HpEts, an ets-related transcription factor implicated in primary mesenchyme cell differentiation in the sea urchin embryo

Mechanisms of Development

Volumn 80, Issue 1, 1999, Pages 41-52

  Kurokawa, Daisuke ^a   Kitajima, Takashi ^b   Mitsunaga Nakatsubo, Keiko ^a   Amemiya, Shonan ^c   Shimada, Hiraku ^a   Akasaka, Koji ^a  

^a HIROSHIMA UNIVERSITY   (Japan)

^b TOKYO METROPOLITAN UNIVERSITY   (Japan)

^c UNIVERSITY OF TOKYO   (Japan)

Author keywords

Ets related transcription factor; Primary mesenchyme cells; Sea urchin

Indexed keywords

ARYLSULFATASE; MATRIX PROTEIN; MESSENGER RNA; ONCOPROTEIN; TRANSCRIPTION FACTOR;

ANIMAL CELL; ARTICLE; BINDING SITE; BLASTULA; CELL DIFFERENTIATION; CELL FATE; CELL MIGRATION; CONTROLLED STUDY; ECTODERM; EMBRYO; EMBRYO DEVELOPMENT; ENDODERM; FERTILIZATION; GENE OVEREXPRESSION; MESENCHYME CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEA URCHIN;

AMINO ACID SEQUENCE; ANIMALS; ARYLSULFATASES; BLOTTING, NORTHERN; BLOTTING, SOUTHERN; CELL ADHESION MOLECULES; CELL COUNT; CELL DIFFERENTIATION; CYTOSKELETAL PROTEINS; EXTRACELLULAR MATRIX PROTEINS; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MESODERM; MODELS, GENETIC; MOLECULAR SEQUENCE DATA; OVUM; PHENOTYPE; PROTEINS; SEA URCHINS; SEQUENCE HOMOLOGY, AMINO ACID; TIME FACTORS; TRANSCRIPTION FACTORS; UBIQUITINS;

ANIMALIA; ECHINOIDEA; INVERTEBRATA;

EID: 0032926482     PISSN: 09254773     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4773(98)00192-0     Document Type: Article

References (53)

1. Akasaka K., Ueda T., Higashinakagawa T., Yamada K., Shimada H. Spatial pattern of arylsulfatase mRNA expression in sea urchin embryo. Dev. Growth Differ. 32:1990;9-13.
2. Akasaka K., Nishimura A., Hijikata K., Iuchi Y., Morokuma J., Takahashi M., Morikawa H., Shimada H. Introduction of DNA into sea urchin eggs by particle gun. Mol. Marine Biol. Biotech. 4:1995;255-261.
3. Akasaka K., Uemoto H., Wilt F., Mitsunaga-Nakatsubo K., Shimada H. Oral-aboral ectoderm differentiation of the sea urchin embryos is disrupted in response to calcium ionophore. Dev. Growth Differ. 39:1997;373-379.
4. Akasaka K., Frudakis T.N., Killian C.E., George N.C., Yamasu K., Khaner O., Wilt F.H. Genomic organization of a gene encoding the spicule matrix protein SM30 in the sea urchin Strongylocentrotus purpuratus. J. Biol. Chem. 269:1994;20592-20598.
5. Amemiya S. Complete regulation of development throughout metamorphosis of sea urchin embryos devoid of macromeres. Dev. Growth Differ. 38:1996;465-476.
6. Anstrom J.A., Chin E., Leaf D.S., Parks A.L., Raff R.A. Localization and expression of msp130, a primary mesenchyme lineage-specific cell surface protein in the sea urchin embryo. Development. 101:1987;255-265.
7. Badiani P., Corbella P., Kioussis D., Marvel J., Weston K. Dominant interfering alleles define a role for c-Myb in T-cell development. Genes Dev. 8:1994;770-782.
8. Boulukos K.E., Pognonec P., Begue A., Galiber T.F., Gesquiere J.C., Stehelin D., Ghysdael J. Identification in chickens of an evolutionarily conserved cellular ets-2 gene(c-ets-2) encoding nuclear proteins related to the products of the c-ets proto-oncogene. EMBO J. 7:1988;697-705.
9. Burdett L.A., Qui S.M., Chen Z.Q., Lautenberger J.A., Papas T.S. Characterization of the cDNA sequences of two Xenopus ets-2 proto-oncogenes. Nucleic Acids Res. 20:1992;371-371.
10. Chen Z.-Q., Kan N.C., Pribyl L., Lautenberger J.A., Papas T.S. Molecular cloning of the ets proto-oncogene of the sea urchin and analysis of its developmental. Exp. Dev. Biol. 125:1988;432-440.
11. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162:1987;156-159.
12. Cox K.H., DeLeon D.V., Angerer L.M., Angerer R.C. Detection of mRNAs in sea urchin embryos by in situ hybridization using asymmetric RNA probes. Dev. Biol. 101:1984;485-502.
13. Davidson E.H. Lineage-specific gene expression and the regulative capacities of the sea urchin embryo: a proposed mechanism. Development. 105:1989;421-445.
14. Davidson E.H. Spatial mechanisms of gene regulation in metazoan embryos. Development. 113:1991;1-26.
15. Duval C., Bouvet P., Omilli F., Roghi C., Dorel C., Le Guellec R., Paris J., Osborne H.B. Stablity of maternal mRNA in Xenopus embryos: role of transcription and translation. Mol. Cell. Biol. 10:1990;4123-4129.
16. Emily-Fenouil F., Ghiglione C., Lhomond G., Lepage T., Gache C. GSK3/shaggy mediates patterning along the animal-vegetal axis of the sea urchin embryo. Development. 125:1998;2489-2498.
17. Ettensohn, C.A., 1992. Cell interactions and mesodermal cell fates in the sea urchin embryo. Dev. Suppl. 43-51.
18. Ettensohn C.A., McClay D.R. Cell interactions and mesodermal cell fates in the sea urchin embryo. Cell lineage conversion in the sea urchin embryo. Dev. Biol. 125:1988;396-409.
19. Ettensohn C.A., Ruffins S.W. Mesodermal cell interactions in the sea urchin embryo: properties of skeletogenic secondary mesenchyme cells. Development. 117:1993;1275-1285.
20. Gan L., Wessel G.M., Klein W.H. Regulatory elements from the related Spec genes of Strongylocentrotus purpuratus yield different spatial patterns with a lacZ reporter gene. Dev. Biol. 142:1990;346-359.
21. George N.C., Killian C.E., Wilt F.H. Characterization and expression of a gene encoding a 30.6-kDa Strongylocentrotus purpuratus spicule matrix protein. Dev. Biol. 147:1991;334-342.
22. Gunther C.V., Nye J.A., Bryner R.S., Graves B.J. Sequence-specific DNA binding of the proto-oncoprotein ets-1 defines a transcriptional activator sequence within the long terminal repeat of the Moloney murine sarcoma virus. Genes Dev. 4:1990;667-679.
23. Guss K.A., Ettensohn C.A. Skeletal morphogenesis in the sea urchin embryo: regulation of primary mesenchyme gene expression and skeletal rod growth by ectoderm-derived cues. Development. 124:1997;1899-1908.
24. Harkey M.A., Whiteley H.R., Whiteley A.H. Differential expression of the msp130 gene among skeletal lineage cells in the sea urchin embryo: a three dimensional in situ hybridization analysis. Mech. Dev. 37:1992;173-218.
25. Harkey M.A., Klueg K., Sheppard P., Raff R.A. Structure, expression, and extracellular targeting of PM27, a skeletal protein associated specifically with growth of the sea urchin larval spicule. Dev. Biol. 168:1995;549-566.
26. Henry J.J., Amemiya S., Wray G.A., Raff R.A. Early inductive interactions are involved in restricting cell fates of mesomeres in sea urchin embryos. Dev. Biol. 136:1989;140-153.
27. Horstadius, S., 1973. Experimental Embryology of Echinoderms. Clarendon Press, Oxford.
28. Katoh-Fukui Y., Noce T., Ueda T., Fujiwara Y., Hashimoto N., Tanaka S., Higashinakagawa T. Isolation and characterization of cDNA encoding a spicule matrix protein in Hemicentrotus pulcherrimus micromeres. Int. Dev. Biol. 36:1992;353-361.
29. Khaner O., Wilt F. Interactions of different vegetal cells with mesomeres during early stages of sea urchin development. Development. 112:1991;881-890.
30. Kitajima T., Okazaki K. Spicule formation in vitro by the descendants of precocious micromere formed at the 8-cell stage of sea urchin embryo. Dev. Growth. Diff. 22:1980;265-279.
31. Klambt C. The Drosophila gene pointed encodes two ETS-like proteins which are involved in the development of the midline glial cells. Development. 117:1993;163-176.
32. Kurokawa D., Akasaka K., Mitsunaga-Nakatsubo K., Shimada H. Cloning of cyclin E mRNA of the sea urchin, Hemicentrotus pulcherrimus. Zool. Sci. 14:1997;791-794.
33. LePrince D., Gegonne A., Coll J., DeTaisne C., Schneeberger A., Lagrou C., Stehelin D. A putative second cell-derived oncogene of the avian leukaemia retrovirus E26. Nature. 306:1983;395-397.
34. LePrince D., Duterque-coquillaud M., Li R.-P., Henry C., Flourens A., Debuire B., Stehelin D. Alternative splicing within the chicken c-ets-1 locus: implication for transduction within the E26 retrovirus of the c-ets proto-oncogene. J. Virol. 62:1988;3233-3241.
35. Logan C.Y., McClay D.R. The allocation of early blastomeres to the ectoderm and endoderm is variable in the sea urchin embryo. Development. 124:1997;2213-2223.
36. Makabe K.W., Carmen K.V., Britten R.J., Davidson E.H. Cis-regulatory control of the SM50 gene. an early marker of skeletogenic lineage specification in the sea urchin embryo. Development. 121:1995;1957-1970.
37. Mao C.A., Wikramanayake A.H., Gan L., Chaung C.K., Summers R.G., Klein W.H. Altering cell fates in sea urchin embryos by overexpressing SpOtx, an orthodenticle-related protein. Development. 122:1996;1489-1498.
38. Maroulakou I.G., Papas T.S., Green J.E. Differential expression of ets-1 and ets-2 proto-oncogenes during murine embryogenesis. Oncogene. 9:1994;1551-1565.
39. Meyer D., Stieger P., Hindelang C., Mager A.-M., Remy P. Whole-mount in situ hybridization reveals the expression of the Xl-fli gene in several lineage of migrating cells in Xenopus embryos. Int. J. Dev. Biol. 40:1995;577-589.
40. Meyer D., Durliat M., Senan F., Wolff M., Andre M., Hourdry J., Remy P. Ets-1 and Ets-2 proto-oncogenes exhibit differential and restricted expression patterns during Xenopus laevis oogenesis and embryogenesis. Int. J. Dev. Biol. 41:1997;607-620.
41. Nemer M., Rondinelli E., Infante D., Infante A.A. Polyubiquitin RNA characteristics and conditional induction in sea urchin embryos. Dev. Biol. 145:1991;255-265.
42. Nunn M.F., Seeburg P.H., Moscovici C., Duesberg P.H. Tripartite structure of the avian erythroblastosis virus E26 transforming gene. Nature. 306:1983;391-395.
43. Okazaki K. Spicule formation by isolated micromeres of the sea urchin embryo. Am. Zool. 15:1975;567-581.
44. Qui S., Chen Z.-Q., Papas T.S., Lautenberger J.A. The sea urchin erg homolog defines a highly conserved erg-specific domain. DNA Seq. 3:1992;127-129.
45. Ransick A., Ernst S., Britten R.J., Davidson E.H. Whole mount in situ hybridization shows Endo16 to be a marker for the vegital plate territory in sea urchin embryos. Mech. Dev. 42:1993;117-124.
46. Ransick A., Davidson E.H. A complete second gut induced by transplanted micromeres in the sea urchin embryo. Science. 259:1993;1134-1138.
47. Stiegler P., Wolff C.-M., Baltzinger M., Hirtzlin J., Senan F., Meyer D., Ghysdael J., Stehelin D., Befort N., Remy P. Characterization of Xenopus laevis cDNA clones of the c-ets-1 proto-oncogene. Nucleic Acids Res. 18:1990;5298-5298.
48. Stiegler P., Wolff C.-M., Meyer D., Senan F., Durliat M., Hourdry J., Befort N., Remy P. The c-ets -1 proto-oncogenes in Xenopus laevis: expression during oogenesis and embryogenesis. Mech. Dev. 41:1993;163-174.
49. Wasylyk B., Hahn S.L., Giovane A. The ets family of transcription factors. Eur. J. Biochem. 211:1993;7-18.
50. Watson D.K., McWilliams M.J., Lapis P., Lautenberger J.A., Schweinfest C.W., Papas T.S. Mammalian ets-1 and ets-2 genes encode highly conserved proteins. Proc. Natl. Acad. Sci. USA. 85:1988;7862-7866.
51. Wikramanayake A.H., Brandhorst B.P., Klein W.H. Autonomous and non-autonomous differentiation of ectoderm in different sea urchin species. Development. 100:1995;559-575.
52. Wikramanayake A.H., Klein W.H. Multiple signaling events specify ectoderm and pattern the oral-aboral axis in the sea urchin embryo. Development. 124:1997;13-20.
53. Wikramanayake A.H., Huang L., Klein W.H. b-Catenin is essential for patterning the maternally specified animal-vegetal axis in the sea urchin embryo. Proc. Natl. Acad. Sci. USA. 95:1998;9343-9348.