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An improved whole life cycle culture protocol for the hydrozoan genetic model Clytia hemisphaerica
Lechable, M.; Jan, A.; Duchene, A.; Uveira, J.; Weissbourd, B.; Gissat, L.; Collet, S.; Gilletta, L.; Chevalier, S.; Leclère, L.; Peron, S.; Barreau, C.; Lasbleiz, R.; Houliston, E.; Momose, T. (2020). An improved whole life cycle culture protocol for the hydrozoan genetic model Clytia hemisphaerica. Biology Open 9(11): bio051268. https://dx.doi.org/10.1242/bio.051268
In: Biology Open. The Company of Biologists: Cambridge. ISSN 2046-6390; e-ISSN 2046-6390, more
Peer reviewed article  

Available in  Authors 

Keywords
    Exploitable Scientific Result
    Scientific Publication
    Cnidaria [WoRMS]
Author keywords
    Animal culture, Cnidarian, Developmental biology, Genetics, Jellyfish

Authors  Top 
  • Lechable, M.
  • Jan, A.
  • Duchene, A.
  • Uveira, J.
  • Weissbourd, B.
  • Gissat, L.
  • Collet, S.
  • Gilletta, L.
  • Chevalier, S.
  • Leclère, L.
  • Peron, S.
  • Barreau, C.
  • Lasbleiz, R.
  • Houliston, E.
  • Momose, T.

Abstract
    The jellyfish species Clytia hemisphaerica (Cnidaria, Hydrozoa) has emerged as a new experimental model animal in the last decade. Favorable characteristics include a fully transparent body suitable for microscopy, daily gamete production and a relatively short life cycle. Furthermore, whole genome sequence assembly and efficient gene editing techniques using CRISPR/Cas9 have opened new possibilities for genetic studies. The quasi-immortal vegetatively-growing polyp colony stage provides a practical means to maintain mutant strains. In the context of developing Clytia as a genetic model, we report here an improved whole life cycle culture method including an aquarium tank system designed for culture of the tiny jellyfish form. We have compared different feeding regimes using Artemia larvae as food and demonstrate that the stage-dependent feeding control is the key for rapid and reliable medusa and polyp rearing. Metamorphosis of the planula larvae into a polyp colony can be induced efficiently using a new synthetic peptide. The optimized procedures detailed here make it practical to generate genetically modified Clytia strains and to maintain their whole life cycle in the laboratory.

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