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The genome of the jellyfish Clytia hemisphaerica and the evolution of the cnidarian life-cycle
Leclère, L.; Horin, C.; Chevalier, S.; Lapébie, P.; Druart, P.; Peron, S.; Jager, M.; Condamine, T.; Pottin, K.; Romano, S.; Steger, J.; Sinigaglia, C.; Barreau, C.; Quiroga Artigas, G.; Ruggiero, A.; Fourrage, C.; Kraus, J.E.M.; Poulain, J.; Aury, J.-M.; Wincker, P.; Quéinnec, E.; Technau, U.; Manuel, M.; Momose, T.; Houliston, E.; Copley, R.R. (2019). The genome of the jellyfish Clytia hemisphaerica and the evolution of the cnidarian life-cycle. Nature Ecology & Evolution 3(5): 801-810. https://dx.doi.org/10.1038/s41559-019-0833-2
In: Nature Ecology & Evolution. Springer Nature. ISSN 2397-334X, meer
Is gerelateerd aan:
Schnitzler, C.E. (2019). What makes a jellyfish. Nature Ecology & Evolution 3(5): 724-725. https://dx.doi.org/10.1038/s41559-019-0872-8, meer
Peer reviewed article  

Beschikbaar in  Auteurs 

Author keywords
    Genome evolution; Evolutionary genetics

Auteurs  Top 
  • Leclère, L.
  • Horin, C.
  • Chevalier, S.
  • Lapébie, P.
  • Druart, P., meer
  • Peron, S.
  • Jager, M.
  • Condamine, T.
  • Pottin, K.
  • Romano, S.
  • Steger, J.
  • Sinigaglia, C.
  • Barreau, C.
  • Quiroga Artigas, G.
  • Ruggiero, A.
  • Fourrage, C.
  • Kraus, J.E.M.
  • Poulain, J.
  • Aury, J.-M.
  • Wincker, P.
  • Quéinnec, E.
  • Technau, U.
  • Manuel, M.
  • Momose, T.
  • Houliston, E.
  • Copley, R.R.

Abstract
    Jellyfish (medusae) are a distinctive life-cycle stage of medusozoan cnidarians. They are major marine predators, with integrated neurosensory, muscular and organ systems. The genetic foundations of this complex form are largely unknown. We report the draft genome of the hydrozoan jellyfish Clytia hemisphaerica and use multiple transcriptomes to determine gene use across life-cycle stages. Medusa, planula larva and polyp are each characterized by distinct transcriptome signatures reflecting abrupt life-cycle transitions and all deploy a mixture of phylogenetically old and new genes. Medusa-specific transcription factors, including many with bilaterian orthologues, associate with diverse neurosensory structures. Compared to Clytia, the polyp-only hydrozoan Hydra has lost many of the medusa-expressed transcription factors, despite similar overall rates of gene content evolution and sequence evolution. Absence of expression and gene loss among Clytia orthologues of genes patterning the anthozoan aboral pole, secondary axis and endomesoderm support simplification of planulae and polyps in Hydrozoa, including loss of bilateral symmetry. Consequently, although the polyp and planula are generally considered the ancestral cnidarian forms, in Clytia the medusa maximally deploys the ancestral cnidarian–bilaterian transcription factor gene complement.

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