Role of TSC-22 during early embryogenesis in Xenopus laevis

Development Growth and Differentiation

Volumn 46, Issue 6, 2004, Pages 535-544

  Hashiguchi, Akiko ^a   Okabayashi, Koji ^a   Asashima, Makoto ^a  

^a UNIVERSITY OF TOKYO   (Japan)

Author keywords

Cell cycle; Cell migration; Gastrulation; TSC 22; Xenopus laevis

Indexed keywords

ANTISENSE OLIGONUCLEOTIDE; CYCLIN DEPENDENT KINASE; CYCLINE; LEUCINE ZIPPER PROTEIN; MESSENGER RNA; PROTEIN P27; PROTEIN P27 XIC1; TRANSFORMING GROWTH FACTOR BETA1; TRANSFORMING GROWTH FACTOR BETA1 STIMULATED CLONE 22; UNCLASSIFIED DRUG;

ANIMAL TISSUE; ARTICLE; BLASTULA; CELL CYCLE; CELL DIVISION; CELL INTERACTION; CELL LINEAGE; CELL MIGRATION; CONTROLLED STUDY; ECTODERM; EMBRYO; EMBRYO DEVELOPMENT; EPITHELIUM CELL; GASTRULATION; GENE EXPRESSION; GENE ISOLATION; GENE REPRESSION; GENETIC CONSERVATION; IN SITU HYBRIDIZATION; MESENCHYME CELL; MESODERM; NONHUMAN; NUCLEOTIDE SEQUENCE; PROTEIN PROTEIN INTERACTION; REGULATORY MECHANISM; XENOPUS LAEVIS;

AMINO ACID SEQUENCE; ANIMALS; APOPTOSIS; BRAIN CHEMISTRY; CELL MOVEMENT; EMBRYONIC DEVELOPMENT; EYE; GASTRULA; GENE EXPRESSION; LEUCINE ZIPPERS; MOLECULAR SEQUENCE DATA; OLIGODEOXYRIBONUCLEOTIDES, ANTISENSE; REPRESSOR PROTEINS; TRANS-ACTIVATION (GENETICS); XENOPUS LAEVIS; XENOPUS PROTEINS;

ANIMALIA; XENOPUS LAEVIS;

EID: 11144230815     PISSN: 00121592     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1440-169x.2004.00770.x     Document Type: Article

References (31)

1. Carruthers, S., Mason, J., Papalopulu, N. 2003. Depletion of the cell-cycle inhibitor p27 (Xic1) impairs neuronal differentiation and increases the number of ElrC (+) progenitor cells in Xenopus tropicalis. Mech. Dev. 120, 607-616.
2. Dobens, L. L., Hsu, T., Twombly, V., Gelbart, W. M., Raftery, L. A., Kafatos, F. C. 1997. The Drosophila bunched gene is a homologue of the growth factor stimulated mammalian TSC-22 sequence and is required during oogenesis. Mech. Dev. 65, 197-208.
3. Dohrmann, C. E., Belaoussoff, M., Raftery, L. A. 1999. Dynamic expression of TSC-22 at sites of epithelial-mesenchymal interactions during mouse development. Mech. Dev. 84, 147-151.
4. Gupta, R. A., Sarraf, P., Brockman, J. A. et al. 2003. Peroxisome proliferator-activated receptor gamma and transforming growth factor-beta pathways inhibit intestinal epithelial cell growth by regulating levels of TSC-22. J. Biol. Chem. 278, 7431-7438.
5. Hamil, K. G. & Hall, S. H. 1994. Cloning of rat Sertoli cell follicle-stimulating hormone primary response complementary deoxyribonucleic acid: regulation of TSC-22 gene expression. Endocrinology. 134, 1205-1212.
6. Harland, R. M. 1991. In situ hybridization: an improved whole-mount method for Xenopus embryos. Methods Cell Biol. 36, 685-695.
7. Heasman, J., Kofron, M., Wylie, C. 2000. Beta-catenin signaling activity dissected in the early Xenopus embryo: a novel antisense approach. Dev Biol. 222, 124-134.
8. Hensey, C. & Gautier, J. 1997. A development timer that regulates apoptosis at the onset of gastrulation. Mech. Dev. 69, 183-195.
9. Hino, S., Kawamata, H., Uchida, D. et al. 2000. Nuclear translocation of TSC-22 (TGF-beta-stimulated clone-22) concomitant with apoptosis: TSC-22 as a putative transcriptional regulator. Biochem. Biophys. Res. Commun. 278, 659-664.
10. Hogan, B. L. 1999. Morphogenesis. Cell. 96, 225-233.
11. Kawamata, H., Nakashiro, K., Uchida, D. et al. 1998. Induction of TSC-22 by treatment with a new anti-cancer drug, vesnarinone, in a human salivary gland cancer cell. Br. J. Cancer. 77, 71-78.
12. Kawa-uchi, T., Nose, K., Noda, M. 1995. Fibroblast growth factor enhances expression of TGF-b stimulated clone 22 gene in osteoblastic cells. Endocrine 3, 833-837.
13. Keller, R. & Danilchik, M. 1988. Regional expression, pattern and timing of convergence and extension during gastrulation of Xenopus laevis. Development. 103, 193-209.
14. Kester, H. A., van der Leede, B. M., van der Saag, P. T., van der Burg, B. 1997. Novel progesterone target genes identified by an improved differential display technique suggest that progestin-induced growth inhibition of breast cancer cells coincides with enhancement of differentiation. J. Biol. Chem. 272, 16637-16643.
15. Kimelman, D., Kirschner, M., Scherson, T. 1987. The events of the midblastula transition in Xenopus are regulated by changes in the cell cycle. Cell. 48, 399-407.
16. Leise, W. F. 3rd & Mueller, P. R. 2002. Multiple Cdk1 inhibitory kinases regulate the cell cycle during development. Dev Biol. 249, 156-173.
17. Leise, W. F. 3rd & Mueller, P. R. 2004. Inhibition of the cell cycle is required for convergent extension of the paraxial mesoderm during Xenopus neurulation. Development. 131, 1703-1715.
18. Murakami, M. S., Moody, S. A., Daar, I. O., Morrison, D. K. 2004. Morphogenesis during Xenopus gastrulation requires Wee1-mediated inhibition of cell proliferation. Development. 131, 571-580.
19. Nakashiro, K., Kawamata, H., Hino, S. et al. 1998. Down-regulation of TSC-22 (transforming growth factor beta-stimulated clone 22) markedly enhances the growth of a human salivary gland cancer cell line in vitro and in vivo. Cancer Res. 58, 549-555.
20. Nechiporuk, A. & Keating, M. T. 2002. A proliferation gradient between proximal and msxb-expressing distal blastoma directs zebrafish fin regeneration. Development. 129, 2607-2617.
21. Newport, J. & Kirschner, M. 1982. A major developmental transition in early Xenopus embryos: I. characterization and timing of cellular changes at the midblastula stage. Cell. 30, 675-686.
22. Nieuwkoop, P. D. & Faber, J. 1956. Normal Table of Xenopus Laevis (Daudin). North-Holland Publishing Company, Amsterdam.
23. Nishimatsu, S., Suzuki, A., Shoda, A., Murakami, K., Ueno, N. 1992. Genes for bone morphogenetic proteins are differentially transcribed in early amphibian embryos. Biochem. Biophys. Res. Commun. 186, 1487-1495.
24. Richard-Parpaillon, L., Cosgrove, R. A., Devine, C., Vernon, A. E., Philpott, A. 2004. G1/S phase cyclin-dependent kinase overexpression perturbs early development and delays tissue-specific differentiation in Xenopus. Development. 131, 2577-2586.
25. Saka, Y. & Smith, J. C. 2001. Spatial and temporal patterns of cell division during early Xenopus embryogenesis. Dev Biol. 229, 307-318.
26. Shibanuma, M., Kuroki, T., Nose, K. 1992. Isolation of a gene encoding a putative leucine zipper structure that is induced by transforming growth factor beta 1 and other growth factors. J. Biol. Chem. 267, 10219-10224.
27. Shostak, K. O., Dmitrenko, V. V., Garifulin, O. M. et al. 2003. Downregulation of putative tumor suppressor gene TSC-22 in human brain tumors. J. Surg. Oncol. 82, 57-64.
28. Su, J. Y., Rempel, R. E., Erikson, E. & Mailer, J. L. 1995. Cloning and characterization of the Xenopus cyclin-dependent kinase inhibitor p27XIC1. Proc. Natl Acad. Sci. USA 92, 10187-10191.
29. Takahashi, S., Yokota, C., Takano, K. et al. 2000. Two novel nodal-related genes initiate early inductive events in Xenopus Nieuwkoop center. Development. 127, 5319-5329.
30. Vernon, A. E., Devine, C., Philpott, A. 2003. The cdk inhibitor p27Xic1 is required for differentiation of primary neurones in Xenopus. Development. 130, 85-92.
31. Vernon, A. E. & Philpott, A. 2003. The developmental expression of cell cycle regulators in Xenopus laevis. Gene Exp. Patterns. 3, 179-192.