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Journal of Cell Science, Vol 61, Issue 1 31-70, Copyright © 1983 by Company of Biologists


JOURNAL ARTICLES

Studies of nuclear and cytoplasmic behaviour during the five mitotic cycles that precede gastrulation in Drosophila embryogenesis

VE Foe and BM Alberts

Using differential interference contrast optics, combined with cinematography, we have studied the morphological changes that the living, syncytial embryo undergoes from stage 10 through 14 of Drosophila embryogenesis, that is just prior to and during formation of the cellular blastoderm. We have supplemented these studies with data collected from fixed, stained, whole embryos. The following information has been obtained. The average duration of nuclear cycles 10, 11, 12 and 13 is about 9, 10, 12 and 21 min, respectively (25 degrees C). In these four cycles, the duration of that portion of the mitotic period that lacks a discrete nuclear envelope is 3, 3, 3 and 5 min, respectively. The length of nuclear cycle 14 varies in a position-specific manner throughout the embryo, the shortest cycles being of 65 min duration. During nuclear cycles 10 through 13, it is commonly observed in living embryos that the syncytial blastoderm nuclei enter (and leave) mitosis in one of two waves that originate nearly simultaneously from the opposite anterior and posterior poles of the embryo, and terminate in its midregion. From our preparations of quick-frozen embryos, we estimate that these mitotic waves take on average about half a minute to travel over the embryonic surface from pole to equator. The yolk nuclei, which remain in the core of the embryo when the rest of the nuclei migrate to the periphery, divide in synchrony with the migrating nuclei at nuclear cycles 8 and 9, and just after the now peripherally located nuclei at nuclear cycle 10. After cycle 10, these yolk nuclei cease dividing and become polyploid. The syncytial embryo has at least three distinct levels of cytoskeletal organization: structured domains of cytoplasm are organized around each blastoderm nucleus; radially directed tracks orient colchicine-sensitive saltatory transport throughout the peripheral cytoplasm; and a long-range organization of the core of the embryo makes possible coherent movements of the large inner yolk mass in concert with each nuclear cycle. This highly organized cytoplasm may be involved in providing positional information for the important process of nuclear determination that is known to occur during these stages.
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Development, January 8, 1998; 125(16): 3259 - 3268.
[Abstract] [PDF]


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DevelopmentHome page
W. Rothwell, P Fogarty, C. Field, and W Sullivan
Nuclear-fallout, a Drosophila protein that cycles from the cytoplasm to the centrosomes, regulates cortical microfilament organization
Development, January 4, 1998; 125(7): 1295 - 1303.
[Abstract] [PDF]


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JCBHome page
P. Jordan and R. Karess
Myosin Light Chain-activating Phosphorylation Sites Are Required for Oogenesis in Drosophila
J. Cell Biol., December 29, 1997; 139(7): 1805 - 1819.
[Abstract] [Full Text] [PDF]


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Proc. Natl. Acad. Sci. USAHome page
H. Stanley, J. Botas, and V. Malhotra
The mechanism of Golgi segregation during mitosis is cell type-specific
PNAS, December 23, 1997; 94(26): 14467 - 14470.
[Abstract] [Full Text] [PDF]


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JCBHome page
R. W. Burgess, D. L. Deitcher, and T. L. Schwarz
The Synaptic Protein Syntaxin1 Is Required for Cellularization of Drosophila Embryos
J. Cell Biol., August 25, 1997; 138(4): 861 - 875.
[Abstract] [Full Text] [PDF]


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JCBHome page
P. Buchenau, H. Saumweber, and D. J. Arndt-Jovin
The Dynamic Nuclear Redistribution of an hnRNP K-homologous Protein during Drosophila Embryo Development and Heat Shock. Flexibility of Transcription Sites In Vivo
J. Cell Biol., April 21, 1997; 137(2): 291 - 303.
[Abstract] [Full Text] [PDF]


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DevelopmentHome page
K Ho, O. Dunin-Borkowski, and M Akam
Cellularization in locust embryos occurs before blastoderm formation
Development, January 7, 1997; 124(14): 2761 - 2768.
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Genes Dev.Home page
B A Edgar and S A Datar
Zygotic degradation of two maternal Cdc25 mRNAs terminates Drosophila's early cell cycle program.
Genes & Dev., August 1, 1996; 10(15): 1966 - 1977.
[Abstract] [PDF]


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Genes Dev.Home page
D K Pritchard and G Schubiger
Activation of transcription in Drosophila embryos is a gradual process mediated by the nucleocytoplasmic ratio.
Genes & Dev., May 1, 1996; 10(9): 1131 - 1142.
[Abstract] [PDF]


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J. Cell Sci.Home page
L. Frenz and D. Glover
A maternal requirement for glutamine synthetase I for the mitotic cycles of syncytial Drosophila embryos
J. Cell Sci., January 11, 1996; 109(11): 2649 - 2660.
[Abstract] [PDF]


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DevelopmentHome page
S. Bissen
Expression of the cell cycle control gene, cdc25, is constitutive in the segmental founder cells but is cell-cycle-regulated in the micromeres of leech embryos
Development, January 9, 1995; 121(9): 3035 - 3043.
[Abstract] [PDF]


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DevelopmentHome page
R. Galindo, D. Edwards, S. Gillespie, and S. Wasserman
Interaction of the pelle kinase with the membrane-associated protein tube is required for transduction of the dorsoventral signal in Drosophila embryos
Development, January 7, 1995; 121(7): 2209 - 2218.
[Abstract] [PDF]


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DevelopmentHome page
S Wheatley, S Kulkarni, and R Karess
Drosophila nonmuscle myosin II is required for rapid cytoplasmic transport during oogenesis and for axial nuclear migration in early embryos
Development, January 6, 1995; 121(6): 1937 - 1946.
[Abstract] [PDF]


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J. Cell Sci.Home page
S Gunawardena, E Heddle, and M. Rykowski
'Chromosomal puffing' in diploid nuclei of Drosophila melanogaster
J. Cell Sci., January 5, 1995; 108(5): 1863 - 1872.
[Abstract] [PDF]


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J. Cell Sci.Home page
R Kellum, J. Raff, and B. Alberts
Heterochromatin protein 1 distribution during development and during the cell cycle in Drosophila embryos
J. Cell Sci., January 4, 1995; 108(4): 1407 - 1418.
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J. Cell Sci.Home page
R Kellum and B. Alberts
Heterochromatin protein 1 is required for correct chromosome segregation in Drosophila embryos
J. Cell Sci., January 4, 1995; 108(4): 1419 - 1431.
[Abstract] [PDF]


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DevelopmentHome page
D. Ruden and H Jackle
Mitotic delay dependent survival identifies components of cell cycle control in the Drosophila blastoderm
Development, January 1, 1995; 121(1): 63 - 73.
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Genes Dev.Home page
A Kispert, B G Herrmann, M Leptin, and R Reuter
Homologs of the mouse Brachyury gene are involved in the specification of posterior terminal structures in Drosophila, Tribolium, and Locusta.
Genes & Dev., September 15, 1994; 8(18): 2137 - 2150.
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J. Cell Sci.Home page
M. A. Postner and E. F. Wieschaus
The nullo protein is a component of the actin-myosin network that mediates cellularization in Drosophila melanogaster embryos
J. Cell Sci., July 1, 1994; 107(7): 1863 - 1873.
[Abstract] [PDF]


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Genes Dev.Home page
B A Edgar, F Sprenger, R J Duronio, P Leopold, and P H O'Farrell
Distinct molecular mechanism regulate cell cycle timing at successive stages of Drosophila embryogenesis.
Genes & Dev., February 15, 1994; 8(4): 440 - 452.
[Abstract] [PDF]


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J. Cell Sci.Home page
X Chen, E. Reynolds, G Ranganayakulu, and J. O'Donnell
A maternal product of the Punch locus of Drosophila melanogaster is required for precellular blastoderm nuclear divisions
J. Cell Sci., January 12, 1994; 107(12): 3501 - 3513.
[Abstract] [PDF]




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