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  • 1
    ISSN: 1573-5028
    Keywords: Antibody ; coordinated expression ; genetic engineering ; protein assembly ; root ; secretion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract To explore the feasibility of employing antibodies to obtain disease resistance against plant root pathogens, we have studied the expression of genes encoding antibodies in roots of transgenic plants. A model monoclonal antibody was used that binds to a fungal cutinase. Heavy and light chain cDNAs were amplified by PCR, fused to a signal sequence for secretion and cloned behind CaMV 35S and TR2′ promoters in a single T-DNA. The chimeric genes were cloned both in tandem and in a divergent orientation. The roots of tobacco plants transformed with these constructs produced antibodies that were able to bind antigen in an ELISA. Immunoblotting showed assembly to a full-size antibody. In addition, a F(ab′)2-like fragment was observed, which is probably formed by proteolytic processing. Both antibody species were properly targeted to the apoplast, but the full-size antibody was partially retained by the wall of suspension cells. The construct with divergent promoters showed a better performance than the construct with promoters in tandem. It directed the accumulation of functional antibodies to a maximum of 1.1% of total soluble protein, with half of the plants having levels higher than 0.35%. The high efficiency of this construct probably results from coordinated and balanced expression of light and heavy chain genes, as evidenced by RNA blot hybridization.
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  • 2
    ISSN: 1573-5028
    Keywords: carrot ; cell wall ; suspension culture ; secreted glycoprotein ; root ; nodulin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A 47 kDa glycoprotein, termed EP4, was purified from carrot cell suspension culture medium. An antiserum raised against EP4 also recognized a protein of 45 kDa that was ionically bound to the cell wall. EP4 was detected in culture media from both embryogenic and non-embryogenic cell lines and was found to be secreted by a specific subset of non-embryogenic cells. Secretion of the 47 kDa glycoprotein by embryogenic cells was not evident. The 45 kDa cell wall-bound EP4 protein was specific for non-embryogenic cells and was shown by immunolocalization to occur in the walls of clustered cells, with the highest levels in the walls separating adjacent cells. In seedlings, EP4 proteins were mainly found in roots. EP4 cDNA was cloned by screening a cDNA library with an oligonucleotide derived from an EP4 peptide sequence. The EP4 cDNA sequence was found to be 55% homologous to ENOD8, an early nodulin gene from alfalfa.
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  • 3
    ISSN: 0044-2313
    Keywords: Selenites ; hydrates ; X-ray ; IR ; crystal structure ; pseudosymmetry ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Polymorphic and Pseudosymmetrical Hydrates MSeO3 · H2O (M = Mn, Co, Ni, Zn, Cd)By crystallization from aqueous solutions of MSeO3 and M(HSeO3)2, the selenites MSeO3 · H2O (M = Mn, Co, Ni, Zn, Cd) were obtained and characterized by means of X-ray diffraction and IR-spectroscopy. The crystal structure of ZnSeO3 · H2O was determined. The IR spectra indicate that the hydrates are isotypic and contain H2O molecules of symmetry mm2. However, the X-ray data show different structure types with H2O molecules of site symmetry m or 1. CdSeO3 · H2O and MnSeO3 · H2O are isotypic (o.rh., MnSeO3 · D2O type). CoSeO3 · H2O (mon.) as well as the isotypic NiSeO3 · H2O and ZnSeO3 · H2O (mon.) form new structure types. These findings are discussed on the basis of the crystal structure of ZnSeO3 · H2O (P21/n, a = 477.9(1), b = 1319.4(5), c = 570.1(1) pm, β = 90.84(2)°, Z = 4, Dx = 3.886 g · cm-3, R = 0.035 for 722 reflections with I 〉 2σ1) and the local pseudosymmetry of its components, i.e., layers ∞2[ZnSeO3 · H2O] of ZnO6 octahedra sharing four equatorial vertices, SeO32- anions and H2O molecules.
    Notes: Durch Kristallisation aus MSeO3- und M(HSeO3)2-Lösungen wurden die Selenite MSeO3 · H2O (M = Mn, Co, Ni, Zn, Cd) erhalten und röntgenographisch sowie IR-spektroskopisch charakterisiert. Von ZnSeO3 · H2O wurde die Kristallstruktur bestimmt. Die IR-Spektren deuten auf Isotypie der Hydrate und H2O-Moleküle der Symmetrie mm2. Die Röntgenbeugungsdaten zeigen dagegen das Vorliegen verschiedener Strukturtypen mit H2O-Molekülen der Lagesymmetrie m oder 1. CdSeO3 · H2O und MnSeO3 · H2O sind isotyp (o.rh., MnSeO3 · D2O-Typ). CoSeO3 · H2O (mon.) sowie die isotypen NiSeO3 · H2O und ZnSeO3 · H2O (mon.) kristallisieren in neuen Strukturtypen. Diese Befunde werden auf der Basis der Kristallstruktur von ZnSeO3 · H2O (P21/n, a = 477,9(1), b = 1319,4(5), c = 570,1(1) pm, β = 90,84(2)°, Z = 4, Dx = 3,886 g · cm-3, R = 0,035 für 722 Reflexe mit I 〉 2σ1) und der lokalen Pseudosymmetrie ihrer Bausteine (Schichten ∞2[ZnSeO3 · H2O] aus vierfach eckenverknüpften ZnO6-Oktaedern, SeO32--Anionen und H2O-Moleküle) diskutiert.
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  • 4
    ISSN: 0044-2313
    Keywords: Hydrogen selenites ; crystal structure ; IR ; Raman heating ; thermal analysis ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Hydrates M(HSeO3)2 · 4H2O (M = Mg, Co, Ni, Zn) - Crystal Structures, IR, Raman, and Thermoanalytical InvestigationsFrom aqueous solutions of M(HSeO3)2 single crystals of Mg(HSeO3)2 · 4H2O and of the hitherto unknown compounds Co(HSeO3)2 · 4H2O, Ni(HSeO3)2 · 4H2O and Zn(HSeO3)2 · 4H2O could be obtained. The crystal structures, X-ray powder, IR, Raman and thermoanalytical (DTA, TG, Raman heating) data are presented and discussed. The crystal data of the isotypic compounds are: monoclinic, space group C2/c, Z = 4, Mg: a = 1 464.6(2), b = 755.3(1), c = 1 099.9(1) pm, β = 126.59(1)°, V = 0.9769(1) nm3, Co: a = 1 462.5(2), b = 756.5(2), c = 1 102.2(2) pm, β = 126.53(1)°, V = 0.9798(2) nm3, Ni: a = 1 452.2(2), b = 751.0(1), c = 1 091.5(1) pm, β = 126.28(1)°, V = 0.9595(1) nm3, Zn: a = 1 468.3(2), b = 755.8(1), c = 1 103.1(1) pm, β = 126.79(1)°, V = 0.9804(2) nm3. The crystal structures consist of hexagonal packed [M(HSeO3)2 · 2H2O]n chains of [MO4(H2O)2] octahedra linked by Se atoms. They contain trigonal pyramidal SeO2OH-ions with “free” hydroxyl groups and also “free” molecules of water of crystallization. The hydroxyl groups build strong H-bonds (O—H … O distances: 265-268 pm). The IR spectra show AB doublett bands in the OH stretching mode region of the hydroxyl groups. The water molecules of crystallization are linked to planar (H2O)4 tetramers by H-bonds with unusually short O—H … O bond distances of 271-273 pm. DTA and TG measurements indicate that thermal decomposition results in the direct formation of the respective diselenite MSe2O5. Raman heating measurements show under quasi static conditions the intermediate formation of the anhydrous hydrogen selenites.
    Notes: Aus M(HSeO3)2-Lösungen konnten erstmals Einkristalle von Mg(HSeO3)2 · 4H2O sowie die bisher nicht bekannten Verbindungen Co(HSeO3)2 · 4H2O, Ni(HSeO3)2 · 4H2O und Zn(HSeO3)2 · 4H2O erhalten werden. Die Kristallstrukturen, Röntgenpulverdaten, IR- und Raman-Spektren sowie die Ergebnisse thermoanalytischer (DTA, TG, Raman-Heizaufnahmen) Untersuchungen werden mitgeteilt und diskutiert. Die Kristalldaten der isotypen Verbindungen sind: monoklin, Raumgruppe C2/c, Z = 4, Mg: a = 1 464,6(2), b = 755,3(1), c = 1 099,9(1) pm, β = 126,59(1)°, V = 0,9769(1) nm3, Co: a = 1 462,5(2), b = 756,5(2), c = 1 102,2(2) pm, β = 126,53(1)°, V = 0,9798(2) nm3, Ni: a = 1 452,2(2), b = 751,0(1), c = 1 091,5(1) pm, β = 126,28(1)°, V = 0,9595(1) nm3, Zn: a = 1 468,3(2), b = 755,8(1), c = 1 103,1(1) pm, β = 126,79(1)°, V = 0,9804(2) nm3. Die Kristallstrukturen bestehen aus hexagonal gepackten [M(HSeO3)2 · 2H2O]n-Ketten Se-verbrückter [MO4(H2O)2]-Oktaeder. Sie enthalten trigonal pyramidale SeO2OH--Ionen mit „freien“ Hydroxylgruppen und „freie“ Kristallwassermoleküle. Die Hydroxylgruppen bilden starke H-Brücken (O—H … O-Abstände: 265-268 pm). Die IR-Spektren zeigen im Bereich der OH-Streckschwingungen der Hydroxylgruppen AB-Doublett-Banden. Die Kristallwassermoleküle sind zu planaren (H2O)4-Tetrameren mit ungewöhnlich kurzen O—H … Ow-Abständen (271 - 273 pm) H-verbrückt. Die thermische Zersetzung führt nach DTA- und TG-Messungen direkt zum jeweiligen Diselenit MSe2O5. Mittels Raman-Heizaufnahmen unter Quasi-Gleichgewichtsbedingungen konnte erstmals die intermediäre Bildung wasserfreier Hydrogenselenite beobachtet werden.
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  • 5
    Publication Date: 2009-07-15
    Description: The formation of a complex nervous system requires the intricate interaction of neurons and glial cells. Glial cells generally migrate over long distances before they initiate their differentiation, which leads to wrapping and insulation of axonal processes. The molecular pathways coordinating the switch from glial migration to glial differentiation are largely unknown. Here we demonstrate that, within the Drosophila eye imaginal disc, fibroblast growth factor (FGF) signalling coordinates glial proliferation, migration and subsequent axonal wrapping. Glial differentiation in the Drosophila eye disc requires a succession from glia-glia interaction to glia-neuron interaction. The neuronal component of the fly eye develops in the peripheral nervous system within the eye-antennal imaginal disc, whereas glial cells originate from a pool of central-nervous-system-derived progenitors and migrate onto the eye imaginal disc. Initially, glial-derived Pyramus, an FGF8-like ligand, modulates glial cell number and motility. A switch to neuronally expressed Thisbe, a second FGF8-like ligand, then induces glial differentiation. This switch is accompanied by an alteration in the intracellular signalling pathway through which the FGF receptor channels information into the cell. Our findings reveal how a switch from glia-glia interactions to glia-neuron interactions can trigger formation of glial membrane around axonal trajectories. These results disclose an evolutionarily conserved control mechanism of axonal wrapping, indicating that Drosophila might serve as a model to understand glial disorders in humans.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Franzdottir, Sigridur Rut -- Engelen, Daniel -- Yuva-Aydemir, Yeliz -- Schmidt, Imke -- Aho, Annukka -- Klambt, Christian -- England -- Nature. 2009 Aug 6;460(7256):758-61. doi: 10.1038/nature08167. Epub 2009 Jul 13.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Institut fur Neurobiologie, Universitat Munster, Badestr. 9, D-48149 Munster, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19597479" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Axons/metabolism ; *Cell Differentiation ; Cell Movement ; Cell Proliferation ; Drosophila Proteins/metabolism ; Drosophila melanogaster/cytology/genetics/growth & development/*metabolism ; Eye/*cytology/growth & development/innervation/metabolism ; Fibroblast Growth Factors/*metabolism ; Guinea Pigs ; Ligands ; Neuroglia/*cytology/*metabolism ; *Signal Transduction
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2015-05-23
    Description: Marine plankton support global biological and geochemical processes. Surveys of their biodiversity have hitherto been geographically restricted and have not accounted for the full range of plankton size. We assessed eukaryotic diversity from 334 size-fractionated photic-zone plankton communities collected across tropical and temperate oceans during the circumglobal Tara Oceans expedition. We analyzed 18S ribosomal DNA sequences across the intermediate plankton-size spectrum from the smallest unicellular eukaryotes (protists, 〉0.8 micrometers) to small animals of a few millimeters. Eukaryotic ribosomal diversity saturated at ~150,000 operational taxonomic units, about one-third of which could not be assigned to known eukaryotic groups. Diversity emerged at all taxonomic levels, both within the groups comprising the ~11,200 cataloged morphospecies of eukaryotic plankton and among twice as many other deep-branching lineages of unappreciated importance in plankton ecology studies. Most eukaryotic plankton biodiversity belonged to heterotrophic protistan groups, particularly those known to be parasites or symbiotic hosts.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉de Vargas, Colomban -- Audic, Stephane -- Henry, Nicolas -- Decelle, Johan -- Mahe, Frederic -- Logares, Ramiro -- Lara, Enrique -- Berney, Cedric -- Le Bescot, Noan -- Probert, Ian -- Carmichael, Margaux -- Poulain, Julie -- Romac, Sarah -- Colin, Sebastien -- Aury, Jean-Marc -- Bittner, Lucie -- Chaffron, Samuel -- Dunthorn, Micah -- Engelen, Stefan -- Flegontova, Olga -- Guidi, Lionel -- Horak, Ales -- Jaillon, Olivier -- Lima-Mendez, Gipsi -- Lukes, Julius -- Malviya, Shruti -- Morard, Raphael -- Mulot, Matthieu -- Scalco, Eleonora -- Siano, Raffaele -- Vincent, Flora -- Zingone, Adriana -- Dimier, Celine -- Picheral, Marc -- Searson, Sarah -- Kandels-Lewis, Stefanie -- Tara Oceans Coordinators -- Acinas, Silvia G -- Bork, Peer -- Bowler, Chris -- Gorsky, Gabriel -- Grimsley, Nigel -- Hingamp, Pascal -- Iudicone, Daniele -- Not, Fabrice -- Ogata, Hiroyuki -- Pesant, Stephane -- Raes, Jeroen -- Sieracki, Michael E -- Speich, Sabrina -- Stemmann, Lars -- Sunagawa, Shinichi -- Weissenbach, Jean -- Wincker, Patrick -- Karsenti, Eric -- New York, N.Y. -- Science. 2015 May 22;348(6237):1261605. doi: 10.1126/science.1261605.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉CNRS, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. Sorbonne Universites, Universite Pierre et Marie Curie (UPMC) Paris 06, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. vargas@sb-roscoff.fr pwincker@genoscope.cns.fr karsenti@embl.de. ; CNRS, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. Sorbonne Universites, Universite Pierre et Marie Curie (UPMC) Paris 06, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. ; Department of Ecology, University of Kaiserslautern, Erwin-Schroedinger Street, 67663 Kaiserslautern, Germany. CNRS, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. Sorbonne Universites, Universite Pierre et Marie Curie (UPMC) Paris 06, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. ; Department of Marine Biology and Oceanography, Institute of Marine Science (ICM)-Consejo Superior de Investigaciones Cientificas (CSIC), Passeig Maritim de la Barceloneta 37-49, Barcelona E08003, Spain. ; Laboratory of Soil Biology, University of Neuchatel, Rue Emile-Argand 11, 2000 Neuchatel, Switzerland. ; CNRS, FR2424, Roscoff Culture Collection, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. Sorbonne Universites, UPMC Paris 06, FR 2424, Roscoff Culture Collection, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. ; CNRS, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. Sorbonne Universites, Universite Pierre et Marie Curie (UPMC) Paris 06, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. Ecole Normale Superieure, Institut de Biologie de l'ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris, F-75005 France. ; Commissariat a l'Energie Atomique et aux Energies Alternatives (CEA), Institut de Genomique, GENOSCOPE, 2 rue Gaston Cremieux, 91000 Evry, France. ; CNRS FR3631, Institut de Biologie Paris-Seine, F-75005, Paris, France. Sorbonne Universites, UPMC Paris 06, Institut de Biologie Paris-Seine, F-75005, Paris, France. Ecole Normale Superieure, Institut de Biologie de l'ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris, F-75005 France. CNRS, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. Sorbonne Universites, Universite Pierre et Marie Curie (UPMC) Paris 06, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. ; Department of Microbiology and Immunology, Rega Institute, KU Leuven, Herestraat 49, 3000 Leuven, Belgium. Center for the Biology of Disease, VIB, Herestraat 49, 3000 Leuven, Belgium. Department of Applied Biological Sciences, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium. ; Department of Ecology, University of Kaiserslautern, Erwin-Schroedinger Street, 67663 Kaiserslautern, Germany. ; Institute of Parasitology, Biology Centre, Czech Academy of Sciences, Branisovska 31, 37005 Ceske Budejovice, Czech Republic. Faculty of Science, University of South Bohemia, Branisovska 31, 37005 Ceske Budejovice, Czech Republic. ; CNRS, UMR 7093, Laboratoire d'Oceanographie de Villefranche-sur-Mer (LOV), Observatoire Oceanologique, F-06230, Villefranche-sur-Mer, France. Sorbonne Universites, UPMC Paris 06, UMR 7093, LOV, Observatoire Oceanologique, F-06230, Villefranche-sur-Mer, France. ; Commissariat a l'Energie Atomique et aux Energies Alternatives (CEA), Institut de Genomique, GENOSCOPE, 2 rue Gaston Cremieux, 91000 Evry, France. CNRS, UMR 8030, CP5706, Evry, France. Universite d'Evry, UMR 8030, CP5706, Evry, France. ; Institute of Parasitology, Biology Centre, Czech Academy of Sciences, Branisovska 31, 37005 Ceske Budejovice, Czech Republic. Faculty of Science, University of South Bohemia, Branisovska 31, 37005 Ceske Budejovice, Czech Republic. Canadian Institute for Advanced Research, 180 Dundas Street West, Suite 1400, Toronto, Ontario M5G 1Z8, Canada. ; Ecole Normale Superieure, Institut de Biologie de l'ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris, F-75005 France. ; MARUM, Center for Marine Environmental Sciences, University of Bremen, 28359 Bremen, Germany. CNRS, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. Sorbonne Universites, Universite Pierre et Marie Curie (UPMC) Paris 06, UMR 7144, Station Biologique de Roscoff, Place Georges Teissier, 29680 Roscoff, France. ; Stazione Zoologica Anton Dohrn, Villa Comunale, 80121 Naples, Italy. ; Ifremer, Centre de Brest, DYNECO/Pelagos CS 10070, 29280 Plouzane, France. ; Center for the Biology of Disease, VIB, Herestraat 49, 3000 Leuven, Belgium. Ecole Normale Superieure, Institut de Biologie de l'ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris, F-75005 France. ; Structural and Computational Biology, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, 69117 Heidelberg, Germany. Directors' Research, EMBL, Meyerhofstrasse 1, 69117 Heidelberg, Germany. ; Structural and Computational Biology, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, 69117 Heidelberg, Germany. Max-Delbruck-Centre for Molecular Medicine, 13092 Berlin, Germany. ; CNRS UMR 7232, Biologie Integrative des Organismes Marins (BIOM), Avenue du Fontaule, 66650 Banyuls-sur-Mer, France. Sorbonne Universites Paris 06, Observatoire Oceanologique de Banyuls (OOB) UPMC, Avenue du Fontaule, 66650 Banyuls-sur-Mer, France. ; Aix Marseille Universite, CNRS IGS UMR 7256, 13288 Marseille, France. ; Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan. ; PANGAEA, Data Publisher for Earth and Environmental Science, University of Bremen, Bremen, Germany. MARUM, Center for Marine Environmental Sciences, University of Bremen, 28359 Bremen, Germany. ; Bigelow Laboratory for Ocean Sciences, East Boothbay, ME 04544, USA. National Science Foundation, Arlington, VA 22230, USA. ; Department of Geosciences, Laboratoire de Meteorologie Dynamique (LMD), Ecole Normale Superieure, 24 rue Lhomond, 75231 Paris Cedex 05, France. Laboratoire de Physique des Oceans, Universite de Bretagne Occidentale (UBO)-Institut Universitaire Europeen de la Mer (IUEM), Place Copernic, 29820 Plouzane, France. ; Structural and Computational Biology, European Molecular Biology Laboratory (EMBL), Meyerhofstrasse 1, 69117 Heidelberg, Germany. ; Commissariat a l'Energie Atomique et aux Energies Alternatives (CEA), Institut de Genomique, GENOSCOPE, 2 rue Gaston Cremieux, 91000 Evry, France. CNRS, UMR 8030, CP5706, Evry, France. Universite d'Evry, UMR 8030, CP5706, Evry, France. vargas@sb-roscoff.fr pwincker@genoscope.cns.fr karsenti@embl.de. ; Directors' Research, EMBL, Meyerhofstrasse 1, 69117 Heidelberg, Germany. Ecole Normale Superieure, Institut de Biologie de l'ENS (IBENS), and Inserm U1024, and CNRS UMR 8197, Paris, F-75005 France. vargas@sb-roscoff.fr pwincker@genoscope.cns.fr karsenti@embl.de.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25999516" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Biodiversity ; DNA Barcoding, Taxonomic ; DNA, Ribosomal/genetics ; Eukaryota/*classification/genetics ; Oceans and Seas ; Phylogeny ; Plankton/*classification/genetics ; Ribosomes/genetics ; Sequence Analysis, DNA ; Sunlight
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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