Crosstalk between the phosphatidylinositol cycle and MAP kinase signaling pathways in xenopus mesoderm induction

Development Growth and Differentiation

Volumn 40, Issue 2, 1998, Pages 231-241

  Rose, Linda ^a   Busa, William B ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

Crosstalk; MAP kinase; Mesoderm induction; Phosphoinositide; Xenopus

Indexed keywords

BASIC FIBROBLAST GROWTH FACTOR; MITOGEN ACTIVATED PROTEIN KINASE; PHOSPHATIDYLINOSITIDE;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; ENZYME REGULATION; FEMALE; GROWTH REGULATION; MESODERM; NONHUMAN; PHOSPHOINOSITIDE METABOLISM; PROTEIN CROSS LINKING; SIGNAL TRANSDUCTION; XENOPUS;

ANIMALIA; VERTEBRATA;

EID: 0031952856     PISSN: 00121592     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1440-169X.1998.00012.x     Document Type: Article

References (52)

1. Amaya, E., Musci, T. J. & Kirschner, M. W. 1991. Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos. Cell 66, 257-270.
2. Anderson, N. G., Maller, J. L., Tonks, N. K. & Sturgill, T. W. 1990. Requirement for integration of signals from two distinct phosphorylation pathways for activation of MAP kinase. Nature 343, 651-653.
3. Ault, K. T., Durmowicz, G., Galione, A., Harger, P. L. & Busa, W. B. 1996. Modulation of Xenopus embryo mesoderm-specific gene expression and dorsoanterior patterning by receptors that activate the phosphatidylinositol cycle signal transduction pathway. Development 122, 2033-2041.
4. Baker, P. C. 1965. Changing serotonin levels in developing Xenopus laevis. Acta Embryol. Morphol. Exp. 8, 197-204.
5. Berridge, M. J. 1984 Inositol trisphosphate and diacylglycerol as second messengers. Biochem. J. 220, 345-360.
6. Berridge, M. J., Downes, C. P. & Hanley, M. R. 1989. Neural and developmental actions of lithium: A unifying hypothesis. Cell 59, 411-419.
7. Blenis, J. 1993. Review: Signal transduction via the MAPK kinases: Proceed at your own RSK. Proc. Natl Acad. Sci. USA 90, 5889-5892.
8. Busa, W. B. & Gimlich, R. L. 1989. Lithium-induced teratogenesis in frog embryos prevented by a polyphosphoinositide cycle intermediate or a diacylglycerol analog. Dev. Biol. 132, 315-324.
9. Cai, H., Smola, U., Wixler, V. et al. 1997. Role of diacylglycerol-regulated protein kinase C isotypes in growth factor activation of the raf-1 protein kinase. Mol. Cell. Biol. 17, 732-741.
10. Christian, J. L. & Moon, R. T. 1993. When cells take fate into their own hands: Differential competence to respond to inducing signals generates diversity in the embryonic mesoderm. Bioessays 15, 135-139.
11. Cohen, P. 1992. Signal integration at the level of protein kinases, protein phosphatases, and their substrates. Trends Biochem. Sci. 17, 408-413.
12. Cooke, J., Symes, K. & Smith, E. J. 1989. Potentiation by the lithium ion of morphogenetic responses to a Xenopus inducing factor. Development 105, 549-558.
13. Cunliffe, V. & Smith, J. C. 1994. Specification of mesodermal pattern in Xenopus laevis by interactions between Brachyury, noggin, and Xwnt-8. EMBO J. 13, 349-359.
14. De Meyts, P., Christoffersen, C., Urso, B. et al. 1995. Role of the time factor in signaling specificity: Application to mitogenic and metabolic signaling by the insulin and insulin-like growth factor-I receptor tyrosine kinases. Metabolism 44, 2-11.
15. Denhardt, D. T. 1996. Review article: Signal-transducing protein phosphorylation cascades mediated by the ras/rho proteins in the mammalian cell: The potential for multiplex signaling. Biochem. J. 318, 729-747.
16. Gillespie, L. L., Paterno, G. D., Mahadevan, L. C. & Slack, J. M. W. 1992. Intracellular signaling pathways involved in mesoderm induction by FGF. Mech. Dev. 38, 99-108.
17. Gotoh, Y., Masuyama, N., Suzuki, A., Ueno, N. & Nishida, E. 1995. The involvement of the MAP kinase cascade in Xenopus mesoderm induction. EMBO J. 14, 2491-2498.
18. Gotoh, Y., Nishida, E., Matsuda, S. et al. 1991. In vitro effects on microtubule dynamics of purified Xenopus M phase-activated MAP kinase. Nature 349, 251-254.
19. Gotoh, Y., Nishida, E., Yamashita, T., Hoshi, M., Kawakami, M. & Sakai, H. 1990. Microtubule-associated-protein (MAP) kinase activated by nerve growth factor and epidermal growth factor in PC 12 cells. Eur. J. Biochem. 193, 661-669.
20. Graves, L. M., Northrop, J. L., Potts, B. C., Krebs, E. G. & Kimmelman, D. 1994. Fibroblast growth factor, but not activin, is a potent activator of mitogen-activated protein kinase in Xenopus explants. Proc. Natl Acad. Sci. USA 91, 1662-1666.
21. Hartley, R. S., Lewellyn, A. L. & Maller, J. L. 1994. MAP kinase is activated during mesoderm induction in Xenopus laevis. Dev. Biol. 163, 521-524.
22. Hedgepeth, C. M., Conrad, L. J., Zhang, J. Huang, H-C., Lee, V. M. Y. & Klein, P. S. 1997. Activation of the Wnt signaling pathway: A molecular mechanism for lithium action. Dev. Biol. 185, 82-91.
23. Jones, E. A. & Woodland, H. R. 1987. The development of animal cap cells in Xenopus: A measure of the start of animal cap competence to form mesoderm. Development 101, 557-563.
24. Kahan, C., Seuwen, K., Meloche, S. & Pouyssegur, J. 1992. Coordinate, biphasic activation of p44 mitogen-activated protein kinase and S6 kinase by growth factors in hamster fibroblasts. J. Biol. Chem. 267, 13369-13375.
25. Kameshita, I. & Fujisawa, H. 1989. A sensitive method for detection of calmodulin-dependent protein kinase II activity in sodium dodecyl sulfate-polyacrylamide gels. Anal. Biochem. 183, 139-143.
26. Kao, K. R., Masui, Y. & Ellinson, R. P. 1986. Lithium-induced respecification of pattern in Xenopus laevis embryos. Nature 322, 371-373.
27. Kessler, D. S. & Melton, D. A. 1994. Vertebrate embryonic induction: Mesodermal and neural patterning. Science 266, 596-604.
28. Kimmelman, D. 1993. Peptide growth factors and the regulation of early amphibian development. Biochem. Biophys. Acta 1155, 227-237.
29. Klein, P. S. & Melton, D. A. 1996. A molecular mechanism for the effect of lithium on development. Proc. Natl Acad. Sci. USA. 93, 8455-8459.
30. Kolch, W., Heldecker, G., Kochs, G. et al. 1993. Protein kinase C activates raf-1 by direct phosphorylation. Nature 364, 249-252.
31. Kume, S., Muto, A., Inoue, T., Suga, K., Okano, H. & Mikoshiba, K. 1997. Role of inositol 1,4,5-trisphosphate receptor in ventral signaling in Xenopus embryos. Science 278, 1940-1942.
32. La Bonne, C., Burke, B. & Whitman, M. 1995. Role of MAP kinase in mesoderm induction and axial patterning during Xenopus development. Development 121, 1475-1486.
33. La Bonne, C. & Whitman, M. 1997. Localization of MAP kinase activity in early Xenopus embryos: Implications for endogenous FGF signaling. Dev. Biol. 183, 9-20.
34. Lamb, T. M. & Harland, R. M. 1995. Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior neural pattern. Development 121, 3627-3636.
35. MacNicol, A. M., Muslin, A. J. & Williams, L. T. 1993. Raf-1 kinase is essential for early Xenopus development and mediates the induction of mesoderm by FGF. Cell 73, 571-583.
36. Manji, H. K., Potter, W. Z. & Lenox, R. H. 1995. Signal transduction pathways: Molecular targets for lithium's actions. Arch. Gen. Psychiatry 52, 531-543.
37. Maslanski, J. A., Leshko, L. & Busa, W. B. 1992. Lithium-sensitive production of inositol phosphates during amphibian embryonic mesoderm induction. Science 256, 243-245.
38. MAPK (ERK1) by growth factors: Correlation between late phase activation and mitogenicity. Mol. Endocrinol. 6, 845-854.
39. Niehrs, C., Steinbeisser, H. & De Robertis, E. M. 1994. Mesodermal patterning by a gradient of the vertebrate homeobox gene goosecoid. Science 263, 817-820.
40. Nieuwkoop, P. D. & Faber, J. 1975. Normal Table of Xenopus laevis (Daudin). North-Holland. Amsterdam.
41. Otte, A. P., Kramer, I. M., Mannesse, M., Lambrachts, C. & Durston, A. J. 1990. Characterization of protein kinase C in early Xenopus embryogenesis. Development 110, 461-470.
42. Perry, M., Thomsen, G. H. & Roeder, R. G. 1985. Genomic organization and nucleotide sequence of two distinct histone gene clusters from Xenopus laevis: Identification of novel conserved upstream sequence elements. J. Mol. Biol. 185, 479-499.
43. Posada, J. & Cooper, J. A. 1992. Requirements for phosphorylation of MAP kinase during meiosis in Xenopus oocytes. Science 255, 212-215.
44. Posada, J., Sanghera, J., Pelech, S., Aebersold, R. & Cooper, J. A. 1991. Tyrosine phosphorylation and activation of homologous protein kinases during oocyte maturation and mitogenic activation of fibroblasts. Mol. Cell. Biol. 11, 2517-2528.
45. Ryan, P. J. & Gillepsie, L. L. 1994. Phosphorylation of phospholipase Cγ1 and its association with the FGF receptor is developmentally regulated and occurs during mesoderm induction in Xenopus laevis. Dev. Biol. 166, 101-111.
46. Seger, R. & Krebs, E. 1995. The MAPK signaling cascade. FASEB J. 9, 726-735.
47. Slack, J. M. W., Isaacs, H. V. & Darlington, B. G. 1988. Inductive effects of fibroblast growth factor and lithium ion on Xenopus blastula ectoderm. Development 103, 581-590.
48. Smith, J. C., Price, B. M. J., Green, J. B. A., Weigel, D. & Herrmann, B. G. 1991. Expression of a Xenopus homolog of Brachyury (T) is an immediate-early response to mesoderm induction. Cell 67, 79-87.
49. Sun, H., Charles, C., Lau, L. & Tonks, N. 1993. MKP-1 (3CH134) an immediate early gene product, is a dual specificity phosphatase that dephosphorylates MAP kinase in vivo. Cell 75, 487-493.
50. Uedo, Y., Hirai, Si., Osada, Si., Suzuki, A., Mizuno, K. & Ohno, S. 1996. Protein kinase C activates the MEK-ERK pathway in a manner independent of Ras and dependent on Raf. J. Biol. Chem. 271, 23512-23519.
51. Umbhauer, M., Marshall, C. J., Mason, C. S., Old, R. W. & Smith, J. C. 1995. Mesoderm induction in Xenopus caused by activation of MAPK kinase. Nature 376, 58-62.
52. ras in Xenopus mesoderm induction. Nature 357, 252-254.