Genetic transformation of somatic cells. VI. Transfer of the trait of the rate of loss of transformant phenotype by means of DNA from cells containing the thymidine kinase gene of the herpes simplex virus

Using dot-hybridization with thymidine kinase gene (tk gene) of Herpes simplex virus type 1 (HSV 1) of DNA preparations obtained from isolated metaphase chromosomes and lysate fractions of metaphase cells, which presumably contain smaller particles compared to metaphase chromosomes, it has been shown that the tk gene of HSV 1 is localized in chromosomes of cells of transformant clones unstable in TK+-phenotype. The DNA isolated from the metaphase chromosomes from cells of transformant clones is 1.5- or 2-fold more efficient in transforming TK-Chinese hamster cells than is the total high molecular weight DNA from the same cells. Upon transformation of TK- cells by the high molecular weight DNA from the tk gene of HSV 1-containing clones, varying in the rate of the loss of TK+-phenotypes, the character "rate of the loss of transformant phenotype" is transferred together with the tk gene of HSV 1 in 22% of cases. Cells of rerevertant clones, produced from TK- subclones of transformant clones, display the rate of the loss of transformant phenotype characteristic of cells of parental TK+-clones. A comparison of the results allows a conclusion that DNA sequences, determining the character "rate of the loss of transformant phenotype", are linked tightly with the transforming DNA proper containing the tk gene of HSV 1, but are not localized inside such a DNA.     

Effect of dopamine and dopamine mimetics on Na, K-ATPase of corpus striatum synaptosomes

Dopamine (DA) and DA-mimetics (apomorphine, midantan, piribedil) have a dual effect on Na, K-ATPase of the rat brain striate synaptosomes: activating at micromolar concentrations and inhibitory at higher concentrations (less than or equal to 30 microM). In the presence of Ca2+ (1 mM EGTA + 2.5 mM Ca2+) DA activating effect completely disappears and the inhibitory effect becomes even more pronounced. In the presence of cAMP (50 microM) which has no effect of its own on Na, K-ATPase, DA activation maximum is shifted towards lower concentrations, and the inhibitory effect remains unchanged. The above mentioned effects of DA persist in the presence of ouabain (1 mM), i.e. during measuring of Na, K-ATPase activity by an "ouabain" method, with DA activation maximum shifted towards higher concentrations.     

Interaction of isolated synaptic vesicles with synaptic contacts in the rat brain

The effects of Mg-ATP, EGTA, EDTA and dicyclohexylcarbodiimide on the changes in the intensity of light scattering were studied in rat brain synaptic vesicles (SV) suspended in saccharose-buffer medium. Specific interactions between SV and isolated synaptic junctional complex were observed in the presence of Mg-ATP and calmodulin. An in vitro model of exocytosis is discussed.     

Distinct molecular mechanisms control levels of synaptic F‐actin

Polymerization of filamentous (F)‐actin at the neuronal synapse plays an important role in neuronal function. However, the regulatory mechanisms controlling the levels of synaptic actin remain incompletely understood. Here, I used established pharmacological blockers to acutely disrupt the function of actin polymerization machinery, then quantified their effect on synaptic F‐actin levels. Synaptic F‐actin was modestly decreased by inhibition of Arp2/3‐dependent actin branching. Blockade of formin‐dependent actin elongation resulted in an Arp2/3‐dependent increase in synaptic actin that could be mimicked by limited actin depolymerization. Limited actin depolymerization was also sufficient to reverse a decrease in synaptic F‐actin caused by prolonged blockade of synaptic NMDA‐type glutamate receptors. These results suggest that interplay between different actin polymerization pathways may regulate synaptic actin dynamics.     

Erratum to: Transoceanic Migration of Pacific Lamprey,Entosphenus tridentatus

Journal of Ichthyology -     

Inter- and Intra-Species Relationships of Greenland Halibut Reinhardtius hippoglossoides (Pleuronectidae) Based on the Analysis of Nuclear and Mitochondrial Genetic Markers

Journal of Ichthyology - Samples of Greenland halibut Reinhardtius hippoglossoides (Jordan and Snyder, 1901) from the Atlantic, Arctic, and Pacific Oceans were compared using eight microsatellite...     

Distribution and some features of biology of representatives of the genus Lycodes in the western part of the Bering Sea in the summer period

Based on materials of bottom inventory trawl survey performed in summer 2008 in the western part of the Bering Sea, we show that representatives of the genus Lycodes in the summer period occur almost throughout the study water area of the sea from the sublittoral to the drop-off. The pattern of distribution and abundance of particular species depend on the depth and specific features of the hydrological regime of the given area. The most numerous species??Lycodes brevipes and L. palearis??are found in warm intermediate and in cold demersal water masses, are distributed over a vast stretch, and there form considerable concentrations. Deep-water species??L. beringi and L. concolor??are more stenothermal, occur along the narrow band of the continental slope, and are considerably inferior to stretch species in numbers. Of shallow species dwelling at depths smaller than 100 m, only L. raridens has high numbers and occurs over a considerable area in the northern part of the study area, the remaining species (L. mucosus, L. polaris, and L. turneri) are caught in small amounts at local sites. The largest sizes are in L. raridens and L. concolor, their maximum length in catches is more than 70 cm, the former species reaches maximum length in the seventh year of life, and the latter reaches maximum length in the ninth year. The smallest and slowest-growing among the studied fish is L. brevipes: its maximum length in catches does not exceed 39 cm and maximum age is 7 years.     

Effect of the Ca ionophore A-23187 on the plasmatic and mitochondrial potentials of the brain synaptosomes in rats: fluorescence measurements

The applicability of the potential-sensitive dye diS-C3-(5) for the study of A23187 + Ca2+ induced plasma membrane hyperpolarization was tested in rat brain synaptosomes. An appropriate dye synaptosome ratio was chosen for the fluorescence titration dye in Ca-free Krebs-Ringer solution. The fluorescence intensity of the probe was increased upon the addition of Ca2+ (1 microM) to the synaptosomes in the presence of A23187 (1 microM). The effect of Ca2+ + A23187 persisted in a Na+-free medium or when Na+ channels were inhibited by tetrodotoxin as well as in high K+-depolarized synaptosomes (75 microM KCl). In the presence of oligomycin or a protonophore (1 microM) the effect of Ca2+ + A23187 was suppressed. This suggests that the A23187-induced fluorescence increase is due to a depolarization of intrasynaptosomal mitochondria. Therefore, the use of the dye diS-C3-(5) for the study of Ca-induced hyperpolarization does not seem to be feasible unless a quantitative model of changes in fluorescence related to the plasma and mitochondrial membrane potentials is elaborated.     

Low nekton abundance in the western Bering Sea according to trawl survey data and model estimates

Complex trawl surveys were conducted in the upper epipelagic zone of the western Bering Sea and adjacent Pacific waters in the summer and fall seasons of 2002–2006. The abundance of small nekton (micronekton) was estimated using two independent methods: traditional trawling and a mathematical model of selective feeding by fish. According to the trawl data, total micronekton density varied from 1 to 158 (average 40) mg/m³ on the northwestern Bering Sea shelf and from 6 to 151 (37) mg/m³ in deep-water areas of the southwestern Bering Sea and adjacent Pacific waters. According to model calculations, micronekton density was higher—72–193 (141) mg/m³ on the shelf and 78–507 (228) mg/m³ in the deep-water part of the studied area. Both trawl and model data showed that small nekton on the northwestern shelf mostly consisted of larval and juvenile walleye pollock, as well as small fish species, such as capelin and Pacific sand lance. In the deepwater areas, mesopelagic fish and squid (northern lampfish, northern smoothtongue, and boreopacific gonate squid), which migrate to the surface at night, juvenile Atka mackerel, and shortarm gonate squid dominated among micronekton. The advantages and disadvantages of both the trawl and model methods for calculating the abundance of small fish and squid were considered. Comparison of abundance estimates for mass fish species, obtained through trawl and model methods, enabled us to analyze trawl catchability coefficients and propose a more differentiated division of micronekton into size classes than had been done earlier. A function that characterizes the dependence of the catchability coefficient (CC) on body length was offered for juvenile Atka mackerel. This equation can be also used for evaluation of CC for other fishes that have similar size and behavior.     

A der(8)t(8;11) chromosome in the Karpas-620 myeloma cell line expresses only Cyclin D1: Yet both Cyclin D1 and MYC are repositioned in close proximity to the 3′ IGH enhancer

The Karpas-620 human myeloma cell line (HMCL) expresses high levels of Cyclin D1 (CCND1), but has a der(8)t(8;11) and a der(14)t(8;14), and not a conventional t(11;14). Fluorescent in situ hybridization (FISH) and array comparative genomic hybridization (aCGH) studies suggest that der(14)t(11;14) from a primary translocation underwent a secondary translocation with chromosome 8 to generate der(8)t(8;[14];11) and der(14)t(8;[11];14). Both secondary derivatives share extensive identical sequences from chromosomes 8, 11, and 14, including MYC and the 3′ IgH enhancers. Der(14), with MYC located ～700 kb telomeric to the 3′ IGH enhancer, expresses MYC. By contrast, der(8), with both CCND1 and MYC repositioned near a 3′ IGH enhancer, expresses CCND1, which is telomeric of the enhancer, but not MYC, which is centromeric to the enhancer. The secondary translocation that dysregulated MYC resulted in extensive regions from both donor chromosomes being transmitted to both derivative chromosomes, suggesting a defect in DNA recombination or repair in the myeloma tumor cell.