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Cell surface changes in an egg at fertilization are essential to begin development and for protecting the zygote. Most fertilized eggs construct a barrier around themselves by modifying their original extracellular matrix. This construction usually results from calcium-induced exocytosis of cortical granules, the contents of which in sea urchins function to form the fertilization envelope (FE), an extracellular matrix of cortical granule contents built upon a vitelline layer scaffold. Here, we examined the molecular mechanism of this process in sea stars, a close relative of the sea urchins, and analyze the evolutionary changes that likely occurred in the functionality of this structure between these two organisms. We find that the FE of sea stars is more permeable than in sea urchins, allowing diffusion of molecules in excess of 2 megadaltons. Through a proteomic and transcriptomic approach, we find that most, but not all, of the proteins present in the sea urchin envelope are present in sea stars, including SFE9, proteoliaisin, and rendezvin. The mRNAs encoding these FE proteins accumulated most densely in early oocytes, and then beginning with vitellogenesis, these mRNAs decreased in abundance to levels nearly undetectable in eggs. Antibodies to the SFE9 protein of sea stars showed that the cortical granules in sea star also accumulated most significantly in early oocytes, but different from sea urchins, they translocated to the cortex of the oocytes well before meiotic initiation. These results suggest that the preparation for cell surface changes in sea urchins has been shifted to later in oogenesis, and perhaps reflects the meiotic differences among the species-sea star oocytes are stored in prophase of meiosis and fertilized during the meiotic divisions, as in most animals, whereas sea urchins are one of the few taxons in which eggs have completed meiosis prior to fertilization.
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23331915 ???displayArticle.pmcLink???PMC3888873 ???displayArticle.link???Evol Dev ???displayArticle.grants???[+]
Briggs,
In the beginning...animal fertilization and sea urchin development.
2006, Pubmed,
Echinobase
Briggs,
In the beginning...animal fertilization and sea urchin development.
2006,
Pubmed
,
Echinobase Brooks,
Selective transport and packaging of the major yolk protein in the sea urchin.
2003,
Pubmed
,
Echinobase Carroll,
Isolation and biological activity of the proteases released by sea urchin eggs following fertilization.
1975,
Pubmed
,
Echinobase Daiyasu,
Molecular evolution of the myeloperoxidase family.
2000,
Pubmed Ducibella,
Quantification and localization of cortical granules during oogenesis in the mouse.
1994,
Pubmed Foerder,
Release of ovoperoxidase from sea urchin eggs hardens the fertilization membrane with tyrosine crosslinks.
1977,
Pubmed
,
Echinobase Greenberg,
Transglutaminases: multifunctional cross-linking enzymes that stabilize tissues.
1991,
Pubmed Haley,
Proteolytic cleavage of the cell surface protein p160 is required for detachment of the fertilization envelope in the sea urchin.
2004,
Pubmed
,
Echinobase Haley,
Regulated proteolysis by cortical granule serine protease 1 at fertilization.
2004,
Pubmed
,
Echinobase Haley,
The cortical granule serine protease CGSP1 of the sea urchin, Strongylocentrotus purpuratus, is autocatalytic and contains a low-density lipoprotein receptor-like domain.
1999,
Pubmed
,
Echinobase Hinman,
Developmental gene regulatory network architecture across 500 million years of echinoderm evolution.
2003,
Pubmed
,
Echinobase LaFleur,
Sea urchin ovoperoxidase: oocyte-specific member of a heme-dependent peroxidase superfamily that functions in the block to polyspermy.
1998,
Pubmed
,
Echinobase Laidlaw,
Cortical granule biogenesis is active throughout oogenesis in sea urchins.
1994,
Pubmed
,
Echinobase Lee,
Changes in internal pH associated with initiation of motility and acrosome reaction of sea urchin sperm.
1983,
Pubmed
,
Echinobase Matsunaga,
Role of specialized microvilli and the fertilization envelope in the spatial positioning of blastomeres in early development of embryos of the starfish Astropecten scoparius.
2002,
Pubmed
,
Echinobase Minokawa,
Expression patterns of four different regulatory genes that function during sea urchin development.
2004,
Pubmed
,
Echinobase Nagahara,
Transduction of full-length TAT fusion proteins into mammalian cells: TAT-p27Kip1 induces cell migration.
1998,
Pubmed Reimer,
Identification and partial characterization of yolk and cortical granule proteins in eggs and embryos of the starfish, Pisaster ochraceus.
1995,
Pubmed
,
Echinobase Showman,
Removal of the fertilization membrane of sea urchin embryos employing aminotriazole.
1979,
Pubmed
,
Echinobase Smith,
Testing the molecular clock: molecular and paleontological estimates of divergence times in the Echinoidea (Echinodermata).
2006,
Pubmed
,
Echinobase Steinhardt,
Intracellular calcium release at fertilization in the sea urchin egg.
1977,
Pubmed
,
Echinobase Towbin,
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
1979,
Pubmed Vacquier,
Isolation of bindin: the protein responsible for adhesion of sperm to sea urchin eggs.
1977,
Pubmed
,
Echinobase Vacquier,
Sea urchin eggs release protease activity at fertilization.
1972,
Pubmed
,
Echinobase Vacquier,
Evolution of gamete recognition proteins.
1998,
Pubmed Ward,
Chemotaxis of Arbacia punctulata spermatozoa to resact, a peptide from the egg jelly layer.
1985,
Pubmed
,
Echinobase Weidman,
Purification and characterization of proteoliaisin, a coordinating protein in fertilization envelope assembly.
1987,
Pubmed
,
Echinobase Wessel,
SFE1, a constituent of the fertilization envelope in the sea urchin is made by oocytes and contains low-density lipoprotein-receptor-like repeats.
2000,
Pubmed
,
Echinobase Wessel,
The biology of cortical granules.
2001,
Pubmed Wessel,
A protein of the sea urchin cortical granules is targeted to the fertilization envelope and contains an LDL-receptor-like motif.
1995,
Pubmed
,
Echinobase Wessel,
Use of sea stars to study basic reproductive processes.
2010,
Pubmed
,
Echinobase Wong,
Major components of a sea urchin block to polyspermy are structurally and functionally conserved.
2004,
Pubmed
,
Echinobase Wong,
Free-radical crosslinking of specific proteins alters the function of the egg extracellular matrix at fertilization.
2008,
Pubmed
,
Echinobase Wong,
Defending the zygote: search for the ancestral animal block to polyspermy.
2006,
Pubmed Wong,
Reactive oxygen species and Udx1 during early sea urchin development.
2005,
Pubmed
,
Echinobase Wong,
The oxidative burst at fertilization is dependent upon activation of the dual oxidase Udx1.
2004,
Pubmed
,
Echinobase Wong,
Extracellular matrix modifications at fertilization: regulation of dityrosine crosslinking by transamidation.
2009,
Pubmed
,
Echinobase