Association of the sea urchin EGF-related peptide, EGIP-D, with fasciclin I-related ECM proteins from the sea urchin Anthocidaris crassispina

Development Growth and Differentiation

Volumn 41, Issue 4, 1999, Pages 483-494

  Hirate, Yoshikazu ^a   Tomita, Kazuo ^a   Yamamoto, Shinji ^a   Kobari, Kazuki ^a   Uemura, Isao ^b   Yamasu, Kyo ^a   Suyemitsu, Takashi ^a  

^a SAITAMA UNIVERSITY   (Japan)

^b TOKYO METROPOLITAN UNIVERSITY   (Japan)

Author keywords

Exogastrula inducing peptide; Exogastrula inducing peptide D binding protein; Extracellular matrix; Fasciclin I; Sea urchin embryo

Indexed keywords

EPIDERMAL GROWTH FACTOR; FASCICLIN I; SCLEROPROTEIN;

ANIMAL CELL; ARTICLE; BINDING SITE; BLASTOMERE; ECTODERM; EMBRYO DEVELOPMENT; GASTRULA; NONHUMAN; NUCLEOTIDE SEQUENCE; PROTEIN ANALYSIS; PROTEIN INTERACTION; PROTEIN PURIFICATION; PROTEIN STRUCTURE; SEA URCHIN;

AMINO ACID SEQUENCE; ANIMALS; CELL ADHESION MOLECULES, NEURONAL; DNA, COMPLEMENTARY; EMBRYO, NONMAMMALIAN; GENE EXPRESSION; INVERTEBRATE HORMONES; MOLECULAR SEQUENCE DATA; PHYLOGENY; PROTEIN BINDING; RECEPTORS, INVERTEBRATE PEPTIDE; SEA URCHINS; SEQUENCE HOMOLOGY, AMINO ACID;

ANIMALIA; ANTHOCIDARIS CRASSISPINA; ECHINOIDEA; INSECTA; INVERTEBRATA; PLUTEUS;

EID: 0032811547     PISSN: 00121592     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-169x.1999.00446.x     Document Type: Article

References (46)

1. Adelson, D. L. & Humphreys, I. 1988. Sea urchin morphogenesis and cell-hyalin adhesion are perturbed by a monoclonal antibody specific for hyatin. Development 104, 391-402.
2. Alliegro, M. C., Ettensohn, C. A., Burdsal, C. A., Erickson, H. P. & McClay, D. R. 1988. Echinonectin: A new embryonic substrate adhesion protein. J. Cell Biol. 107, 2319-2327.
3. Altschul, S. F., Gish, W., Miller, W., Myers, E. W. & Lipman, D. J. 1990. Basic local alignment search tool. J. Mol. Biol. 215, 403-410.
4. Appelle, E., Weber, I. I. & Blasi, F. 1988. Structure and function of epidermal growth factor-like regions in proteins. FEBS Lett. 231, 1-4.
5. Bisgrove, B. W., Andrews, M. E. & Raff, R. A. 1991. Fibropellins, products of an EGF repeat-containing gene, form a unique extracellular matrix structure that surrounds the sea urchin embryo. Dev. Biol. 146, 89-99.
6. Brennan, C. & Robinson, J. J. 1994. Cloning and characterization of HLC-32, a 32-kDa protein component of the sea urchin extra-embryonic matrix, the hyaline layer. Dev. Biol. 165, 556-565.
7. Burke, R. D., Myers, R. L., Sexton, T. L. & Jackson, C. 1991. Cell movements during the initial phase of gastrulation in the sea urchin embryo. Dev. Biol. 146, 542-557.
8. Cameron, A. & Holland, N. D. 1985. Demonstration of the granular layer and the fate of the hyaline layer during the development of a sea urchin (Lytechinus variegatus). Cell. Tissue Res. 239, 455-458.
9. Cervello, M. & Matranga, V. 1989. Evience of a precursor-product relationship between vitellogenin and toposome, a glycoprotein complex mediating cell adhesion. Cell Differ. Dev. 26, 67-76.
10. Chomczynski, P. & Sacchi, N. 1987. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162, 156-159.
11. Church, G. M. & Gilbert, W. 1984. Genomic sequencing. Proc. Natl Acad. Sci. USA 81, 1991-1995.
12. Dan, K. & Okazaki, K. 1956. Cyto-embryological studies of sea urchins: III. Role of the secondary mesenchyme cells in the formation of the primitive gut in sea urchin larvae. Biol. Bull. 110, 29-42.
13. Davidson, L. A., Koehl, M. A. R., Keller, R. & Oster, G. F. 1995. How do sea urchins invaginate? Using biomechanics to distinguish between mechanisms of primary invagination. Development 121, 2005-2018.
14. Di Carlo, M., Montana, G. & Bonura, A. 1990. Analysis of the sequence and expression during sea urchin development of two members of a multigenic family, coding for butanol-extractable proteins. Mol. Reprod. Dev. 25, 28-36.
15. Di Carlo, M., Perriera, S., Montana, G., Romancino, D. P. & Reale, S. 1994a. Cloning and sequencing of a cell surface protein-encoding gene conserved in sea urchin species. Gene 141, 243-248.
16. Di Carlo, M., Romancino, D. P., Montana, G. & Ghersi, G. 1994b. Spatial distribution of two maternal messengers in Paracentrotus lividus during oogenesis and embryogenesis. Proc. Natl Acad. Sci. USA 91, 5622-5626.
17. Elkins, I., Hortsch, M., Bieber, A. J., Snow, P. M. & Goodman, C. S. 1990. Drosophila fasciclin I is a novel homophilic adhesion molecule that along with fasciclin III can mediate cell sorting. J. Cell Biol. 110, 1825-1832.
18. Engel, J. 1989. EGF-like domains in extracellular matrix proteins: Localized signals for growth and differentiation? FEBS Lett. 251, 1-7.
19. Fujita, Y., Hirate, Y., Hiyama, T., Yamasu, K., Suyemitsu, I. & Ishihara, K. 1997. Purification of EGIP-D-binding protein from the embryos of the sea urchin Anthocidaris crassispina. Zool. Sci. 14, 931-934.
20. Fujita, Y., Yamasu, K., Suyemitsu, T. & Ishihara, K. 1994. A protein that binds an exogastrula-inducing peptide, EGIP-D, in the hyaline layer of sea urchin embryos. Develop. Growth Differ. 36, 275-280.
21. Gratwohl, E. K-M., Kellenberger, E., Lorand, L. & Noll, H. 1991. Storage, ultrastructural targeting and function of toposomes and hyalin in sea urchin embryogenesis. Mech. Dev. 33, 127-138.
22. Gustafson, T. & Wolpert, L. 1967. Cellular movement and contact in sea urchin morphogenesis. Biol. Rev. Camb. Philos. Soc. 42, 442-498.
23. Hardin, J. 1989. Local shifts in position and polarized motility drive cell rearrangement during sea urchin gastrulation. Dev. Biol. 136, 430-445.
24. Hashimoto, K., Noshiro, M., Ohno, S. et al. 1997. Characterization of a cartilage-derived 66-kDa protein (RGD-CAP/βig-h3) that binds to collagen. Biochim. Biophys. Acta 1355, 303-314.
25. Huber, O. & Sumper, M. 1994. Algal-CAMs: Isoforms of a cell adhesion molecule in embryos of the alga Volvox with homology to Drosophila fasciclin I. EMBO J. 13, 4212-4222.
26. Hunter, D. D., Porter, B. E., Bulock, J. W., Adams, S. P., Merlie, J. P. & Sanes, J. R. 1989. Primary sequence of a motor neuron-selective adhesive site in the synaptic basal lamina protein S-laminin. Cell 59, 905-913.
27. Ishihara, K., Tonegawa, Y., Suyemitsu, T. & Kubo, H. 1982. The blastocoelic fluid of sea urchin embryo induces exogastrulation. J. Exp. Zool. 220, 227-233.
28. Kozak, M. 1989. The scanning model for translation: An update. J. Cell Biol. 108, 229-241.
29. Laemmli, U. K. 1970, Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 277, 680-685.
30. McClay, D. R. & Fink, R. D. 1982. Sea urchin hyalin: Appearance and function in development. Dev. Biol. 92, 285-293.
31. Matsumoto, S., Matsuo, T., Ohara, N. et al. 1995. Cloning and sequencing of a unique antigen MPT70 from Mycobacterium tuberculosis H37Rv and expression in BCG using E coli-mycobacteria shuttle vector. Scand. J. Immunol 41, 281-287.
32. Mizuno, N., Uemura, I., Yamasu, K., Suyemitsu, T. & Ishihara, K. 1993. Localization of an exogastrula-inducing peptide (EGIP) in embryos of the sea urchin (Anthocidaris crassispina). Develop. Growth Differ. 35, 539-549.
33. Onodera, H., Kobari, K., Sakuma, M., Sato, M., Suyemitsu, T. & Yamasu, K. 1999. Expression of a src-type protein tyrosine kinase gene, AcSrc 1, in the sea urchin embryo. Develop. Growth Differ. 41, 19-28.
34. Romancino, D. P., Ghersi, G., Montana, G., Bonura, A., Perriera, S. & Di Carlo, M. 1992. Characterization of bep 1 and bep4 antigens involved in cell interactions during Paracentrotus lividus development. Differentiation 50, 67-74.
35. Sambrook, J., Fritsch, E. F. & Maniatis, T. 1989. Molecular Cloning: A Laboratory Manual, 2nd edn. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY.
36. Sardet, C. & Chang, P. 1987. The egg cortex: From maturation through fertilization. Cell Differ. 21, 1-19.
37. Skonier, J., Bennett, K., Rothwell, V. et al. 1994. βig-h3: A transforming growth factor-β-responsive gene encoding a secreted protein that inhibits cell attachment in vitro and suppresses the growth of CHO cells in nude mice. DNA Cell Biol. 13, 571-584.
38. Skonier, J., Neubauer, M., Madisen, L., Bennett, K., Plowman, G. D. & Purchio, A. F. 1992. cDNA cloning and sequence analysis of βig-h3, a novel gene induced in a human adenocarcinoma cell line after treatment with transforming growth factor-β. DNA Cell Biol. 11, 511-522.
39. Suyemitsu, T. 1991. The positions of the disulfide bonds in exogastrula-inducing peptide D (EGIP-D) purified from embryos of the sea urchin, Anthocidaris crassispina. Zool. Sci. 8, 505-509.
40. Suyemitsu, T., Tonegawa, Y. & Ishihara, K. 1990. Similarities between the primary structures of exogastrula-inducing peptides and peptide B purified from embryos of the sea urchin, Anthocidaris crassispina. Zool. Sci. 7, 831-839.
41. Takeshita, S., Kikuno, R., Iezuka, K. & Amann, E. 1993. Osteoblast-specific factor 2: Cloning of a putative bone adhesion protein with homology with the insect protein fasciclin I. Biochem. J. 294, 271-278.
42. Thain, A., Gaston, K., Jenkins, O. & Clarke, A. R. 1996. A method for the separation of GST fusion proteins from co-purifying GroEL. Trends Genet. 12, 209-210.
43. Ulstrup, J. C., Jeansson, S., Wiker, H. G., Harboe, M. 1995. Relationship of secretion pattern and MPB70 homclogy with osteoblast-specific factor 2 to osteitis following Mycobacterium bovis BCG vaccination. Infect. Immunol. 63, 672-675.
44. Yamasu, K., Watanabe, H., Kohchi, C. et al. 1995. Molecular cloning of a cDNA that encodes the precursor to several exogastrula-inducing peptides, epidermal-growth-factor-related polypeptides of the sea urchin Anthocidaris crassispina. Eur. J. Biochem. 228, 515-523.
45. Yang, Q., Angerer, L. M. & Angerer, R. C. 1989. Unusual pattern of accumulation of mRNA encoding EGF-related protein in sea urchin embryos. Science 246, 806-808.
46. Zinn, K., McAllister, L. & Goodman, C. S. 1988. Sequence analysis and neuronal expression of fasciclin I in grasshopper and Drosophila. Cell 53, 577-587.