Scrapping of nuclear surface ships in the Primorsky Kray

Cytochalasin B, a mould metabolite from Helminthosporium dermatioideum has been shown to interfere with specific cell activities such as cytoplasmic cleavage and cell movement. Cells undergoing nuclear division in the presence of cytochalasin B are unable to complete the separation of the resulting daughter cells. In time-lapse studies, the daughter cells coalesce after an initial unsuccessful attempt at separation and form large multinucleate polyploid cells. The present report describes the fine structure of the large polyploid cells induced in Earle's L-cell monolayer cultures by exposure to cytochalasin B (lγ/ml) for 92 hours.In the present material we have seen as many as 7 nuclei in these polyploid cells. Treatment with cytochalasin B for longer periods of time (6 to 7 days, with one medium change on the 3rd day) did not increase the number of nuclei beyond the 7 nuclei stage. Figure 1 shows a large polyploid cell with four nuclei. These nuclei are indistinguishable in their fine structure from those of the cells from control cultures but often show unusually large numbers of cytoplasmic invaginations and extensions of the nuclear surface (Figure 2).

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Detection and mapping of interactions between chromatin and the nuclear envelope in drosophila embryos

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100140191 ◽

1995 ◽

Vol 53 ◽

pp. 764-765

Author(s):

W.F. Marshall ◽

A.F. Dernburg ◽

B. Harmon ◽

J.W. Sedat

Keyword(s):

Nuclear Envelope ◽

Chromatin Condensation ◽

Three Dimensional ◽

Physiological Role ◽

Nuclear Surface ◽

Intact Cells ◽

Molecular Determinants ◽

Surface Harmonic ◽

Drosophila Embryos

Interactions between chromatin and nuclear envelope (NE) have been implicated in chromatin condensation, gene regulation, nuclear reassembly, and organization of chromosomes within the nucleus. To further investigate the physiological role played by such interactions, it will be necessary to determine which loci specifically interact with the nuclear envelope. This will not only facilitate identification of the molecular determinants of this interaction, but will also allow manipulation of the pattern of chromatin-NE interactions to probe possible functions. We have developed a microscopic approach to detect and map chromatin-NE interactions inside intact cells.Fluorescence in situ hybridization (FISH) is used to localize specific chromosomal regions within the nucleus of Drosophila embryos and anti-lamin immunofluorescence is used to detect the nuclear envelope. Widefield deconvolution microscopy is then used to obtain a three-dimensional image of the sample (Fig. 1). The nuclear surface is represented by a surface-harmonic expansion (Fig 2). A statistical test for association of the FISH spot with the surface is then performed.

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The Chemical Composition of Cometary Nuclei

Symposium - International Astronomical Union ◽

10.1017/s0074180900006628 ◽

1972 ◽

Vol 45 ◽

pp. 265-270

Author(s):

L. M. Shul'man

Keyword(s):

Chemical Composition ◽

Cosmic Rays ◽

Organic Molecules ◽

Solid Phase ◽

Critical Concentration ◽

Energy Output ◽

Time Interval ◽

Nuclear Surface ◽

Solar Cosmic Rays ◽

Cometary Nuclei

The probable parent-molecules of radicals such as C3 and N2+ are discussed, and it is concluded that cometary nuclei may contain complicated organic molecules, such as C3H4, CH2N2, and C4H2. It is suggested that these molecules are formed by radiation synthesis in solid phase. In a time interval of order 107 to 109 yr bombardment from cosmic rays would be expected to transform the chemical composition to a depth of 1 m. Solar cosmic rays do not penetrate as far, and as a result the surface layer of the nucleus can be enriched with unsaturated hydrocarbons. After a critical concentration of this explosive material is reached a further burst of solar cosmic rays can initiate an explosion and thus an outburst in the comet's brightness. This mechanism is the only one advanced to date that can explain the synchronism of the energy output over the whole nuclear surface.

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