Developmental changes in genome activity in Drosophila lebanonensis casteeli pipkin

Puparium formation in Drosophila lebanonensis casteeli is obviously restricted to a certain phase in circadian oscillation. The question whether or not the release of molting hormone is the actual process which is controlled by the circadian oscillation could be approached by using molting hormone-specific changes in genome activity as indication for changes in hormone titer. The identification of hormone specific changes in the puffing pattern of polytene chromosomes should provide a basis for this study.—To this end, a chromosome map of the 7 polytene chromosome arms (1 acrocentric and 3 metacentric chromosomes) of the species was made. Changes in the puffing pattern associated with puparium formation are described and compared with those occurring in response to experimental administration of -ecdysone.—89 puffs were regularly observed in midthird instar larvae. Prior to puparium formation 5 new puffs arise, one at an early stage and 4 attaining their maximum size immediately before puparium formation. Concomitantly, 5 puffs increase considerably in size. These changes in the puffing pattern can be reproduced by injection of ecdysone.—Upon injection of the hormone a clear differentiation between fast reacting loci (within 30–60 min) and slow reacting loci (after 3–4 hours) can be found. As in other Drosophila species the immediate response (within 30–60 min) comprises more than one (5) locus.In memory of Professor Dr. J. Schultz.     

Serious-mindedness and the effect of self-induced respiratory changes upon parietal EEG

The role of serious-mindedness (so-called telic dominance) in regulation of parietal cortex EEG was investigated. Ten telic (serious-minded) and 10 paratelic (playful state-dominant) individuals were selected on the basis of their responses to the Telic Dominance Scale. They all performed instructed breath-holding (hypopnea) and excessive breathing (hyperpnea) in counterbalanced order. The paratelic individuals yielded relatively high scores of integral EEG power; theta power was markedly increased in the left hemisphere during hyperpnea, and reduced in the right hemisphere during hypopnea. Both hyperpnea and hypopnea were reported to be more aversive to the paratelic than to the telic subjects, but no group difference in respiratory activity was found. The electrocortical and hedonic tone differences between the groups are discussed in relation to the distinction between the prefrontal (dopamine) activation pathway and frontoparietal (noradrenalin) arousal pathway, as well as in relation to changes in cortical blood flow and proprioceptive feedback.This research is part of a project supported by the Norwegian Research Council for Social Science and the Humanities and by funds at the University of Bergen. Mary R. Cook and two anonymous reviewers helped to improve an earlier version of this report.     

Serious-mindedness and the effect of self-induced respiratory changes upon parietal EEG

The role of serious-mindedness (so-called telic dominance) in regulation of parietal cortex EEG was investigated. Ten telic (serious-minded) and 10 paratelic (playful state-dominant) individuals were selected on the basis of their responses to the Telic Dominance Scale. They all performed instructed breathholding (hypopnea) and excessive breathing (hyperpnea) in counterbalanced order. The paratelic individuals yielded relatively high scores of integral EEG power; theta power was markedly increased in the left hemisphere during hyperpnea, and reduced in the right hemisphere during hypopnea. Both hyperpnea and hypopnea were reported to be more aversive to the paratelic than to the telic subjects, but no group difference in respiratory activity was found. The electrocortical and hedonic tone differences between the groups are discussed in relation to the distinction between the prefrontal (dopamine) activation pathway and frontoparietal (noradrenalin) arousal pathway, as well as in relation to changes in cortical blood flow and proprioceptive feedback.     

Spatial and developmental changes in the respiratory activity of mitochondria in early Drosophila embryos.

Mitochondria of early Drosophila embryos were observed with a transmission electron microscope and a fluorescent microscope after vital staining with rhodamine 123, which accumulates only in active mitochondria. Rhodamine 123 accumulated particularly in the posterior pole region in early cleavage embryos, whereas the spatial distribution of mitochondria in an embryo was uniform throughout cleavage stages. In late cleavage stages, the dye showed very weak and uniform accumulation in all regions of periplasm. Polar plasm, sequestered in pole cells, restored the ability to accumulate the dye. Therefore, it is concluded that the respiratory activity of mitochondria is higher in the polar plasm than in the other regions of periplasm in early embryos, and this changes during development. The temporal changes in rhodamine 123-staining of polar plasm were not affected by u.v. irradiation at the posterior of early cleavage embryos at a sufficient dosage to prevent pole cell formation. This suggests that the inhibition of pole cell formation by u.v. irradiation is not due to the inactivation of the respiratory activities of mitochondria. In addition, we found that the anterior of Bicaudal-D mutant embryos at cleavage stage was stained with rhodamine 123 with the same intensity as the posterior of wild-type embryos. No pole cells form in the anterior of Bic-D embryos, where no restoration of mitochondrial activity occurs in the blastoderm stage. The posterior group mutations that we tested (staufen, oskar, tudor, nanos) and the terminal mutation (torso) did not alter staining pattern of the posterior with rhodamine 123.     

The Drosophila genome

The past year has been a spectacular one for Drosophila research. The sequencing and annotation of the Drosophila melanogaster genome has allowed a comprehensive analysis of the first three eukaryotes to be sequenced-yeast, worm and fly-including an analysis of the fly's influences as a model for the study of human disease. This year has also seen the initiation of a full-length cDNA sequencing project and the first analysis of Drosophila development using high-density DNA microarrays containing several thousand Drosophila genes. For the first time homologous recombination has been demonstrated in flies and targeted gene disruptions may not be far off.     

The effect of intermediate respiratory chain inhibitors upon the tetrazolium-reductase activity of human polymorphonuclear leukocytes.

Intact human phagocytes are capable of reducing tetrazolium salts in their cytoplasm. The exact mechanism that reduces the dye is not well understood. It has been suggested that increased NADH and stimulation of NADH-oxidase may be responsible for tetrazolium reduction. This reaction is insensitive to terminal respiratory inhibitors such as cyanide, but the effect of intermediate respiratory inhibitors has not been explored. Amytal and Antimycin A were used in blood from 60 healthy subjects to study its effect upon the biochemical and histochemical tetrazolium-reductase reactions. It was found that Amytal and Antimycin block the reaction, while azide and cyanide have no effect. It was concluded that electrons are trapped between cytochromes b and C₁ and that this portion of the respiratory chain is essential for tetrazolium reduction. Since CoQ is the main constituent of that portion of the chain, we assume that this compound could be of prime importance in the biochemical events that lead to intracytoplasmic tetrazolium reduction. The possibility of CoQ participation in some phagocytic functions and in phagocytic disorders is discussed.     

The distribution of genes in the Drosophila genome

In the present work we show that in the Drosophila genome (which covers a 37-51% GC range at a DNA size of approx.50kb) a linear correlation holds between GC (or GC(3)50kb) genomic sequences embedding them. This correlation allows us to position the two compositional distributions of (a) coding sequences, and (b) of long DNA segments relative to each other and to calculate gene concentration across the compositional range of the Drosophila genome. Using this approach, we show that gene concentration increases with increasing GC of the regions embedding the genes, reaching a 7-fold higher level in the GC-richest regions compared with the GC-poorest regions. The gene distribution of the Drosophila genome is, therefore, similar to (although less striking than) that of the human genome, whereas it is very different from those of the Arabidopsis genome, which has about the same size as the Drosophila genome.     

The effect of A23187 upon calcium metabolism in the human lymphocyte

Treatment of human peripheral lymphocytes with mitogenic concentrations of the divalent cation ionophore A23187 led to an initial marked increased in the uptake of calcium by these cells, but the amount of accumulated calcium retained decreased with time so that after 8–12 h of culture, the calcium content of treated cells was only 1.5–2.0-fold higher than that of control cells. Three possible explanations for the biphasic nature of ionophore-induced calcium uptake were considered: (1) the ionophore underwent chemical or metabolic inactivation upon prolonged incubation; (2) massive accumulation of calcium caused irreversible uncouplingof mitochondria in these cells with consequent loss of accumulated calcium; or (3) with time there was a redistribution of ionophore within the cell, and sufficient ionophore was taken up by internal, most likely mitochondrial, membranes to cause an efflux of calcium from internal stores. By developing a bioassay for ionophore and examining the time-dependent effects of ionophore in the presence and absence of calcium, it was concluded that the third explanation was the most likely. The general implications of these results are discused.     

The effect of A23187 upon calcium metabolism in the human lymphocyte.

Treatment of human peripheral lymphocytes with mitogenic concentrations of the divalent cation ionophore A23187 led to an initial marked increase in the uptake of calcium by these cells, but the amount of accumulated calcium retained decreased with time so that after 8-12 h of culture, the calcium content of treated cells was only 1.5-2.0-fold higher than that of control cells. Three possible explanations for the biphasic nature of ionophore-induced calcium uptake were considered: (1) the ionophore underwent chemical or metabolic inactivation upon prolonged incubation; (2) massive accumulation of calcium caused irreversible uncoupling of mitochondria in these cells with consequent loss of accumulated calcium; or (3) with time there was a redistribution of ionophore within the cell, and sufficient ionophore was taken up by internal, most likely mitochondrial, membranes to cause an efflux of calcium from internal stores. By developing a bioassay for ionophore and examining the time-dependent effects of ionophore in the presence and absence of calcium, it was concluded that the third explanation was the most likely. The general implications of these results are discussed.