Developmental regulation of NAD+ kinase in Neurospora crassa

The specific activity of NAD⁺ kinase (ATP:NAD⁺ 2-phosphotransferase, EC 2.7.1.23) from Neurospora crassa shows sharp peaks when the organism enters a new developmental stage of the asexual life cycle: the peaks are observed during hydration and germination of conidia, at the transition from exponential to stationary growth and at the photostimulated conidiation. As stimulation of NAD⁺ kinase activity by light in conidiating mycelium is not sensitive to translation inhibitors, the activiation of pre-existing molecules, rather than induction of protein synthesis de novo may be supposed. Enzyme electrophoresis revealed the presence of four forms of NAD⁺ kinase having different apparent molecular weights (I=333,000; II=306,000; III=229,000 and IV=203,000). Manifestation of the activity of individual forms of NAD⁺ kinase is developmentally controlled: form III is most abundant during vegetative growth, forms I and II prevail in conidia. At the conidial germination the increase of NAD⁺ kinase activity is associated with the activation of form III, whereas during photostimulation of conidiation form II is the most activated one. Therefore, certain molecular forms of the enzyme may be regarded as biochemical markers for different developmental stages of N. crassa.     

Hollow structures in radiolarian skeletons

Spines are the major element of radiolarian skeletons; they are usually solid or, rarely, hollow. Subcylindrical hollow spines and other hollow structures of radiolarian skeletons appeared in the Middle Cambrian. Later, hollow skeletal structures repeatedly developed in the evolution of all radiolarian classes of the subphylum Polycystina throughout the Phanerozoic to the Recent. The analysis of appearance and distribuion in the Phanerozoic of morphotypes with hollow spines has shown that the formation of hollow skeletal structures allowed better adaptation for the planktonic mode of life and could become a key adaptation in struggle for life under stressful conditions.     

Effects of Ebola virus glycoproteins on endothelial cell activation and barrier function

Ebola virus causes severe hemorrhagic fever with high mortality rates in humans and nonhuman primates. Vascular instability and dysregulation are disease-decisive symptoms during severe infection. While the transmembrane glycoprotein GP(1,2) has been shown to cause endothelial cell destruction, the role of the soluble glycoproteins in pathogenesis is largely unknown; however, they are hypothesized to be of biological relevance in terms of target cell activation and/or increase of endothelial permeability. Here we show that virus-like particles (VLPs) consisting of the Ebola virus matrix protein VP40 and GP(1,2) were able to activate endothelial cells and induce a decrease in barrier function as determined by impedance spectroscopy and hydraulic conductivity measurements. In contrast, the soluble glycoproteins sGP and delta-peptide did not activate endothelial cells or change the endothelial barrier function. The VLP-induced decrease in barrier function was further enhanced by the cytokine tumor necrosis factor alpha (TNF-alpha), which is known to induce a long-lasting decrease in endothelial cell barrier function and is hypothesized to play a key role in Ebola virus pathogenesis. Surprisingly, sGP, but not delta-peptide, induced a recovery of endothelial barrier function following treatment with TNF-alpha. Our results demonstrate that Ebola virus GP(1,2) in its particle-associated form mediates endothelial cell activation and a decrease in endothelial cell barrier function. Furthermore, sGP, the major soluble glycoprotein of Ebola virus, seems to possess an anti-inflammatory role by protecting the endothelial cell barrier function.     

Mutation processes in natural populations of <Emphasis Type="Italic">Drosophila melanogaster</Emphasis> and <Emphasis Type="Italic">Hirundo rustica</Emphasis> from radiation-contaminated regions of Ukraine

Natural populations of Drosophila melanogaster and Hirundo rustica from regions of Ukraine exhibiting different levels of radiation contamination are investigated. Genetic monitoring was performed with respect to such parameters as the frequency of visible sex-linked mutations, frequency of gonad reduction in Drosophila, and rate of interphase manifestations of chromosomal instability in the erythrocytes of the birds. The results attest to a possible opposite dependence of the level of chromosomal instability among swallows and that of the rate of lethal mutations in the sex chromosome of Drosophila on the density of radiation contamination.     

Deviations in skeletons of radiolarians

Deviations in the skeleton structure of radiolarians are extremely rare in the fossil record. They are known from the Devonian to Recent. This is a very ancient and periodically repeated phenomenon, which should be regarded as a regularity or “lost chance” rather than exotic or accident. Emergence of deviant “mutants” in radiolarians is probably connected with two main causes, i.e., disturbance during reproduction and mutations in particular modules. From the point of view of the morphogenesis of skeletal structures, deviancy facilitates the recognition of relatively “weak” modules–blocks in the general skeleton pattern, which are subject to structural changes. Nonheritable deviant variants have been revealed in skeletons of 61 radiolarian in all of three subphyla of the phylum Radiolaria: Polycystina, Phaeodaria, and Collodaria. Three deviant types are recognized: multiplicative, posterioric and supplemental.     

Apophyses,verticiles, and denticles in skeletons of Late Paleozoic radiolarians of the subfamily Entactiniinae

Morphostructural analysis of secondary skeletal elements, such as apophyses on the main spines and verticiles on the secondary spines of certain Late Paleozoic radiolarians of the subfamily Entactiniinae allow their taxonomic rank to be raised to genus. The presence of denticles on the secondary spines is only evidence of particular species. Three skeleton morphotypes are established: primary morphotype A, verticillate morphotype B, and apophyseal morphotype C. A new species, Entactinia mariannae sp. nov., and two new genera, Apophysiacus gen. nov. with five species, A. ichikawai (Caridroit et De Wever, 1984), A. minuta (Feng, 2007), A. praepycnoclada (Nazarov et Ormiston, 1983), A. pycnoclada (Nazarov et Ormiston, 1985), and A. sakmaraensis (Kozur et Mostler, 1989), and Verticillides gen. nov. with three species, V. nazarovi nom. nov., V. nestellae sp. nov., and V. verticillatus sp. nov., are described.     

Interspecies transmission of prions

Mammalian prions are infectious agents of proteinaceous nature that cause several incurable neurodegenerative diseases. Interspecies transmission of prions is usually impeded or impossible. Barriers in prion transmission are caused by small interspecies differences in the primary structure of prion proteins. The barriers can also depend on the strain (variant) of a transmitted prion. Interspecies barriers were also shown for yeast prions, which define some heritable phenotypes. Yeast prions reproduce all the main traits of prion transmission barriers observed for mammals. This allowed to show that the barrier in prion transmission can be observed even upon copolymerization of two prionogenic proteins. Available data allow elucidation of the mechanisms that impede prion transmission or make it impossible.