Cryopreservation of Sea Urchin (Lytechinus pictus) Embryos and Development Through Metamorphosis

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Abstract

Background Sea urchins have contributed to knowledge of fertilization, embryonic development and cell physiology for 150 years. Their evolutionary position, as basal deuterostomes, and their long background in developmental biology, motivate establishing a genetically-enabled sea urchin species. Because of its relatively short generation time of 4-6 months and ease of culture, our lab has focused on the California sea urchin Lytechinus pictus as a multigenerational model, and produced knockout and transgenic lines using this species. To ensure that diverse genetic lines can be preserved, methods must be developed to cryopreserve gametes and embryos. We have previously reported methods for cryopreservation of sperm, but robust methods to preserve embryos remained lacking. Results Here, we describe a relatively simple method to cryopreserve late gastrulae embryos of L. pictus . Importantly we show that, after thawing and culturing, the embryos progress through larval development, undergo metamorphosis and yield juvenile adults, indicating the method is robust. Conclusion The cryopreservation of embryos is an important advance that will facilitate the biobanking, sharing and long-term preservation of diverse genetic lines. This method may also eventually prove useful for cryopreservation of embryos of other marine invertebrates.
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Abstract

Background Sea urchins have contributed to knowledge of fertilization, embryonic development and cell physiology for 150 years. Their evolutionary position, as basal deuterostomes, and their long background in developmental biology, motivate establishing a genetically-enabled sea urchin species. Because of its relatively short generation time of 4-6 months and ease of culture, our lab has focused on the California sea urchin Lytechinus pictus as a multigenerational model, and produced knockout and transgenic lines using this species. To ensure that diverse genetic lines can be preserved, methods must be developed to cryopreserve gametes and embryos. We have previously reported methods for cryopreservation of sperm, but robust methods to preserve embryos remained lacking.

Results

Here, we describe a relatively simple method to cryopreserve late gastrulae embryos of L. pictus. Importantly we show that, after thawing and culturing, the embryos progress through larval development, undergo metamorphosis and yield juvenile adults, indicating the method is robust.

Conclusion

The cryopreservation of embryos is an important advance that will facilitate the biobanking, sharing and long-term preservation of diverse genetic lines. This method may also eventually prove useful for cryopreservation of embryos of other marine invertebrates. Competing Interest Statement The authors have declared no competing interest. Footnotes The images and legends for Figures 1 and 2 were switched.

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License: CC-BY-NC-ND-4.0