Tissue-specific regulation of the number of cell division rounds by inductive cell interaction and transcription factors during ascidian embryogenesis

Developmental Biology

Volumn 355, Issue 2, 2011, Pages 313-323

  Fujikawa, Tetsuya ^a   Takatori, Naohito ^a   Kuwajima, Mami ^a   Kim, Gil Jung ^b   Nishida, Hiroki ^a  

^a OSAKA UNIVERSITY   (Japan)

^b Gangneung Wonju National University   (South Korea)

Author keywords

Ascidian; Brachyury; Cell division count; FGF; Notochord

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR BRACHYURY; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; ASCIDIACEA; BLASTOMERE; CELL COUNT; CELL CYCLE REGULATION; CELL DIVISION; CELL FATE; CELL INTERACTION; CELL LINEAGE; CONTROLLED STUDY; DEVELOPMENTAL STAGE; EMBRYO; EMBRYO CELL; EMBRYO DEVELOPMENT; FERTILIZATION; HALOCYNTHIA RORETZI; HATCHING; LARVA; MESENCHYME CELL; MITOSIS; NERVE CORD; NONHUMAN; NOTOCHORD; PRIORITY JOURNAL; PROTEIN EXPRESSION; REGULATORY MECHANISM; SIGNAL TRANSDUCTION; TISSUE DIFFERENTIATION;

ASCIDIA; HALOCYNTHIA RORETZI;

EID: 80955177675     PISSN: 00121606     EISSN: 1095564X     Source Type: Journal    
DOI: 10.1016/j.ydbio.2011.04.033     Document Type: Article

References (40)

1. Chiba S., Jiang D., Satoh N., Smith W.C. Brachyury null mutant-induced defects in juvenile ascidian endodermal organs. Development 2009, 136:35-39.
2. Clayton J.E., van den Heuvel S.J.L., Saito R.M. Transcriptional control of cell-cycle quiescence during C. elegans development. Dev. Biol. 2008, 313:603-613.
3. Dan-Sohkawa M., Satoh N. Studies on dwarf larvae developed from isolated blastomeres of the starfish, Asterina pectinifera. J. Embryol. Exp. Morphol. 1978, 46:171-185.
4. Darras S., Nishida H. The BMP signaling pathway is required together with the FGF pathway for notochord induction in the ascidian embryo. Development 2001, 128:2629-2638.
5. Deng X., Mercer S.E., Shah S., Ewton D.Z., Friedman E. The cyclin-dependent kinase inhibitor p27Kip1 is stabilized in G0 by Mirk/dyrk1B kinase. J. Biol. Chem. 2004, 279:22498-22504.
6. de Nooij J.C., Letendre M.A., Hariharan I.K. A Cyclin-dependent kinase inhibitor, Dacapo, is necessary for timely exit from the cell cycle during Drosophila embryogenesis. Cell 1996, 87:1237-1247.
7. Favata M.F., Horiuchi K.Y., Manos E.J., Daulerio A.J., Stradley D.A., Feeser W.S., Van Dyk D.E., Pitts W.J., Earl R.A., Hobbs F., Copeland R.A., Magolda R.L., Scherle P.A., Trzaskos J.M. Identification of a novel inhibitor of mitogen-activated protein kinase kinase. J. Biol. Chem. 1998, 273:18623-18632.
8. Hörstadius S. Experimental Embryology of Echinoderms 1973, Oxford University Press, London.
9. Hotta K., Takahashi H., Erives A., Levine M., Satoh N. Temporal expression pattern of 39 Brachyury-downstream genes associated with notochord formation in the Ciona intestinalis embryos. Dev. Growth Differ. 1999, 41:657-664.
10. Imai K.S., Satoh N., Satou Y. A Twist-like bHLH gene is a downstream factor of an endogenous FGF and determines mesenchymal fate in the ascidian embryos. Development 2003, 130:4461-4472.
11. Kim G.J., Nishida H. Role of FGF and MEK signaling pathway in the ascidian embryo. Dev. Growth Differ. 2001, 43:521-533.
12. Kim G.J., Yamada A., Nishida H. An FGF signal from endoderm and localized factors in the posterior-vegetal egg cytoplasm pattern the mesodermal tissues in the ascidian. Development 2000, 127:2853-2862.
13. Kim G.J., Kumano G., Nishida H. Cell fate polarization in ascidian mesenchyme/muscle precursors by directed FGF signaling and role for an additional ectodermal FGF antagonizing signal in notochord/nerve cord precursors. Development 2007, 134:1509-1518.
14. Kispert A., Herrmann B.G. The Brachyury gene encodes a novel DNA binding protein. EMBO J. 1993, 12:3211-3220.
15. Kispert A., Koschorz B., Herrmann B.G. The T protein encoded by Brachyury is a tissue-specific transcription factor. EMBO J. 1995, 14:4763-4772.
16. Kobayashi K., Sawada K., Yamamoto H., Wada S., Saiga H., Nishida H. Maternal macho-1 is an intrinsic factor that makes cell response to the same FGF signal differ between mesenchyme and notochord induction in ascidian embryos. Development 2003, 130:5179-5190.
17. Kumano G., Nishida H. Ascidian embryonic development: an emerging model system for the study of cell fate specification in chordates. Dev. Dyn. 2007, 236:1732-1747.
18. Kumano G., Yamaguchi S., Nishida H. Overlapping expression of FoxA and Zic confers responsiveness to FGF signaling to specify notochord in ascidian embryos. Dev. Biol. 2006, 30:770-784.
19. Lane M.E., Sauer K., Wallace K., Jan Y.N., Lehner C.F., Vaessin H. Dacapo, a cyclin-dependent kinase inhibitor, stops cell proliferation during Drosophila development. Cell 1996, 87:1225-1235.
20. Matsumoto J., Kumano G., Nishida H. Direct activation by Ets and Zic is required for initial expression of the Brachyury gene in the ascidian notochord. Dev. Biol. 2007, 306:870-882.
21. Minokawa T., Yagi K., Makabe K.W., Nishida H. Binary specification of nerve cord and notochord cell fates in ascidian embryos. Development 2001, 128:2007-2017.
22. Mitani Y., Takahashi H., Satoh N. An ascidian T-box gene As-T2 is related to the Tbx6 subfamily and is associated with embryonic muscle cell differentiation. Dev. Dyn. 1999, 215:62-68.
23. Nakatani Y., Nishida H. Induction of notochord during ascidian embryogenesis. Dev. Biol. 1994, 166:289-299.
24. Nakatani Y., Yasuo H., Satoh N., Nishida H. Basic fibroblast growth factor induces notochord formation and the expression of As-T, a Brachyury homolog, during ascidian embryogenesis. Development 1996, 122:2023-2031.
25. Newport J., Kirschner M. A major developmental transition in early Xenopus embryo: I. Characterization and timing of cellular changes at the midblastula stage. Cell 1982, 30:675-686.
26. Newport J., Kirschner M. A major developmental transition in early Xenopus embryo: II. Control of the onset of transcription. Cell 1982, 30:687-696.
27. Nicol D., Meinertzhagen I.A. Development of the central nervous system of the larva of the ascidian, Ciona intestinalis L.: I. The early lineages of the neural plate. Dev. Biol. 1988, 130:737-766.
28. Nishida H. Cell lineage analysis in ascidian embryos by intracellular injection of a tracer enzyme. III. Up to the tissue restricted stage. Dev. Biol. 1987, 121:526-541.
29. Nishida H. Developmental potential for tissue differentiation of fully dissociated cells of the ascidian embryo. Roux's Arch. Dev. Biol. 1992, 201:81-87.
30. Nishida H. Specification of embryonic axis and mosaic development in ascidians. Dev. Dyn. 2005, 233:1177-1193.
31. Nishida H., Satoh N. Cell lineage analysis in ascidian embryos by intracellular injection of tracer enzyme. I. Up to the eight-cell stage. Dev. Biol. 1983, 99:382-394.
32. Nishikata T., Satoh N. Specification of notochord cells in the ascidian embryo analysed with a specific monoclonal antibody. Cell Differ. Dev. 1990, 30:43-53.
33. Niwano T., Takatori N., Kumano G., Nishida H. Wnt5 is required for notochord cell intercalation in the ascidian Halocynthia roretzi. Biol. Cell 2009, 101:645-659.
34. Slack J.M.W. The mysterious mechanism of growth. Curr. Biol. 1996, 6:348.
35. Takahashi H., Hotta K., Erives A., Di Gregorio A., Zeller R.W., Levine M., Satoh N. Brachyury downstream notochord differentiation in the ascidian embryos. Genes Dev. 1999, 13:1519-1523.
36. Vervoorts J., Luscher B. Post-translational regulation of the tumor suppressor p27KIP1. Cell. Mol. Life Sci. 2008, 65:3255-3264.
37. Yagi K., Takatori N., Satou Y., Satoh N. Ci-Tbx6b and Ci-Tbx6c are key mediators of the maternal effect gene Ci-macho1 in muscle cell differentiation in Ciona intestinalis embryos. Dev. Biol. 2005, 282:535-549.
38. Yamada A., Nishida H. Distinct parameters are involved in controlling the number of rounds of cell division in each tissue during ascidian embryogenesis. J. Exp. Zool. 1999, 284:379-391.
39. Yasuo H., Satoh N. An ascidian homolog of the mouse Brachyury (T) gene is expressed exclusively in notochord cells at the fate restricted stage. Dev. Growth Differ. 1994, 36:9-18.
40. Yasuo H., Satoh N. Conservation of the developmental role of Brachyury in notochord formation in a urochordate, the ascidian Halocynthia roretzi. Dev. Biol. 1998, 200:158-170.