Gibberellin and nucleic acid metabolism duringZea mays fertilization

Summary Either by direct GA supply or by release of glycosidic bound GA, pollination causes partial opening of double-stranded DNA in somatic maize kernel tissues, as evidenced by increased Tm profiles. This phenomenon is associated with enhanced RNA and protein production.Acknowledgments: The authors wish to thank Dr.Y. Wurzburger for her aid and advice in extraction and biossay procedure. This research was financed by a grant from the Bar-Ilan Research Council.     

Modulation of natural killer cell cytotoxicity and cytokine release by the drug glatiramer acetate

Glatiramer acetate (GA or Copaxone) is a drug used to treat experimental autoimmune encephalomyelitis in mice and multiple sclerosis in human. Here, we describe a new mechanism of action for this drug. GA enhanced the cytolysis of human NK cells against autologous and allogeneic immature and mature monocyte-derived dendritic cells (DCs). This drug reduced the percentages of mature DCs expressing CD80, CD83, HLA-DR or HLA-I. In contrast, it did not modulate the percentages of NK cells expressing NKG2D, NKp30, or NKp44. Nonetheless, anti-NKp30 or anti-CD86 inhibited GA-enhanced human NK cell lysis of immature DCs. Hence, CD86, and NKp30 are important for NK cell lysis of immature DCs, whereas CD80, CD83, HLA-DR and HLA-I are important for the lysis of mature DCs when GA is used as a stimulus. Further, GA inhibited the release of IFN-γ 24 h but increased the release of TNF-α 48 h after incubation with NK cells. Received 13 November 2008; received after revision 10 February 2009; accepted 18 February 2009     

The cucumber tendril — a new test organ for gibberellic acid

Résumé On peut se servir de tronçons de vrilles de concombre en voie de dévelopmentin vitro, pour déterminer d'après leurs réactions la présence d'acide gibberellique (GA). L'avantage de cette méthode réside dans le fait qu'on peut l'employer en la combinant avec la chromatographie sur papier et ainsi évaluer le GA dans l'extrait des plantes.     

Molluscicidal and insecticidal activities of isobutylamides isolated fromFagara macrophylla

Summary Five isobutylamides were isolated as insect growth inhibitors and toxicants fromFagara macrophylla and identified from their spectroscopic data.Insects were kindly supplied by the agencies of the USDA in Tifton, GA; Phoenix, AZ and Brownsville TX. The authors thank Professor D. Heyneman forB. glabratus supply. This work was partly supported by a PHS Biomedical Grant to I.K.     

Stimulation of ribonuclease activity and its isoenzymes in germinating seeds of cowpea (Vigna sinensis) by gibberellic acid and adenosine-3',5-cyclic monophosphate.

Application of GA3 and cyclic AMP to cowpea seedings caused a 2-3 fold stimulation of RNAase activity, together with the augmentation of RNAase isoenzymes. Inhibitor studies indicated the requirement of fresh RNA and protein synthesis for enzyme stimulation.     

基于新的树编码方式用免疫遗传算法解决DCMST问题

本文提出了一种新的树编码方式，可以方便地表达一棵树，简化了树在遗传算法中的编码表达。且新的树编码方式清楚地表达了边的信息，有利于疫苗的设计。此外，本文使用免疫遗传算法，有效地克服了传统遗传算法中解退化的现象。数值实验表明，解的振荡相对于传统遗传算法减小了，且收敛速度更快。     

Influence of Growth-Regulating substances onPhymatotrichum omnivorum (Shear) dugg

Zusammenfassung Die drei wachstumregulierenden Substanzen Indolessigsäure (IAA), Gibberellinsäure (GA) und Kinetin (K), wurden im Wachstumsversuch mitPhymatotrichum omnivorum (Shear) Dugg. miteinander verglichen. Die Resultate zeigen, dass Kinetin das Wachstum dieses Pilzes stärker anregt als Indolessigrenäs oder Gibberellinsäure.     

Dissection of a novel molecular determinant mediating Golgi to trans-Golgi network transition

Two major functions of the Golgi apparatus (GA) are formation of complex glycans and sorting of proteins destined for various subcellular compartments or secretion. To fulfill these tasks proper localization of the accessory proteins within the different sub-compartments of the GA is crucial. Here we investigate structural determinants mediating transition of the two glycosyltransferases β-1,4- galactosyltransferase 1 (gal-T1) and the α-1,3-fucosyltransferase 6 (fuc-T6) from the trans-Golgi cisterna to the trans-Golgi network (TGN). Upon treatment with the ionophore monensin both glycosyltransferases are found in TGN-derived swollen vesicles, as determined by confocal fluorescence microscopy and density gradient fractionation. Both enzymes carry a signal consisting of the amino acids E₅P₆ in gal-T1 and D₂P₃ in fuc-T6 necessary for the transition of these glycosyltransferases from the trans-Golgi cisterna to the TGN, but not for their steady state localization in the trans-Golgi cisterna. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users. Received 30 July 2008; received after revision 17 September 2008; accepted 29 September 2008     

GSK-3β is essential for physiological electric field-directed Golgi polarization and optimal electrotaxis

Endogenous electrical fields (EFs) at corneal and skin wounds send a powerful signal that directs cell migration during wound healing. This signal therefore may serve as a fundamental regulator directing cell polarization and migration. Very little is known of the intracellular and molecular mechanisms that mediate EF-induced cell polarization and migration. Here, we report that Chinese hamster ovary (CHO) cells show robust directional polarization and migration in a physiological EF (0.3–1 V/cm) in both dissociated cell culture and monolayer culture. An EF of 0.6 V/cm completely abolished cell migration into wounds in monolayer culture. An EF of higher strength (≥1 V/cm) is an overriding guidance cue for cell migration. Application of EF induced quick phosphorylation of glycogen synthase kinase 3β (GSK-3β) which reached a peak as early as 3 min in an EF. Inhibition of protein kinase C (PKC) significantly reduced EF-induced directedness of cell migration initially (in 1–2 h). Inhibition of GSK-3β completely abolished EF-induced GA polarization and significantly inhibited the directional cell migration, but at a later time (2–3 h in an EF). Those results suggest that GSK-3β is essential for physiological EF-induced Golgi apparatus (GA) polarization and optimal electrotactic cell migration.     

Diagnosis of diabetes mellitus using artificial neural network and classification and regression tree optimized with genetic algorithm

Diabetes mellitus is one of the most important public health problems affecting millions of people worldwide. An early and accurate diagnosis of diabetes mellitus has critical importance for the medical treatments of patients. In this study, first, artificial neural network (ANN) and classification and regression tree (CART)-based approaches are proposed for the diagnosis of diabetes. Hybrid ANN-GA and CART-GA approaches are then developed using a genetic algorithm (GA) to improve the classification accuracy of these approaches. Finally, the performances of the developed approaches are evaluated with a Pima Indian diabetes data set. Experimental results show that the developed hybrid CART-GA approach outperforms the ANN, CART, and ANN-GA approaches in terms of classification accuracy, and this approach provides an efficient methodology for diagnosis of diabetes mellitus.     

Molecular and functional heterogeneity of GABAergic synapses

Knowledge of the functional organization of the GABAergic system, the main inhibitory neurotransmitter system, in the CNS has increased remarkably in recent years. In particular, substantial progress has been made in elucidating the molecular mechanisms underlying the formation and plasticity of GABAergic synapses. Evidence available ascribes a key role to the cytoplasmic protein gephyrin to form a postsynaptic scaffold anchoring GABA(A) receptors along with other transmembrane proteins and signaling molecules in the postsynaptic density. However, the mechanisms of gephyrin scaffolding remain elusive, notably because gephyrin can auto-aggregate spontaneously and lacks PDZ protein interaction domains found in a majority of scaffolding proteins. In addition, the structural diversity of GABA(A) receptors, which are pentameric channels encoded by a large family of subunits, has been largely overlooked in these studies. Finally, the role of the dystrophin-glycoprotein complex, present in a subset of GABAergic synapses in cortical structures, remains ill-defined. In this review, we discuss recent results derived mainly from the analysis of mutant mice lacking a specific GABA(A) receptor subtype or a core protein of the GABAergic postsynaptic density (neuroligin-2, collybistin), highlighting the molecular diversity of GABAergic synapses and its relevance for brain plasticity and function. In addition, we discuss the contribution of the dystrophin-glycoprotein complex to the molecular and functional heterogeneity of GABAergic synapses.     

Lipopeptaibols, a novel family of membrane active, antimicrobial peptides

Lipopeptaibols are members of a novel group of naturally occurring, short peptides with antimicrobial activity, characterized by a lipophilic acyl chain at the N-terminus, a high content of the turn/helix forming α-aminoisobutyric acid and a 1,2-amino alcohol at the C-terminus. The amino acid sequences range from 6 to 10 residues and the fatty acyl moieties from 8 to 15 carbon atoms. The peptide portion of lipopeptaibols can be shorter than those of the nonlipidated peptaibols that range from 10 to 19 amino acid residues. The longest peptides fold into a mixed 3₁₀/α helix, whereas the shortest peptides tend to adopt a β-turn/sheet structure. Using solution methodologies, a series of analogues of trichogin GA IV was synthesized which allowed determination of the minimal lipid chain and peptide main-chain lengths for the onset of membrane activity and exploitation of a number of spectroscopic techniques aimed at determining its preferred conformation under a variety of conditions and investigating in detail its mode of interaction with, and its effect on, the phospholipid membranes. Received 26 January 2001; received after revision 7 March 2001; accepted 15 March 2001     

Genetic control of hippocampal cholinergic and dynorphinergic mechanisms regulating novelty-induced exploratory behavior in house mice

Summary Neurobehavioral genetics endeavors to trace the pathways from genetic and eenvironmental determinants to neuroanatomical and neurophysiological systems and, thence, to behavior. Exploiting genetic variation as a tool, the behavioral sequelae of manipulating these neuronal systems by drugs and antisera are analyzed. Apart from research in rats, this paper deals mainly with the genetically-influenced regulation in mice of exploratory behaviors that are adaptive in novel surroundings and are hippocampally-mediated. Special attention is paid to neuropeptidergic, GABAergic, and cholinergic synaptic functions in the mouse hippocampus.The behaviorally different inbred mouse strains C57BL/6 and DBA/2 show opposite reactions (reductions and increases, respectively, in exploration rates) to peripheral and intrahippocampal injections with agents that interfere with peptidergic, cholinergic, and GABAergic neurotransmission. These findings can be explained by an interdependent over-release of opioids, arrested GABA release, and excess acetylcholine in the hippocampal neuronal network of DBA/2 mice, as compared to C57BL/6 mice where these systems are functionally well balanced. Very similar results have been obtained with the lines SRH and SRL, derived from C57BL/6 and DBA/2, and genetically selected for rearing behavior. Most probably, the opioids act to disinhibit exploratory responses. An additional genetic approach is mentioned, in which four inbred mouse strains and one derived heterogeneous stock are used for estimating genetic correlations between structural properties of the hippocampal mossy fibers and levels of hippocampal dynorphin B, on the one hand, and frequencies of exploratory responses to environmental novelty, on the other.     

Role of serum components in the binding and phagocytosis of oxidatively damaged erythrocytes by autologous mouse macrophages

To investigate the role of autologous serum components in the recognition of damaged cells by macrophages, we examined the binding and phagocytosis of damage oxidatively damaged red blood cells with Cu2+ and ascorbate (oxRBCs) by autologous resident mouse peritoneal macrophages. The binding of oxRBCs by macrophages was independent of the presence of serum. However, phagocytosis by macrophages increased with serum concentration, and macrophages showed little ingestion of oxRBCs in a serum-free medium. Macrophages neither bound nor appreciably ingested native RBCs (before oxidation) in either the absence or presence of autologous serum. Mouse macrophages ingested significantly more native as well as oxRBCs in the presence of heat-inactivated fetal calf serum than in the presence of heat-inactivated mouse serum. Pretreated oxRBCs with normal serum were rarely ingested by macrophages in a serum-free medium. Phagocytosis of oxRBCs was significantly inhibited by depletion of IgG or calcium from serum, by heat inactivation of complement, or by antiserum against mouse C3. These results demonstrate that serum components such as IgG, C3, and calcium are involved in phagocytosis of oxRBCs by autologous macrophages.     

Hydrogen peroxide and hydroxyl radical involvement in the activation of caspase-3 in chemically induced apoptosis of HL-60 cells

Apoptosis of HL-60 cells induced by actinomycin D, H7, or daunorubicin was shown to involve the activation of caspase-3-like protease, 2 h after the addition of these drugs, based on microassay of enzyme activity by high-performance liquid chromatography. Catalase and a spin trap, N-t-butyl--phenylnitrone, which effectively inhibited the apoptosis induced by these drugs, also inhibited the activation of caspase-3-like protease. These results suggest that hydrogen peroxide and the hydroxyl radical are common mediators of caspase-3 activation caused by these chemicals, with apparently different functional mechanisms. Based on mitochondrial activity determined by oxygen consumption, complexes I, II, and IV were inhibited by actinomycin D. H7 inhibited complexes I and IV, 1 and 1.5 h respectively, after the addition of the drug to HL-60 cells. Daunorubicin inhibited complex IV, 1.5 h after the addition of the drug to HL-60 cells. Inhibition of complex IV by actinomycin D, H7, and daunorubicin were almost fully restored by the addition of cytochrome c. The release to the cytosol of cytochrome c by these drugs was also demonstrated by Western blot analysis. Addition of catalase inhibited the depression of complex IV activity induced by actinomycin D and H7. These observations indicate a direct relationship between hydrogen peroxide and the release of cytochrome c during apoptosis caused by actinomycin D, H7, and daunorubicin. Received 24 November 2000; received after revision 2 January 2001; accepted 30 January 2001     

Some characteristics of urokinase released in organ culture of human kidney.

Plasminogen activator produced in organ culture of human kidney, i.e. in the histotypical arrangement of the tissue, was partially purified by affinity chromatography on para-aminobenzamidine coupled to Sepharose by a 6-carbon spacer, followed by gel chromatography on Sephadex G-100. The molecular weight of 2 active peaks were 27,000 and 52,000 daltons respectively. It was inhibited by DFP and by IgG antiurokinase.     

Über die durch Licht bedingte «Missweisung» bei den Tänzen im Bienenstock

Summary Bees are able to indicate direction to their hive comrades by means of a waggling dance of 2 kinds: in the horizontal plane with regard to the sun they point directly towards the goal by a waggling walk using the same angle to the sun as they took in their flight. Inside the dark hive in the vertical honey-comb, they transpose the angle between goal and sun to the field of gravity, whereby the sun's direction is shown by a waggling walk upwards, and the angle to the right or left of the sun's position is given by a dance-direction in the corresponding angle to the right or left of the zenith.If a piece of blue sky is made visible in an observation hive to the bees which are dancing in orientation by gravity, they recognise the position of the sun by this polarisation sample, and the effort to orientate themselves directly by the sun (as in the horizontal plane) comes into conflict with the orientation by gravity. The result is a dance direction which corresponds remarkably well with the halving of the angle between what the dance direction should have been by gravity and what it should have been by light orientation (Figure 1). This is also true when the bee is orientating itself by polarised sky light over its back, while the sun is at the other side of the honey-comb under its front (Figure 2), a situation which does not occur during flight but which is important for its dance in the swarm. The bees receiving the information compensate the deviation of the angle determined by light, and fly to the right goal.As the sun itself, as well as the piece of blue sky, was made visible to the dancers, its influence dominated and they orientated themselves by its light (Figure 3).     

Natural and experimental interspecific hybridization between populations ofDolichopoda cave crickets

Summary Evidence of hybridization between 2 pairs of allopatricDolichopoda species is provided by electrophoretic analysis. Occurrence of hybrids was revealed by laboratory crosses and in nature both by occasional co-existence due to passive dispersal and by transplantation experiments.This research was supported by the National Research Council, Italy, grant No. 78.01441.04, and by funds of the Faculty of Sciences, University of Rome. Acknowledgments are due to Drs G. Carchini, M. Rampini and G. Sammuri for substantial help in collecting in caves and to Professor B. Baccetti for SEL micrographs.     

Lysis of Rous sarcoma virus in the presence of anti-chicken fibroblast serum and complement]

Rous sarcoma virus produced by Chick embryo fibroblasts is inactivated by an antiserum prepared against uninfected fibroblasts in the presence, but not in the absence, of complement. This inactivation which demonstrates the presence of one or more antigens of the surface of the producer cell on the viral envelope, is due to virolysis. This is demonstrated by the release of the viral internal proteins and by the fact that the viral RNA becomes entirely degradable by RNase.