Cytofluorimetric analysis of nuclear DNA during meiosis, fertilization and macronuclear development in the ciliate Tetrahymena pyriformis, syngen 1

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.

1965 ◽  
Vol 25 (2) ◽  
pp. 9-19 ◽  
Author(s):  
Ivan L. Cameron

Tetrahymena pyriformis were brought to a non-growing state by removal of pyrimidines from their growth medium. During pyrimidine deprivation cell number increased 3- to 4 fold, and this increase was accompanied by one or more complete cycles of macronuclear DNA replication. Autoradiographic studies show that endogenous protein and RNA were turning over throughout starvation and that RNA breakdown products were used to support the DNA synthesis that occurred during the early period of starvation. However, after 72 hours of starvation all DNA synthesis and cell division had ceased. Feulgen microspectrophotometry shows the macronuclei of these cells to have been stopped at a point prior to DNA replication (G1 stage). After pyrimidine replacement the incorporation of H3-uridine, H3-adenosine, and H3-leucine was measured by the autoradiographic grain counting method. The results indicate that RNA synthesis began to increase almost immediately, but that there was a lag of almost an hour before an increase in protein synthesis. In agreement with the autoradiographic data, chemical data also show that cellular content of RNA began to increase shortly after pyrimidine replacement but that cellular protein content did not increase until about one hour later. Pulse labeling of the cells with H3-thymidine at intervals after pyrimidine replacement shows that labeled macronuclei first began to appear at 150 minutes; that 98 per cent of the macronuclei were in DNA synthesis at 240 to 270 minutes; and that the percentage then began to decrease from 300 to 390 minutes, at which time only 25 per cent of the macronuclei were labeled. Cellular content of DNA did not increase for at least 135 minutes after pyrimidine replacement; however, just before the first cells divided (360 minutes) the DNA content had doubled. After pyrimidine replacement the cells first began to divide at 360 minutes, and 50 per cent had divided at 420 minutes; however, all cells had not divided until 573 minutes. This technique of chemical synchronization of cells in mass cultures makes feasible detailed biochemical analysis of events leading to nuclear DNA replication and cell division.


1974 ◽  
Vol 14 (2) ◽  
pp. 289-300
Author(s):  
H. A. ANDERSEN

Previous experiments showed that a synchronous population of Tetrahymena could divide even though DNA replication was blocked during the latter half of the preceding S-period by addition of methotrexate plus uridine (M + U). Furthermore, it was found that the DNA fraction which was in replication at the time of inhibition became localized in the cytoplasm following elimination from the nucleus at the time of division. When the inhibitory treatment (M + U) was removed prior to or at the time of the cell division the cells were found to engage in new DNA replication and continue growth. Two questions arose from these studies. First, is the DNA replication normal following release from M + U? Second, what is the fate of the cytoplasmic DNA? In the present paper DNA replication has been studied using incorporation of 5-bromodeoxyuridine and centrifugation of the labelled DNA in CsCl gradients. It is concluded that the DNA which finished replication prior to the effect of the M + U treatment replicates again during the S-period of the next cell generation. On the other hand, the DNA fraction which was stalled in replication and subsequently eliminated from the nucleus also replicates in the cytoplasm in the next generation but during G2 period, out of phase with the undamaged nuclear DNA. The cytoplasmic DNA replication appeared to be a continuation of the replication initiated in the nucleus in the previous generation.


1973 ◽  
Vol 13 (2) ◽  
pp. 479-509 ◽  
Author(s):  
K. G. MURTI

This report describes an ultrastructural investigation of macronuclear development following conjugation in Stylonychia mytilus (a spirotrichous ciliate) and Tetrahymena pyriformis (a holotrichous ciliate). In S. mytilus, polytene chromosomes are formed in the young macronucleus (macronuclear Anlage). They are subsequently broken between the bands by ‘membranous’ partitions; the assembly of the membranes appears to be concomitant with the formation of the polytene chromosomes. The membranes in the Anlage appear to originate from fibrous material seen in the early Anlage. This fibrous material in the earlier stages is seen concentrated at several points along the border of the inner nuclear membrane. In the later stages it is seen in the interior of the Anlage, outlining the developing polytene chromosomes. As the chromosomes reach the maximum degree of polyteny, the fibrous material condenses to acquire a membranous appearance and extends into the interband regions. The Anlage throughout this period shows a progressive increase in size. Subsequently, the membranes enclose individually each band plus portions of the 2 adjacent interband regions of the polytene chromosomes to form a large number of vesicles. After vesicle formation the Anlage shrinks, and the chromatin inside the vesicles shows degradative changes. Finally, the vesicles disappear, the membrane degradation products appear at the nuclear membrane, and the Anlage now contains nucleoli. The Anlage increases its DNA content by multiple rounds of replication to become a mature macronucleus. The ultra-structural changes observed in the Anlage support the idea of genetic diminution (i.e. extensive DNA synthesis, elimination of many DNA nucleotide sequences, and amplification of the remaining DNA nucleotide sequences in a second period of DNA synthesis) proposed earlier on the basis of cytochemical, biochemical, and limited electron-microscope studies. In T. pyriformis, the macronuclear development differs substantially from that of Stylonychia. Features such as the formation and degradation of polytene chromosomes are absent in the macronuclear development of Tetrahymena; the young macronucleus in this cell becomes a mature macronucleus by progressive increment in size and chromatin content with no apparent genetic diminution. These observations agree with cytochemical studies on the macronuclear development of Tetrahymena.


1970 ◽  
Vol 46 (3) ◽  
pp. 533-543 ◽  
Author(s):  
William R. Jeffery ◽  
Kenneth D. Stuart ◽  
Joseph Frankel

The effect of supraoptimal temperature on macronuclear DNA synthesis in Tetrahymena was studied by radioautography during prolonged heat and heat-shock synchronization treatments. Prolonged heat treatments (34°C) delayed the initiation of S, but did not appreciably delay DNA synthesis in progress. Return to optimal temperature (28°C) 50 or 100 min later resulted in initiation of S, in delayed cells, at a rate greater than in controls. During the synchronization treatment, most cells were unable to enter S during a heat shock, but initiated S with a slight delay during the following intershock period. These cells were not appreciably delayed in completion of S by subsequent heat shocks. Supraoptimal temperature appears to affect the DNA synthetic cycle near the G1 to S transition. Cells subjected to the heat-shock treatment in early G1 all participated in one S period, and many underwent a succession of two S periods. DNA synthesis occurred in about 50% of the cells between EST and the first synchronous division, with the likelihood of DNA synthesis becoming greater the longer the interval between these two events. In some cells no detectable DNA synthesis occurred between EST and the second synchronous division. It was concluded that a precise temporal alternation of DNA replication and cell division is not obligatory in Tetrahymena.


1999 ◽  
Vol 26 (3) ◽  
pp. 273 ◽  
Author(s):  
Manuel Le Bris ◽  
Nicole Michaux-Ferrière ◽  
Yves Jacob ◽  
Alain Poupet ◽  
Philippe Barthe ◽  
...  

In vitro cultures showed that the proximal buds isolated from a rose (Rosa hybrida L. cv. Ruidriko Vivaldi®) stem were endodormant. Growth and a high percentage of bud break could be observed when cultures were treated with fluridone, an inhibitor of carotenoid synthesis. Flow cytometry determination of nuclear DNA content revealed that cell cycle activity of endodormant buds was arrested in the G 1 phase. Upon culture, the large decrease in bud ABA content was responsible for the progress from G1 to G2 phase whatever the culture medium. However, in control culture, neither cell division nor leaf primordium initiation could be observed and cells appeared stably arrested in G2 . By contrast, with fluridone, an additional ABA decrease was observed resulting from an inhibition of its synthesis inside the bud. New leaf primordia were initiated and many figures of mitosis could be observed, indicating that intense activity of cell division occurred after DNA replication. Therefore, the results indicate that, as long as ABA was synthesized inside the buds, cell cycle was arrested in G2 phase and buds remained dormant. Continued in situ ABA biosynthesis appears, therefore, to be required for the maintenance of bud dormancy.


The anther is useful for the study of development because it provides comparisons between mitotic and meiotic divisions; between nuclear behaviour during the sporophyte and gametophyte stages; and between cell cycles and divisions involving cells with different nuclear DNA contents. The duration of the period from the immediately premeiotic mitosis until the start of leptotene at 20 °C was estimated to be about 48 h in hexaploid Chinese Spring wheat ( Triticum aestivum ), and about 42 h in diploid Petkus Spring rye ( Secale cereale ). Comparisons of the durations of meiosis and of pollen maturation in wheat, in rye and in Triticale genotypes showed that in all three the durations of these stages of development decreased as ploidy level increased. Within each ploidy level, genotypes with higher nuclear DNA content had longer meiotic durations. Differences in both meiotic duration and pollen maturation resulted from proportional differences in the duration of all component stages. These results obtained from comparisons of a closely related group of species in the Gramineae are similar to the results obtained previously (Bennett 1971) from comparisons of plant species taken from widely different families. Data in animals showing positive linear relationship between meiotic duration and the duration of spermatogenesis are collected. Possible causes of the faster rates of development during meiosis and pollen maturation in polyploid cereal species, and of the constant proportions between the durations of all their constituent stages, are discussed.


1968 ◽  
Vol 37 (3) ◽  
pp. 683-693 ◽  
Author(s):  
John A. Parsons ◽  
Ronald C. Rustad

A squash technique was developed for log phase Tetrahymena pyriformis which permitted the resolution of over 100 individual mitochondria from a single cell. Mitochondria incorporated thymidine at all stages of the cell cycle, even when nuclear DNA synthesis was not occurring. During the stage of macronuclear DNA synthesis, however, there was a significant increase in the extent of mitochondrial labeling. Low radioautograph background suggests that mitochondrial DNA is synthesized at the mitochondria themselves. All mitochondria incorporated thymidine-3H within one population-doubling time. Grain counts also showed that the amount of mitochondrial label was retained for four generations and that this label remained randomly distributed among all mitochondria during this time. The results are not consistent with any theory of de-novo or "microbody" origin of mitochondria, but do support the hypothesis that mitochondria are produced by the growth and division of preexisting mitochondria. The stability of the mitochondrial DNA and its distribution among daughter mitochondria satisfy two prerequisites for a genetic material. The possibility is discussed that some of the genetic information for the mitochondrion is contained in the DNA associated with this organelle.


1982 ◽  
Vol 9 (2) ◽  
pp. 179 ◽  
Author(s):  
T.L Setter ◽  
H Greenway ◽  
J Kuo

Effects of high external NaCl concentrations on growth were examined in the unicellular freshwater alga Cldorella emevsonii during different phases of cell development, using synchronized cultures obtained by alternating light-dark cycles. Growth of cultures synchronized at 1 mM NaCl [external osmotic pressure (next=) 0.08 MPa] was compared with (i) cultures synchronized at 200 mM NaCl (n,,, = 1.01 MPa) and (ii) cultures synchronized at 1 mM NaCl from which the daughter cells were suddenly transferred to 100, 150 or 200 mM NaCl. The effects of these two treatments on synthesis of protein, RNA and DNA during cell cycles were similar, and are attributed to the high nexta nd not to specific effects of Na+ and C1-. Growth inhibitions in cells at 200 mM NaCl relative to 1 mM NaCl occurred mainly via effects on cell division; this was confirmed by electron microscopy. There was a lag before net DNA synthesis commenced, and there were reductions in rates of net DNA synthesis in cells at 200 mM NaCl relative to 1 mM NaC1. Rates of increase in cell volume and in protein and RNA content per cell were little affected by high external NaCl concentrations. Consequently, daughter cells at 200 mM NaCl were approximately twice the volume and contained twice as much protein and RNA as daughter cells at 1 mM NaCl, while DNA content was equal in daughter cells at 1 and 200 mM NaCl.


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