Endo16 is required for gastrulation in the sea urchin Lytechinus variegatus

Development Growth and Differentiation

Volumn 48, Issue 8, 2006, Pages 487-497

  Romano, Laura A ^a,b   Wray, Gregory A ^a  

^a DUKE UNIVERSITY   (United States)

^b DENISON UNIVERSITY   (United States)

Author keywords

Antisense; Endo16; Endoderm; Morpholino; Sea urchin

Indexed keywords

ANTIBODY; ENDO16 PROTEIN; ENHANCED GREEN FLUORESCENT PROTEIN; MESSENGER RNA; MORPHOLINE DERIVATIVE; PROTEIN; UNCLASSIFIED DRUG;

ARTICLE; BLASTOCYTE; CELL DIFFERENTIATION; CELL STRUCTURE; CONTROLLED STUDY; DNA SEQUENCE; ECTODERM; EMBRYO; EMBRYO DEVELOPMENT; ENDODERM; EXTRACELLULAR MATRIX; GASTRULATION; LYTECHINUS; MESENCHYME CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PROTEIN EXPRESSION; SEA URCHIN; SPECIES; STAINING;

AMINO ACID SEQUENCE; ANIMALS; CELL DIFFERENTIATION; EMBRYO, NONMAMMALIAN; EXTRACELLULAR MATRIX PROTEINS; GASTRULA; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GERM LAYERS; LYTECHINUS; MOLECULAR SEQUENCE DATA;

ECHINOIDEA; LYTECHINUS VARIEGATUS;

EID: 33749382352     PISSN: 00121592     EISSN: 1440169X     Source Type: Journal    
DOI: 10.1111/j.1440-169X.2006.00884.x     Document Type: Article

References (45)

1. Angerer, L. M. & Angerer, R. C. 2004. Disruption of gene function using antisense morpholinos. Meth. Cell Biol. 74, 699-711.
2. Angerer, L. M., Oleksyn, D. W., Levine, A. M., Li, X., Klein, W. H. & Angerer, R. C. 2001. Sea urchin goosecoid function links fate specification along the animal-vegetal and oral-aboral embryonic axes. Development 128, 4393-4404.
3. Anstrom, J. A., Chin, J. E., Leaf, D. S., Parks, A. L. & Raff, R. A. 1987. Localization and expression of msp130, a primary mesenchyme lineage-specific cell surface protein in the sea urchin embryo. Development 101, 255-265.
4. Benson, S., Rawson, R., Killian, C. & Wilt, F. 1991. The role of the extracellular matrix and tissue specific gene expression in the sea urchin. Mol. Rep. Dev. 29, 220-226.
5. Berg, L., Chen, S. W. & Wessel, G. M. 1996. An extracellular matrix molecule that is selectively expressed during development is important for gastrulation in the sea urchin embryo. Development 122, 703-713.
6. Bhalerao, J., Tylzanowski, P., Filie, J. D., Kozak, C. A. & Merregaert, J. 1995. Molecular cloning, characterization, and genetic mapping of the cDNA coding for a novel secretory protein of mouse. Demonstration of alternative splicing in skin and cartilage. J. Biol. Chem. 270, 16385-16394.
7. Burdsal, C. A., Alliegro, M. C. & McClay, D. R. 1991. Tissue-specific, temporal changes in cell adhesion to echinonectin in the sea urchin embryo. Dev. Biol. 144, 327-334.
8. 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.
9. Coffman, J. A. & McClay, D. R. 1990. A hyaline layer protein that becomes localized to the oral ectoderm and foregut of sea urchin embryos. Dev. Biol. 140, 93-104.
10. Dobias, S., Ma, L., Wu, H., Bell, J. & Maxson, R. 1997. The evolution of Msx gene function: expression and regulation of a sea urchin Msx class homeobox gene. Mech. Dev. 61, 37-48.
11. Duboc, V., Rottinger, E., Lapraz, F., Besnardeau, L. & Lepage, T. 2005. Left-right asymmetry in the sea urchin embryo is regulated by nodal signaling on the right side. Dev. Cell. 9, 147-158.
12. Ekker, S. C. & Larson, J. D. 2001. Morphant technology in model developmental systems. Genesis 30, 89-93.
13. Fatemi, S. H. 2005. Reelin glycoprotein: structure, biology, and roles in health and disease. Mol. Psychiatry 10, 251-257.
14. Godin, R. E., Klinzing, D. C., Porcaro, W. A. & Ernst, S. G. 1997. Specification of endoderm in the sea urchin embryo. Mech. Dev. 67, 35-47.
15. Govindarajan, V., Ramachandran, R., George, J., Shakes, D. & Tomlinson, C. 1995. An ECM-bound, PDGF-like growth factor and a TGF-α-like growth factor are required for gastrulation and spiculogenesis in the Lytechinus embryo. Dev. Biol. 172, 541-551.
16. Harada, Y., Akasaka, K., Shimada, H., Peterson, K. J., Davidson, E. H. & Satoh, N. 1996. Spatial expression of a forkhead homologue in the sea urchin embryo. Mech. Dev. 60, 163-173.
17. Howard, E. W., Newman, L. A., Oleksyn, D. W., Angerer, R. C. & Angerer, L. M. 2001. SpKrl: a direct target of β-catenin regulation required for endoderm differentiation in sea urchin embryos. Development 128, 365-375.
18. Kragh-Hansen, U. 1990. Structure and ligand binding properties of human serum albumin. Dan. Med. Bull. 37, 57-84.
19. Luke, N. H., Killian, C. E. & Livingston, B. T. 1997. Spfkh1 encodes a transcription factor implicated in gut formation during sea urchin development. Dev. Growth Differ. 39, 285-294.
20. Marsden, M. & Burke, R. D. 1998. The betaL integrin subunit is necessary for gastrulation in sea urchin embryos. Dev. Biol. 203, 134-148.
21. Martinez, P. & Davidson, E. H. 1997. SpHmx, a sea urchin homeobox gene expressed in embryonic pigment cells. Dev. Biol. 181, 213-222.
22. Maurer, P., Hohenester, E. & Engel, J. 1996. Extracellular calciumbinding proteins. Curr. Opin. Cell Biol. 8, 609-617.
23. McClay, D. R. & Logan, C. Y. 1996. Regulative capacity of the archenteron during gastrulation in the sea urchin. Development 122, 607-616.
24. McClay, D. R., Wessel, G. M. & Marchase, R. B. 1981. Intercellular recognition: quantitation of initial binding events. Proc. Natl Acad. Sci. USA 78, 4975-4979.
25. Nasevicius, A., Larson, J. & Ekker, S. C. 2000. Distinct requirements for zebrafish angiogenesis revealed by a VEGF-A morphant. Yeast. 17, 294-301.
26. Nocente-McGrath, C., Brenner, C. A. & Ernst, S. G. 1989. Endo16, a lineage-specific protein of the sea urchin embryo, is first expressed just prior to gastrulation. Dev. Biol. 136, 264-272.
27. Ramachandran, R. K., Govindarajan, V., Seid, C. A., Patil, S. & Tomlinson, C. R. 1995. Role for platelet-derived growth factor-like and epidermal growth factor-like signaling pathways in gastrulation and spiculogenesis in the Lytechinus sea urchin embryo. Dev. Dyn. 204, 77-88.
28. Ransick, A., Ernst, S., Britten, R. J. & Davidson, E. H. 1993. Whole mount in situ hybridization shows Endo16 to be a marker for the vegetal plate territory in sea urchin embryos. Mech. Dev. 42, 117-124.
29. Romano, L. A. & Wray, G. A. 2003. Conservation of Endo16 expression despite evolutionary divergence in cis- and trans-acting components of transcriptional regulation. Development 130, 4187-4199.
30. Ruffins, S. W. & Ettensohn, C. A. 1996. A fate map of the vegetal plate of the sea urchin (Lytechinus variegatus) mesenchyme blastula. Development 122, 253-263.
31. Ruoslahti, E. 1996. RGD and other recognition sequences for integrins. Annu. Rev. Cell Dev. Biol. 12, 697-715.
32. Soltysik-Espanola, M., Klinzing, D. C., Pfarr, K., Burke, R. D. & Ernst, S. G. 1994. Endo16, a large multidomain protein found on the surface and ECM of endodermal cells during sea urchin gastrulation, binds calcium. Dev. Biol. 165, 73-85.
33. Summerton, J. 1999. Morpholino antisense oligomers: the case for an RNase H-independent structural type. Biochem. Biophys. Acta 1489, 141-158.
34. Sweet, H. C., Hodor, P. G. & Ettensohn, C. A. 1999. The role of micromere signaling in Notch activation and mesoderm specification during sea urchin embryogenesis. Development 126, 5255-5265.
35. Wang, W., Wikramanayake, A., Gonzalez-Rimbau, M., Vlahou, A., Flytzanis, C. & McClay, D. R. 1996. Very early and transient vegetal plate expression of SpKrox1, a Kruppel/Krox gene from Strongylocentrotus purpuratus. Mech. Dev. 60, 185-195.
36. Wessel, G. M., Goldberg, L., Lennarz, W. J. & Klein, W. H. 1989. Gastrulation in the sea urchin embryo is accompanied by the accumulation of an endoderm-specific mRNA. Dev. Biol. 136, 526-536.
37. Wessel, G. M. & McClay, D. R. 1985. Sequential expression of germ-layer specific molecules in the sea urchin embryo. Dev. Biol. 111, 451-463.
38. Wessel, G. M. & 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.
39. Wessel, G. M. & Wikramanayakem, A. 1999. How to grow a gut: ontogeny of the endoderm in the sea urchin embryo. Bioessays 21, 459-471.
40. Yang, F., Luna, V. J., McAnelly, R. D., Naberhaus, K. H., Cupples, R. L. & Bowman, B. H. 1985. Evolutionary and structural relationships among the group-specific component, albumin, and alpha-fetoprotein. Nucl. Acid. Res. 22, 8007-8017.
41. Yuh, C.-H., Bolouri, H. & Davidson, E. H. 1998. Genomic cisregulatory logic: experimental and computational analysis of a sea urchin gene. Science 279, 1896-1902.
42. Yuh, C.-H., Bolouri, H. & Davidson, E. H. 2001. Cis-regulatory logic in the Endo16 gene: switching from a specification to a differentiation mode of control. Development 128, 617-629.
43. Yuh, C.-H. & Davidson, E. H. 1996. Modular cis-regulatory organization of Endo16, a gut-specific gene of the sea urchin embryo. Development 122, 1069-1082.
44. Yuh, C.-H., Moore, J. G. & Davidson, E. H. 1996. Quantitative functional interrelations within the cis-regulatory system of the S. purpuratus Endo16 gene. Development 122, 4045-4056.
45. Yuh, C.-H., Ransick, A., Martinez, P., Britten, R. J. & Davidson, E. H. 1994. Complexity and organization of DNA-protein interactions in the 5′-regulatory region of an endoderm-specific marker gene in the sea urchin embryo. Mech. Dev. 47, 165-186.