The effect of X-radiation on fumarase activity during different stages of cell division in Tetrahymena pyriformis GL

1962 ◽  
Vol 28 (2) ◽  
pp. 239-247 ◽  
Author(s):  
W.D. Sullivan ◽  
Rita L. Snyder
1975 ◽  
Vol 17 (3) ◽  
pp. 471-493 ◽  
Author(s):  
F.P. Doerder ◽  
L.E. Debault

Fluorescence cytophotometry was used to study nuclear DNA content and synthesis patterns during meiosis, fertilization and macronuclear development in the ciliated protozoon, Tetrahymena pyriformis, syngen 1. It was found that cells entered conjugation with a G1 (45C) macronucleus and a G2 (4C) micronucleus. During meiosis the micronucleus was reduced to 4 haploid nuclei, each with a 1C amount of DNA; each meiotic product then replicated to 2C, but only the nucleus next to the attachment membrane in each conjugant divided to form the two 1C gametic nuclei. The gametic nuclei replicated to 2C prior to fertilization; hence there was no S-period in the 4C fertilization nucleus (synkaryon). The first postzygotic division products immediately entered an S-period to become 4C, and at the second postzygotic division, each of the two 4C nuclei in each conjugant divided to form one 2C micronucleus and one 2C macronuclear Anlage. The macronuclear Anlagen began DNA synthesis immediately and were about 8C at the completion of conjugation; the micronuclei did not undergo rapid DNA doubling and measured between 2C and 3C when the conjugants separated. The old macronucleus did not participate in any S-period during conjugation and began to decompose after the second postzygotic division; it contained an average of 24C at the end of conjugation. From this sequence of nuclear divisions a pattern emerges that, unless a general cytoplasmic signal for DNA synthesis is suppressed, DNA synthesis always occurs in micronuclear division products immediately following separation of sister chromatids. Nuclear development continued in the first two cell cycles after conjugation. In exconjugants (the first cycle), macronuclear Anlagen underwent two rounds of DNA synthesis to become 32C and both micronuclei also underwent DNA synthesis. However, prior to the first cell division, one micronucleus and the old macronucleus completely disintegrated, and at the first cell division the remaining 4C micronucleus divided and one macronuclear Anlage was distributed to each resulting caryonide. At the end of the second cell cycle, the dividing macronucleus of each caryonide contained about 128C. These results relate to the question of ploidy of macronuclear subunits. It is argued that the G1 macronucleus contains 22 or 23 diploid subunits, each subunit being a copy of the diploid micronuclear genome. It is suggested that unequal macronuclear division relates to the question of subunit ploidy by playing a role in the phenomenon of macronuclear assortment.


Science ◽  
1970 ◽  
Vol 168 (3929) ◽  
pp. 385-386 ◽  
Author(s):  
C. Elson ◽  
H. A. Hartmann ◽  
A. L. Shug ◽  
E. Shrago

The reasons that have led to a search for DNA in the basal body of Tetrahymena pyriformis are twofold: the well-known property of proliferation of this organelle and the possibility that basal body DNA might be involved in its morphogenesis. After a brief review of earlier work the methods employed in this paper are described. To ensure large numbers of cells in a particular state of development organisms were grown in synchronized culture. Animals required for autoradiographic studies were appropriately treated with tritiated thymidine. All investigations were made on the cell cortex or 'ghost’ in order to avoid confusion from cell contents. In addition to autoradiography of ghosts, tests were made with acridine orange in the fluorescence microscope. It is concluded from fluorescence tests that basal bodies of T. pyriformis strain S contain DNA . This DNA is not detectable for the first 2h of the temperature-shock cycle, but is detect­able thereafter until cell division. The presence of DNA is confirmed by the autoradiography experiments. The amount of DNA per basal body is estimated very roughly in order of magnitude as 2 × 10 -16 g. The origin of basal body DNA is discussed and the possibilities and consequences of the existence of DNA in the homologous centriole are examined in terms of the mitotic cycle, the amoeba-flagellate transformation in Naegleria , and artificial parthenogenesis. The paper concludes with a brief discussion of the genetic implications of basal body DNA .


1983 ◽  
Vol 61 (1) ◽  
pp. 273-287
Author(s):  
K.K. Hjelm

The relative daughter cell volume (RDCV) values for Tetrahymena pyriformis were determined at division on live cells. It was found that the anterior cell is generally larger than the posterior cell, and that the RDCV values are distributed in groups 5–6% apart. The RDCV value was found to be independent of predivision cell volume, indicating that the mother cell is divided into proportional volumes. The cells seem, however, not to assess volume directly but rather a parameter related to the cell volume. Furthermore, the RDCV value was found to increase during cell division, so that the final value is not reached until actual separation of daughter cells. It is suggested that the division furrow is positioned so that the area of the cell surface lying between the old oral apparatus and the posterior pole of the cell is divided into equal parts. It is further suggested that several alternative values of the RDCV are possible, only one of which is expressed in each cell. The early division furrow is placed anteriorly to its final position, and its location is adjusted during cytokinesis.


1979 ◽  
Vol 37 (1) ◽  
pp. 109-116
Author(s):  
D.N. Wheatley ◽  
L. Rasmussen ◽  
E. Zeuthen

We exposed division-synchronized Tetrahymena pyriformis to pulse treatments with the structural amino acid analogue p-fluorophenylalanine. We related the timing of the treatments to the delays in onset or completion of division, or both. The results enable us to distinguish between early and late phases in cell division in which the cells bring into action proteins which contribute to initiate and complete division, respectively. Normally, these events are separated by 25–30 min.


1974 ◽  
Vol 16 (1) ◽  
pp. 39-47
Author(s):  
J. R. NILSSON

Increasing concentrations of dimethyl sulphoxide (DMSO) affect vacuole formation in Tetrahymena, as measured quantitatively by the uptake of carmine particles. The rate of vacuole formation decreased to about 50% of the control value in 5.0% DMSO (v/v) and to zero in 7.5%. At the latter concentration, the inhibition was expressed immediately; however, the effect of 1-h exposure was reversible after removal of DMSO by washing. In vivo observations revealed abnormal function of the contractile vacuole in 7.5% DMSO, while cell motility and cell division appeared to be unaffected. Although cell division occurred there was little or no increase in cell number, as studied over a cell generation time. Feulgen preparations showed that nuclear division was inhibited and that cell division resulted in one anucleate and one nucleate daughter cell. This effect was also observed in some dividing cells at lower concentrations of DMSO. The effect of DMSO on Tetrahymena was dependent not only on the concentration of the compound but also on the physiological state of the cells.


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