Cell tracking supports secondary gastrulation in the moon jellyfish Aurelia
Abstract
The moon jellyfish Aurelia exhibits a dramatic reorganization of tissue during its metamorphosis from planula larva to polyp. There are currently two competing hypotheses regarding the fate of embryonic germ layers during this metamorphosis. In one scenario, the original endoderm undergoes apoptosis and is replaced by a secondary endoderm derived from ectodermal cells. In the second scenario, both ectoderm and endoderm remain intact through development. In this study, we performed a pulse-chase experiment to trace the fate of larval ectodermal cells. We observed that prior to metamorphosis, ectodermal cells that proliferated early in larval development concentrate at the future oral end of the polyp. During metamorphosis, these cells migrate into the endoderm, extending all the way to the aboral portion of the gut. We therefore reject the hypothesis that larval endoderm remains intact during metamorphosis and provide additional support for the "secondary gastrulation" hypothesis. Aurelia appears to offer the first and only described case where a cnidarian derives its endoderm twice during normal development, adding to a growing body of evidence that germ layers can be dramatically reorganized in cnidarian life cycles.
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Several studies support a major ectodermal contribution to the gastrodermis of the Aurelia scyphistoma.
“Notably, several studies have supported a major ectodermal contribution to the gastrodermis of the Aurelia scyphistoma (Gold et al. 2016; Mayorova et al. 2012; Yuan et al. 2008).”
From A non-bilaterian perspective on the development and evolution of animal digestive systems (2019) · cites this paper as Gold et al. 2016
The gastrodermis of sea anemones, scyphozoans and ctenophores is derived from endoderm, and secondarily internalised pharyngeal ectoderm.
“The gastrodermis of sea anemones, scyphozoans and ctenophores is derived from endoderm, and secondarily internalised pharyngeal ectoderm.”
From A non-bilaterian perspective on the development and evolution of animal digestive systems (2019) · cites this paper as Gold et al. 2016
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References 24 · Cited by 18
- Authors
- Gold, D. A., Nakanishi, N., Hensley, N. M., Hartenstein, V., & Jacobs, D. K.
- Affiliations
- California Institute of Technology (US)
- University of California, Los Angeles (US)
- University of California, Santa Barbara (US)
- Corresponding author
- Jacobs, David K.
- Venue
- Development Genes and Evolution
- Published
- 2016-08-18
- Volume
- 226
- Issue
- 6
- Pages
- 383-387
- ISSN
- 0043-5546 (ISSN-L)
- 0949-944X
- 1432-041X
- OpenAlex
- W2510730256
- Cited by
- 18
- References
- 24
- Citations by year
- 2025: 2 · 2023: 2 · 2022: 8 · 2020: 1 · 2019: 2 · 2018: 2 · 2017: 1
- FWCI
- 1.39
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Development Genes and Evolution (publishedVersion)
- PubMed (publishedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- Funders
- NASA Astrobiology: Foundations of Complex Life: Evolution, Preservation and Detection on Earth and Beyond
- Topics
- Physical Sciences › Earth and Planetary Sciences › Paleontology › Marine Invertebrate Physiology and Ecology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Agricultural and Biological Sciences › Aquatic Science › Echinoderm biology and ecology
- Keywords
- Aurelia, Aurelia aurita, metamorphosis, planula larvae, polyp development, endoderm, cell migration, cell proliferation, cnidarian development
- MeSH terms
- Animals, Cell Movement, Female, Larva, Scyphozoa, Gastrulation, Cell Tracking
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