589 research outputs found

    Transcriptome analysis of hepatic gene expression and DNA methylation in methionine- and betaine-supplemented geese (Anser cygnoides domesticus)

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    Dietary methionine (Met) restriction produces a coordinated series of transcriptional responses in the liver that limits growth performance and amino acid metabolism. Methyl donor supplementation with betaine (Bet) may protect against this disturbance and affect the molecular basis of gene regulation. However, a lack of genetic information remains an obstacle to understand the mechanisms underlying the relationship between Met and Bet supplementation and its effects on genetic mechanisms. The goal of this study was to identify the effects of dietary supplementation of Met and Bet on growth performance, transcriptomic gene expression, and epigenetic mechanisms in geese on a Met-deficient diet. One hundred and fifty 21-day-old healthy male Yangzhou geese of similar body weight were randomly distributed into 3 groups with 5 replicates per treatment and 10 geese per replicate: Met-deficient diet (Control), Control+1.2 g/kg of Met (Met), and Control+0.6 g/kg of Bet (Bet). All geese had free access to the diet and water throughout rearing. Our results indicated that supplementation of 1.2 g/kg of Met in Met-deficient feed increased growth performance and plasma homocysteine (HCY) levels, indicating increased transsulfuration flux in the liver. Supplementation of 0.6 g/kg Bet had no apparent sparing effect on Met needs for growth performance in growing geese. The expression of many genes critical for Met metabolism is increased in Met supplementation group. In the Bet-supplemented group, genes involved in energy production and conversion were up-regulated. Dietary supplementation with Bet and Met also altered DNA methylation. We observed changes in the methylation of the LOC106032502 promoter and corresponding changes in mRNA expression. In conclusion, Met and Bet supplementation in geese affects the transcriptional regulatory network and alters the hepatic DNA methylation of LOC106032502

    Observation of Two New N* Peaks in J/psi -> ppinˉp pi^- \bar n and pˉπ+n\bar p\pi^+n Decays

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    The πN\pi N system in decays of J/ψNˉNπJ/\psi\to\bar NN\pi is limited to be isospin 1/2 by isospin conservation. This provides a big advantage in studying NπNN^*\to \pi N compared with πN\pi N and γN\gamma N experiments which mix isospin 1/2 and 3/2 for the πN\pi N system. Using 58 million J/ψJ/\psi decays collected with the Beijing Electron Positron Collider, more than 100 thousand J/ψpπnˉ+c.c.J/\psi \to p \pi^- \bar n + c.c. events are obtained. Besides two well known NN^* peaks at 1500 MeV and 1670 MeV, there are two new, clear NN^* peaks in the pπp\pi invariant mass spectrum around 1360 MeV and 2030 MeV. They are the first direct observation of the N(1440)N^*(1440) peak and a long-sought "missing" NN^* peak above 2 GeV in the πN\pi N invariant mass spectrum. A simple Breit-Wigner fit gives the mass and width for the N(1440)N^*(1440) peak as 1358±6±161358\pm 6 \pm 16 MeV and 179±26±50179\pm 26\pm 50 MeV, and for the new NN^* peak above 2 GeV as 2068±340+152068\pm 3^{+15}_{-40} MeV and 165±14±40165\pm 14\pm 40 MeV, respectively

    Inclusive J/Psi photoproduction and polarization at HERA in the kt-factorization approach

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    We investigate the inclusive photoproduction of J/Psi mesons at HERA within the framework of the kt-factorization QCD approach. Our consideration is based on the color singlet model supplemented with the relevant off-shell matrix elements and the CCFM and KMR unintegrated gluon densities in a proton and in a photon. Both the direct and resolved photon contributions are taken into account. Our predictions are compared with the recent experimental data taken by the H1 and ZEUS collaborations. Special attention is put on the J/Psi polarization parameters lambda and nu which are sensitive to the production dynamics.Comment: 21 pages, 15 figure

    On the deflection of asteroids with mirrors

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    This paper presents an analysis of an asteroid deflection method based on multiple solar concentrators. A model of the deflection through the sublimation of the surface material of an asteroid is presented, with simulation results showing the achievable orbital deflection with, and without, accounting for the effects of mirror contamination due to the ejected debris plume. A second model with simulation results is presented analyzing an enhancement of the Yarkovsky effect, which provides a significant deflection even when the surface temperature is not high enough to sublimate. Finally the dynamical model of solar concentrators in the proximity of an irregular celestial body are discussed, together with a Lyapunov-based controller to maintain the spacecraft concentrators at a required distance from the asteroid

    On the mechanisms of heavy-quarkonium hadroproduction

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    We discuss the various mechanisms potentially at work in hadroproduction of heavy quarkonia in the light of computations of higher-order QCD corrections both in the Colour-Singlet (CS) and Colour-Octet (CO) channels and the inclusion of the contribution arising from the s-channel cut in the CS channel. We also discuss new observables meant to better discriminate between these different mechanisms.Comment: Invited review talk at 3rd International Conference On Hard And Electromagnetic Probes Of High-Energy Nuclear Collisions (HP2008), 8-14 June 2008, Illa da Toxa, Galicia, Spain. 11 pages, 21 figures, LaTeX, uses svjour.cls and svepj.clo (included

    Genome-wide functional perturbation of human microsatellite repeats using engineered zinc finger transcription factors.

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    Repeat elements can be dysregulated at a genome-wide scale in human diseases. For example, in Ewing sarcoma, hundreds of inert GGAA repeats can be converted into active enhancers when bound by EWS-FLI1. Here we show that fusions between EWS and GGAA-repeat-targeted engineered zinc finger arrays (ZFAs) can function at least as efficiently as EWS-FLI1 for converting hundreds of GGAA repeats into active enhancers in a Ewing sarcoma precursor cell model. Furthermore, a fusion of a KRAB domain to a ZFA can silence GGAA microsatellite enhancers genome wide in Ewing sarcoma cells, thereby reducing expression of EWS-FLI1-activated genes. Remarkably, this KRAB-ZFA fusion showed selective toxicity against Ewing sarcoma cells compared with non-Ewing cancer cells, consistent with its Ewing sarcoma-specific impact on the transcriptome. These findings demonstrate the value of ZFAs for functional annotation of repeats and illustrate how aberrant microsatellite activities might be regulated for potential therapeutic applications

    Direct Measurements of the Branching Fractions for D0Ke+νeD^0 \to K^-e^+\nu_e and D0πe+νeD^0 \to \pi^-e^+\nu_e and Determinations of the Form Factors f+K(0)f_{+}^{K}(0) and f+π(0)f^{\pi}_{+}(0)

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    The absolute branching fractions for the decays D0Ke+νeD^0 \to K^-e ^+\nu_e and D0πe+νeD^0 \to \pi^-e^+\nu_e are determined using 7584±198±3417584\pm 198 \pm 341 singly tagged Dˉ0\bar D^0 sample from the data collected around 3.773 GeV with the BES-II detector at the BEPC. In the system recoiling against the singly tagged Dˉ0\bar D^0 meson, 104.0±10.9104.0\pm 10.9 events for D0Ke+νeD^0 \to K^-e ^+\nu_e and 9.0±3.69.0 \pm 3.6 events for D0πe+νeD^0 \to \pi^-e^+\nu_e decays are observed. Those yield the absolute branching fractions to be BF(D0Ke+νe)=(3.82±0.40±0.27)BF(D^0 \to K^-e^+\nu_e)=(3.82 \pm 0.40\pm 0.27)% and BF(D0πe+νe)=(0.33±0.13±0.03)BF(D^0 \to \pi^-e^+\nu_e)=(0.33 \pm 0.13\pm 0.03)%. The vector form factors are determined to be f+K(0)=0.78±0.04±0.03|f^K_+(0)| = 0.78 \pm 0.04 \pm 0.03 and f+π(0)=0.73±0.14±0.06|f^{\pi}_+(0)| = 0.73 \pm 0.14 \pm 0.06. The ratio of the two form factors is measured to be f+π(0)/f+K(0)=0.93±0.19±0.07|f^{\pi}_+(0)/f^K_+(0)|= 0.93 \pm 0.19 \pm 0.07.Comment: 6 pages, 5 figure

    Holographic dilatonic model of dark energy

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    We present a dilatonic description of the holographic dark energy by connecting the holographic dark energy density with the dilaton scalar field energy density in a flat Friedmann-Robertson-Walker universe. We show that this model can describe the observed accelerated expansion of our universe with the choice c1c\geq1 and reconstruct the kinetic term as well as the dynamics of the dilaton scalar field.Comment: 7 pages, 3 figures, changed content, added references, accepted for publication at Eur.Phys.J.
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