Distinct functions for ERK1 and ERK2 in cell migration processes during zebrafish gastrulation

Developmental Biology

Volumn 319, Issue 2, 2008, Pages 370-383

  Krens, S F Gabby ^a   He, Shuning ^a   Lamers, Gerda E M ^a   Meijer, Annemarie H ^a   Bakkers, Jeroen ^c,d   Schmidt, Thomas ^b   Spaink, Herman P ^a   Snaar Jagalska, B Ewa ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

^b LEIDEN UNIVERSITY   (Netherlands)

^c HUBRECHT INSTITUTE   (Netherlands)

^d ROYAL NETHERLANDS ACADEMY OF ARTS AND SCIENCES   (Netherlands)

Author keywords

Cell migration; Development; Epiboly; ERK1; ERK2; Gastrulation; MAPK

Indexed keywords

ACTIN; FIBROBLAST GROWTH FACTOR; MESSENGER RNA; MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; TUBULIN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BLASTULA; CELL MIGRATION; EMBRYO; EMBRYO DEVELOPMENT; GASTRULATION; NONHUMAN; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN PHOSPHORYLATION; ZEBRA FISH;

DANIO RERIO;

EID: 46349109999     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2008.04.032     Document Type: Article

References (74)

1. Babb S.G., and Marrs J.A. E-cadherin regulates cell movements and tissue formation in early zebrafish embryos. Dev. Dyn. 230 (2004) 263-277
2. Bakkers J., Kramer C., Pothof J., Quaedvlieg N.E.M., Spaink H.P., and Hammerschmidt M. Has2 is required upstream of Rac1 to govern dorsal migration of lateral cells during zebrafish gastrulation. Development 131 (2004) 525-537
3. Betchaku T., and Trinkaus J.P. Contact relations, surface-activity, and cortical microfilaments of marginal cells of enveloping layer and of yolk syncytial and yolk cytoplasmic layers of Fundulus before and during epiboly. J. Exp. Zool. 206 (1978) 381-426
4. Bottcher R.T., and Niehrs C. Fibroblast growth factor signaling during early vertebrate development. Endocr. Rev. 26 (2005) 63-77
5. Carballada R., Yasuo H., and Lemaire P. Phosphatidylinositol-3 kinase acts in parallel to the ERK MAP kinase in the FGF pathway during Xenopus mesoderm induction. Development 128 (2001) 35-44
6. Cheng J.C., Miller A.L., and Webb S.E. Organization and function of microfilaments during late epiboly in zebrafish embryos. Dev. Dyn. 231 (2004) 313-323
7. Corson L.B., Yamanaka Y., Lai K.M.V., and Rossant J. Spatial and temporal patterns of ERK signaling during mouse embryogenesis. Development 130 (2003) 4527-4537
8. Coumoul X., and Deng C.-X. Roles of FGF receptors in mammalian development and congenital diseases. Birth Defects Res. (Part C) 69 4 (2003) 286-304
9. Crawford B.D., Henry C.A., Clason T.A., Becker A.L., and Hille M.B. Activity and distribution of paxillin, focal adhesion kinase, and cadherin indicate cooperative roles during zebrafish morphogenesis. Mol. Biol. Cell 14 (2003) 3065-3081
10. D'Amico L.A., and Cooper M.S. Morphogenetic domains in the yolk syncytial layer of axiating zebrafish embryos. Dev. Dyn. 222 (2001) 611-624
11. Daggett D.F., Boyd C.A., Gautier P., Bryson-Richardson R.J., Thisse C., Thisse B., Amacher S.L., and Currie P.D. Developmentally restricted actin-regulatory molecules control morphogenetic cell movements in the zebrafish gastrula. Curr. Biol. 14 (2004) 1632-1638
12. Delfini M.C., Dubrulle J., Malapert P., Chal J., and Pourquie O. Control of the segmentation process by graded MAPK/ERK activation in the chick embryo. PNAS 102 (2005) 11343-11348
13. Deng T., and Karin M. c-Fos transcriptional activity stimulated by H-Ras-activated protein kinase distinct from JNK and ERK. Nature 371 (1994) 171-175
14. Draper B.W., Stock D.W., and Kimmel C.B. Zebrafish fgf24 functions with fgf8 to promote posterior mesodermal development. Development 130 (2003) 4639-4654
15. Furthauer M., Lin W., Ang S.L., Thisse B., and Thisse C. Sef is a feedback-induced antagonist of Ras/MAPK-mediated FGF signalling. Nat. Cell Biol. 4 (2002) 170-174
16. Furthauer M., Van Celst J., Thisse C., and Thisse B. Fgf signalling controls the dorsoventral patterning of the zebrafish embryo. Development 131 (2004) 2853-2864
17. Gabay L., Seger R., and Shilo B.Z. MAP kinase in situ activation atlas during Drosophila embryogenesis. Development 124 (1997) 3535-3541
18. Pagès G., Guérin S., Grall D., Bonino F., Smith A., Anjuere F., Auberger P., and Pouysségur J. Defective thymocyte maturation in p44 MAP kinase (Erk 1) knockout mice. Science 286 (1999) 1374-1377
19. Glickman N.S., Kimmel C.B., Jones M.A., and Adams R.J. Shaping the zebrafish notochord. Development 130 (2003) 873-887
20. Gotoh Y., Masuyama N., Suzuki A., Ueno N., and Nishida E. Involvement of the map kinase cascade in Xenopus mesoderm induction. Embo J. 14 (1995) 2491-2498
21. Griffin K.J.P., and Kimelman D. Interplay between FGF, one-eyed pinhead, and T-box transcription factors during zebrafish posterior development. Dev. Biol. 264 (2003) 456-466
22. Griffin K., Patient R., and Holder N. Analysis of FGF function in normal and no tail zebrafish embryos reveals separate mechanisms for formation of the trunk and the tail. Development 121 (1995) 2983-2994
23. Grotegut S., von Schweinitz D., Christofori G., and Lehembre F. Hepatocyte growth factor induces cell scattering through MAPK/Egr-1-mediated upregulation of Snail1. Embo J. 25 (2006) 3534-3545
24. Gryzik T., and Muller H.A.J. FGF8-like1 and FGF8-like2 encode putative ligands of the FGF receptor Htl for mesoderm migration and are required in the Drosophila gastrula. Curr. Biol. 14 (2004) 659-667
25. Hammerschmidt M., Pelegri F., Mullins M.C., Kane D.A., Brand M., vanEeden F.J.M., FurutaniSeiki M., Granato M., Haffter P., Heisenberg C.P., Jiang Y.J., Kelsh R.N., Odenthal J., Warga R.M., and NussleinVolhard C. Mutations affecting morphogenesis during gastrulation and tail formation in the zebrafish, Danio rerio. Development 123 (1996) 143-151
26. Harrison R.E., and Turley E.A. Active erk regulates microtubule stability in H-ras-transformed cells. Neoplasia 3 (2001) 385-394
27. Hongo I., Kengaku M., and Okamoto H. FGF signaling and the anterior neural induction in Xenopus. Dev. Biol. 216 (1999) 561-581
28. Ishibe S., Joly D., Liu Z.X., and Cantley L.G. Paxillin serves as an ERK-regulated scaffold for coordinating FAK and Rac activation in epithelial morphogenesis. Mol. Cell 16 (2004) 257-267
29. Johnson G.L., and Lapadat R. Mitogen-activated protein kinase pathways mediated by ERK, JNK, and p38 protein kinases. Science 298 (2002) 1911-1912
30. Johnson G.L., Dohlman H.G., and Graves L.M. MAPK kinase kinases (MKKKs) as a target class for small-molecule inhibition to modulate signaling networks and gene expression. Curr. Opin. Chem. Biol. 9 (2005) 325-331
31. Jopling C., and den Hertog J. Fyn/Yes and non-canonical Wnt signalling converge on RhoA in vertebrate gastrulation cell movements. Embo Rep. 6 (2005) 426-431
32. Kane D.A., Hammerschmidt M., Mullins M.C., Maischein H.M., Brand M., van Eeden F.J., Furutani-Seiki M., Granato M., Haffter P., Heisenberg C.P., Jiang Y.J., Kelsh R.N., Odenthal J., Warga R.M., and Nusslein-Volhard C. The zebrafish epiboly mutants. Development 123 (1996) 47-55
33. Kane D.A., McFarland K.N., and Warga R.M. Mutations in half baked/E-cadherin block cell behaviors that are necessary for teleost epiboly. Development 132 (2005) 1105-1116
34. Kato T., Ohtani-kaneko R., Ono K., Okado N., and Shiga T. Developmental regulation of activated ERK expression in the spinal cord and dorsal root ganglion of the chick embryo. Neurosci. Res. 52 (2005) 11-19
35. Kim G.J., and Nishida H. Role of the FGF and MEK signaling pathway in the ascidian embryo. Dev. Growth Differ. 43 (2001) 521-533
36. Kolch W. Coordinating ERK/MAPK signalling through scaffolds and inhibitors. Nat. Rev. Mol. Cell Biol. 6 (2005) 827-837
37. Köppen M., Fernandez B.G., Carvalho L., Jacinto A., and Heisenberg C.P. Coordinated cell-shape changes control epithelial movement in zebrafish and Drosophila. Development 133 (2006) 2671-2681
38. Kozlowski D.J., Murakami T., Ho R.K., and Weinberg E.S. Regional cell movement and tissue patterning in the zebrafish embryo revealed by fate mapping with caged fluorescein. Biochem. Cell Biol.-Biochimie et Biologie Cellulaire 75 (1997) 551-562
39. Krens S.F.G., He S., Spaink H.P., and Snaar-Jagalska B.E. Characterization and expression patterns of the MAPK family in zebrafish. Gene Expr. Patterns 6 (2006) 1019-1026
40. LaBonne C., Burke B., and Whitman M. Role of MAP kinase in mesoderm induction and axial patterning during Xenopus development. Development 121 (1995) 1475-1486
41. Lloyd A. Distinct functions for ERKs?. J. Biol. 5 (2006) 13
42. Mathieu J., Griffin K., Herbomel P., Dickmeis T., Strahle U., Kimelman D., Rosa F.M., and Peyrieras N. Nodal and Fgf pathways interact through a positive regulatory loop and synergize to maintain mesodermal cell populations. Development 131 (2004) 629-641
43. Mazzucchelli C., Vantaggiato C., Ciamei A., Fasano S., Pakhotin P., Krezel W., Welzl H., Wolfer D.P., Pages G., and Valverde O. Knockout of ERK1 MAP kinase enhances synaptic plasticity in the striatum and facilitates striatal-mediated learning and memory. Neuron 34 (2002) 807-820
44. Medici D., Hay E.D., and Goodenough D.A. Cooperation between snail and LEF-1 transcription factors is essential for TGF-beta 1-induced epithelial-mesenchymal transition. Mol. Biol. Cell 17 (2006) 1871-1879
45. Mohammadi M., McMahon G., Sun L., Tang C., Hirth P., Yeh B.K., Hubbard S.R., and Schlessinger J. Structures of the tyrosine kinase domain of fibroblast growth factor receptor in complex with inhibitors. Science 276 (1997) 955-960
46. Montero J.A., and Heisenberg C.P. Gastrulation dynamics: cells move into focus. Trends Cell Biol. 14 (2004) 620-627
47. Myers D.C., Sepich D.S., and Solnica-Krezel L. Convergence and extension in vertebrate gastrulae: cell movements according to or in search of identity?. Trends Genet. 18 (2002) 447-455
48. Ornitz, D., Itoh, N., 2001. Fibroblast growth factors. Genome Biol., 2, reviews 3005.1-3005.
49. Poulain M., Furthauer M., Thisse B., Thisse C., and Lepage T. Zebrafish endoderm formation is regulated by combinatorial Nodal, FGF and BMP signalling. Development 133 (2006) 2189-2200
50. Pozios K.C., Ding J., Degger B., Upton Z., and Duan C. IGFs stimulate zebrafish cell proliferation by activating MAP kinase and PI3-kinase-signaling pathways. Am. J. Physiol. Regul. Integr. Comp. Physiol. 280 (2001) R1230-R1239
51. Pullikuth A., McKinnon E., Schaeffer H.J., and Catling A.D. The MEK1 scaffolding protein MP1 regulates cell spreading by integrating PAK1 and Rho signals. Mol. Cell. Biol. 25 (2005) 5119-5133
52. Raible F., and Brand M. Tight transcriptional control of the ETS domain factors Erm and Pea3 by Fgf signaling during early zebrafish development. Mech. Dev. 107 (2001) 105-117
53. Saba-El-Leil M.K., Vella F.D.J., Vernay B., Voisin L., Chen L., Labrecque N., Ang S.L., and Meloche S. An essential function of the mitogen-activated protein kinase Erk2 in mouse trophoblast development. Embo Rep. 4 (2003) 964-968
54. Sawada A., Shinya M., Jiang Y.J., Kawakami A., Kuroiwa A., and Takeda H. Fgf/MAPK signalling is a crucial positional cue in somite boundary formation. Development 128 (2001) 4873-4880
55. Schier A.F., and T.W.S. Molecular genetics of axis formation in zebrafish. Annu. Rev. Genet. 39 (2005) 561-613 12-15-2005
56. Sepich D.S., Myers D.C., Short R., Topczewski J., Marlow F., and Solnica-Krezel L. Role of the zebrafish trilobite locus in gastrulation movements of convergence and extension. Genesis 27 (2000) 159-173
57. Shimizu T., Yabe T., Muraoka O., Yonemura S., Aramaki S., Hatta K., Bae Y.K., Nojima H., and Hibi M. E-cadherin is required for gastrulation cell movements in zebrafish. Mech. Dev. 122 (2005) 747-763
58. Shinya M., Koshida S., Sawada A., Kuroiwa A., and Takeda H. Fgf signalling through MAPK cascade is required for development of the subpallial telencephalon in zebrafish embryos. Development 128 (2001) 4153-4164
59. Snaar-Jagalska B.E., Krens S.F.G., Robina I., Wang L.X., and Spaink H.P. Specific activation of ERK pathways by chitin oligosaccharides in embryonic zebrafish cell lines. Glycobiology 13 (2003) 725-732
60. Solnica-Krezel L. Gastrulation in zebrafish - all just about adhesion?. Curr. Opin. Genet. Dev. 16 (2006) 433-441
61. Solnica-Krezel L., and Driever W. Microtubule arrays of the zebrafish yolk cell: organization and function during epiboly. Development 120 (1994) 2443-2455
62. Stathopoulos A., Tam B., Ronshaugen M., Frasch M., and Levine M. pyramus and thisbe: FGF genes that pattern the mesoderm of Drosophila embryos. Genes Dev. 18 (2004) 687-699
63. Sun X., Meyers E.N., Lewandoski M., and Martin G.R. Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo. Genes Dev. 13 (1999) 1834-1846
64. Thisse B., and Thisse C. Functions and regulations of fibroblast growth factor signaling during embryonic development. Dev. Biol. 287 (2005) 390-402
65. Thisse C., Thisse B., Schilling T.F., and Postlethwait J.H. Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos. Development 119 (1993) 1203-1215
66. Tsang M., Friesel R., Kudoh T., and Dawid I.B. Identification of Sef, a novel modulator of FGF signalling. Nat. Cell Biol. 4 (2002) 165-169
67. Tsang M., Maegawa S., Kiang A., Habas R., Weinberg E., and Dawid I.B. A role for MKP3 in axial patterning of the zebrafish embryo. Development 131 (2004) 2769-2779
68. Turner C.E. Paxillin interactions. J. Cell Sci. 113 (2000) 4139-4140
69. Umbhauer M., Marshall C.J., Mason C.S., Old R.W., and Smith J.C. Mesoderm induction in Xenopus caused by activation of Map kinase. Nature 376 (1995) 58-62
70. Uzgare A.R., Uzman J.A., El Hodiri H.M., and Sater A.K. Mitogen-activated protein kinase and neural specification in Xenopus. PNAS 95 (1998) 14833-14838
71. Vantaggiato C., Formentini I., Bondanza A., Bonini C., Naldini L., and Brambilla R. ERK1 and ERK2 mitogen-activated protein kinases affect Ras-dependent cell signaling differentially. J. Biol. 5 5 (2006) 14.1-14.15
72. Wilson R., Vogelsang E., and Leptin M. FGF signalling and the mechanism of mesoderm spreading in Drosophila embryos. Development 132 (2005) 491-501
73. Yang X., Dormann D., Munsterberg A.E., and Weijer C.J. Cell movement patterns during gastrulation in the chick are controlled by positive and negative chemotaxis mediated by FGF4 and FGF8. Dev. Cell 3 (2002) 425-437
74. Yao Y., Li W., Wu J., Germann U.A., Su M.S.S., Kuida K., and Boucher D.M. Extracellular signal-regulated kinase 2 is necessary for mesoderm differentiation. PNAS 100 (2003) 12759-12764