Analysis of sea urchin embryo gene expression by immunocytochemistry

Methods in Cell Biology

Volumn 2004, Issue 74, 2004, Pages 333-369

  Venuti, Judith M ^a   Pepicelli, Carmen ^b   Flowers, Vera Lynn ^a  

^a LOUISIANA STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CURIS INC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBODY;

ANIMAL; ANIMAL EMBRYO; ARTIFACT; FEMALE; GENE EXPRESSION REGULATION; GENETICS; IMMUNOHISTOCHEMISTRY; IMMUNOLOGY; METHODOLOGY; MICRODISSECTION; PHYSIOLOGY; PRENATAL DEVELOPMENT; REVIEW; SEA URCHIN; STAINING;

ANIMALS; ANTIBODIES; ARTIFACTS; EMBRYO, NONMAMMALIAN; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; IMMUNOHISTOCHEMISTRY; MICRODISSECTION; SEA URCHINS; STAINING AND LABELING;

EID: 16644401918     PISSN: 0091679X     EISSN: None     Source Type: Book Series    
DOI: 10.1016/s0091-679x(04)74015-7     Document Type: Review

References (42)

1. Adelson, D. L., and Humphreys, T. (1988). Sea urchin morphogenesis and cell-hyalin adhesion are perturbed by a monoclonal antibody specific for hyalin. Development 104, 391-402.
2. Alliegro, M. C., Burdsal, C. A., and McClay, D. R. (1990). In vitro biological activities of echinonectin. Biochem. 29, 2135-2141.
3. Hodor, P. G., Illies, M. R., Broadley, S., and Ettensohn, C. A. (2000). Cell-substrate interactions during sea urchin gastrulation: Migrating primary mesenchyme cells interact with and align extracellular matrix fibers that contain ECM3, a molecule with NG2-like and multiple calcium-binding domains. Dev. Biol. 222, 181-194.
4. Hsu, S. M., Raine, L., and Fanger, H. (1981). The use of antiavidin antibody and avidinbiotin-peroxidase complex in immunoperoxidase techniques. Am. J. Clin. Pathol. 75, 816-821.
5. Humason, G. L. (1972). "Animal Tissue Techniques," p. 641. W. H. Freeman and Company, San Francisco.
6. Ingersoll, E. P., and Ettensohn, C. A. (1994). An N-linked carbohydrate-containing extracellular matrix determinant plays a key role in sea urchin gastrulation. Dev. Biol. 163, 351-366.
7. Kanoh, K., Aizu, G., and Katow, H. (2001). Disappearance of an epithelial cell surface-specific glycoprotein (Epith-1) associated with epithelial-mesenchymal conversion in sea urchin embryogenesis. Dev. Growth Diff. 43, 83-95.
8. Katow, H. (1995). Pamlin, a primary mesenchyme cell adhesion protein, in the basal lamina of the sea urchin embryo. Exp. Cell Res. 218, 469-478.
9. Katow, H., and Sofuku, S. (2001). An RGDS peptide-binding receptor, FR-1R, localizes to the basal side of the ectoderm and to primary mesenchyme cells in sand dollar embryos. Dev. Growth Diff. 43, 601-610.
10. Kenny, A. P., Kozlowski, D., Oleksyn, D. W., Angerer, L. M., and Angerer, R. C. (1999). SpSoxB1, a maternally encoded transcription factor asymmetrically distributed among early sea urchin blastomeres. Development 126, 5473-5483.
11. LaFleur, G. J., Jr, Horiuchi, Y., and Wessel, G. M. (1998). Sea urchin ovoperoxidase: oocyte-specific member of a heme-dependent peroxidase superfamily that functions in the block to polyspermy. Mech. Dev. 70, 77-89.
12. Laidlaw, M., and Wessel, G. M. (1994). Cortical granule biogenesis is active throughout oogenesis in sea urchins. Development 120, 1325-1333.
13. Leguia, M., and Wessel, G. M. (2004). Selective expression of a sec1/munc18 member in sea urchin eggs and embryos. Mech. Dev. in press.
14. Logan, C. Y., Miller, J. R., Ferkowicz, M. J., and-McClay, D. R. (1999). Nuclear beta-catenin is required to specify vegetal cell fates in the sea urchin embryo. Development 126, 345-357.
15. Lowe, C. J., and Wray, G. A. (1997). Radical alterations in the roles of homeobox genes during echinoderm evolution. Nature 389, 718-721.
16. Lowe, C. J., Issel-Tarverm, L., and Wray, G. A. (2002). Gene expression and larval evolution: Changing roles of distal-less and orthodenticle in echinoderm larvae. Evol. Dev. 4, 111-123.
17. Matranga, V., Kuwasaki, B., and Noll, H. (1986). Functional characterization of toposomes from sea urchin blastula embryos by a morphogenetic cell aggregation assay. EMBO J. 5, 3125-3132.
18. Matranga, V., Yokota, Y., Zito, F., Tesoro, V., and Nakano, E. (1995). Biochemical and immunological relationships among fibronectin-like proteins from different sea urchin species. Roux's Arch. Dev. Biol. 204, 413-418.
19. McClay, D. R., Peterson, R. E., Range, R. C., Winter-Vann, A. M., and Ferkowicz, M. J. (2000). Micromere induction signal is activated by beta-catenin and acts through notch to initiate specification of secondary mesenchyme cells in the sea urchin embryo. Development 127, 5113-5122.
20. Mujumdar, R. B., Ernst, L. A., Mujumdar, S. R., Lewis, C. J., and Waggoner, A. S. (1993). Cyanine dye labeling reagents: Sulfoindocyanine succinimidyl esters. Bioconjug. Chem. 4, 105-111.
21. Noll, H., Matranga, V., Cervello, M., Humphreys, T., Kuwasaki, B., and Adelson, D. (1985). Characterization of toposome from sea urchin blastula cells: A cell organelle mediating adhesion and expressing positional information. Proc. Natl. Acad. Sci. USA 82, 8062-8066.
22. Oliveri, P., Davidson, E. H., and McClay, D. R. (2003). Activation of pmarl controls specification of micromeres in the sea urchin embryo. Dev. Biol. 258, 32-43.
23. Panchuk-Voloshina, N., Haugland, R. P., Bishop-Stewart, J., Bhalgat, M. K., Millard, P. J., Mao, F., Leung, W. Y., and Haugland, R. P. (1999). Alexa dyes, a series of new fluorescent dyes that yield exceptionally bright, photostable conjugates. J. Histochem. Cytochem. 47, 1179-1188.
24. Sherwood, D. R., and McClay, D. R. (1999). LvNotch signaling mediates secondary mesenchyme specification in the sea urchin embryo. Development 126, 1703-1713.
25. Somers, C. E., Battaglia, D. E., and Shapiro, B. M. (1989). Localization and developmental fate of ovoperoxidase and proteoliaisin, two proteins involved in fertilization envelope assembly. Dev Biol. 131, 226-235.
26. Sweet, H. C., Hodor, P. G., and Ettensohn, C. A. (1999). The role of micromere signaling in Notch activation and mesoderm specification during sea urchin embryogenesis. Development 126, 5255-5265.
27. Urry, L. A., Hamilton, P. C., Killian, C. E., and Wilt, F. H. (2000). Expression of spicule matrix proteins in the sea urchin embryo during normal and experimentally altered spiculogenesis. Dev. Biol. 225, 201-213.
28. Vonica, A., Weng, W., Gumbiner, B. M., and Venuti, J. M. (2000). TCF is the nuclear effector of the beta-catenin signal that patterns the sea urchin animal-vegetal axis. Dev. Biol. 217, 230-243.
29. Voronina, E., Marzluff, W. F., and Wessel, G. M. (2003). Cyclin B synthesis is required for sea urchin oocyte maturation. Dev. Biol. 256, 258-275.
30. Voronina, E., and Wessel, G. M. (2004). Regulatory contribution of heterotrimeric G-proteins to oocyte maturation in the sea urchin. Mech. Dev. 121, 247-259.
31. Wessel, G. M., and McClay, D. R. (1985). Sequential expression of germ-layer specific molecules in the sea urchin embryo. Dev. Biol. 111, 451-463.
32. Wessel, G. M., and McClay, D. R. (1986). Two embryonic, tissue-specific molecules identified by a double-label immunofiuorescence technique for monoclonal antibodies. J. Histochem. Cytochem. 34, 703-706.
33. Wessel, G. M., and McClay, D. R. (1987). Gastrulation in the sea urchin embryo requires the deposition of crosslinked collagen within the extracellular matrix. Dev. Biol. 121, 149-165.
34. Wessel, G. M., Zhang, W., and Klein, W. H. (1990). Myosin heavy chain accumulates in dissimilar cell types of the macromere lineage in the sea urchin embryo. Dev. Biol. 140, 447-454.
35. Wessel, G. M. (1995). A protein of the sea urchin cortical granules is targeted to the fertilization envelope and contains an LDL-receptor-like motif. Dev. Biol. 167, 388-397.
36. Wessel, G. M., Berg, L., Adelson, D. L., Cannon, G., and McClay, D. R. (1998). A molecular analysis of hyalin - a substrate for cell adhesion in the hyaline layer of the sea urchin embryo. Dev. Biol. 193, 115-126.
37. Wessel, G. M., Brooks, J. M., Green, E., Haley, S., Voronina, E., Wong, J., Zaydfudim, V., and Conner, S. (2001). The biology of cortical granules. Int. Rev. Cytol. 209, 117-206.
38. Wikramanayake, A. H., Huang, L., and Klein, W. H. (1998). β-Catenin is essential for patterning the maternally specified animal-vegetal axis in the sea urchin embryo. Proc. Natl. Acad. Sci. USA 95, 9343-9348.
39. Wray, G. A., and McClay, D. R. (1989). Molecular heterochronies and heterotropies in early echinoid development. Evolution. 43, 803-813.
40. Wright, B. D., and Scholey, J. M. (1993). Nonfluorescent immunolocalization of antigens in mitotic sea urchin blastomeres. Meth. Cell. Biol. 37, 223-240.
41. Zito, F., Tesoro, V., McClay, D. R., Nakano, E., and Matranga, V. (1998). Ectoderm cell-ECM interaction is essential for sea urchin embryo skeletogenesis. Dev. Biol. 196, 184-192.
42. Zito, F., Nakano, E., Sciarrino, S., and Matranga, V. (2000). Regulative specification of ectoderm in skeleton disrupted sea urchin embryos treated with monoclonal antibody to P1-nectin. Growth Diff. 42, 499-506.