Induction by ouabain of hemoglobin synthesis in cultured friend erythroleukemic cells

Induction of erythroid differentiation in ouabain-resistant murine erythroleukemia cells by ouabain is reported. Ouabain induction results in the appearance of hemoglobin-containing cells 12–24 hr earlier than induction of the same clone by dimethyl sulfoxide. The levels of globin mRNA after ouabain induction are similar in amount to the globin mRNA levels observed after induction by dimethyl sulfoxide. The concentration of ouabain required to induce hemoglobin synthesis depends upon the K⁺ ion levels in the culture medium. Lowering the extracellular K⁺ ion concentration 2–4 fold reduced by 10–40 fold the ouabain concentration necessary for the induction of hemoglobin synthesis. In low K⁺ medium (1.8 mM), ouabain is an effective inducer of hemoglobin synthesis at a concentration of 0.02 mM. This K⁺ effect is specific for ouabain induction, since induction by other inducers, such as dimethyl sulfoxide and dimethyl acetamide, does not exhibit this marked sensitivity to the levels of K⁺ ions in the culture medium. These results suggest that the binding of ouabain to the plasma membrane enzyme, $\text{Na}\text{K}$ ATPase, is required for the induction of erythroid differentiation by ouabain. A small but significant proportion of wild-type, ouabain-sensitive cells also can be induced by ouabain, below ouabain concentrations that are toxic to these cells. The observation that the binding of ouabain to the $\text{Na}\text{K}$ ATPase induces hemoglobin synthesis suggests that changes in the intracellular concentration of K⁺ ions may be involved in the control of erythroid differentiation in Friend erythroleukemic cells.     

Purification of adenovirus messenger ribonucleic acid by an aqueous polymer two-phase system.

An aqueous polymer phase system containing 6.3% (w/w) dextran and 3.5% (w/w) poly(ethylene glycol) in 10 mM phosphate buffer (pH 8.0) was developed to select RNA-DNA hybrids from unhybridized RNA. The top phase of this phase system, which contains DNA and the RNA-DNA hybrids, can be used to purify adenovirus messenger RNA both early and late in the infectious cycle. The hybrids can be melted by heat in the top phase and the messenger RNA selected by oligo(dT)cellulose chromatography whereupon the polymers and the DNA percolate and the polyadenylated messenger RNA absorb to the column. The isolated messenger RNA appears to be almost quantitatively recovered at a purity from 70 to 90% depending on the concentration of the specific messenger RNA in the starting material. Early and late viral messenger RNA were selected on the complementary strands of adenovirus DNA according to this procedure.     

Trgrps — an interactive algorithm for group recogniton with an example from spartinetea

Summary TRGRPS can detect groups or signal if discrete groups cannot be found in a sample. The present paper elaborates on the concepts, describes the algorithm and provides illustrations from syntaxonomy. A computer program (TRGRPS.BAS) is available from the author upon request.Contribution from the Working Group for Data Processing in Phytosociology, International Society for Vegetation Science. For nomenclature of species see Lausi, Beeftink & Kortekaas (1975).The research project, from which this paper summarizes partial results, is supported by a National Research Council of Canada grant. Computer time was provided by the University of Western Ontario.     

A heuristic test for homogeneity in species populations

Summary This paper elaborates on the notion of homogeneity in plant populations and its quantification. It describes a method for testing homogeneity without the need to make assumptions about generalized distributions. The implementation of the method is illustrated through actual numerical examples.This paper presents results from a study of plant populations for which a National Research Council of Canade grant has been received (L. Orlóci).     

Regulation of synthesis of ribosomal proteins during pyrimidine starvation in Escherichia coli.

The synthesis of ribosomal proteins during pyrimidine starvation was investigated. A progressive turn-off of protein synthesis, with a decay half-time of about 5 min, was observed when Escherichia coli cells were starved of uridine. By means of double-labelling, the syntheses of different ribosomal proteins were shown to be turned off unequally during the starvation. Comparison of the turn-off patterns for some proteins and the known polycistronic organization of the structural genes for these proteins suggests that a major cause of the unequal turn-off was the degradation of mRNA molecules for the ribosomal proteins from the 5'-end toward the 3'-end.     

The effect of microhabitats on the leaf litter decomposition and on the distribution of soil animals

Earthworm burrows as microhabitats for other soil fauna were studied in a hornbeam-oak mixed forest in Hungary. Comparative chemical analysis and feeding experiments were carried out to find out whether the leaves in the burrows of large-bodied earthworms are more decomposed than those from the surrounding areas. The total organic matter content, the C/N ratio, the stability coefficient and the percentage of tannins and lipids indicate that the chemical breakdown of the litter material is more advanced in the burrows than on the other parts of the forest floor especially in autumn. No consistent differences were observed in the amounts of other organic components. Feeding experiments showed that three species of the fauna preferred the leaves pulled into the burrows to those from the surrounding areas and the preference was greater in autumn than in spring.
It is suggested that the high density of some soil animals in the burrows in autumn is due to the more palatable food there; in summer the microclimate of the burrows is favoured, whereas spring can be considered as a transition period.     

Kinetics and dynamics of annealing during sub-gel phase formation in phospholipid bilayers: A saturation transfer electron spin resonance study

The saturation transfer electron spin resonance (STESR) spectra of spin-labeled phosphatidylcholine have been used to follow the kinetics of conversion from the gel phase to the sub-gel phase in aqueous bilayers of dipalmitoyl phosphatidylcholine. This is a simple, well-defined model system for lipid domain formation in membranes. The integrated intensity of the STESR spectrum from the chain-labeled lipid first increases and then decreases with time of incubation in the gel phase at 0°C. The first, more rapid phase of the kinetics is attributed to the conversion of germ nuclei to growth nuclei of the sub-gel phase. The increase in STESR intensity corresponds to the reduction in chain mobility of spin labels located in the gel phase at the boundaries of the growth nuclei and correlates with the increase in the diagnostic STESR line height ratios over this time range. The second, slower phase of the kinetics is attributed to growth of the domains of the sub-gel phase. The decrease in STESR intensity over this time regime corresponds to exclusion of the spin-labeled lipids from the tightly packed sub-gel phase and correlates quantitatively with calibrations of the spin label concentration dependence of the STESR intensity in the gel phase. The kinetics of formation of the sub-gel phase are consistent with the classical model for domain formation and growth. At 0°C, the half-time for conversion of germ nuclei to growth nuclei is ∼7.7 h and domain growth of the sub-gel phase is characterized by a rate constant of 0.025 h^-1. The temperature dependence of the STESR spectra from samples annealed at 0°C suggests that the subtransition takes place via dissolution of sub-gel phase domains, possibly accompanied by domain fission.     

Ultrastructural studies of amphibian neural fold fusion.

The fusion of neural folds to form the neural tube is a process in which presumptive contacting surfaces become adhering. An ultrastructural examination of regions of neural folds in the neurulae of three amphibian species (Hyla regilla, Rana pipiens, and Xenopus laevis), using both transmission and scanning electron microscopy, revealed that, prior to fusion, there is formation of vesicles within cells lining the neural groove, development of extracellular vesicles, changes in the surface morphology of the cells forming the fusion area, and extension of projections (filopodia) from cells lining the neural groove. The association of intra- and extracellular vesicles and filopodia with cells of the neural groove and folds suggests that these organelles may be involved in preparing the neural folds for initial contact, adhesion, and fusion. Ultrastructural differences in reaction of neural fold cell surfaces to staining by ruthenium red, colloidal iron, Alcian blue-lanthanum nitrate, and concanavalin A-hemocyanin indicate that the glycosaminoglycan compositions of these cell surfaces differ from those of presumptive epidermal cells.