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<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd> <responseDate>2018-01-15T18:26:25Z</responseDate> <request identifier=oai:HAL:hal-01224215v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:hal-01224215v1</identifier> <datestamp>2018-01-12</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:sdv</setSpec> <setSpec>collection:UPMC</setSpec> <setSpec>collection:CNRS</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:UNICE</setSpec> <setSpec>collection:EVOLUTION_PARIS_SEINE</setSpec> <setSpec>collection:UPMC_POLE_4</setSpec> <setSpec>collection:UCA-TEST</setSpec> <setSpec>collection:IBPS</setSpec> <setSpec>collection:EVOL_PARIS_SEINE-AIRE</setSpec> <setSpec>collection:UNIV-COTEDAZUR</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>Studying Genome Heterogeneity within the Arbuscular Mycorrhizal Fungal Cytoplasm</title> <creator>Boon, Eva</creator> <creator>Halary, Sébastien</creator> <creator>Bapteste, Eric</creator> <creator>Hijri, Mohamed</creator> <contributor>Département de Sciences Biologiques [Montreal] ; Université de Montréal</contributor> <contributor>Evolution Paris Seine ; Université Nice Sophia Antipolis (UNS) ; Université Côte d'Azur (UCA) - Université Côte d'Azur (UCA) - Centre National de la Recherche Scientifique (CNRS) - Université des Antilles et de la Guyane (UAG) - Université Pierre et Marie Curie - Paris 6 (UPMC)</contributor> <contributor>Institut de Biologie Paris-Seine</contributor> <description>International audience</description> <source>ISSN: 1759-6653</source> <source>EISSN: 1759-6653</source> <source>Genome Biology and Evolution</source> <publisher>Society for Molecular Biology and Evolution</publisher> <identifier>hal-01224215</identifier> <identifier>http://hal.upmc.fr/hal-01224215</identifier> <identifier>http://hal.upmc.fr/hal-01224215/document</identifier> <identifier>http://hal.upmc.fr/hal-01224215/file/Genome%20Biol%20Evol-2015-Boon-505-21.pdf</identifier> <source>http://hal.upmc.fr/hal-01224215</source> <source>Genome Biology and Evolution, Society for Molecular Biology and Evolution, 2015, 7 (2), pp.505-521. 〈10.1093/gbe/evv002〉</source> <identifier>DOI : 10.1093/gbe/evv002</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.1093/gbe/evv002</relation> <language>en</language> <subject lang=en>next generation sequencing</subject> <subject lang=en>symbiosis</subject> <subject lang=en>genome heterogeneity</subject> <subject lang=en>arbuscular mycorrhizal fungi</subject> <subject lang=en>genome evolution</subject> <subject lang=en>network analysis</subject> <subject>[SDV.GEN] Life Sciences [q-bio]/Genetics</subject> <subject>[SDV.BC] Life Sciences [q-bio]/Cellular Biology</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>Although heterokaryons have been reported in nature, multicellular organisms are generally assumed genetically homogeneous. Here, we investigate the case of arbuscular mycorrhizal fungi (AMF) that form symbiosis with plant roots. The growth advantages they confer to their hosts are of great potential benefit to sustainable agricultural practices. However, measuring genetic diversity for these coenocytes is a major challenge: Within the same cytoplasm, AMF contain thousands of nuclei and show extremely high levels of genetic variation for some loci. The extent and physical location of polymorphism within and between AMF genomes is unclear. We used two complementary strategies to estimate genetic diversity in AMF, investigating polymorphism both on a genome scale and in putative single copy loci. First, we used data from whole-genome pyrosequencing of four AMF isolates to describe genetic diversity, based on a conservative network-based clustering approach. AMF isolates showed marked differences in genome-wide diversity patterns in comparison to a panel of control fungal genomes. This clustering approach further allowed us to provide conservative estimates of Rhizophagus spp. genomes sizes. Second, we designed new putative single copy genomic markers, which we investigated by massive parallel amplicon sequencing for two Rhizophagus irregularis and one Rhizophagus sp. isolates. Most loci showed high polymorphism, with up to 103 alleles per marker. This polymorphism could be distributed within or between nuclei. However, we argue that the Rhizophagus isolates under study might be heterokaryotic, at least for the putative single copy markers we studied. Considering that genetic information is the main resource for identification of AMF, we suggest that special attention is warranted for the study of these ecologically important organisms.</description> <rights>http://creativecommons.org/licenses/by/</rights> <date>2015-01-05</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>