2,855 research outputs found

    Sphingosine Phosphate Lyase Expression Is Essential for Normal Development in Caenorhabditis elegans

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    Sphingolipids are ubiquitous membrane constituents whose metabolites function as signaling molecules in eukaryotic cells. Sphingosine 1-phosphate, a key sphingolipid second messenger, regulates proliferation, motility, invasiveness, and programmed cell death. These effects of sphingosine 1-phosphate and similar phosphorylated sphingoid bases have been observed in organisms as diverse as yeast and humans. Intracellular levels of sphingosine 1-phosphate are tightly regulated by the actions of sphingosine kinase, which is responsible for its synthesis and sphingosine-1-phosphate phosphatase and sphingosine phosphate lyase, the two enzymes responsible for its catabolism. In this study, we describe the cloning of the Caenorhabditis elegans sphingosine phosphate lyase gene along with its functional expression in Saccharomyces cerevisiae. Promoter analysis indicates tissue-specific and developmental regulation of sphingosine phosphate lyase gene expression. Inhibition of C. elegans sphingosine phosphate lyase expression by RNA interference causes accumulation of phosphorylated and unphosphorylated long-chain bases and leads to poor feeding, delayed growth, reproductive abnormalities, and intestinal damage similar to the effects seen with exposure to Bacillus thuringiensis toxin. Our results show that sphingosine phosphate lyase is an essential gene in C. elegans and suggest that the sphingolipid degradative pathway plays a conserved role in regulating animal development

    Parallel Metric Tree Embedding based on an Algebraic View on Moore-Bellman-Ford

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    A \emph{metric tree embedding} of expected \emph{stretch~α1\alpha \geq 1} maps a weighted nn-node graph G=(V,E,ω)G = (V, E, \omega) to a weighted tree T=(VT,ET,ωT)T = (V_T, E_T, \omega_T) with VVTV \subseteq V_T such that, for all v,wVv,w \in V, dist(v,w,G)dist(v,w,T)\operatorname{dist}(v, w, G) \leq \operatorname{dist}(v, w, T) and operatornameE[dist(v,w,T)]αdist(v,w,G)operatorname{E}[\operatorname{dist}(v, w, T)] \leq \alpha \operatorname{dist}(v, w, G). Such embeddings are highly useful for designing fast approximation algorithms, as many hard problems are easy to solve on tree instances. However, to date the best parallel (polylogn)(\operatorname{polylog} n)-depth algorithm that achieves an asymptotically optimal expected stretch of αO(logn)\alpha \in \operatorname{O}(\log n) requires Ω(n2)\operatorname{\Omega}(n^2) work and a metric as input. In this paper, we show how to achieve the same guarantees using polylogn\operatorname{polylog} n depth and O~(m1+ϵ)\operatorname{\tilde{O}}(m^{1+\epsilon}) work, where m=Em = |E| and ϵ>0\epsilon > 0 is an arbitrarily small constant. Moreover, one may further reduce the work to O~(m+n1+ϵ)\operatorname{\tilde{O}}(m + n^{1+\epsilon}) at the expense of increasing the expected stretch to O(ϵ1logn)\operatorname{O}(\epsilon^{-1} \log n). Our main tool in deriving these parallel algorithms is an algebraic characterization of a generalization of the classic Moore-Bellman-Ford algorithm. We consider this framework, which subsumes a variety of previous "Moore-Bellman-Ford-like" algorithms, to be of independent interest and discuss it in depth. In our tree embedding algorithm, we leverage it for providing efficient query access to an approximate metric that allows sampling the tree using polylogn\operatorname{polylog} n depth and O~(m)\operatorname{\tilde{O}}(m) work. We illustrate the generality and versatility of our techniques by various examples and a number of additional results

    Vanishing of Gravitational Particle Production in the Formation of Cosmic Strings

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    We consider the gravitationally induced particle production from the quantum vacuum which is defined by a free, massless and minimally coupled scalar field during the formation of a gauge cosmic string. Previous discussions of this topic estimate the power output per unit length along the string to be of the order of 106810^{68} ergs/sec/cm in the s-channel. We find that this production may be completely suppressed. A similar result is also expected to hold for the number of produced photons.Comment: 10 pages, Plain LaTex. Minor improvements. To appear in PR

    Regulation of Sphingosine-1-phosphate Lyase Gene Expression by Members of the GATA Family of Transcription Factors

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    Sphingosine-1-phosphate is a bioactive sphingolipid that regulates proliferation, differentiation, migration, and apoptosis. Sphingosine-1-phosphate is irreversibly degraded by the highly conserved enzyme sphingosine-1-phosphate lyase. Recent studies have suggested that sphingosine-1-phosphate lyase expression affects animal development and cell fate decisions. Despite its crucial role, mechanisms affecting expression of sphingosine-1-phosphate lyase remain poorly understood. In this study, regulation of sphingosine-1-phosphate lyase gene expression was investigated in Caenorhabditis elegans, where lyase expression is spatially restricted to cells of the developing and adult gut and is essential for normal development. Deletion analysis and generation of transgenic worms combined with fluorescence microscopy identified a 350-nucleotide sequence upstream of the ATG start site necessary for maximal lyase expression in adult worms. Site-specific mutagenesis of a GATA transcription factor-binding motif in the promoter led to loss of reporter expression. Knockdown of the gut-specific GATA transcription factor ELT-2 by RNA interference similarly led to loss of reporter expression. ELT-2 interacted with the GATA factor-binding motif in vitro and was also capable of driving expression of a Caenorhabditis elegans lyase promoter-{beta}-galactosidase reporter in a heterologous yeast system. These studies demonstrate that ELT-2 regulates sphingosine-1-phosphate lyase expression in vivo. Additionally, we demonstrate that the human sphingosine-1-phosphate lyase gene is regulated by a GATA transcription factor. Overexpression of GATA-4 led to both an increase in activity of a reporter gene as well as an increase in endogenous sphingosine-1-phosphate lyase protein

    Using level-2 fuzzy sets to combine uncertainty and imprecision in fuzzy regions

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    In many applications, spatial data need to be considered but are prone to uncertainty or imprecision. A fuzzy region - a fuzzy set over a two dimensional domain - allows the representation of such imperfect spatial data. In the original model, points of the fuzzy region where treated independently, making it impossible to model regions where groups of points should be considered as one basic element or subregion. A first extension overcame this, but required points within a group to have the same membership grade. In this contribution, we will extend this further, allowing a fuzzy region to contain subregions in which not all points have the same membership grades. The concept can be used as an underlying model in spatial applications, e.g. websites showing maps and requiring representation of imprecise features or websites with routing functions needing to handle concepts as walking distance or closeby

    Protein engineering of Pseudomonas fluorescens peroxidase Dyp1B for oxidation of phenolic and polymeric lignin substrates

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    Directed evolution was applied to dye-decolourizing peroxidase Dyp1B from Pseudomonas fluorescens Pf-5, in order to enhance the activity for oxidation of phenolic and lignin substrates. Saturation mutagenesis was used to generate focused libraries at 7 active site residues in the vicinity of the heme cofactor, and the libraries were screened for activity towards 2,6-dichlorophenol. Mutants N193 L and H169 L were found to show 7–8 fold enhanced kcat/KM towards DCP, and replacements at Val205 and Ala209 also showed enhanced activity towards alkali Kraft lignin. Residues near the predicted Mn(II) binding site were also investigated by site-directed mutagenesis, and mutants S223 N and H127R showed 4-7-fold increased kcat/KM for Mn(II) oxidation. Mutant F128R also showed enhanced thermostability, compared to wild-type Dyp1B. Testing of mutants for low molecular weight product release from Protobind alkali lignin revealed that mutant H169 L showed enhanced product release, compared with WT enzyme, and the formation of three low molecular weight metabolites by this mutant was detected by reverse phase HPLC analysis

    The Savvidy ``ferromagnetic vacuum'' in three-dimensional lattice gauge theory

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    The vacuum effective potential of three-dimensional SU(2) lattice gauge theory in an applied color-magnetic field is computed over a wide range of field strengths. The background field is induced by an external current, as in continuum field theory. Scaling and finite volume effects are analyzed systematically. The first evidence from lattice simulations is obtained of the existence of a nontrivial minimum in the effective potential. This supports a ``ferromagnetic'' picture of gluon condensation, proposed by Savvidy on the basis of a one-loop calculation in (3+1)-dimensional QCD.Comment: 9pp (REVTEX manuscript). Postscript figures appende
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