148 research outputs found

    The Ecm11-Gmc2 complex promotes synaptonemal complex formation through assembly of transverse filaments in budding yeast

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    During meiosis, homologous chromosomes pair at close proximity to form the synaptonemal complex (SC). This association is mediated by transverse filament proteins that hold the axes of homologous chromosomes together along their entire length. Transverse filament proteins are highly aggregative and can form an aberrant aggregate called the polycomplex that is unassociated with chromosomes. Here, we show that the Ecm11-Gmc2 complex is a novel SC component, functioning to facilitate assembly of the yeast transverse filament protein, Zip1. Ecm11 and Gmc2 initially localize to the synapsis initiation sites, then throughout the synapsed regions of paired homologous chromosomes. The absence of either Ecm11 or Gmc2 substantially compromises the chromosomal assembly of Zip1 as well as polycomplex formation, indicating that the complex is required for extensive Zip1 polymerization. We also show that Ecm11 is SUMOylated in a Gmc2-dependent manner. Remarkably, in the unSUMOylatable ecm11 mutant, assembly of chromosomal Zip1 remained compromised while polycomplex formation became frequent. We propose that the Ecm11-Gmc2 complex facilitates the assembly of Zip1 and that SUMOylation of Ecm11 is critical for ensuring chromosomal assembly of Zip1, thus suppressing polycomplex formation

    GeV electron beams from a laser-plasma accelerator

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    Abstract-High-quality electron beams with up to 1 GeV energy have been generated by a laser-driven plasma-based accelerator by guiding a 40 TW peak power laser pulse in a 3.3 cm long gas-filled capillary discharge waveguide [1]

    GeV electron beams from a laser-plasma accelerator

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    High-quality electron beams with up to 1 GeV energy havebeen generated by a laser-driven plasma-based accelerator by guiding a 40TW peak power laser pulse in a 3.3 cm long gas-filled capillary dischargewaveguide

    GeV electron beams from a centimeter-scale channel guided laser wakefield accelerator

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    Laser wakefield accelerators can produce electric fields of order 10-100 GV/m, suitable for acceleration of electrons to relativistic energies. The wakefields are excited by a relativistically intense laser pulse propagating through a plasma and have a phase velocity determined by the group velocity of the light pulse. Two important effects that can limit the acceleration distance and hence the net energy gain obtained by an electron are diffraction of the drive laser pulse and particle-wake dephasing. Diffraction of a focused ultrashort laser pulse can be overcome by using preformed plasma channels. The dephasing limit can be increased by operating at a lower plasma density, since this results in an increase in the laser group velocity. Here we present detailed results on the generation of GeV-class electron beams using an intense femtosecond laser beam and a 3.3 cm long preformed discharge-based plasma channel [W. P. Leemans et al., Nature Physics 2, 696 (2006)]. The use of a discharge-based waveguide permitted operation at an order of magnitude lower density and 15 times longer distance than in previous experiments that relied on laser preformed plasma channels. Laser pulses with peak power ranging from 10-40 TW were guided over more than 20 Rayleigh ranges and high quality electron beams with energy up to 1 GeV were obtained by channeling a 40 TW peak power laser pulse. The dependence of the electron beam characteristics on capillary properties, plasma density, and laser parameters are discussed. (C) 2007 American Institute of Physics

    High Quality Electron Bunches up to 1 GeV from Laser Wakefield Acceleration at LBNL

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    Experiments at the LOASIS laboratory of LBNL havedemonstrated production of 100 MeV to 1 GeV electron bunches with lowenergy spread and low divergence from laser wakefield acceleration. Theradiation pressure of a 10 TW laser pulse, guided over 10 diffractionranges by a few-mm long plasma density channel, was used to drive anintense plasma wave (wakefield), producing electron bunches with energieson the order of 100 MeV and acceleration gradients on the order of 100GV/m. Beam energy was increased from 100 MeV to 1 GeV by using a few-cmlong guiding channel at lower density, driven by a 40 TW laser,demonstrating the anticipated scaling to higher beam energies. Particlesimulations indicate that the low energy spread beams were produced fromself-trapped electrons through the interplay of trapping, loading, anddephasing. Other experiments and simulations are also underway to controlinjection of particles into the wake, and hence improve beam quality andstability further

    Thar She Blows! A Novel Method for DNA Collection from Cetacean Blow

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    Background: Molecular tools are now widely used to address crucial management and conservation questions. To date, dart biopsying has been the most commonly used method for collecting genetic data from cetaceans; however, this method has some drawbacks. Dart biopsying is considered inappropriate for young animals and has recently come under scrutiny from ethical boards, conservationists, and the general public. Thus, identifying alternative genetic collection techniques for cetaceans remains a priority, especially for internationally protected species. Methodology/Principal Findings: In this study, we investigated whether blow-sampling, which involves collecting exhalations from the blowholes of cetaceans, could be developed as a new less invasive method for DNA collection. Our current methodology was developed using six bottlenose dolphins, Tursiops truncatus, housed at the National Aquarium, Baltimore (USA), from which we were able to collect both blow and blood samples. For all six individuals, we found that their mitochondrial and microsatellite DNA profile taken from blow, matched their corresponding mitochondrial and microsatellite DNA profile collected from blood. This indicates that blow-sampling is a viable alternative method for DNA collection. Conclusion/Significance: In this study, we show that blow-sampling provides a viable and less invasive method for collection of genetic data, even for small cetaceans. In contrast to dart biopsying, the advantage of this method is that it capitalizes on the natural breathing behaviour of dolphins and can be applied to even very young dolphins. Both biopsy and blow-sampling require close proximity of the boat, but blow-sampling can be achieved when dolphins voluntarily bowride and involves no harmful contact

    Fungal Endophyte Diversity in Sarracenia

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    Fungal endophytes were isolated from 4 species of the carnivorous pitcher plant genus Sarracenia: S. minor, S. oreophila, S. purpurea, and S. psittacina. Twelve taxa of fungi, 8 within the Ascomycota and 4 within the Basidiomycota, were identified based on PCR amplification and sequencing of the internal transcribed spacer sequences of nuclear ribosomal DNA (ITS rDNA) with taxonomic identity assigned using the NCBI nucleotide megablast search tool. Endophytes are known to produce a large number of metabolites, some of which may contribute to the protection and survival of the host. We speculate that endophyte-infected Sarracenia may benefit from their fungal associates by their influence on nutrient availability from within pitchers and, possibly, by directly influencing the biota within pitchers

    A Battle Lost? Report on Two Centuries of Invasion and Management of Lantana camara L. in Australia, India and South Africa

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    Recent discussion on invasive species has invigorated the debate on strategies to manage these species. Lantana camara L., a shrub native to the American tropics, has become one of the worst weeds in recorded history. In Australia, India and South Africa, Lantana has become very widespread occupying millions of hectares of land. Here, we examine historical records to reconstruct invasion and management of Lantana over two centuries and ask: Can we fight the spread of invasive species or do we need to develop strategies for their adaptive management? We carried out extensive research of historical records constituting over 75% of records on invasion and management of this species in the three countries. The records indicate that governments in Australia, India and South Africa have taken aggressive measures to eradicate Lantana over the last two centuries, but these efforts have been largely unsuccessful. We found that despite control measures, the invasion trajectory of Lantana has continued upwards and that post-war land-use change might have been a possible trigger for this spread. A large majority of studies on invasive species address timescales of less than one year; and even fewer address timescales of >10 years. An understanding of species invasions over long time-scales is of paramount importance. While archival records may give only a partial picture of the spread and management of invasive species, in the absence of any other long-term dataset on the ecology of Lantana, our study provides an important insight into its invasion, spread and management over two centuries and across three continents. While the established paradigm is to expend available resources on attempting to eradicate invasive species, our findings suggest that in the future, conservationists will need to develop strategies for their adaptive management rather than fighting a losing battle

    Alteration in P-glycoprotein Functionality Affects Intrabrain Distribution of Quinidine More Than Brain Entry—A Study in Rats Subjected to Status Epilepticus by Kainate

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    This study aimed to investigate the use of quinidine microdialysis to study potential changes in brain P-glycoprotein functionality after induction of status epilepticus (SE) by kainate. Rats were infused with 10 or 20 mg/kg quinidine over 30 min or 4 h. Plasma, brain extracellular fluid (brain ECF), and end-of-experiment total brain concentrations of quinidine were determined during 7 h after the start of the infusion. Effect of pretreatment with tariquidar (15 mg/kg, administered 30 min before the start of the quinidine infusion) on the brain distribution of quinidine was assessed. This approach was repeated in kainate-treated rats. Quinidine kinetics were analyzed with population modeling (NONMEM). The quinidine microdialysis assay clearly revealed differences in brain distribution upon changes in P-glycoprotein functionality by pre-administration of tariquidar, which resulted in a 7.2-fold increase in brain ECF and a 40-fold increase in total brain quinidine concentration. After kainate treatment alone, however, no difference in quinidine transport across the blood–brain barrier was found, but kainate-treated rats tended to have a lower total brain concentration but a higher brain ECF concentration of quinidine than saline-treated rats. This study did not provide evidence for the hypothesis that P-glycoprotein function at the blood–brain barrier is altered at 1 week after SE induction, but rather suggests that P-glycoprotein function might be altered at the brain parenchymal level
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