Abstract
Reproduction underpins the life cycles, population dynamics, and ecology of marine organisms which have a wide variety of strategies, including sexual and asexual, gonochorism and hermaphroditism, as well as internal or external fertilization. It is often easy to collect a large quantity of gametes from species with external fertilization. In some species, such as many Echinodermata, female gametes (oocytes and eggs) are semitransparent, which makes it possible to observe changes in intracellular structures during fertilization. For these reasons, gametes from marine organisms have contributed to the general knowledge of biology, e.g., the first observation of sperm penetration into an egg and studies on the motile machinery of flagella (microtubules and dyneins), hormonal regulation of spawning in marine invertebrates, and oocyte maturation and cell cycles. Sexual maturation in marine organisms varies among species and their habitats; however, most Japanese species are seasonal and spawn once a year. For experiments using gametes and their fertilization, it is important to know the time of the spawning or copulation. In this chapter, we focus on the gametes and fertilization of marine species, especially marine invertebrates. Reproduction of marine algae is described in Chap. 12.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Similar content being viewed by others
References
Christiaen, L., Wagner, E., Shi, W., & Levine, M. (2009). The sea squirt Ciona intestinalis. Cold Spring Harbor Protocols, 2009(12), 138. https://doi.org/10.1101/pdb.emo138
Dzyuba, V., & Cosson, J. (2014). Motility of fish spermatozoa: From external signaling to flagella response. Reproductive Biology, 14(3), 165–175. https://doi.org/10.1016/j.repbio.2013.12.005
Harada, Y., et al. (2007). Characterization of a sperm factor for egg activation at fertilization of the newt Cynops pyrrhogaster. Developmental Biology, 306, 797–808. https://doi.org/10.1016/j.ydbio.2007.04.01
Inaba, K. (2003). Molecular architecture of the sperm flagella: Molecules for motility and signaling. Zoological Science, 20(9), 1043–1056.
Inaba, K., & Mizuno, K. (2009). Purification of dyneins from sperm flagella. In S. M. King & G. J. Pazour (Eds.), Methods in cell biology (Vol. 92, pp. 49–63). Amsterdam: Elsevier.
Kyozuka, K., Deguchi, R., Mohri, T., & Miyazaki, S. (1998). Injection of sperm extract mimics spatiotemporal dynamics of Ca2+ responses and progression of meiosis at fertilization of ascidian oocytes. Development, 125, 4099–4105.
Miyazaki, S., & Ito, M. (2006). Calcium signals for egg activation in mammals. Journal of Pharmacological Sciences, 100, 545–552.
Mizuno, K., Shiba, K., Okai, M., Takahashi, Y., Shitaka, Y., Oiwa, K., et al. (2012). Calaxin drives sperm chemotaxis by Ca2+-mediated direct modulation of a dynein motor. Proceedings of the National Academy of Sciences of the United States of America, 109, 20497–20502. https://doi.org/10.1073/pnas.1217018109
Morisawa, M., & Yoshida, M. (2005). Activation of motility and chemotaxis in the spermatozoa: From invertebrates to humans. Reproductive Medicine Biology, 4(2), 101–114. https://doi.org/10.1111/j.1447-0578.2005.00099.x
Rakow, T. L., & Shen, S. S. (1990). Multiple stores of calcium are released in the sea urchin egg during fertilization. Proceedings of the National Academy of Sciences of the United States of America, 87, 9285–9289.
Runft, L. L., Jaffe, L. A., & Mehlmann, L. M. (2002). Egg activation at fertilization: Where it all begins. Developmental Biology, 245, 237–254. https://doi.org/10.1006/dbio.2002.0600
Saito, T., Shiba, K., Inaba, K., Yamada, L., & Sawada, H. (2012). Self-incompatibility response induced by calcium increase in sperm of the ascidian Ciona intestinalis. Proceedings of the National Academy of Sciences of the United States of America, 109, 4158–4162.
Sato, K., Fukami, Y., & Stith, B. J. (2006). Signal transduction pathways leading to Ca2+ release in a vertebrate model system: Lessons from Xenopus eggs. Seminars in Cell & Developmental Biology, 17, 285–292. https://doi.org/10.1016/j.semcdb.2006.02.008
Saunders, C. M., et al. (2002). PLC zeta: A sperm-specific trigger of Ca2+ oscillations in eggs and embryo development. Development, 129, 3533–3544.
Shiba, K., Baba, S. A., Inoue, T., & Yoshida, M. (2008). Ca2+ bursts occur around a local minimal concentration of attractant and trigger sperm chemotactic response. Proceedings of the National Academy of Sciences of the United States of America, 105, 19312–19317. https://doi.org/10.1073/pnas.0808580105
Stricker, S. A. (1999). Comparative biology of calcium signaling during fertilization and egg activation in animals. Developmental Biology, 211, 157–176. https://doi.org/10.1006/dbio.1999.9340
Swann, K. (1990). A cytosolic sperm factor stimulates repetitive calcium increases and mimics fertilization in hamster eggs. Development, 110, 1295–1302.
Tsien, R. Y. (1980). New calcium indicators and buffers with high selectivity against magnesium and protons: Design, synthesis, and properties of prototype structures. Biochemistry, 19, 2396–2404.
Wessel, G. M., & Vacquier, V. D. (2004). Isolation of organelles and components from sea urchin eggs and embryos. In C. A. Ettensohn, G. A. Wray, & G. M. Wessel (Eds.), Methods in cell biology (Vol. 74, pp. 491–522). Amsterdam: Elsevier.
Yoshida, M., Sensui, N., Inoue, T., Morisawa, M., & Mikoshiba, K. (1998). Role of two series of Ca2+ oscillations in activation of ascidian eggs. Developmental Biology, 203, 122–133. https://doi.org/10.1006/dbio.1998.9037
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
1 Electronic Supplementary Material
Sperm chemotaxis to the tip of capillary filled with sperm attractant in the ascidian C. intestinalis (play at 1.8× speed) (MOV 8556 kb).
Formation of fertilization membrane in the sea urchin Hemicentrotus pulcherrimus (play at 3× speed) (MOV 6482 kb).
Ca2+ oscillation patterns of a fertilized egg of C. intestinalis. Probed with Calcium Green-1. Note that fertilization accompanies the first large Ca2+ increase that cause egg deformation, followed by several spikes of Ca2+ increases (MOV 6535 kb).
Ca2+ oscillation patterns of a fertilized egg of C. intestinalis. Probed with Fura-2 (MOV 3565 kb).
Rights and permissions
Copyright information
© 2020 Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Inaba, K., Sawada, H., Yoshida, M., Shiba, K., Shirae-Kurabayashi, M. (2020). Gametes and Fertilization. In: Inaba, K., Hall-Spencer, J. (eds) Japanese Marine Life. Springer, Singapore. https://doi.org/10.1007/978-981-15-1326-8_9
Download citation
DOI: https://doi.org/10.1007/978-981-15-1326-8_9
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-15-1325-1
Online ISBN: 978-981-15-1326-8
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)