have constrained evolution of C4 in Moricandia

    Comprehensive transcriptome analysis of the highly complex Pisum sativum genome using next generation sequencing

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    <p>Abstract</p> <p>Background</p> <p>The garden pea, <it>Pisum sativum</it>, is among the best-investigated legume plants and of significant agro-commercial relevance. <it>Pisum sativum </it>has a large and complex genome and accordingly few comprehensive genomic resources exist.</p> <p>Results</p> <p>We analyzed the pea transcriptome at the highest possible amount of accuracy by current technology. We used next generation sequencing with the Roche/454 platform and evaluated and compared a variety of approaches, including diverse tissue libraries, normalization, alternative sequencing technologies, saturation estimation and diverse assembly strategies. We generated libraries from flowers, leaves, cotyledons, epi- and hypocotyl, and etiolated and light treated etiolated seedlings, comprising a total of 450 megabases. Libraries were assembled into 324,428 unigenes in a first pass assembly.</p> <p>A second pass assembly reduced the amount to 81,449 unigenes but caused a significant number of chimeras. Analyses of the assemblies identified the assembly step as a major possibility for improvement. By recording frequencies of Arabidopsis orthologs hit by randomly drawn reads and fitting parameters of the saturation curve we concluded that sequencing was exhaustive. For leaf libraries we found normalization allows partial recovery of expression strength aside the desired effect of increased coverage. Based on theoretical and biological considerations we concluded that the sequence reads in the database tagged the vast majority of transcripts in the aerial tissues. A pathway representation analysis showed the merits of sampling multiple aerial tissues to increase the number of tagged genes. All results have been made available as a fully annotated database in fasta format.</p> <p>Conclusions</p> <p>We conclude that the approach taken resulted in a high quality - dataset which serves well as a first comprehensive reference set for the model legume pea. We suggest future deep sequencing transcriptome projects of species lacking a genomics backbone will need to concentrate mainly on resolving the issues of redundancy and paralogy during transcriptome assembly.</p

    Antimicrobials: a global alliance for optimizing their rational use in intra-abdominal infections (AGORA)

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    Plastid transport and metabolism of C 3 and C 4 plants- comparative analysis and possible biotechnological exploitation

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    Recent progress in genomics has provided complete or near complete genome sequences of several C3 (e.g. Arabidopsis, rice, and poplar) and C4 (e.g. sorghum and maize) plant species. These genome sequences enabled comparative quantitative proteomic and transcriptomic analyses of C3 and C4 plants, in particular of their chloroplasts. Such analyses have revealed a comprehensive picture of the distribution of C4 pathway components between bundle sheath and mesophyll cell chloroplasts and they permitted the prediction of novel pathway components. A comprehensive understanding of the C4 photosynthetic mechanism is required for the transfer of C4-like photosynthesis into C3 crop plants, such as rice

    Photorespiration: origins and metabolic integration in interacting compartments

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    Hagemann M, Weber APM, Eisenhut M. Photorespiration: origins and metabolic integration in interacting compartments. Journal of Experimental Botany. 2016;67(10):2915-2918
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