Apextrin, a novel extracellular protein associated with larval ectoderm evolution in Heliocidaris erythrogramma

Developmental Biology

Volumn 211, Issue 1, 1999, Pages 77-87

  Haag, Eric S ^a   Sly, Belinda J ^a   Andrews, Mary E ^a   Raff, Rudolf A ^a  

^a INDIANA UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; ANTISERUM; APEXTRIN; DNA; HYALIN; PROTEIN; RNA; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL TISSUE; ARTICLE; CELL ADHESION; ECTODERM; EMBRYO; EXTRACELLULAR MATRIX; GENE; GENE EXPRESSION; IMMUNOBLOTTING; IMMUNOHISTOCHEMISTRY; LARVA; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; SEA URCHIN;

ANIMALIA; ECHINOIDEA; HELIOCIDARIS ERYTHROGRAMMA; HELIOCIDARIS TUBERCULATA; HEXAPODA;

EID: 0033168060     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1006/dbio.1999.9283     Document Type: Article

References (42)

1. Adelson D. L., Humphreys T. Sea urchin morphogenesis and cell-hyalin adhesion are perturbed by a monoclonal antibody specific for hyalin. Development. 104:1988;391-402.
2. Alliegro M. C., Ettensohn C. A., Burdsal C. A., Erickson H. P., McClay D. R. Echinonectin: A new embryonic substrate adhesion protein. J. Cell Biol. 107:1988;2319-2327.
3. Alliegro M. C., McClay D. R. Storage and mobilization of extracellular matrix proteins during sea urchin development. Dev. Biol. 125:1988;208-216.
4. Bisgrove B. W., Andrews M. E., Raff R. A. Fibropellins, products of an EGF repeat-containing gene, form a unique extracellular matrix structure that surrounds the sea urchin embryo. Dev. Biol. 146:1991;89-99.
5. Bisgrove B. W., Andrews M. E., Raff R. A. Evolution of the fibropellin gene family and patterns of fibropellin gene expression in sea urchin phylogeny. J. Mol. Evol. 41:1995;34-45.
6. Bisgrove B. W., Raff R. A. The SpEGF III gene encodes a member of the fibropellins: EGF repeat-containing proteins that form the apical lamina of the sea urchin embryo. Dev. Biol. 157:1993;526-538.
7. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:1987;156-159.
8. Citkowitz E. The hyaline layer: Its isolation and role in echinoderm development. Dev. Biol. 24:1971;348-362.
9. Citkowitz E. Analysis of the isolated hyaline layer of sea urchin embryos. Dev. Biol. 27:1972;494-503.
10. Coffman J. A., McClay D. R. A hyaline layer protein that becomes localized to the oral ectoderm and foregut of sea urchin embryos. Dev. Biol. 140:1990;93-104.
11. Denny M. W. Biology and the Mechanics of the Wave-Swept Environment. 1988;Princeton Univ. Press, Princeton.
12. Emlet R. B., Hoegh-Guldberg O. Effects of egg size on post-larval performance: Experimental evidence from a sea urchin. Evolution. 51:1997;141-152.
13. Engel J., Efimov V. P., Maurer P. Domain organizations of extracellular matrix proteins and their evolution. Development. 1994 Suppl. 1994;35-42.
14. Furlow J. D., Berry D. L., Wang Z., Brown D. D. A set of novel tadpole-specific genes expressed only in the epidermis are down-regulated by thyroid hormone during Xenopus laevis metamorphosis. Dev. Biol. 182:1997;284-298.
15. Galione A., McDougall A., Busa W. B., Willmott N., Gillot I., Whitaker M. Redundant mechanisms of calcium-induced calcium release underlying calcium waves during fertilization of sea urchin eggs. Science. 261:1993;348-352.
16. Giga Y., Ikai A., Takahashi K. The complete amino acid sequence of echinoidin, a lectin from the coelomic fluid of the sea urchin Anthocidaris crassispina. J. Biol. Chem. 262:1987;6197-6203.
17. Guo L., Stepien P. P., Tso J. Y., Brousseau R., Narang S., Thomas D. Y., Wu R. Synthesis of human insulin gene. VIII. Construction of expression vectors for fused proinsulin production in Escherichia coli. Gene. 29:1984;251-254.
18. Haag E. S., Raff R. A. Isolation and characterization of three mRNAs enriched in embryos of the direct-developing sea urchin Heliocidaris erythrogramma: Evolution of larval ectoderm. Dev. Genes Evol. 208:1998;188-204.
19. Hahn J.-H., Kissinger J. C., Raff R. A. Structure and evolution of CyI cytoplasmic actin-encoding genes in the indirect- and direct-developing sea urchins Heliocidaris tuberculata and Heliocidaris erythrogramma. Gene. 153:1995;219-224.
20. Hall H. G., Vacquier V. D. The apical lamina of the sea urchin embryo: Major glycoproteins associated with the hyaline layer. Dev. Biol. 89:1982;168-178.
21. Hinegardner R. Growth and development of the laboratory cultured sea urchin. Biol. Bull. 137:1969;465-475.
22. Kissinger J. C., Raff R. A. Evolutionary changes in sites and timing of actin gene expression in embryos of the direct- and indirect-developing sea urchins, Heliocidaris erythrogramma and H. tuberculata. Dev. Genes Evol. 208:1998;82-93.
23. Lowe C. J., Wray G. A. Radical alterations in the roles of homeobox genes during echinoderm evolution. Nature. 389:1997;718-721.
24. MacBride E. W. Development of Echinus. Philos. Trans. R. Soc. London. 195B:1903.
25. Matese J. C., Black S., McClay D. R. Regulated exocytosis and sequential construction of the extracellular matrix surrounding the sea urchin zygote. Dev. Biol. 186:1997;16-26.
26. McClay D. R., Fink R. D. Sea urchin hyalin: Appearance and function in development. Dev. Biol. 92:1982;285-293.
27. Miller J., McClay D. R. Characterization of the role of cadherin in regulating cell adhesion during sea urchin development. Dev. Biol. 192:1997;323-339.
28. Numata O., Takemasa T., Takagi I., Hirono M., Hirano H., Chiba J., Watanabe Y. Tetrahymena 14-nM filament-forming protein has citrate synthase activity. Biochem. Biophys. Res. Commun. 174:1991;1028-1034.
29. Parks A. L., Parr B. A., Chin J., Leaf D. S., Raff R. A. Molecular analysis of heterochronic changes in the evolution of direct developing sea urchins. J. Evol. Biol. 1:1988;27-44.
30. Pearse J. S., Cameron R. A. Echinodermata: Echinoidea. Giese A. C., Pearse J. S., Pearse V. B. Reproduction of Marine Invertebrates. 1991;514-663 Boxwood Press, Pacific Grove.
31. Piatagorsky J., Wistow G. J. Enzyme/crystallins: Gene sharing as an evolutionary strategy. Cell. 57:1989;197-199.
32. Sambrook J., Fritsch E. F., Maniatis T. Molecular Cloning. 1989;Cold Spring Harbor Laboratory Press, Cold Spring Harbor.
33. Sasaki H., Yamada K., Akasaka K., Kawasaki H., Suzuki K., Saito A., Sato M., Shimada H. cDNA cloning, nucleotide sequence and expression of the gene for arylsulfatase in the sea urchin (Hemicentrotus pulcherrimus) embryo. Eur. J. Biochem. 177:1988;9-13.
34. Sharon-Friling R., Richardson J., Sperbeck S., Lee D., Rauchman M., Maas R., Swaroop A., Wistow G. Lens-specific gene recruitment of ζ-crystallin through Pax-6, Nrl-Maf, and brain suppressor sites. Mol. Cell. Biol. 18:1998;2067-2076.
35. Spilsbury K., O'Mara M. A., Wu W. M., Rowe P. B., Symonds G., Takayama Y. Isolation of a novel macrophage-specific gene by differential cDNA analysis. Blood. 85:1995;1620-1629.
36. Stephens R. E., Kane R. E. Some properties of hyalin, the calcium-insoluble protein of the hyaline layer of the sea urchin egg. J. Cell Biol. 44:1970;611-617.
37. Takeichi M. Cadherins: A molecular family important in selective cell-cell adhesion. Annu. Rev. Biochem. 59:1990;237-252.
38. von Ubisch L. Die Anlage und Ausbildung des Skeletsystems einiger Echiniden. Z. Wiss. Zool. 104:1913.
39. Whalley T., Crossley I., Whitaker M. Phosphoprotein inhibition of calcium-stimulated exocytosis in sea urchin eggs. J. Cell Biol. 113:1991;769-778.
40. Wray G. A., Raff R. A. Heliocidaris erythrogramma. Dev. Biol. 141:1990;41-54.
41. Yang Q., Angerer L. M., Angerer R. C. Structure and tissue-specific developmental expression of a sea urchin arylsulfatase gene. Dev. Biol. 135:1989;53-65.
42. Yang Q., Kingsley P. D., Kozlowski D. J., Angerer R. C., Angerer L. M. Immunochemical analysis of arylsulfatase accumulation in sea urchin embryos. Dev. Growth Differ. 35:1993;139-151.