Sur l'action de l'acide 2,4-dichlorophénoxyacétique sur la croissance des racines deZea mays et dePisum cultivéesin vitro

Summary (1) A response ofZea mays andPisum roots cultured aseptically to 2,4-dichlorophenoxyacetic acid has been observed.Depending on the concentrationZea mays shows an increase of the growth rate (optimal concentration 10^–11 mol) which turns over to an inhibition (above 10^–7 mol). The curve is similar to that obtained by 3-indoleacetic acid, which proves the phytohormonal character of 2,4-D.(2) ThePisum root is more sensitive than theZea mays root. A concentration of 10^–7 molinhibitsPisum in a high degree, whileZea mays is no more inhibited, thus demonstrating the selective herbicidal action of 2,4-D against isolated roots of Dicotyledons culturedin vitro.     

Unstable genetic system inDrosophila melanogaster: I. Instability at theCinnabar locus

Summary A mutant strain containing acinnabar allele (cn ^rbr ,rojo brillante) is reported, that produces wild-type revertants at thecinnabar (cn) locus. Incn ^rbr /cn heterozygotes the rate of mutation is highly increased. The presence of a mutator agent acting premeiotically is indicated.D.L. Lindsley and E.H. Grell, Genetic variations ofDrosophila melanogaster. Carnegie Institution of Washington, Washington, 1968; Publication No. 627.     

A potent attractant of zoospores ofAphanomyces cochlioides isolated from its host,Spinacia oleracea

A highly potent attractant of zoospores ofAphanomyces cochlioides, a causal fungus of the root rot disease of spinach (Spinacia oleracea), was isolated from spinach roots, and its structure was determined by spectroscopic evidence and chemical synthesis as cochliophilin A (5-hydroxy-6,7-methylenedioxyflavone,1). A chromosorb particle prepared by soaking in solution of1 showed a potent attracting activity toward the zoospores using concentrations of1 above 10^–9 or 10^–10 M.     

Naringenin inhibition on expiants in vitro ofCichorium intybus (Chicory)

Riassunto La naringenina alla concentrazione di 10^–4 M inibisce in modo totale l'emissione di gemme in radici diCichorium intybus in vitro senza tuttavia bloccare completamente la callogenesi. A concentrazioni scalari minori (10^–5, 10^–6, 10^–7 M) questa sostanza causa una inibizione solo nella fase iniziale dell'esperienza.     

Repressible alkaline phosphotase inAspergillus niger

Summary ALP fromA. niger is a) P_i repressible enzyme; b) stimulated by addition of Zn⁺⁺ to the growth medium, and c) that EDTA inhibits the enzyme reversibly, which could be restored by addition of Zn⁺⁺ and perhaps Mg⁺⁺. This property is in contrast to the enzyme fromN. crassa, which is independent of any metal requirement.     

Spermatozoid-attracting substance in hermaphrodite brown algae,Pelvetia wrightii andFucus evanescens

Summary A spermatozoid-attracting substance of the hermaphrodite brown algae,Pelvetia wrightii andFucus evanescens, was identified as 1, trans-3, cis-5-octatriene, respectively, by¹H-NMR and¹³C-NMR data and biological activities.Acknowledgments. The authors would like to express their thanks to Mr A. Nishikawa for technical assistance, to Dr M. Abe (Yamagata Univ.) for valuable discussion on biological work and to Prof. Y. Sakai (Hokkaido Univ. Director of the Institute of Algological Research, Muroran) for the facilities during the investigation ofP. wrightii andF. evanescens. Financial support from the Ministry of Education Science, and Culture (Grant-in Aid for Scientific Research No. 556092) is gratefully acknowledged.     

Radical yields in X-irradiated aqueous solutions

Résumé La valeur deGh+Goh peut être obtenue en utilisant des solutions aqueuses de certains composés organiques contenant Cu²⁺ et/ou Fe³⁺. Les ions métalliques sont réduits par H et par les radicaux produits par l'oxydation des composés organiques par OH. A concentration convenable des réactifs, on a;G _Fe ²⁺ =G _H+G _OH.     

Targeting O 6-methylguanine-DNA methyltransferase with specific inhibitors as a strategy in cancer therapy

O ⁶-methylguanine-DNA methyltransferase (MGMT) repairs the cancer chemotherapy-relevant DNA adducts, O ⁶-methylguanine and O ⁶-chloroethylguanine, induced by methylating and chloroethylating anticancer drugs, respectively. These adducts are cytotoxic, and given the overwhelming evidence that MGMT is a key factor in resistance, strategies for inactivating MGMT have been pursued. A number of drugs have been shown to inactivate MGMT in cells, human tumour models and cancer patients, and O ⁶-benzylguanine and O ⁶-[4-bromothenyl]guanine have been used in clinical trials. While these agents show no side effects per se, they also inactivate MGMT in normal tissues and hence exacerbate the toxic side effects of the alkylating drugs, requiring dose reduction. This might explain why, in any of the reported trials, the outcome has not been improved by their inclusion. It is, however, anticipated that, with the availability of tumour targeting strategies and hematopoetic stem cell protection, MGMT inactivators hold promise for enhancing the effectiveness of alkylating agent chemotherapy.     

Genetic variation at the alcohol dehydrogenase locus inDrosophila melanogaster: A third ubiquitous allele

Summary A 3rd allele at theAdh locus,Adh ^FCh.D., has been found at polymorphic frequencies in natural populations ofD. melanogaster. The ADH-FChD enzyme has properties distinct from those of the 2 more common forms of ADH. TheAdh polymorphism should now be analyzed as a triallelic system.     

Disruption of clc-5 leads to a redistribution of annexin A2 and promotes calcium crystal agglomeration in collecting duct epithelial cells

Mutations in CLCN5, which encodes the voltage-dependent Cl⁻/H⁺antiporter, CLC-5, cause Dent’s disease. This disorder is characterized by low molecularweight proteinuria, hypercalciuria, nephrocalcinosis and nephrolithiasis. Using a collecting duct cell model (mIMCD-3) in which endogenous clc-5 is disrupted by antisense clc-5 or overexpression of truncated clc-5, we demonstrate altered expression of the crystal adhesion molecule, annexin A2. Endogenously expressed annexin A2 is intracellular with limited plasma membrane localization. Following clc-5 disruption, there is both a marked increase in plasma membrane annexin A2 and an increase in cell surface crystal retention and agglomeration, which may be attenuated using pretreatment with anti-annexin A2 antibodies or wheat germ agglutinin lectin but not by concanavalin A. We hypothesize that in Dent’s disease, endocytic failure leads to an accumulation at the plasma membrane of crystal-binding molecules that include annexin A2 leading to retention of calcium crystals and ultimately nephrocalcinosis and nephrolithiasis. Received 22 October 2005; received after revision 26 November 2005; accepted 2 December 2005     

Über eine selektive Mitosehemmung und -schädigung bei jungen Ratten durch Synthalin A

Summary A single subcutaneous injection of synthalin-A does not affect the cytoplasma ofA-cells in pancreatic islets of the rat during the 1^st–5^th day of life, in contrast to adult animals. Selective action was found on mitoticA-cells: reduction of mitotic frequency to 25% of the normal rate, and pathological mitoses in the sense of the so-called primary effect. The mitoses ofB-cells, exocrine pancreatic cells and intestinal epithelia seemed to be unchanged, although the mitotic rate was higher than inA-cells.     

The use of fungal protoplasts in the study of aflatoxin biosynthesis

Summary Protoplasts derived fromAspergillus flavus are shown to be capable of synthesizing aflatoxins when incubated in a chemically defined medium.¹⁴C-Acetate and¹⁴C-Versicolorin A, added to protoplasts from 3-day-old mycelium, are incorporated into aflatoxin B₁.     

Inhibition of riboflavin-sensitized photoinactivation of taka-amylase a by some inhibitors

Zusammenfassung Durch Gegenwart von Co⁺⁺ oder J^– oder Tryptophan oderp-Phenylendiamin wird die durch Riboflavin sensibilisierte Photoinaktivierung der Taka-Amylase A stark gehemmt. Die möglichen Mechanismen der Hemmungswirkung dieser Inhibitoren werden diskutiert.     

Effect of sulpiride on oxygen uptake by rat's brain tissue in vitro

Resumen El Sulpiride in vitro a la concentración de 1×10^–2 M disminuye el consumo de Oxígeno en cortes de cerebro de rata. El exceso de potasio o ausencia de calcio en el medio de incubación, no modifican este efecto. En homogeneizado de cerebro total, unicamente a la concentración de 1×10^–2 M deprime el consumo de oxígeno. A las concentraciones 1×10^–3 y 1×10^–4 M no modifica el consumo de oxígeno en cortes ni homogeneizados de cerebro.     

Iridophore development in wild-type and periodic albinoXenopus larvae

Summary Light microscopic studies of iridophore preparations from a^p mutantXenopus larvae revealed abnormalities in the morphology and size distribution of reflecting platelets; purine synthesis is normal. A pleiotropic effect of the a^p gene on melanoblasts and iridoblasts is proposed.     

Does an inhibitor of mitochondrial adenylate kinase also affect oxidative phosphorylation?

Summary Adenylate kinase activity of intact mitochondria is strongly inhibited by Ap₅A, i.e.p ¹,p ⁵-Di (adenosine-5-) pentaphosphate, whereas oxidative phosphorylation is not affected. Therefore, Ap₅A is a useful tool to distinguish between oxidative and non oxidative ATP generating reactions.Acknowledgment. The generous support of Prof. Dr.Walther Lamprecht is gratefully acknowledged. J. L. thanks the Stipendienfonds des Verbandes der Chemische Industrie for a scholarship.     

Über das komplexchemische Verhalten von aromatischen Karbonsäurehydraziden

Summary A simple method to evaluate rough values of complex-formation constants has been developed. We have determinedk ₁*-values for Cu⁺² and aromatic hydrazides.k ₁* is suitable for comparison with biological results.     

Specific precipitins for type XIV pneumococcus polysaccharide fromAbrus precatorius seeds

Zusammenfassung Präzipitine ausAbrus precatorius-Samen scheinen folgende Spezifität zu besitzen: 1. gegen Pneumococcus-Polysaccharide des Typus XIV; 2. gegen die menschlichen blutgruppenspezifischen Substanzen A, B, H und Le^a      

Multiple roles of the DSCR1 (Adapt78 or RCAN1) gene and its protein product Calcipressin 1 (or RCAN1) in disease

The DSCR1 (Adapt78) gene¹ is transiently induced by stresses to temporarily protect cells against further potentially lethal challenges. However, chronic expression of the DSCR1 (Adapt78) gene has now been implicated in several pathological conditions including Alzheimer’s disease, Down syndrome and cardiac hypertrophy. Calcipressin 1 has been shown to function through direct binding and inhibition of the serine threonine protein phosphatase Calcineurin. Pharmacological inhibition of calcineurin, by the immunosuppressive drugs cyclosporin A and FK506, affects a wide variety of diseases. It is, therefore, likely that this endogenous calcineurin inhibitor, calcipressin 1, may also play a role in a variety of human diseases. ¹Please note that the mammalian DSCR1 gene is also called Adapt78 or RCAN1, and its protein products have been named Calcipressin1, MCIP1 and RCAN1. A proposal to adopt a single gene name of RCAN1 and a protein name RCAN1 (for Regulator of Calcineurin) has been endorsed by the HUGO Gene Nomenclature Committee, but final approval must await agreement from a majority of researchers in the field. Received 2 March 2005; received after revision 27 May 2005; accepted 19 July 2005     

Recognition of very low concentrations of ATP byGlossina tachinoides Westwood

Summary Like many other blood feeders,Glossina tachinoides is stimulated to gorge by the presence of ATP in its diet. A concentration of 1.3×10^–8 M ATP induces 50% feeding. The ability ofG. tachinoides to detect ATP is the highest recorded so far among insects.