Associative sequential recall in a synaptic matrix

An adaptive neuronal network (synaptic matrix) was simulated. After learning a number of randomly generated scenes, the network was tested for associative sequential recall in a stimulus-bound mode and in an image-bound mode. It is demonstrated that neuronal mechanisms of this kind can exhibit orderliness or looseness of associative response suggestive of human recall behavior.     

Temperature-dependent ovariole and testis maturation in the yellow dung fly

Temperature is one of the abiotic environmental factors most strongly affecting animal behaviour, physiology, and life history. In insects, lower temperatures generally slow down most physiological processes, reducing growth rate and prolonging the juvenile period. Here, we investigate temperature‐dependent ovariole and testis maturation in the anautogenous yellow dung fly, Scathophaga stercoraria L. (Diptera: Scathophagidae), and relate it to corresponding temperature effects on pre‐adult development time and the adult pre‐reproductive period. Flies were reared in the laboratory at three constant temperatures (18, 22, and 26 °C), and the size of the developing ovarioles and testes (reflecting sperm production) was measured over time (i.e., age). Ovariole size increased asymptotically over the first 12 days of adult life, while the testes continued to fill after day 10. In accordance with the temperature‐size rule, warmer temperatures resulted in smaller ovarioles (eggs) and smaller testes, independent of body size. Warmer temperatures also greatly reduced pre‐adult development time by more than half, from 12 to 25 °C, the larger males always taking 1–3 days longer than the females. Corresponding temperature effects on the adult pre‐reproductive period were small (<1 day between 15 and 25 °C), with males taking 5–6 days and females 10–13 days to first reproduction. Time lost by males during the pre‐adult stage, when ovaries and testes are produced, can thus be more than compensated‐for by time gained during the pre‐reproductive period, when eggs and sperm are produced, so males can nevertheless start reproducing sooner than females.     

Preventing desert locust plagues: optimizing management interventions

Solitarious desert locusts, Schistocerca gregaria (Forskål) (Orthoptera: Acrididae), inhabit the central, arid, and semi‐arid parts of the species’ invasion area in Africa, the Middle East, and South‐West Asia. Their annual migration circuit takes them downwind to breed sequentially where winter, spring, and summer rains fall. In many years, sparse and erratic seasonal rains support phase change and local outbreaks at only a few sites. Less frequently, seasonal rains are widespread, frequent, heavy, and long lasting, and many contemporaneous outbreaks occur. When such seasonal rains fall sequentially, populations develop into an upsurge and eventually into a plague unless checked by drought, migration to hostile habitats, or effective control. Increases in the proportion of gregarious populations as the plague develops alter the effectiveness of control. As an upsurge starts, only a minority of locusts is aggregated into treatable targets and spraying them leaves sufficient unsprayed individuals to continue the upsurge. Spraying all individuals scattered within an entire infested zone is arguably both financially and environmentally unacceptable. More of the population gregarizes and forms sprayable targets after each successive season of good rains and successful breeding. Eventually, unless the rains fail, the entire upsurge population becomes aggregated at high densities so that the infested area diminishes and a plague begins. These populations must continue to increase numerically and spread geographically to achieve peak plague levels, a stage last reached in the 1950s. Effective control, aided by poor rains, accompanied each subsequent late upsurge and early plague stage and all declined rapidly. The control strategy aims to reduce populations to prevent plagues and damage to crops and grazing. Differing opinions on the optimum stage to interrupt pre‐plague breeding sequences are reviewed.     

cAMP-dependent phosphorylation sites and macroscopic activity of recombinant cardiac L-type calcium channels

The involvement of cAMP-dependent phosphorylation sites in establishing the basal activity of cardiac L-type Ca²⁺ channels was studied in HEK 293 cells transiently cotransfected with mutants of the human cardiac ₁ and accessory subunits. Systematic individual or combined elimination of high consensus protein kinase A (PKA) sites, by serine to alanine substitutions at the amino and carboxyl termini of the ₁ subunit, resulted in Ca²⁺ channel currents indistinguishable from those of wild type channels. Dihydropyridine (DHP)-binding characteristics were also unaltered. To explore the possible involvement of nonconsensus sites, deletion mutants were used. Carboxyl-terminal truncations of the ₁ subunit distal to residue 1597 resulted in increased channel expression and current amplitudes. Modulation of PKA activity in cells transfected with the wild type channel or any of the mutants did not alter Ca²⁺ channel functions suggesting that cardiac Ca²⁺ channels expressed in these cells behave, in terms of lack of PKA control, like Ca²⁺ channels of smooth muscle cells.     

Wide distribution of the cysteine string proteins in Drosophila tissues revealed by targeted mutagenesis

The “cysteine string protein” (CSP) genes of higher eukaryotes code for a novel family of proteins characterized by a “J” domain and an unusual cysteine-rich region. Previous studies had localized the proteins in neuropil and synaptic terminals of larval and adult Drosophila and linked the temperature-sensitive paralysis of the mutants described here to conditional failure of synaptic transmission. We now use the null mutants as negative controls in order to reliably detect even low concentrations of CSPs by immunohistochemistry, employing three monoclonal antibodies. In wild-type flies high levels of cysteine string proteins are found not only in apparently all synaptic terminals of the embryonic, larval, and adult nervous systems, but also in the “tall cells” of the cardia, in the follicle cells of the ovary, in specific structures of the female spermatheca, and in the male testis and ejaculatory bulb. In addition, low levels of CSPs appear to be present in all tissues examined, including neuronal perikarya, axons, muscles, Malpighian tubules, and salivary glands. Western blots of isolated tissues demonstrate that of the four isoforms expressed in heads only the largest is found in non-neural organs. The wide expression of CSPs suggests that at least some of the various phenotypes of the null mutants observed at permissive temperatures, such as delayed development, short adult lifespan, modified electroretinogram, and optomotor behavior, may be caused by the lack of CSPs outside synaptic terminals.     

Purification and characterization of a dextranase from Sporothrix schenckii

A dextranase (EC 3.2.1.11) was purified and characterized from the IP-29 strain of Sporothrix schenckii, a dimorphic pathogenic fungus. Growing cells secreted the enzyme into a standard culture medium (20 °C) that supports the mycelial phase. Soluble bacterial dextrans substituted for glucose as substrate with a small decrease in cellular yield but a tenfold increase in the production of dextranase. This enzyme is a monomeric protein with a molecular mass of 79 kDa, a pH optimum of 5.0, and an action pattern against a soluble 170-kDa bacterial dextran that leads to a final mixture of glucose (38%), isomaltose (38%), and branched oligosaccharides (24%). In the presence of 200 mM sodium acetate buffer (pH 5.0), the K _m for soluble dextran was 0.067 ± 0.003% (w/v). Salts of Hg²⁺, (UO₂)²⁺, Pb²⁺, Cu²⁺, and Zn²⁺ inhibited by affecting both V _max and K _m. The enzyme was most stable between pH values of 4.50 and 4.75, where the half-life at 55 °C was 18 min and the energy of activation for heat denaturation was 99 kcal/mol. S. schenckii dextranase catalyzed the degradation of cross-linked dextran chains in Sephadex G-50 to G-200, and the latter was a good substrate for cell growth at 20 °C. Highly cross-linked grades (i.e., G-10 and G-25) were refractory to hydrolysis. Most strains of S. schenckii from Europe and North America tested positive for dextranase when grown at 20 °C. All of these isolates grew on glucose at 35 °C, a condition that is typically associated with the yeast phase, but they did not express dextranase and were incapable of using dextran as a carbon source at the higher temperature. Received: 29 December 1997 / Accepted: 4 March 1998     

Exclusion of five subunits of cGMP phosphodiesterase in Leber’s congenital amaurosis

Leber’s congenital amaurosis (LCA) is the earliest and most severe of all inherited retinal dystrophies. Recently, we mapped an LCA gene to chromosome 17p13.1 (LCA1) and ascribed the disease to mutations of the retinal guanylate cyclase (ret GC) gene in a subset of families of North African ancestry. Owing to the genetic heterogeneity of LCA and considering that LCA1 results from an impaired production of cGMP in the retina (with permanent closure of cGMP-gated cation channels), we hypothesized that the activation of the cGMP phosphodiesterase (PDE) could trigger the disease by lowering the intracellular cGMP level in the retina. The rod and cone cGMP-PDE inhibitory subunits were regarded therefore as candidate genes in LCA. Here, we report the exclusion of five rod and cone cGMP-PDE subunits in LCA families unlinked to chromosome 17p13. Received: 7 April 1997 / Accepted: 3 November 1997     

Das Pyrenoid als Ort der Chlorophyllbildung im Algenchloroplasten. II

Die Pyrenoidstärke von Mesotaenium caldariorum enthält Chlorophyll mit Extinktionsmaxima bei λ = 435 und 675 nm. Zugabe von 5-Aminolävulinsäure (ALA, 10^?3 M/L) erhöht die Chlorophyllkonzentration in der Pyrenoidstärke und mit zeitlicher Verzögerung auch im Chloroplastenraum. Am Pyrenoid tritt das Konzentrationsmaximum neun Stunden nach Zugabe der ALA auf, im Chloroplastenraum erst nach 60 Stunden. Nach Behandlung mit ¹⁴C-ALA ist Radioaktivität mikroautoradiographisch zunächst nur am Pyrenoid (Maximum nach neun Stunden) nachzuweisen, im Chloroplastenraum erst zeitlich verzögert (Maximum nach 60 Stunden). 84 Stunden nach Zugabe der ALA hat sich die Radioaktivität gleichmäßig über den Chloroplasten verteilt.