scholarly journals Different effects of thymidine and 5-fluorouracil 2′-deoxyriboside on biosynthetic events in cultured P815Y mast cells

1971 ◽  
Vol 123 (3) ◽  
pp. 385-390 ◽  
Author(s):  
J. J. M. Bergeron
Keyword(s):  
Cell Cycle ◽  
Protein Synthesis ◽  
Cell Division ◽  
Mast Cells ◽  
Cell Volume ◽  
Mean Cell Volume

1. Addition of 2mm-thymidine, although resulting in the cessation of cell division, allows the continuation of phospholipid and protein synthesis and results in an increase in mean cell volume for at least 15h. 2. 5-Fluorouracil 2′-deoxyriboside inhibits cell division but differs from thymidine by inhibiting the synthesis of phospholipid and protein in a more marked manner. 3. The relation between these results and the P815Y cell cycle is discussed.

Effects of Chloramphenicol on Growth, Size Distribution, Chlorophyll Synthesis and Ultrastructure of Euglena Gracilis

1969 ◽  
Vol 4 (3) ◽  
pp. 627-644
Author(s):  
Y. BEN-SHAUL ◽  
Y. MARKUS
Keyword(s):  
Protein Synthesis ◽  
Cell Division ◽  
Cell Volume ◽  
Chlorophyll Synthesis ◽  
Secondary Effect ◽  
Mean Cell Volume ◽  
Initial Rise ◽  
Dividing Cells ◽  
Light Inhibition ◽  
The Mean

Multiplication of Euglena cells treated by 0.5-1.0 mg/ml chloramphenicol was not disturbed for the first 36 h and inhibition appeared only at later stages. The mean cell volume of treated dividing cells was decreased, although the initial rise in cell volume, which normally occurred during the first 12 h of incubation, was not prevented. The antibiotic also lowered the chlorophyll content of green dividing cells. In dard-grown cells transferred to light, inhibition of chlorophyll synthesis was immediate but not complete, and was followed by a decreased rate of plastid elongation and thylakoid formation. Our findings suggest that chloramphenicol does not cause the loss of existing pigment and that impaired chlorophyll synthesis is a secondary effect of inhibition of protein synthesis. The results also indicate that the greening process is more sensitive than cell division to the antibiotic.

scholarly journals Intracellular free calcium oscillates during cell division of Xenopus embryos.

1991 ◽  
Vol 112 (4) ◽  
pp. 711-718 ◽  
Author(s):  
N Grandin ◽  
M Charbonneau
Keyword(s):  
Cell Cycle ◽  
Cell Division ◽  
Cell Volume ◽  
Intracellular Ph ◽  
Calcium Ions ◽  
Volume Ratio ◽  
Mean Amplitude ◽  
Free Calcium ◽  
Periodic Oscillations ◽  
Xenopus Embryos

In Xenopus embryos, previous results failed to detect changes in the activity of free calcium ions (Ca2+i) during cell division using Ca2(+)-selective microelectrodes, while experiments with aequorin yielded uncertain results complicated by the variation during cell division of the aequorin concentration to cell volume ratio. We now report, using Ca2(+)-selective microelectrodes, that cell division in Xenopus embryos is accompanied by periodic oscillations of the Ca2+i level, which occur with a periodicity of 30 min, equal to that of the cell cycle. These Ca2+i oscillations were detected in 24 out of 35 experiments, and had a mean amplitude of 70 nM, around a basal Ca2+i level of 0.40 microM. Ca2+i oscillations did not take place in the absence of cell division, either in artificially activated eggs or in cleavage-blocked embryos. Therefore, Ca2+i oscillations do not represent, unlike intracellular pH oscillations (Grandin, N., and M. Charbonneau. J. Cell Biol. 111:523-532. 1990), a component of the basic cell cycle ("cytoplasmic clock" or "master oscillator"), but appear to be more likely related to some events of mitosis.

Wachstumsparameter in normalen und durch Actinomycin verlängerten Zellzyklen von Tetrahymena / Growth Parameters in Normal and Actinomycin-induced prolonged Cell Cycles of Tetrahymena

1969 ◽  
Vol 24 (12) ◽  
pp. 1624-1629 ◽  
Author(s):  
Günter Cleffmann
Keyword(s):  
Cell Cycle ◽  
Protein Synthesis ◽  
Cell Division ◽  
Dna Replication ◽  
Cell Growth ◽  
Rna Synthesis ◽  
Growth Parameters ◽  
Average Duration ◽  
Cell Cycles ◽  
Growing Cell

Actinomycin in low concentration (0,2 μg/ml — 0,5 μg/ml) prolongs the average duration of the cell cycle of Tetrahymena considerably, but does not inhibit cell division completely. Some parameters of the growing cell have been tested in cell cycles extended in this way and compared to those of normally growing cells. The RNA synthesis of treated cells is reduced to such an extent that the RNA content per cell decreases during the prolonged cell cycle. Nevertheless cell growth, protein synthesis and DNA replication proceed at almost the same rate as in untreated cells. These findings indicate that the presence of actinomycin does not interfere with RNA fractions necessary for growth but reduce the synthesis of RNA fractions which are essential for cell division. Therefore a longer period is needed for their accumulation.

Periodic cell cycle changes in the rate of CO2 production in the fission yeast Schizosaccharomyces pombe persist after a block to protein synthesis

1987 ◽  
Vol 87 (2) ◽  
pp. 323-325
Author(s):  
B. Novak ◽  
J.M. Mitchison
Keyword(s):  
Cell Cycle ◽  
Protein Synthesis ◽  
Cell Division ◽  
Schizosaccharomyces Pombe ◽  
Co2 Production ◽  
Normal Cycle ◽  
Periodic Cell ◽  
Asynchronous Control ◽  
Initial Culture ◽  
The Difference

CO2 production has been followed by manometry in synchronous and asynchronous control cultures of Schizosaccharomyces pombe prepared by elutriation from the same initial culture. Earlier results showed a periodic change in the rate of production, which took place once per cell cycle. These changes were most clearly shown as oscillations in the difference between values of the second differential (acceleration) for the synchronous and asynchronous cultures. This paper shows that the oscillations continue for at least three cycles in the presence of cycloheximide (with and without chloramphenicol). Protein synthesis is virtually absent and there is no cell division. The control of this metabolic oscillation is therefore not directly dependent on translation. The period of the oscillation under these conditions is about 60% of the normal cycle time.

Periodic sensitivity of mechanisms of cytodifferentiation in cleaving eggs of Limnaea stagnalis

Development ◽  
1964 ◽  
Vol 12 (2) ◽  
pp. 183-195
Author(s):  
W. L. M. Geilenkirchen
Keyword(s):  
Cell Cycle ◽  
Protein Synthesis ◽  
Cell Division ◽  
Dna Replication ◽  
Time Course ◽  
Chromosome Doubling ◽  
Daughter Cells ◽  
Morphogenetic Factors ◽  
Limnaea Stagnalis

Investigations on cellular reproduction have led to a highly resolved and integrated picture of the cell cycle in a morphological and physiological sense. The various preparations for division, doubling of components or syntheses, follow their own time course parallel to one another. It has become evident that the various factors involved in cell division are dissociable, for example chromosome doubling and reproduction of centrioles (Bucher & Mazia, 1960), DNA replication and protein synthesis (Zeuthen, 1961). The conditions for cell division in general are applicable to division of egg cells. However, in addition in egg cells there is a complicating system of morphogenetic factors acting, as must be postulated from the observation that in ‘mosaic’ eggs the fate of the blastomeres is fixed. In dividing eggs differences between daughter cells may be due to local differences established during oögenesis in the mother which are parcelled out during cleavages.

Cell Volume and the Control of the Chlamydomonas Cell Cycle

1982 ◽  
Vol 54 (1) ◽  
pp. 173-191 ◽  
Author(s):  
R. A. CRAIGIE ◽  
T. CAVALIER-SMITH
Keyword(s):  
Cell Cycle ◽  
Cell Wall ◽  
Cell Division ◽  
Simple Model ◽  
Cell Volume ◽  
Mother Cell ◽  
Dark Period ◽  
Size Fractions ◽  
Daughter Cells ◽  
Mother Cell Wall

Chlamydomonas reinhardii divides by multiple fission to produce 2n daughter cells per division burst, where n is an integer. By separating predivision cells from synchronous cultures into fractions of differing mean cell volumes, and electronically measuring the numbers and volume distributions of the daughter cells produced by the subsequent division burst, we have shown that n is determined by the volume of the parent cell. Control of n can occur simply, if after every cell division the daughter cells monitor their volume and divide again if, and only if, their volume is greater than a fixed minimum value. In cultures synchronized by 12-h light/12-h dark cycles, the larger parent cells divide earlier in the dark period than do smaller cells. This has been shown by two independent methods: (1) by separating cells into different size fractions by Percoll density-gradient centrifugation and using the light microscope to see when they divide; and (2) by studying changes in the cell volume distribution of unfractioned cultures. Since daughter cells remain within the mother-cell wall for some hours after cell division, and cell division causes an overall swelling of the mother-cell wall, the timing of division can be determined electronically by measuring this increase in cell volume that occurs in the dark period in the absence of growth; we find that cells at the large end of the size distribution range undergo this swelling first, and are then followed by successively smaller size fractions. A simple model embodying a sizer followed by a timer gives a good quantitative fit to these data for 12-h light/12-h dark cycles if cell division occurs 12-h after attaining a critical volume of approximately 140 μm3. However, this simple model is called into question by our finding that alterations in the length of the light period alter the rate of progress towards division even of cells that have attained their critical volume. We discuss the relative roles of light and cell volume in the control of division timing in the Chlamydomonas cell cycle.

scholarly journals Translational control of MPS1 links protein synthesis with the initiation of cell division and spindle pole body duplication in yeast

2020 ◽  
Author(s):  
Heidi M. Blank ◽  
Annabel Alonso ◽  
Mark Winey ◽  
Michael Polymenis
Keyword(s):  
Cell Cycle ◽  
Protein Synthesis ◽  
Cell Division ◽  
Translational Control ◽  
Spindle Pole Body ◽  
Spindle Pole ◽  
Microtubule Organizing Center ◽  
Structured Illumination Microscopy ◽  
Couple Growth ◽  
Pole Body

ABSTRACTProtein synthesis underpins cell growth and controls when cells commit to a new round of cell division at a point in late G1 of the cell cycle called Start. Passage through Start also coincides with the duplication of the microtubule-organizing centers, the yeast spindle pole bodies, which will form the two poles of the mitotic spindle that segregates the chromosomes in mitosis. The conserved Mps1p kinase governs the duplication of the spindle pole body in Saccharomyces cerevisiae. Here, we show that the MPS1 transcript has a short upstream open reading frame that represses the synthesis of Mps1p. Mutating the MPS1 uORF makes the cells smaller, accelerates the appearance of Mps1p in late G1, and promotes completion of Start. The accelerated Start of MPS1 uORF mutants depends on the G1 cyclin Cln3p. Monitoring the spindle pole body in the cell cycle using structured illumination microscopy revealed that mutating the MPS1 uORF enabled cells to duplicate their spindle pole body earlier, at a smaller cell size. For the first time, these results identify growth inputs in mechanisms that control duplication of the microtubule-organizing center and implicate these processes in general mechanisms that couple growth with division.

Cell growth kinetics, division asymmetry and volume control at division in the marine dinoflagellate Gonyaulax polyedra: a model of circadian clock control of the cell cycle

1989 ◽  
Vol 92 (2) ◽  
pp. 303-318 ◽  
Author(s):  
K. Homma ◽  
J.W. Hastings
Keyword(s):  
Cell Cycle ◽  
Cell Division ◽  
Cell Growth ◽  
Circadian Clock ◽  
Cell Volume ◽  
Conditional Probability ◽  
Growth Patterns ◽  
Time Interval ◽  
Dark Cycle ◽  
Gonyaulax Polyedra

A new method of determining the dependence of cell growth on the initial cell volume in the absence of cell division is presented. The assumptions are that volume in a certain period of time is either increasing or decreasing, but not both, and is independent of the history of cells. Applying this method to Gonyaulax polyedra in a 12h light-12h dark cycle, growth in volume between the 3rd and 12th hours of the light period is found to be more exponential-like than linear. The magnitude of growth in the time period is determined solely by cell volume and environmental conditions, not by cell age. All cells decrease in volume slightly in the dark from the 12th to 23rd hour, and then increase a little from the 23rd to 3rd hour of the following day. Cell division in this species is significantly asymmetric, and the extent of asymmetry is estimated mathematically. Simulations based on the growth patterns and the asymmetric division reveal that cell division must at least partly depend on the volume of cells. The dependence of conditional cell division probability on cell volume is then experimentally determined. The probability is zero up to a certain cell volume, and then it gradually increases to a plateau level, which is less than unity. Neither the strict size control model nor the transition probability model is fully consistent with the observed shape of the conditional probability function. A hybrid model postulating a ‘sloppy’ critical volume with a constant probability of division above that volume adequately accounts for the conditional probability. With the use of the observed volume growth law, cell division dependence on volume, and the extent of asymmetry in cell division, cell volume distributions are successfully simulated for cells growing in a 12h light-12h dark cycle. Another simulation reveals that the true coefficient of variation in generation time is 33%. On the basis of these findings, a model of the cell cycle is presented that incorporates the circadian clock as a cyclic G1 phase. According to this scheme, cells satisfying the minimum cell volume requirement between the 12th and the 18th hour probably exit to the replication/segregation sequence ending in division, and re-enter the cyclic portion after a fixed time interval.

scholarly journals Protein synthesis requirements for nuclear division, cytokinesis, and cell separation in Saccharomyces cerevisiae.

1991 ◽  
Vol 11 (7) ◽  
pp. 3691-3698 ◽  
Author(s):  
D J Burke ◽  
D Church
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Cell Cycle ◽  
Protein Synthesis ◽  
Cell Division ◽  
Cell Separation ◽  
Nuclear Division ◽  
S Phase ◽  
Protein Synthesis Inhibitors ◽  
Yeast Saccharomyces Cerevisiae ◽  
Chemical Inhibitors

Protein synthesis inhibitors have often been used to identify regulatory steps in cell division. We used cell division cycle mutants of the yeast Saccharomyces cerevisiae and two chemical inhibitors of translation to investigate the requirements for protein synthesis for completing landmark events after the G1 phase of the cell cycle. We show, using cdc2, cdc6, cdc7, cdc8, cdc17 (38 degrees C), and cdc21 (also named tmp1) mutants, that cells arrested in S phase complete DNA synthesis but cannot complete nuclear division if protein synthesis is inhibited. In contrast, we show, using cdc16, cdc17 (36 degrees C), cdc20, cdc23, and nocodazole treatment, that cells that arrest in the G2 stage complete nuclear division in the absence of protein synthesis. Protein synthesis is required late in the cell cycle to complete cytokinesis and cell separation. These studies show that there are requirements for protein synthesis in the cell cycle, after G1, that are restricted to two discrete intervals.

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