Chromatin structure contribution to the synaptonemal complex formation

Meiosis is a key cellular and molecular process for sexual reproduction contributing to the genetic variability of organisms. This process takes place after DNA replication and consists in a double cellular division, giving rise to four haploid daughter cells or gametes. Meiotic recombination between homologous chromosomes, in the meiotic prophase I, is mediated by a tripartite structure named Synaptonemal Complex (SC). The SC is a peptidic scaffold in which the chromatin of homologous chromosomes is organized during the pachytene stage, holding chromosomes together until the meiotic recombination and genetic exchange have taken place. The role of chromatin structure in formation of the SC and the meiotic recombination at meiotic prophase I remain largely unknown. In this review we address the epigenome contribution to the SC formation at meiotic prophase I, with particular attention on the chromatin structure modifications occurring during the sub-stages of meiotic prophase I. Received 18 September 2008; received after revision 10 October 2008; accepted 24 October 2008     

Origin of the differences of superficial potentials in Rana esculenta]

The spatial distributions of superficial D.C. potentials on the skin of Rana esculenta have been compared to those of the intensity of short-circuit current (S.C.C.) expressing the transcutaneous active transport of sodium ions. It has been observed that the sites of maximum D.C. potentials coincide with the localisations of maximum S.C.C. values. Moreover, superficial D.C. potentials and S.C.C. are similarly modified by the depression of metabolic activity due to lowered temperature or poisoning by dinitrophenol (DNP). It is thus proposed that the spatial distribution of the transcutaneous active transport system for sodium ions is the origin of the electric generator of superficial D.C. potentials.     

Origin of ovarian follicle cells in birds

Summary In the embryonic Japanese quail ovary, transplanted on chicken chorioallantoic membrane (CAM), follicle cells are derived from somatic cells of the ovarian surface epithelium. No evidence was found for a contribution of other cell groups of the quail ovary in the formation of follicle cells. This may be demonstrated on PAS stained sections, by following the transfer of carbon particles, initially applied on the surface epithelium.The author is very grateful to Prof.L. Vakaet, R.U.C.A. Antwerp, for his valuables suggestions, and to MissC. van Hoecke for her technical assistance.     

Mitotic regulation of the anaphase-promoting complex

Orderly progression through mitosis is regulated by the anaphase-promoting complex/cyclosome (APC/C), a large multiprotein E3 ubiquitin ligase that targets key mitotic regulators for destruction by the proteasome. APC/C has two activating subunits, Cdc20 and Cdh1. The well-established view is that Cdc20 activates APC/C from the onset of mitosis through the metaphase-anaphase transition, and that Cdh1 does so from anaphase through G1. Recent work, however, indicates that Cdh1 also activates APC/C in early mitosis and that this APC/C pool targets the anaphase inhibitor securin. To prevent premature degradation of securin, the nuclear transport factors Nup98 and Rae1 associate with APC/C^Cdh1-securin complexes. In late metaphase, when all kinetochores are attached to spindle microtubules and the spindle assembly checkpoint is satisfied, Nup98 and Rae1 are released from these complexes, thereby allowing for prompt ubiquitination of securin by APC/C^Cdh1. This, and other mechanisms by which the catalytic activity of APC/C is tightly regulated to ensure proper timing of degradation of each of its mitotic substrates, are highlighted. Received 8 October 2006; received after revision 24 November 2006; accepted 8 January 2007     

Origin of organic molecules and biomolecular homochirality

Theories about the origin of biomolecular homochirality, which seems to be a prerequisite for the creation of life, are discussed. First, possible terrestrial and extraterrestrial sources of organic molecules are outlined. Then, mechanisms for the formation of enantiomerically enriched compounds and for the amplification of their chirality are described.     

Investigations on the ACTH-protamine complex

Zusammenfassung Der Mechanismus der Verhinderung des ACTH-Effektes durch Protaminsulfat wurde untersucht. Papierchromatographisch konnte festgestellt werden, dass beide Substanzen einen Komplex bilden und infolgedessen ACTH seine Aktivität verliert. Während die proteinartigen ACTH-Präparate starke komplexibldende Eigenschaft besitzen, vermögen die peptidartigen Präparate nur in geringem Masse Komplexe zu bilden. Dies konnte auch durchin-vivo-Verhinderungsversuche (Sayers test) mit beiden Präparaten bestätigt werden.     

Composition and conservation of the telomeric complex

The telomere is composed of telomeric DNA and telomere-associated proteins. Recently, many telomere-associated proteins have been identified, and various telomere functions have been uncovered. In budding yeast, scRap1 binds directly to telomeric DNA, and other telomere regulators (Sir proteins and Rif proteins) are recruited to the telomeres by interacting with scRap1. Cdc13 binds to the most distal end of the chromosome and recruits telomerase to the telomeres. In fission yeast and humans, TTAGGG repeat binding factor (TRF) family proteins bind directly to telomeric DNA, and Rap1 proteins and other telomere regulators are recruited to the telomeres by interacting with the TRF family proteins. Both organisms have Pot1 proteins at the most distal end of the telomere instead of a budding-yeast Cdc13-like protein. Therefore, fission yeast and humans have in part common telomeric compositions that differ from that of budding yeast, a result that suggests budding yeast has lost some telomere components during the course of evolution.     

Scanning Electron Microscopy of the antigen-antibody complex

Zusammenfassung Elektronenmikroskopischer Beitrag für die Verwendung des Scanning-Mikroskops zur Darstellung von Antigen-Antikörper-Bindungen.     

Ethanol and the benzodiazepine-GABA receptor-ionophore complex

Ethanol has a pharmacological profile similar to that of classes of drugs like benzodiazepines and barbiturates, which enhance GABAergic transmission in the mammalian CNS. Several lines of behavioral, electrophysiological and biochemical studies suggest that ethanol may bring about most of its effects by enhancing GABAergic transmission. Recently, ethanol at relevant pharmacological concentrations has been shown to enhance GABA-induced 36Cl-fluxes in cultured spinal cord neurons, synaptoneurosomes and microsacs. These enhancing effects of ethanol were blocked by GABA antagonists. Ro15-4513, an azido analogue of classical BZ antagonist Ro15-1788, reversed most of the behavioral effects of ethanol and other effects involving 36Cl-flux studies. The studies summarized below indicate that most of the pharmacological effects of ethanol can be related to its effects on GABAergic transmission.     

Ethanol and the benzodiazepine-GABA receptor-ionophore complex

Summary Ethanol has a pharmacological profile similar to that of classes of drugs like benzodiazepines and barbiturates, which enhance GABAergic transmission in the mammalian CNS. Several lines of behavioral, electrophysiological and biochemical studies suggest that ethanol may bring about most of its effects by enhancing GABAergic transmission. Recently, ethanol at relevant pharmacological concentrations has been shown to enhance GABA-induced³⁶Cl-fluxes in cultured spinal cord neurons, synaptoneurosomes and microsacs. These enhancing effects of ethanol were blocked by GABA antagonists. Ro15-4513, an azido analogue of classical BZ antagonist Ro15-1788, reversed most of the behavioral effects of ethanol and other effects involving³⁶Cl-flux studies. The studies summarized below indicate that most of the pharmacological effects of ethanol can be related to its effects on GABAergic transmission.     

Origin and course of an afferent component of the facial nerve within the central nervous system

Summary The mesencephalic nucleus of trigeminal gives rise to an afferent component of the facial nerve. This nucleus contains large unipolar afferent cell bodies which give rise to an axon which courses caudally through the brainstem and exits via the facial nerve to terminate distal to the stylomastoid foramen.This work was supported by National Aeronautics and Space Administration Grant No. NAS 9-15213.     

The cloacal gland complex of the Japanese quail

Résumé Chez les cailles japonaises, le complexe glandulaire du cloaque est en fait localisé dans la lèvre dorsale du cloaque et non de l'anus. Il existe un complexe glandulaire similaire et très petit du côté ventral. La glande active se colore intensément avec le réactif périodique «acide Schiff», avec la fuchsine aldéhyde, avec le bleu d'alciane et métachromatiquement avec le bleu de toluidine. Ceci indique la présence d'une sécrétion de glycomucoprotéines. Le liquide transparent sécrété est transformé en masse blanche mousseuse au contact des bactériesE. coli etProteus mirabilis, présentes en quantités équivalentes dans le proctodeum. Les gaz émis consistent probablement en H₂ et CO₂, ce dernier peut agir comme tampon et stabiliser le pH de la sécrétion autour de la valeur 6,5.

---

---

This work was supported by U.S.P.H.S. grant No. ES 00054, Support for Toxicology Center, and by NASA research grant No. NGR 05-004-028.     

Photooxidation,reduction of the ferric ion-glucose complex

Summary Ferric ions in an acid solution of glucose are reduced by irradiation with light of wavelengths less than 400 nm. The action spectrum for this reaction and the oxidation products of glucose have been determined.