Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
???displayArticle.abstract???
The extracellular matrix of the early sea urchin embryo is known to have an important functional role in morphogenesis and in the regulation of cell type specific gene expression. We have undertaken an immuno-cDNA screen to identify the constituents of the embryonic blastocoelic-extracellular matrix. Here we describe a newly identified member of the extracellular matrix that we have designated ECM 3. The transcript encoding ECM 3 is approximately 9.5 kb in length and partial DNA sequence contains no significant similarity to other sequences in the Genbank. This transcript is present in eggs and early embryos, and early in gastrulation the transcript accumulation increases approximately 25 fold. In situ RNA hybridization shows that the mRNA is present uniformly throughout eggs and early embryos, but beginning at mesenchyme blastula stage, RNA accumulation is selective to cells of the ectoderm except at the animal pole, where ECM 3 mRNA is greatly reduced. In this species, Lytechinus variegatus, the animal pole ectoderm is the site of fusion with the invaginating endoderm during formation of the mouth. In situ analysis of protein expression using a monospecific polyclonal antisera made against recombinant ECM 3 polypeptides shows that during gastrulation the ECM 3 protein accumulates selectively in the basal lamina and blastocoelar regions adjacent to the ectoderm in all regions except for the ectoderm at the animal pole. The ECM 3 protein is not detected in other regions of the blastocoel e.g. adjacent to the endoderm. ECM 3 is also contributed maternally; the ECM 3 protein is synthesized during oogenesis and stored in oocytes within membrane-bound vesicles in the vicinity of Golgi complexes. Following fertilization ECM 3 is selectively secreted basally into the nascent blastocoel. No accumulation is detected in apical regions of the blastomeres or in the hyaline layer/apical lamina. This newly described molecule of the extracellular matrix thus demonstrates expression regulated both by secretion and by cell type specific gene expression, and shows a correlation between a microenvironment of the extracellular matrix and a morphogenetic event.
Alliegro,
Storage and mobilization of extracellular matrix proteins during sea urchin development.
1988, Pubmed,
Echinobase
Alliegro,
Storage and mobilization of extracellular matrix proteins during sea urchin development.
1988,
Pubmed
,
Echinobase
Benson,
Role of the extracellular matrix in tissue-specific gene expression in the sea urchin embryo.
1991,
Pubmed
,
Echinobase
Bisgrove,
The SpEGF III gene encodes a member of the fibropellins: EGF repeat-containing proteins that form the apical lamina of the sea urchin embryo.
1993,
Pubmed
,
Echinobase
Brennan,
Cloning and characterization of HLC-32, a 32-kDa protein component of the sea urchin extraembryonic matrix, the hyaline layer.
1994,
Pubmed
,
Echinobase
Bruskin,
Accumulation in embryogenesis of five mRNAs enriched in the ectoderm of the sea urchin pluteus.
1981,
Pubmed
,
Echinobase
D'Alessio,
Cloning of a fibrillar collagen gene expressed in the mesenchymal cells of the developing sea urchin embryo.
1990,
Pubmed
,
Echinobase
Edelman,
Cell adhesion molecules: implications for a molecular histology.
1991,
Pubmed
Exposito,
Identification of a cell lineage-specific gene coding for a sea urchin alpha 2(IV)-like collagen chain.
1994,
Pubmed
,
Echinobase
Feinberg,
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.
1983,
Pubmed
Gong,
Structure and expression of the polyubiquitin gene in sea urchin embryos.
1991,
Pubmed
,
Echinobase
Guo,
Synthesis of human insulin gene. VIII. Construction of expression vectors for fused proinsulin production in Escherichia coli.
1984,
Pubmed
Hardin,
Target recognition by the archenteron during sea urchin gastrulation.
1990,
Pubmed
,
Echinobase
Hylander,
An ultrastructural immunocytochemical localization of hyalin in the sea urchin egg.
1982,
Pubmed
,
Echinobase
Ingersoll,
An N-linked carbohydrate-containing extracellular matrix determinant plays a key role in sea urchin gastrulation.
1994,
Pubmed
,
Echinobase
Karp,
Acid mucopolysaccharide metabolism, the cell surface, and primary mesenchyme cell activity in the sea urchin embryo.
1974,
Pubmed
,
Echinobase
Leaf,
The secretory pathway is blocked between the trans-Golgi and the plasma membrane during meiotic maturation in Xenopus oocytes.
1990,
Pubmed
Martin,
Cutaneous nerves of the embryonic chick wing do not develop in regions denuded of ectoderm.
1989,
Pubmed
Nocente-McGrath,
Endo16, a lineage-specific protein of the sea urchin embryo, is first expressed just prior to gastrulation.
1989,
Pubmed
,
Echinobase
Sanger,
DNA sequencing with chain-terminating inhibitors.
1977,
Pubmed
Somers,
Localization and developmental fate of ovoperoxidase and proteoliaisin, two proteins involved in fertilization envelope assembly.
1989,
Pubmed
,
Echinobase
Spiegel,
Fibronectin and laminin in the extracellular matrix and basement membrane of sea urchin embryos.
1983,
Pubmed
,
Echinobase
Spurr,
A low-viscosity epoxy resin embedding medium for electron microscopy.
1969,
Pubmed
Tabor,
DNA sequence analysis with a modified bacteriophage T7 DNA polymerase.
1987,
Pubmed
Towbin,
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
1979,
Pubmed
Venkatesan,
Structure and developmentally regulated expression of a Strongylocentrotus purpuratus collagen gene.
1986,
Pubmed
,
Echinobase
Wessel,
Primary mesenchyme cells of the sea urchin embryo require an autonomously produced, nonfibrillar collagen for spiculogenesis.
1991,
Pubmed
,
Echinobase
Wessel,
Cortical granule-specific components are present within oocytes and accessory cells during sea urchin oogenesis.
1989,
Pubmed
,
Echinobase
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,
Sequential expression of germ-layer specific molecules in the sea urchin embryo.
1985,
Pubmed
,
Echinobase
Wessel,
Gastrulation in the sea urchin embryo requires the deposition of crosslinked collagen within the extracellular matrix.
1987,
Pubmed
,
Echinobase
Wessel,
Ontogeny of the basal lamina in the sea urchin embryo.
1984,
Pubmed
,
Echinobase
Wessel,
Gastrulation in the sea urchin is accompanied by the accumulation of an endoderm-specific mRNA.
1989,
Pubmed
,
Echinobase