<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Plomion C</submitter><funding>European Research Council</funding><pagination>440-452</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6086335</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(7)</volume><pubmed_abstract>Oaks are an important part of our natural and cultural heritage. Not only are they ubiquitous in our most common landscapes&lt;sup>1&lt;/sup> but they have also supplied human societies with invaluable services, including food and shelter, since prehistoric times&lt;sup>2&lt;/sup>. With 450 species spread throughout Asia, Europe and America&lt;sup>3&lt;/sup>, oaks constitute a critical global renewable resource. The longevity of oaks (several hundred years) probably underlies their emblematic cultural and historical importance. Such long-lived sessile organisms must persist in the face of a wide range of abiotic and biotic threats over their lifespans. We investigated the genomic features associated with such a long lifespan by sequencing, assembling and annotating the oak genome. We then used the growing n</pubmed_abstract><journal>Nature plants</journal><pubmed_title>Oak genome reveals facets of long lifespan.</pubmed_title><pmcid>PMC6086335</pmcid><funding_grant_id>339728</funding_grant_id><pubmed_authors>Dossat C</pubmed_authors><pubmed_authors>Salin F</pubmed_authors><pubmed_authors>Belser C</pubmed_authors><pubmed_authors>Luyten I</pubmed_authors><pubmed_authors>Duplessis S</pubmed_authors><pubmed_authors>Chancerel E</pubmed_authors><pubmed_authors>Martin F</pubmed_authors><pubmed_authors>Francillonne N</pubmed_authors><pubmed_authors>Desprez-Loustau ML</pubmed_authors><pubmed_authors>Gaspin C</pubmed_authors><pubmed_authors>Murat F</pubmed_authors><pubmed_authors>Faye S</pubmed_authors><pubmed_authors>Herrmann S</pubmed_authors><pubmed_authors>Faivre-Rampant P</pubmed_authors><pubmed_authors>Bodenes C</pubmed_authors><pubmed_authors>Lasserre E</pubmed_authors><pubmed_authors>Chantret N</pubmed_authors><pubmed_authors>Hummel I</pubmed_authors><pubmed_authors>Madoui MA</pubmed_authors><pubmed_authors>Picault N</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Dievart A</pubmed_authors><pubmed_authors>Lascoux M</pubmed_authors><pubmed_authors>Rue O</pubmed_authors><pubmed_authors>Mangenot S</pubmed_authors><pubmed_authors>Ehrenmann F</pubmed_authors><pubmed_authors>Tarkka M</pubmed_authors><pubmed_authors>Grima-Pettenati J</pubmed_authors><pubmed_authors>Leroy T</pubmed_authors><pubmed_authors>Soler M</pubmed_authors><pubmed_authors>Quesneville H</pubmed_authors><pubmed_authors>Lesur I</pubmed_authors><pubmed_authors>Klopp C</pubmed_authors><pubmed_authors>Plomion C</pubmed_authors><pubmed_authors>Leple JC</pubmed_authors><pubmed_authors>Maumus F</pubmed_authors><pubmed_authors>Amselem J</pubmed_authors><pubmed_authors>Brachi B</pubmed_authors><pubmed_authors>Wincker P</pubmed_authors><pubmed_authors>Alaeitabar T</pubmed_authors><pubmed_authors>Da Silva C</pubmed_authors><pubmed_authors>Zanne AE</pubmed_authors><pubmed_authors>Couloux A</pubmed_authors><pubmed_authors>Le Provost G</pubmed_authors><pubmed_authors>Bouffaud ML</pubmed_authors><pubmed_authors>Michotey C</pubmed_authors><pubmed_authors>Rustenholz C</pubmed_authors><pubmed_authors>Panaud O</pubmed_authors><pubmed_authors>Rouhier N</pubmed_authors><pubmed_authors>Guichoux E</pubmed_authors><pubmed_authors>Berges H</pubmed_authors><pubmed_authors>Salse J</pubmed_authors><pubmed_authors>Labadie K</pubmed_authors><pubmed_authors>Mercier J</pubmed_authors><pubmed_authors>Aury JM</pubmed_authors><pubmed_authors>Kohler A</pubmed_authors><pubmed_authors>Lalanne C</pubmed_authors><pubmed_authors>Marchal C</pubmed_authors><pubmed_authors>Lemainque A</pubmed_authors><pubmed_authors>Barbe V</pubmed_authors><pubmed_authors>Bogeat-Triboulot MB</pubmed_authors><pubmed_authors>Velt A</pubmed_authors><pubmed_authors>Kremer A</pubmed_authors><pubmed_authors>Cohen D</pubmed_authors><pubmed_authors>Bartholome J</pubmed_authors><pubmed_authors>Hecker A</pubmed_authors><pubmed_authors>Hugueney P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Oak genome reveals facets of long lifespan.</name><description>Oaks are an important part of our natural and cultural heritage. Not only are they ubiquitous in our most common landscapes&lt;sup>1&lt;/sup> but they have also supplied human societies with invaluable services, including food and shelter, since prehistoric times&lt;sup>2&lt;/sup>. With 450 species spread throughout Asia, Europe and America&lt;sup>3&lt;/sup>, oaks constitute a critical global renewable resource. The longevity of oaks (several hundred years) probably underlies their emblematic cultural and historical importance. Such long-lived sessile organisms must persist in the face of a wide range of abiotic and biotic threats over their lifespans. We investigated the genomic features associated with such a long lifespan by sequencing, assembling and annotating the oak genome. We then used the growing n</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jul</publication><modification>2026-05-02T08:51:38.759Z</modification><creation>2019-03-26T22:28:44Z</creation></dates><accession>S-EPMC6086335</accession><cross_references><pubmed>29915331</pubmed><doi>10.1038/s41477-018-0172-3</doi></cross_references></HashMap>