The dynamic genome of Hydra

Jarrod Chapman(Joint Genome Institute), Ewen F. Kirkness(J. Craig Venter Institute), Oleg Simakov(Heidelberg University), Steven E. Hampson(University of California, Irvine), Therese Mitros(University of California, Berkeley), Thomas Weinmaier(Technical University of Munich), Thomas Rattei(Technical University of Munich), Prakash G. Balasubramanian(Heidelberg University), Jon Borman(J. Craig Venter Institute), Dana Busam(J. Craig Venter Institute), Kathryn Disbennett(J. Craig Venter Institute), Cynthia Pfannkoch(J. Craig Venter Institute), Nadezhda Sumin(J. Craig Venter Institute), Granger G. Sutton(J. Craig Venter Institute), Lakshmi Viswanathan(J. Craig Venter Institute), Brian P. Walenz(J. Craig Venter Institute), David Goodstein(Joint Genome Institute), Uffe Hellsten(Joint Genome Institute), Takeshi Kawashima(University of California, Berkeley), Simon Prochnik(Joint Genome Institute), Nicholas H. Putnam(Joint Genome Institute), Shengqiang Shu(Joint Genome Institute), Bruce Blumberg(University of California, Irvine), Catherine E. Dana(University of California, Irvine), Lydia Gee(University of California, Irvine), Dennis Kibler(University of California, Irvine), Lee Law(University of California, Irvine), Dirk Lindgens(University of California, Irvine), Daniel E. Martínez(Pomona College), Jisong Peng(University of California, Irvine), Philip A. Wigge(Salk Institute for Biological Studies), Bianca Bertulat(Heidelberg University), Corina Guder(Heidelberg University), Yukio Nakamura(Heidelberg University), Suat Özbek(Heidelberg University), Hiroshi Watanabe(Heidelberg University), Konstantin Khalturin(Christian-Albrechts-Universität zu Kiel), Georg Hemmrich(Christian-Albrechts-Universität zu Kiel), André Franke(Christian-Albrechts-Universität zu Kiel), René Augustin(Christian-Albrechts-Universität zu Kiel), Sebastian Fraune(Christian-Albrechts-Universität zu Kiel), Eisuke Hayakawa(National Institute of Genetics), Shiho Hayakawa(National Institute of Genetics), Mamiko Hirose(National Institute of Genetics), Jung Shan Hwang(National Institute of Genetics), Kazuho Ikeo(National Institute of Genetics), Chiemi Nishimiya‐Fujisawa(National Institute of Genetics), Atshushi Ogura(National Institute of Genetics), Toshio Takahashi(Suntory Foundation for Life Sciences), Patrick R. H. Steinmetz(University of Vienna), Xiaoming Zhang(University of Kansas Medical Center), Roland Aufschnaiter(Universität Innsbruck), Marie-Kristin Eder(Universität Innsbruck), Anne-Kathrin Gorny(Universität Innsbruck), Willi Salvenmoser(Universität Innsbruck), Alysha M. Heimberg(Dartmouth College), Benjamin M. Wheeler(North Carolina State University), Kevin J. Peterson(Dartmouth College), Angelika Böttger(Ludwig-Maximilians-Universität München), Patrick Tischler(Technical University of Munich), Alexander Wolf(Ludwig-Maximilians-Universität München), Takashi Gojobori(National Institute of Genetics), Karin Remington(J. Craig Venter Institute), Robert L. Strausberg(J. Craig Venter Institute), J. Craig Venter(J. Craig Venter Institute), Ulrich Technau(University of Vienna), Bert Hobmayer(Universität Innsbruck), Thomas C. G. Bosch(Christian-Albrechts-Universität zu Kiel), Thomas W. Holstein(Heidelberg University), Toshitaka Fujisawa(National Institute of Genetics), Hans R. Bode(University of California, Irvine), Charles N. David(Ludwig-Maximilians-Universität München), Daniel S. Rokhsar(Joint Genome Institute), Robert E. Steele(University of California, Irvine)
Nature
March 1, 2010
Cited by 818Open Access
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Abstract

Hydra, first described by Anton van Leeuwenhoek in a letter to the Royal Society in 1702, has been studied by biologists for centuries and now is an important model for work on axial patterning, stem cell biology and regeneration. Its genome, over half of which is made up of mobile elements, has now been sequenced, as has the genome of a Curvibacter sp. bacterium stably associated with Hydra magnipapillata. Comparisons of the Hydra genome with those of other animals provide insights into the evolution of epithelia, contractile tissues, developmentally regulated transcription factors, pluripotency genes and the neuromuscular junction, as well as the Spemann–Mangold organizer, the region in the early embryo that establishes the embryo's axis. The freshwater cnidarian Hydra is a significant model for studies of axial patterning, stem cell biology and regeneration. Its (A+T)-rich genome has now been sequenced. Comparison of this genome with those of other animals provides insights into the evolution of epithelia, contractile tissues, developmentally regulated transcription factors, pluripotency genes and more. The freshwater cnidarian Hydra was first described in 17021 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 animals2. Today, Hydra is an important model for studies of axial patterning3, stem cell biology4 and regeneration5. Here we report the genome of Hydra magnipapillata and compare it to the genomes of the anthozoan Nematostella vectensis6 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 Hydra life cycle. We also report the sequence of the genome of a novel bacterium stably associated with H. magnipapillata. Comparisons of the Hydra genome to the genomes of other animals shed light on the evolution of epithelia, contractile tissues, developmentally regulated transcription factors, the Spemann–Mangold organizer, pluripotency genes and the neuromuscular junction.


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