FoxM1-driven cell division is required for neuronal differentiation in early Xenopus embryos

Development

Volumn 135, Issue 11, 2008, Pages 2023-2030

  Ueno, Hiroyuki ^a   Nakajo, Nobushige ^a   Watanabe, Minoru ^b   Isoda, Michitaka ^a   Sagata, Noriyuki ^a,c  

^a KYUSHU UNIVERSITY   (Japan)

^b UNIVERSITY OF TOKUSHIMA   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

BMP; Cdc25B; Cell division; FoxM1; Neural differentiation; Xenopus

Indexed keywords

BONE MORPHOGENETIC PROTEIN; CYCLIN B; CYCLIN B3; FORKHEAD TRANSCRIPTION FACTOR; PROTEIN TYROSINE PHOSPHATASE; TRANSCRIPTION FACTOR FOXM1;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL CYCLE; CELL CYCLE G2 PHASE; CELL CYCLE M PHASE; CELL DIFFERENTIATION; CELL DIVISION; CELL FATE; CELL PROLIFERATION; CONTROLLED STUDY; ECTODERM; EMBRYO; EMBRYO DEVELOPMENT; INHIBITION KINETICS; NERVE CELL; NERVE CELL DIFFERENTIATION; NEURAL STEM CELL; NEUROECTODERM; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; SIGNAL TRANSDUCTION; VERTEBRATE; XENOPUS;

ANIMALS; BONE MORPHOGENETIC PROTEINS; CARRIER PROTEINS; CELL CYCLE; CELL DIFFERENTIATION; CELL DIVISION; CELL PROLIFERATION; EMBRYO, NONMAMMALIAN; FORKHEAD TRANSCRIPTION FACTORS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; IMMUNOBLOTTING; IN SITU HYBRIDIZATION; MODELS, BIOLOGICAL; NEURONS; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; XENOPUS LAEVIS; XENOPUS PROTEINS;

VERTEBRATA;

EID: 46749092599     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: 10.1242/dev.019893     Document Type: Article

References (42)

1. Bertrand, N., Castro, D. S. and Guillemot, F. (2002). Proneural genes and the specification of neural cell types. Nat. Rev. Neurosci. 3, 517-530.
2. Chitnis, A., Henrique, D., Lewis, J., Ish-Horowicz, D. and Kintner, C. (1995). Primary neurogenesis in Xenopus embryos regulated by a homologue of the Drosophila neurogenic gene Delta. Nature 375, 761-766.
3. Cremisi, F., Philpott, A. and Ohnuma, S. (2003). Cell cycle and cell fate interactions in neural development. Curr. Opin. Neurobiol. 13, 26-33.
4. Dasso, M. and Newport, J. W. (1990). Completion of DNA replication is monitored by a feedback system that controls the initiation of mitosis in vitro: studies in Xenopus. Cell 61, 811-823.
5. Feng, X. H. and Derynck, R. (2005). Specificity and versatility in TGF-β signaling through Smads. Annu. Rev. Cell Dev. Biol. 21, 659-693.
6. Graff, J. M., Thies, R. S., Song, J. J., Celeste, A. J. and Melton, D. A. (1994). Studies with a Xenopus BMP receptor suggest that ventral mesoderm-inducing signals override dorsal signals in vivo. Cell 79, 169-179.
7. Graham, V., Khudyakov, J., Ellis, P. and Pevny, L. (2003). SOX2 functions to maintain neural progenitor identity. Neuron 39, 749-765.
8. Harris, W. A. and Hartenstein, V. (1991). Neuronal determination without cell division in Xenopus embryos. Neuron 6, 499-515.
9. Hartenstein, V. (1989). Early neurogenesis in Xenopus: the spatio-temporal pattern of proliferation and cell lineages in the embryonic spinal cord. Neuron 3, 399-411.
10. Hemmati-Brivanlou, A. and Melton, D. A. (1992). A truncated activin receptor inhibits mesoderm induction and formation of axial structures in Xenopus embryos. Nature 359, 609-614.
11. Hochegger, H., Klotzbücher, A., Kirk, J., Howell, M., Guellec, K. L., Fletcher, K., Duncan, T., Sohail, M. and Hunt, T. (2001). New B-type cyclin synthesis is required between meiosis I and II during Xenopus oocyte maturation. Development 128, 3795-3807.
12. Hogan, B. L. (1996). Bone morphogenetic proteins: multifunctional regulators of vertebrate development. Genes Dev. 10, 1580-1594.
13. Hollyday, M. (2001). Neurogenesis in the vertebrate neural tube. Int. J. Dev. Neurosci. 19, 161-173.
14. Hopwood, N. D., Pluck, A. and Gurdon, J. B. (1989). MyoD expression in the forming somites is an early response to mesoderm induction in Xenopus embryos. EMBO J. 8, 3409-3417.
15. Howe, J. A., Howell, M., Hunt, T. and Newport, J. W. (1995). Identification of developmental timer regulating the stability of embryonic cyclin A and a new somatic A-type cyclin at gastrulation. Genes Dev. 9, 1164-1176.
16. Karsten, S. L., Kudo, L. C., Jackson, R., Sabatti, C., Kornblum, H. I. and Geschwind, D. H. (2003). Global analysis of gene expression in neural progenitors reveals specific cell-cycle, signaling, and metabolic networks. Dev. Biol. 261, 165-182.
17. Katoh, M. and Katoh, M. (2004). Human FOX gene family. Int. J. Oncol. 25, 1495-1500.
18. Kishi, M., Mizuseki, K., Sasai, N., Yamazaki, H., Shiota, K., Nakanishi, S. and Sasai, Y. (2000). Requirement of Sox2-mediated signaling for differentiation of early Xenopus neuroectoderm. Development 127, 791-800.
19. Ko, T. C., Sheng, H. M., Reisman, D., Thompson, E. A. and Beauchamp, R. D. (1995). Transforming growth factor-β1 inhibits cyclin D1 expression in intestinal epithelial cells. Oncogene 10, 177-184.
20. Krupczak-Hollis, K., Wang, X., Kalinichenko, V. V., Gusarova, G. A., Wang, I. C., Dennewitz, M. B., Yoder, H. M., Kiyokawa, H., Kaestner, K. H. and Costa, R. H. (2004). The mouse Forkhead Box m1 transcription factor is essential for hepatoblast mitosis and development of intrahepatic bile ducts and vessels during liver morphogenesis. Dev. Biol. 276, 74-88.
21. Lamborghini, J. E. (1980). Rohon-Beard cells and other large neurons in Xenopus embryos originate during gastrulation. J. Comp. Neurol. 189, 323-333.
22. Laoukill, J., Kooistra, M. R. H,, Bris, A., Kauw, J., Kerkhoven, R. M., Morrison, A., Clevers, H. and Medema, R. H. (2005). FoxM1 is required for execution of the mitotic programme and chromosome stability. Nat. Cell Biol. 7, 126-136.
23. Lee, J. E., Hollenberg, S. M., Snider, L., Turner, D. L., Lipnick, N. and Weintraub, H. (1995). Conversion of Xenopus ectoderm into neurons by NeuroD, a basic helix-loop-helix protein. Science 268, 836-844.
24. Lüscher-Firzlaff, J. M., Lilischkis, R. and Lüscher, B. (2006). Regulation of the transcription factor FOXM1c by Cyclin E/CDK2. FEBS Lett. 580, 1716-1722.
25. Ma, Q., Kintner, C. and Anderson, D. J. (1996). Identification of neurogenin, a vertebrate neuronal determination gene. Cell 87, 43-52.
26. Massagué, J., Blain, S. W. and Lo, R. S. (2000). TGF-β signaling in growth control, cancer, and heritable disorders. Cell 103, 295-309.
27. Mizuseki, K., Kishi, M., Matsui, M., Nakanishi, S. and Sasai, Y. (1998). Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction. Development 125, 579-587.
28. Muñoz-Sanjuin, I. and Brivanlou, A. H. (2002). Neural induction, the default model and embryonic stem cells. Nat Rev. Neurosci. 3, 271-280.
29. Nakajo, N., Yoshitome, S., Iwashita, J., Iida, M., Uto, K., Ueno, S., Okamoto, K. and Sagata, N. (2000). Absence of Wee1 ensures the meiotic cell cycle in Xenopus oocytes. Genes Dev. 14, 328-338.
30. Pohl, B. S., Rössner, A. and Knöchel, W. (2005). The Fox gene family in Xenopus laevis: Foxl2, FoxM1 and FoxP1 in early development. Int. J. Dev. Biol. 49, 53-58.
31. Rollins, M. B. and Andrews, M. T. (1991). Morphogenesis and regulated gene activity are independent of DNA replication in Xenopus embryos. Development 112, 559-569.
32. Saka, Y. and Smith, J. C. (2001). Spatial and temporal patterns of cell division during early Xenopus embryogenesis. Dev Biol. 229, 307-318.
33. Schüller, U., Zhao, Q., Godinho, S. A., Heine, V. M., Medema, R. H., Pellman, D. and Rowitch, D. H. (2007). Forkhead transcription factor FoxM1 regulates mitotic entry and prevents spindle defects in cerebellar granule neuron precursors, Mol. Cell. Biol. 27, 8259-8270.
34. Shimuta, K., Nakajo, N., Uto, K., Hayano, Y., Okazaki, K. and Sagata, N. (2002). Chk1 is activated transiently and targets Cdc25A for degradation at the Xenopus midblastula transition. EMBO J. 21, 3694-3703.
35. Sive, H. L., Grainger, R. M. and Harland, R. M. (2000). Early Development of Xenopus laevis: A Laboratory Manual. New York: Cold Spring Harbor Laboratory Press.
36. Smith, W. C. and Harland, R. M. (1992). Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos. Cell 70, 829-840.
37. Stern, C. D. (2005). Neural induction: old problem, new findings, yet more questions. Development 132, 2007-2021.
38. Vernon, A. E., Devine, C. and Philpott, A. (2003). The cdk inhibitor p27Xic1 is required for differentiation of primary neurones in Xenopus. Development 130, 85-92.
39. Wang, I. C., Chen, Y. J., Hughes, D., Petrovic, V., Major, M. L., Park, H. Y., Tan, Y., Ackerson, T. and Costa, R. H. (2005). Forkhead Box M1 regulates the transcriptional network of genes essential for mitotic progression and genes encoding the SCF (Skp2-Cks1) ubiquitin ligase. Mol. Cell. Biol. 25, 10875-10894.
40. Watanabe, M. and Whitman, M. (1999). FAST-1 is a key maternal effector of mesoderm inducers in the early Xenopus embryo. Development 126, 5621-5634.
41. Ye, H., Kelly, T F., Samadani, U., Lim, L., Rubio, S., Overdier, D. G., Roebuck, K. A. and Costa, R. H. (1997). Hepatocyte nuclear factor 3/fork head homolog 11 is expressed in proliferating epithelial and mesenchymal cells of embryonic and adult tissues. Mol. Cell. Biol. 17, 1626-1641.
42. Yeo, W. and Gautier, J. (2003). A role for programmed cell death during early neurogenesis in Xenopus. Dev. Biol. 260, 31-45.