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Journal ArticleDOI

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

V.E. Foe, +1 more
- 01 May 1983 - 
- Vol. 61, Iss: 1, pp 31-70
TLDR
Using differential interference contrast optics, combined with cinematography, 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 are studied.
Abstract
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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Citations
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Journal ArticleDOI

A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback.

TL;DR: A non-radioactive in situ hybridization technique for the localization of RNA in whole mount Drosophila embryos and revealed translational control of the maternally derived hb mRNA, which was difficult to detect by conventional techniques.
Journal ArticleDOI

The molecular basis for metameric pattern in the Drosophila embryo.

Michael Akam
- 01 Sep 1987 - 
TL;DR: The metameric organization of the Drosophila embryo is generated in the first 5 h after fertilization and an initially rather simple pattern provides the foundation for subsequent development and diversification of the segmented part of the body.
Journal ArticleDOI

A gradient of bicoid protein in Drosophila embryos

TL;DR: The maternal gene bicoid organizes anterior development in Drosophila and its mRNA is localized at the anterior tip of the oocyte and early embryo, distributed in an exponential concentration gradient, reaching background levels in the posterior third of the embryo.
Journal ArticleDOI

The molecular genetics of embryonic pattern formation in Drosophila

Philip W. Ingham
- 01 Sep 1988 - 
TL;DR: Analysis of the genes that control the early events of Drosophila embryogenesis is providing details of the molecular processes underlying the positional specification of cells.
Journal ArticleDOI

Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins.

TL;DR: The most prominent structural feature of both lamins is an α-helical region of repeating heptads of amino acids that shows striking homology with the entire family of cytoplasmic intermediate filament proteins, suggesting that the nuclear envelope is made up of a network of coiled-coil polymers.
References
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Journal ArticleDOI

Positional information and the spatial pattern of cellular differentiation

TL;DR: These concepts provide a unifying framework within which a wide variety of patterns formed from fields may be discussed, and give new meaning to classical concepts such as induction, dominance and field.
Journal ArticleDOI

Filament organization revealed in platinum replicas of freeze-dried cytoskeletons.

TL;DR: Freeze-dried cytoskeletons provide an opportunity to study--at high resolution and in the absence of problems caused by chemical fixation--the detailed organization of filaments in different regions of the cytoplasm and at different stages of cell development.
Book ChapterDOI

Specification of the Basic Body Pattern in Insect Embryogenesis1

TL;DR: This chapter focuses on the problem of pattern specification in early insect embryogenesis, essentially on the formal level characteristic of “classical” developmental physiology.
Journal ArticleDOI

Ultrastructural patterns of RNA synthesis during early embryogenesis of Drosophila melanogaster.

TL;DR: All rRNA loci, whether having complete or incomplete gradients, exhibit high densities of nascent transcripts per unit length, suggesting that the rate of chromatin transcription, rather than the RNA polymarase I pool size, limits rRNA synthesis on individual genes.
Journal ArticleDOI

Autoradiographic study of protein and RNA formation during early development of Drosophila eggs

TL;DR: The results indicate that the expression of zygotic genome before the blastoderm stage is unlikely, and protein labeling of the pole cells, on the contrary, was very strong in the Blastoderm and early gastrula.