Developmental Regulation of Central Spindle Assembly and Cytokinesis during Vertebrate Embryogenesis

Current Biology

Volumn 18, Issue 2, 2008, Pages 116-123

  Kieserman, Esther K ^a   Glotzer, Michael ^b   Wallingford, John B ^a  

^a UNIVERSITY OF TEXAS AT AUSTIN   (United States)

^b UNIVERSITY OF CHICAGO   (United States)

Author keywords

CELLCYCLE

Indexed keywords

ANIMAL; ARTICLE; CYTOKINESIS; EMBRYO DEVELOPMENT; EPIDERMIS; EPITHELIUM CELL; FEMALE; METABOLISM; MITOSIS SPINDLE; NERVOUS SYSTEM; PHYSIOLOGY; PRENATAL DEVELOPMENT; XENOPUS LAEVIS;

ANIMALS; CYTOKINESIS; EMBRYONIC DEVELOPMENT; EPIDERMIS; EPITHELIAL CELLS; FEMALE; MITOTIC SPINDLE APPARATUS; NERVOUS SYSTEM; XENOPUS LAEVIS;

VERTEBRATA;

EID: 38349050937     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cub.2007.12.028     Document Type: Article

References (32)

1. Rappaport R. Experiments concerning the cleavage stimulus in sand dollar eggs. J. Exp. Zool. 148 (1961) 81-89
2. Gong Y., Mo C., and Fraser S.E. Planar cell polarity signalling controls cell division orientation during zebrafish gastrulation. Nature 430 (2004) 689-693
3. Chalmers A.D., Strauss B., and Papalopulu N. Oriented cell divisions asymmetrically segregate aPKC and generate cell fate diversity in the early Xenopus embryo. Development 130 (2003) 2657-2668
4. Glotzer M. Animal cell cytokinesis. Annu. Rev. Cell Dev. Biol. 17 (2001) 351-386
5. Jiang W., Jimenez G., Wells N.J., Hope T.J., Wahl G.M., Hunter T., and Fukunaga R. PRC1: A human mitotic spindle-associated CDK substrate protein required for cytokinesis. Mol. Cell 2 (1998) 877-885
6. Mollinari C., Kleman J.P., Jiang W., Schoehn G., Hunter T., and Margolis R.L. PRC1 is a microtubule binding and bundling protein essential to maintain the mitotic spindle midzone. J. Cell Biol. 157 (2002) 1175-1186
7. Verbrugghe K.J., and White J.G. SPD-1 is required for the formation of the spindle midzone but is not essential for the completion of cytokinesis in C. elegans embryos. Curr. Biol. 14 (2004) 1755-1760
8. Verni F., Somma M.P., Gunsalus K.C., Bonaccorsi S., Belloni G., Goldberg M.L., and Gatti M. Feo, the Drosophila homolog of PRC1, is required for central-spindle formation and cytokinesis. Curr. Biol. 14 (2004) 1569-1575
9. Mollinari C., Kleman J.P., Saoudi Y., Jablonski S.A., Perard J., Yen T.J., and Margolis R.L. Ablation of PRC1 by small interfering RNA demonstrates that cytokinetic abscission requires a central spindle bundle in mammalian cells, whereas completion of furrowing does not. Mol. Biol. Cell 16 (2005) 1043-1055
10. Kurasawa Y., Earnshaw W.C., Mochizuki Y., Dohmae N., and Todokoro K. Essential roles of KIF4 and its binding partner PRC1 in organized central spindle midzone formation. EMBO J. 23 (2004) 3237-3248
11. Bellairs R., and Bancroft M. Midbodies and beaded threads. Am. J. Anat. 143 (1975) 393-398
12. Bancroft M., and Bellairs R. Differentiation of the neural plate and neural tube in the young chick embryo. A study by scanning and transmission electron microscopy. Anat. Embryol. (Berl.) 147 (1975) 309-335
13. Dubreuil V., Marzesco A.M., Corbeil D., Huttner W.B., and Wilsch-Brauninger M. Midbody and primary cilium of neural progenitors release extracellular membrane particles enriched in the stem cell marker prominin-1. J. Cell Biol. 176 (2007) 483-495
14. Wilcock A.C., Swedlow J.R., and Storey K.G. Mitotic spindle orientation distinguishes stem cell and terminal modes of neuron production in the early spinal cord. Development 134 (2007) 1943-1954
15. Cohen E., Binet S., and Meininger V. Ciliogenesis and centriole formation in the mouse embryonic nervous system. An ultrastructural analysis. Biol. Cell 62 (1988) 165-169
16. Haigo S.L., Hildebrand J.D., Harland R.M., and Wallingford J.B. Shroom induces apical constriction and is required for hingepoint formation during neural tube closure. Curr. Biol. 13 (2003) 2125-2137
17. Davidson L.A., and Wallingford J.B. Visualizing cell biology and tissue movements during morphogenesis in the frog embryo. In: Yuste R., and Konnerth A. (Eds). Imaging in Neuroscience and Developement (2005), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
18. Wallingford J.B. Neural tube closure and neural tube defects: Studies in animal models reveal known knowns and known unknowns. Am. J. Med. Genet. 135C (2005) 59-68
19. Saka Y., and Smith J.C. Spatial and temporal patterns of cell division during early Xenopus embryogenesis. Dev. Biol. 229 (2001) 307-318
20. Harris W.A., and Hartenstein V. Neuronal determination without cell division in Xenopus embryos. Neuron 6 (1991) 499-515
21. Gibson M.C., Patel A.B., Nagpal R., and Perrimon N. The emergence of geometric order in proliferating metazoan epithelia. Nature 442 (2006) 1038-1041
22. Kwan K.M., and Kirschner M.W. A microtubule-binding Rho-GEF controls cell morphology during convergent extension of Xenopus laevis. Development 132 (2005) 4599-4610
23. Saxton W.M., and McIntosh J.R. Interzone microtubule behavior in late anaphase and telophase spindles. J. Cell Biol. 105 (1987) 875-886
24. Vize P.D., Melton D.A., Hemmati-Brivanlou A., and Harland R.M. Assays for gene function in developing Xenopus embryos. Methods Cell Biol. 36 (1991) 367-387
25. Zhu C., and Jiang W. Cell cycle-dependent translocation of PRC1 on the spindle by Kif4 is essential for midzone formation and cytokinesis. Proc. Natl. Acad. Sci. USA 102 (2005) 343-348
26. Skop A.R., Liu H., Yates III J., Meyer B.J., and Heald R. Dissection of the mammalian midbody proteome reveals conserved cytokinesis mechanisms. Science 305 (2004) 61-66
27. Krishan A., and Buck R.C. Structure of the Mitotic Spindle in L Strain Fibroblasts. J. Cell Biol. 24 (1965) 433-444
28. Mishima M., Kaitna S., and Glotzer M. Central spindle assembly and cytokinesis require a kinesin-like protein/RhoGAP complex with microtubule bundling activity. Dev. Cell 2 (2002) 41-54
29. Gromley A., Yeaman C., Rosa J., Redick S., Chen C.T., Mirabelle S., Guha M., Sillibourne J., and Doxsey S.J. Centriolin anchoring of exocyst and SNARE complexes at the midbody is required for secretory-vesicle-mediated abscission. Cell 123 (2005) 75-87
30. Sive H.L., Grainger R.M., and Harland R.M. Early Development of Xenopus laevis: A Laboratory Manual (2000), Cold Spring Harbor Press, Cold Spring Harbor, N.Y.
31. Becker B.E., and Gard D.L. Visualization of the cytoskeleton in Xenopus oocytes and eggs by confocal immunofluorescence microscopy. Methods Mol. Biol. 322 (2006) 69-86
32. Potapova T.A., Daum J.R., Pittman B.D., Hudson J.R., Jones T.N., Satinover D.L., Stukenberg P.T., and Gorbsky G.J. The reversibility of mitotic exit in vertebrate cells. Nature 440 (2006) 954-958