University of Basel

About: University of Basel is a education organization based out in Basel, Basel-Stadt, Switzerland. It is known for research contribution in the topics: Population & Gene. The organization has 25084 authors who have published 52975 publications receiving 2388002 citations. The organization is also known as: Universität Basel & Basel University.

Altitudinal increase of mobile carbon pools in Pinus cembra suggests sink limitation of growth at the Swiss treeline

Abstract: Low temperature driven carbon shortage is often assumed to explain slow growth and treeline formation at high elevations. To test this hypothesis, we analysed mobile carbon pools in Pinus cembra across the treeline ecotone in the Swiss Alps. Concentrations of non-structural carbohydrates (NSC) in needles, branches, stems and roots, as well as lipids (acylglycerols) in all woody tissues were measured throughout the growing season. Starch was the most prominent non-structural carbon compound in needles, whereas lipids represented 50–75% of the mobile carbon compounds in wood. The relative seasonal variation of the lipid fraction was very small, but due to the high absolute amount of lipids, the annual variability of carbon in lipids exceeded that of NSC in woody tissues. Mobile carbon compounds were highly abundant throughout the year and were never significantly depleted. Across a 110 m altitudinal transect from timberline to the uppermost site of tree existence, NSC and lipid concentrations generally increased. This trend became even more pronounced when the increasing structural density of tissues at higher elevations was accounted for. An estimation of the whole tree mobile carbon concentration (fraction of mobile carbon compounds within the whole tree biomass) also revealed an increasing trend of NSC and lipid pools with elevation. We therefore conclude that carbon limitation is unlikely to be responsible for reduced tree growth at the alpine treeline studied. Increased concentrations of NSC and lipids at the upper tree limit rather suggest that sink activity is limited. Hence, treeline formation is most likely the result of a direct thermal restriction of tissue formation (investment in structures) under otherwise sufficient carbon assimilation during the growing season.

Actin and fimbrin are required for the internalization step of endocytosis in yeast.

Abstract: In Saccharomyces cerevisiae, alpha-factor is internalized by receptor-mediated endocytosis and transported via vesicular intermediates to the vacuole where the pheromone is degraded. Using beta-tubulin and actin mutant strains, we showed that actin plays a direct role in receptor-mediated internalization of alpha-factor, but is not necessary for transport from the endocytic intermediates to the vacuole. beta-tubulin mutant strains showed no defect in these processes. In addition, cells lacking the actin-binding protein, Sac6p, which is the yeast fimbrin homologue, are defective for internalization of alpha-factor suggesting that actin filament bundling might be required for this step. The actin dependence of endocytosis shows some interesting similarities to endocytosis from the apical membrane in polarized mammalian cells.

Probing the gravitational well: no supernova explosion in spherical symmetry with general relativistic boltzmann neutrino transport

Abstract: We report on the stellar core collapse, bounce, and postbounce evolution of a $13 {\mathrm{M}}_{\ensuremath{\bigodot}}$ star in a self-consistent general relativistic spherically symmetric simulation based on Boltzmann neutrino transport. We conclude that approximations to exact neutrino transport and the omission of general relativistic effects were not alone responsible for the failure of numerous preceding attempts to model supernova explosions in spherical symmetry. Compared to simulations in Newtonian gravity, the general relativistic simulation results in a smaller shock radius. We however argue that the higher neutrino luminosities and rms energies in the general relativistic case could lead to a larger supernova explosion energy.

The activities of current antimalarial drugs on the life cycle stages of Plasmodium: a comparative study with human and rodent parasites.

Abstract: Background: Malaria remains a disease of devastating global impact, killing more than 800,000 people every year—the vast majority being children under the age of 5. While effective therapies are available, if malaria is to be eradicated a broader range of small molecule therapeutics that are able to target the liver and the transmissible sexual stages are required. These new medicines are needed both to meet the challenge of malaria eradication and to circumvent resistance. Methods and Findings: Little is known about the wider stage-specific activities of current antimalarials that were primarily designed to alleviate symptoms of malaria in the blood stage. To overcome this critical gap, we developed assays to measure activity of antimalarials against all life stages of malaria parasites, using a diverse set of human and nonhuman parasite species, including male gamete production (exflagellation) in Plasmodium falciparum, ookinete development in P. berghei, oocyst development in P. berghei and P. falciparum, and the liver stage of P. yoelii. We then compared 50 current and experimental antimalarials in these assays. We show that endoperoxides such as OZ439, a stable synthetic molecule currently in clinical phase IIa trials, are strong inhibitors of gametocyte maturation/gamete formation and impact sporogony; lumefantrine impairs development in the vector; and NPC-1161B, a new 8-aminoquinoline, inhibits sporogony. Conclusions: These data enable objective comparisons of the strengths and weaknesses of each chemical class at targeting each stage of the lifecycle. Noting that the activities of many compounds lie within achievable blood concentrations, these results offer an invaluable guide to decisions regarding which drugs to combine in the next-generation of antimalarial drugs. This study might reveal the potential of life-cycle–wide analyses of drugs for other pathogens with complex life cycles. Please see later in the article for the Editors’ Summary.