<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chapman JA</submitter><funding>Austrian Science Fund FWF</funding><funding>NCRR NIH HHS</funding><pagination>592-6</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4479502</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>464(7288)</volume><pubmed_abstract>The freshwater cnidarian Hydra was first described in 1702 and has been the object of study for 300 years. Experimental studies of Hydra between 1736 and 1744 culminated in the discovery of asexual reproduction of an animal by budding, the first description of regeneration in an animal, and successful transplantation of tissue between animals. Today, Hydra is an important model for studies of axial patterning, stem cell biology and regeneration. Here we report the genome of Hydra magnipapillata and compare it to the genomes of the anthozoan Nematostella vectensis and other animals. The Hydra genome has been shaped by bursts of transposable element expansion, horizontal gene transfer, trans-splicing, and simplification of gene structure and gene content that parallel simplification of the H</pubmed_abstract><journal>Nature</journal><pubmed_title>The dynamic genome of Hydra.</pubmed_title><pmcid>PMC4479502</pmcid><funding_grant_id>R24 RR015088</funding_grant_id><funding_grant_id>P 20734</funding_grant_id><funding_grant_id>P 21108</funding_grant_id><pubmed_authors>Walenz B</pubmed_authors><pubmed_authors>Hirose M</pubmed_authors><pubmed_authors>Hayakawa E</pubmed_authors><pubmed_authors>Gee L</pubmed_authors><pubmed_authors>Rattei T</pubmed_authors><pubmed_authors>Viswanathan LD</pubmed_authors><pubmed_authors>Fraune S</pubmed_authors><pubmed_authors>Holstein TW</pubmed_authors><pubmed_authors>Weinmaier T</pubmed_authors><pubmed_authors>Hellsten U</pubmed_authors><pubmed_authors>Khalturin K</pubmed_authors><pubmed_authors>Balasubramanian PG</pubmed_authors><pubmed_authors>Bottger A</pubmed_authors><pubmed_authors>Shu S</pubmed_authors><pubmed_authors>Hayakawa S</pubmed_authors><pubmed_authors>Disbennett K</pubmed_authors><pubmed_authors>Kibler DF</pubmed_authors><pubmed_authors>Guder C</pubmed_authors><pubmed_authors>Hobmayer B</pubmed_authors><pubmed_authors>Watanabe H</pubmed_authors><pubmed_authors>Dana CE</pubmed_authors><pubmed_authors>Martinez DE</pubmed_authors><pubmed_authors>Bertulat B</pubmed_authors><pubmed_authors>Venter JC</pubmed_authors><pubmed_authors>Salvenmoser W</pubmed_authors><pubmed_authors>Gojobori T</pubmed_authors><pubmed_authors>Hwang JS</pubmed_authors><pubmed_authors>Aufschnaiter R</pubmed_authors><pubmed_authors>Hampson SE</pubmed_authors><pubmed_authors>Chapman JA</pubmed_authors><pubmed_authors>Ikeo K</pubmed_authors><pubmed_authors>Busam D</pubmed_authors><pubmed_authors>Augustin R</pubmed_authors><pubmed_authors>Prochnik SE</pubmed_authors><pubmed_authors>Nakamura Y</pubmed_authors><pubmed_authors>Wheeler BM</pubmed_authors><pubmed_authors>Ozbek S</pubmed_authors><pubmed_authors>Sumin N</pubmed_authors><pubmed_authors>Peterson KJ</pubmed_authors><pubmed_authors>Simakov O</pubmed_authors><pubmed_authors>Mitros T</pubmed_authors><pubmed_authors>Bode HR</pubmed_authors><pubmed_authors>Franke A</pubmed_authors><pubmed_authors>Hemmrich G</pubmed_authors><pubmed_authors>Pfannkoch C</pubmed_authors><pubmed_authors>Lindgens D</pubmed_authors><pubmed_authors>Wigge PA</pubmed_authors><pubmed_authors>Strausberg RL</pubmed_authors><pubmed_authors>Sutton GG</pubmed_authors><pubmed_authors>Goodstein DM</pubmed_authors><pubmed_authors>Takahashi T</pubmed_authors><pubmed_authors>Wolf A</pubmed_authors><pubmed_authors>Heimberg AM</pubmed_authors><pubmed_authors>Gorny AK</pubmed_authors><pubmed_authors>Blumberg B</pubmed_authors><pubmed_authors>Eder MK</pubmed_authors><pubmed_authors>Bosch TC</pubmed_authors><pubmed_authors>Rokhsar DS</pubmed_authors><pubmed_authors>Technau U</pubmed_authors><pubmed_authors>Borman J</pubmed_authors><pubmed_authors>Fujisawa T</pubmed_authors><pubmed_authors>Kawashima T</pubmed_authors><pubmed_authors>David CN</pubmed_authors><pubmed_authors>Nishimiya-Fujisawa C</pubmed_authors><pubmed_authors>Putnam NH</pubmed_authors><pubmed_authors>Law L</pubmed_authors><pubmed_authors>Tischler P</pubmed_authors><pubmed_authors>Kirkness EF</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Remington KA</pubmed_authors><pubmed_authors>Ogura A</pubmed_authors><pubmed_authors>Steinmetz PR</pubmed_authors><pubmed_authors>Peng J</pubmed_authors><pubmed_authors>Steele RE</pubmed_authors></additional><is_claimable>false</is_claimable><name>The dynamic genome of Hydra.</name><description>The freshwater cnidarian Hydra was first described in 1702 and has been the object of study for 300 years. Experimental studies of Hydra between 1736 and 1744 culminated in the discovery of asexual reproduction of an animal by budding, the first description of regeneration in an animal, and successful transplantation of tissue between animals. Today, Hydra is an important model for studies of axial patterning, stem cell biology and regeneration. Here we report the genome of Hydra magnipapillata and compare it to the genomes of the anthozoan Nematostella vectensis and other animals. The Hydra genome has been shaped by bursts of transposable element expansion, horizontal gene transfer, trans-splicing, and simplification of gene structure and gene content that parallel simplification of the H</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Mar</publication><modification>2026-05-30T11:22:26.853Z</modification><creation>2026-04-08T07:10:45.696Z</creation></dates><accession>S-EPMC4479502</accession><cross_references><pubmed>20228792</pubmed><doi>10.1038/nature08830</doi></cross_references></HashMap>