A Periodicity of Tritiated-thymidine Incorporation into Cytoplasmic Deoxyribonucleic Acid during the Cell Cycle of Tetrahymena pyriformis

Nature ◽  
1966 ◽  
Vol 209 (5023) ◽  
pp. 630-631 ◽  
Author(s):  
IVAN L. CAMERON
1975 ◽  
Vol 67 (3) ◽  
pp. 518-522 ◽  
Author(s):  
I L Cameron ◽  
N C Bols

The ciliated protozoan, Tetrahymena pyriformis strain GL-C, has been used to study the effect of cell population density during starvation on the synchrony obtained after refeeding and on the number of cells arrested in G2 phase of the cell cycle. At high cell densities two peaks of division indices were observed after refeeding while only one was observed at low cell densities. Cell division began earlier in cultures starved at high cell densities. Most importantly, the proportion of cells in G2 was considerably higher in populations starved at high cell densities. When tritiated thymidine was present during the refeeding period, radioautographs of cell samples at different times showed that the first cells to exhibit division furrows contained unlabeled nuclei. The first peak in the division index after refeeding was observed only at higher cell densities and is attributed to the cells arrested in G2. These results suggest that Tetrahymena is an excellent organism to study the concept of resting stages in the cell cycle and their control.


RADIOISOTOPES ◽  
1961 ◽  
Vol 10 (1) ◽  
pp. 135-139
Author(s):  
Toyozo SEKIGUCHI ◽  
Takako KANKURA ◽  
Hideo ETO ◽  
Tetuo IWAKURA

1981 ◽  
Vol 51 (1) ◽  
pp. 219-228
Author(s):  
K.I. Mills ◽  
L.G. Bell

The incorporation of tritiated thymidine, uridine and leucine, into the acid-precipitable material of DNA. RNA and proteins, respectively, was studied by autoradiography throughout the cell cycle of Amoeba proteus. DNA synthesis occupied the first 17 h of the cycle (57 h long) and 2 peaks between 0.5 and 9.13 h accounted for the majority of the thymidine incorporation. RNA synthesis was represented by a series of peak uridine grain counts, the 3 major peaks occurring at 10, 26–27 and 47–48 h. The incorporation of leucine also followed a pattern of peaks and dips, the main peaks occurring 1–2 h after the major increases in uridine incorporation. The fraction of label present over the nucleus decreased during the cell cycle, and this was probably due to a lowered incorporation of the leucine label by proteins synthesized in the cytoplasm and destined to become nuclear proteins. The incorporation patterns of 6 amino acids (arginine, aspartic acid, leucine, lysine, serine and valine) were studied individually during 3 periods of the cell cycle: 0-10 h (S phase); 20–30 h (early G2); and 40–50 h (mid-late G2). Variations in the intensity and timings of the incorporation maxima of the amino acids were observed, although the timings of increased grain counts of some of the amino acids frequently coincided. “Unique” incorporation peaks (i.e. only observed in one of the amino acids studied) possibly indicate the synthesis of phase-specific proteins. The amino acid and nucleoside incorporation profiles presented in this paper will enable the results obtained from future studies on amoebae to be related to the macromolecular synthesis patterns.


1988 ◽  
Vol 16 (1) ◽  
pp. 27-31
Author(s):  
Luisa Benassi ◽  
Giovanna Zambruno ◽  
Paola Massimi ◽  
Fabrizio Fantini ◽  
Alberto Gianetti

5-Bromodeoxyuridine (5-BrdU), a pyrimidine analogue of thymidine, is incorporated into the DNA which is actively synthesised during the S-phase of the cell cycle. In the present study, the labelling indices of cultured human keratinocytes, marked by monoclonal antibodies to 5-BrdU and by tritiated thymidine (3H-TdR), were compared. The proportion of cells found to be labelled by the two methods was similar. The immunological method has advantages over 3H-TdR autoradiography, because it does not require radioactive material, and is both faster and less expensive.


1969 ◽  
Vol 5 (2) ◽  
pp. 393-401
Author(s):  
W. K. BLENKINSOPP

Over a 24-h period, groups of mice were given a single injection of colchicine (to collect blocked metaphases) and tritiated thymidine (to label nuclei synthesizing deoxyribonucleic acid). Epithelial nuclei in the oesophagus, trachea and ureter were examined and counted in paraffin sections: the duration of deoxyribonucleic acid synthesis (Ts) was calculated from the numbers of blocked metaphases and labelled nuclei, the duration of the post-synthetic gap (TG2) was estimated from the proportion of blocked mataphases labelled, and the cell cycle time (Tc) was calculated from Ts and the proportion of nuclei labelled. In each epithelium the different layers seen by light microscopy were analysed separately. Ts was probably the same for the basal and superficial cells in the trachea (about 8 h), and was probably the same for the basal, intermediate and superficial cells in the ureter (about 5 h). In the oesophagus Ts was 8.5 h. TG2 was probably the same for the basal and superficial cells in the trachea (3.6 h), and probably the same for the basal, intermediate and superficial cells in the ureter (about 4.6 h). In the oesophagus TG2 was 2.8 h. Tc was about 380 h (basal cells) and 1400 h (superficial cells) in the trachea, and about 8000 h (basal and intermediate cells) and 2700 h (superficial cells) in the ureter. In the oesophagus Tc was 41 h.


1962 ◽  
Vol 13 (2) ◽  
pp. 193-203 ◽  
Author(s):  
Barbara B. McDonald

Evidence as to the times of DNA synthesis in micronucleate Tetrahymena pyriformis (mating type II, variety 1) has been obtained by briefly exposing individuals of different ages to tritiated thymidine, returning them to non-radioactive medium, fixing at division, and preparing autoradiographs. A variable length of interphase, ranging from a few minutes to about 2 hours, has been found to precede the initiation of macronuclear DNA synthesis. Once begun, however, the period of synthesis appears to be similar in all cells, regardless of generation time, and has been estimated at 1 to 1½ hours. Under the conditions of these experiments, the time elapsing between the end of synthesis and subsequent division into daughter cells ranges from approximately 1½ to 2½ hours in generation times long enough to allow such variability. Division of the micronucleus occurs shortly before the cell begins to divide; its DNA synthesis starts immediately and continues after cell division for a total period estimated at about an hour.


1968 ◽  
Vol 42 (3) ◽  
pp. 453-463 ◽  
Author(s):  
ANNE McLAREN

SUMMARY Blastocysts were studied on the 5th and 8th day of pregnancy in lactating mice, in the fresh state, flushed from the uterus, in squash preparations and in serial sections. At the earlier period some mitosis was observed. Tritiated thymidine incorporation studies gave some evidence of DNA synthesis on the 5th and 6th days of pregnancy. By the 8th day the blastocysts were longer, contained more cells, and mitosis had ceased. They were located at the anti-mesometrial end of the uterine lumen, closely apposed to the uterine epithelium, and with their long axes parallel to the long axis of the uterine horn. Implantation could be induced, either by the removal of the litter, or by the injection of an appropriate dose of oestrogen on the 5th or 7th (but not the 4th) day of pregnancy. Both treatments were followed by the appearance of W-bodies in the neighbourhood of the blastocysts, the disappearance of the shed zonae, and the appearance of Pontamine Blue reactivity, oedema of the uterine stroma and formation of the primary decidual zone, in that order.


Sign in / Sign up

Export Citation Format

Share Document