68 research outputs found

    Chemically modified dsRNA induces RNAi effects in insects in vitro and in vivo: a potential new tool for improving RNA-based plant protection

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    Global agriculture loses over $100 billion of produce annually to crop pests such as insects. Many of these crop pests either are not currently controlled by artificial means or have developed resistance against chemical pesticides. Long dsRNAs are capable of inducing RNAi in insects and are emerging as novel, highly selective alternatives for sustainable insect management strategies. However, there are significant challenges associated with RNAi efficacy in insects. In this study, we synthesized a range of chemically modified long dsRNAs in an approach to improve nuclease resistance and RNAi efficacy in insects. Our results showed that dsRNAs containing phosphorothioate modifications demonstrated increased resistance to southern green stink bug saliva nucleases. Phosphorothioate-modified and 2â€Č-fluoro-modified dsRNA also demonstrated increased resistance to degradation by soil nucleases and increased RNAi efficacy in Drosophila melanogaster cell cultures. In live insects, we found chemically modified long dsRNAs successfully resulted in mortality in both stink bug and corn rootworm. These results provide further mechanistic insight into the dependence of RNAi efficacy on nucleotide modifications in the sense or antisense strand of the dsRNA in insects and demonstrate for the first time that RNAi can successfully be triggered by chemically modified long dsRNAs in insect cells or live insects

    A Kinematically Complete Measurement of the Proton Structure Function F2 in the Resonance Region and Evaluation of Its Moments

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    We measured the inclusive electron-proton cross section in the nucleon resonance region (W < 2.5 GeV) at momentum transfers Q**2 below 4.5 (GeV/c)**2 with the CLAS detector. The large acceptance of CLAS allowed for the first time the measurement of the cross section in a large, contiguous two-dimensional range of Q**2 and x, making it possible to perform an integration of the data at fixed Q**2 over the whole significant x-interval. From these data we extracted the structure function F2 and, by including other world data, we studied the Q**2 evolution of its moments, Mn(Q**2), in order to estimate higher twist contributions. The small statistical and systematic uncertainties of the CLAS data allow a precise extraction of the higher twists and demand significant improvements in theoretical predictions for a meaningful comparison with new experimental results.Comment: revtex4 18 pp., 12 figure

    eta-prime photoproduction on the proton for photon energies from 1.527 to 2.227 GeV

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    Differential cross sections for the reaction gamma p -> eta-prime p have been measured with the CLAS spectrometer and a tagged photon beam with energies from 1.527 to 2.227 GeV. The results reported here possess much greater accuracy than previous measurements. Analyses of these data indicate for the first time the coupling of the etaprime N channel to both the S_11(1535) and P_11(1710) resonances, known to couple strongly to the eta N channel in photoproduction on the proton, and the importance of j=3/2 resonances in the process.Comment: 6 pages, 3 figure

    Measurement of the Deuteron Structure Function F2 in the Resonance Region and Evaluation of Its Moments

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    Inclusive electron scattering off the deuteron has been measured to extract the deuteron structure function F2 with the CEBAF Large Acceptance Spectrometer (CLAS) at the Thomas Jefferson National Accelerator Facility. The measurement covers the entire resonance region from the quasi-elastic peak up to the invariant mass of the final-state hadronic system W~2.7 GeV with four-momentum transfers Q2 from 0.4 to 6 (GeV/c)^2. These data are complementary to previous measurements of the proton structure function F2 and cover a similar two-dimensional region of Q2 and Bjorken variable x. Determination of the deuteron F2 over a large x interval including the quasi-elastic peak as a function of Q2, together with the other world data, permit a direct evaluation of the structure function moments for the first time. By fitting the Q2 evolution of these moments with an OPE-based twist expansion we have obtained a separation of the leading twist and higher twist terms. The observed Q2 behaviour of the higher twist contribution suggests a partial cancellation of different higher twists entering into the expansion with opposite signs. This cancellation, found also in the proton moments, is a manifestation of the "duality" phenomenon in the F2 structure function

    A Precise Measurement of the Neutron Magnetic Form Factor GMn in the Few-GeV2 Region

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    The neutron elastic magnetic form factor GMn has been extracted from quasielastic electron scattering data on deuterium with the CEBAF Large Acceptance Spectrometer (CLAS) at Jefferson Lab. The kinematic coverage of the measurement is continuous from Q2=1 GeV2 to 4.8 GeV2. High precision was achieved by employing a ratio technique in which many uncertainties cancel, and by a simultaneous in-situ calibration of the neutron detection efficiency, the largest correction to the data. Neutrons were detected using the CLAS electromagnetic calorimeters and the time-of-flight scintillators. Data were taken at two different electron beam energies, allowing up to four semi-independent measurements of GMn to be made at each value of Q2. The dipole parameterization is found to provide a good description of the data over the measured Q2 range.Comment: 14 pages, 5 figures, revtex4, submitted to Physical Review Letters, Revised version has changes recommended by journal referee

    Tensor Polarization of the phi meson Photoproduced at High t

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    As part of a measurement of the cross section of ϕ\phi meson photoproduction to high momentum transfer, we measured the polar angular decay distribution of the outgoing K+K^+ in the channel ϕ→K+K−\phi \to K^+K^- in the ϕ\phi center-of-mass frame (the helicity frame). We find that s-channel helicity conservation (SCHC) holds in the kinematical range where tt-channel exchange dominates (up to −t∌2.5-t \sim 2.5 GeV2^2 for EÎłE_{\gamma}=3.6 GeV). Above this momentum, uu-channel production of a ϕ\phi meson dominates and induces a violation of SCHC. The deduced value of the ϕNN\phi NN coupling constant lies in the upper range of previously reported values.Comment: 6 pages; 5 figure

    Measurement of the xx- and Q2Q^2-Dependence of the Asymmetry A1A_1 on the Nucleon

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    We report results for the virtual photon asymmetry A1A_1 on the nucleon from new Jefferson Lab measurements. The experiment, which used the CEBAF Large Acceptance Spectrometer and longitudinally polarized proton (15^{15}NH3_3) and deuteron (15^{15}ND3_3) targets, collected data with a longitudinally polarized electron beam at energies between 1.6 GeV and 5.7 GeV. In the present paper, we concentrate on our results for A1(x,Q2)A_1(x,Q^2) and the related ratio g1/F1(x,Q2)g_1/F_1(x,Q^2) in the resonance and the deep inelastic regions for our lowest and highest beam energies, covering a range in momentum transfer Q2Q^2 from 0.05 to 5.0 GeV2^2 and in final-state invariant mass WW up to about 3 GeV. Our data show detailed structure in the resonance region, which leads to a strong Q2Q^2--dependence of A1(x,Q2)A_1(x,Q^2) for WW below 2 GeV. At higher WW, a smooth approach to the scaling limit, established by earlier experiments, can be seen, but A1(x,Q2)A_1(x,Q^2) is not strictly Q2Q^2--independent. We add significantly to the world data set at high xx, up to x=0.6x = 0.6. Our data exceed the SU(6)-symmetric quark model expectation for both the proton and the deuteron while being consistent with a negative dd-quark polarization up to our highest xx. This data setshould improve next-to-leading order (NLO) pQCD fits of the parton polarization distributions.Comment: 7 pages LaTeX, 5 figure

    Beam Spin Asymmetries in DVCS with CLAS at 4 .8 GeV

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    We report measurements of the beam spin asymmetry in Deeply Virtual Compton Scattering (DVCS) at an electron beam energy of 4.8 GeV using the CLAS detector at the Thomas Jefferson National Accelerator Facility. The DVCS beam spin asymmetry has been measured in a wide range of kinematics, 1(GeV/c)2^2 <Q2<2.8<Q^2<2.8(GeV/c)2^2, 0.12<xB<0.480.12<x_B<0.48, and 0.1 (GeV/c)2^2 <−t<0.8<-t<0.8(GeV/c)2^2, using the reaction \pEpX. The number of H(e,eâ€ČÎłp)(e,e^{\prime}\gamma p) and H(e,eâ€Čπ0p)(e,e^{\prime}\pi^0 p) events are separated in each (Q2,xB,t)(Q^2,x_B,t) bin by a fit to the line shape of the H(e,eâ€Čp)X(e,e^{\prime}p)X Mx2M_x^2 distribution. The validity of the method was studied in detail using experimental and simulated data. It was shown, that with the achieved missing mass squared resolution and the available statistics, the separation of DVCS-BH and π0\pi^0 events can reliably be done with less than 5% uncertainty. The Q2Q^2- and tt-dependences of the sinâĄÏ•\sin\phi moments of the asymmetry are extracted and compared with theoretical calculations

    The Coupling of Alternative Splicing and Nonsense-Mediated mRNA Decay

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    Most human genes exhibit alternative splicing, but not all alternatively spliced transcripts produce functional proteins. Computational and experimental results indicate that a substantial fraction of alternative splicing events in humans result in mRNA isoforms that harbor a premature termination codon (PTC). These transcripts are predicted to be degraded by the nonsense-mediated mRNA decay (NMD) pathway. One explanation for the abundance of PTC-containing isoforms is that they represent splicing errors that are identified and degraded by the NMD pathway. Another potential explanation for this startling observation is that cells may link alternative splicing and NMD to regulate the abundance of mRNA transcripts. This mechanism, which we call "Regulated Unproductive Splicing and Translation" (RUST), has been experimentally shown to regulate expression of a wide variety of genes in many organisms from yeast to human. It is frequently employed for autoregulation of proteins that affect the splicing process itself. Thus, alternative splicing and NMD act together to play an important role in regulating gene expression
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