6,065 research outputs found

    Data taking strategy for the phase study in ψK+K\psi^{\prime} \to K^+K^-

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    The study of the relative phase between strong and electromagnetic amplitudes is of great importance for understanding the dynamics of charmonium decays. The information of the phase can be obtained model-independently by fitting the scan data of some special decay channels, one of which is ψK+K\psi^{\prime} \to K^{+}K^{-}. To find out the optimal data taking strategy for a scan experiment in the measurement of the phase in ψK+K\psi^{\prime} \to K^{+} K^{-}, the minimization process is analyzed from a theoretical point of view. The result indicates that for one parameter fit, only one data taking point in the vicinity of a resonance peak is sufficient to acquire the optimal precision. Numerical results are obtained by fitting simulated scan data. Besides the results related to the relative phase between strong and electromagnetic amplitudes, the method is extended to analyze the fits of other resonant parameters, such as the mass and the total decay width of ψ\psi^{\prime}.Comment: 13 pages, 7 figure

    Splicing factor Rbm10 facilitates heterochromatin assembly in fission yeast

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    Splicing factors have recently been shown to be involved in heterochromatin formation, but their role in controlling heterochromatin structure and function remains poorly understood. In this study, we identified a fission yeast homologue of human splicing factor RBM10, which has been linked to TARP syndrome. Overexpression of Rbm10 in fission yeast leads to strong global intron retention. Rbm10 also interacts with splicing factors in a pattern resembling that of human RBM10, suggesting that the function of Rbm10 as a splicing regulator is conserved. Surprisingly, our deep-sequencing data showed that deletion of Rbm10 caused only minor effect on genome-wide gene expression and splicing. However, the mutant displays severe heterochromatin defects. Further analyses confirmed that the heterochromatin defects in the mutant did not result from mis-splicing of heterochromatin factors. Our proteomic data revealed that Rbm10 associates with the histone deacetylase Clr6 complex and chromatin remodeling complexes known to be essential for heterochromatin silencing. Our work together with previous findings further suggests that different splicing subunits may play distinct roles in heterochromatin regulation

    Rbm10 facilitates heterochromatin assembly via the Clr6 HDAC complex

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    Splicing factors have recently been shown to be involved in heterochromatin formation, but their role in controlling heterochromatin structure and function remains poorly understood. In this study, we identified a fission yeast homologue of human splicing factor RBM10, which has been linked to TARP syndrome. Overexpression of Rbm10 in fission yeast leads to strong global intron retention. Rbm10 also interacts with splicing factors in a pattern resembling that of human RBM10, suggesting that the function of Rbm10 as a splicing regulator is conserved. Surprisingly, our deep-sequencing data showed that deletion of Rbm10 caused only minor effect on genome-wide gene expression and splicing. However, the mutant displays severe heterochromatin defects. Further analyses indicated that the heterochromatin defects in the mutant did not result from mis-splicing of heterochromatin factors. Our proteomic data revealed that Rbm10 associates with the histone deacetylase Clr6 complex and chromatin remodelers known to be important for heterochromatin silencing. Deletion of Rbm10 results in significant reduction of Clr6 in heterochromatin. Our work together with previous findings further suggests that different splicing subunits may play distinct roles in heterochromatin regulation

    Spin-filtering and charge- and spin-switching effects in a quantum wire with periodically attached stubs

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    Spin-dependent electron transport in a periodically stubbed quantum wire in the presence of Rashba spin-orbit interaction (SOI) is studied via the nonequilibrium Green's function method combined with the Landauer-Buttiker formalism. The coexistence of spin filtering, charge and spin switching are found in the considered system. The mechanism of these transport properties is revealed by analyzing the total charge density and spin-polarized density distributions in the stubbed quantum wire. Furthermore, periodic spin-density islands with high polarization are also found inside the stubs, owing to the interaction between the charge density islands and the Rashba SOI-induced effective magnetic field. The proposed nanostructure may be utilized to devise an all-electrical multifunctional spintronic device.Comment: 4 pages, 4 figure

    Search for D to phi l nu and measurement of the branching fraction for D to phi pi

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    Using a data sample of integrated luminosity of about 33 pb1^{-1} collected around 3.773 GeV with the BESII detector at the BEPC collider, the semileptonic decays D+ϕe+νeD^+ \to \phi e ^+\nu_e, D+ϕμ+νμD^+ \to \phi \mu^+\nu_\mu and the hadronic decay D+ϕπ+D^+ \to \phi \pi^+ are studied. The upper limits of the branching fractions are set to be BF(D+ϕe+νe)<BF(D^+ \to \phi e ^+\nu_e) < 2.01% and BF(D+ϕμ+νμ)<BF(D^+ \to \phi \mu^+ \nu_\mu) < 2.04% at the 90% confidence level. The ratio of the branching fractions for D+ϕπ+D^+ \to \phi \pi^+ relative to D+Kπ+π+D^+ \to K^-\pi^+\pi^+ is measured to be 0.057±0.011±0.0030.057 \pm 0.011 \pm 0.003. In addition, the branching fraction for D+ϕπ+D^+ \to \phi \pi^+ is obtained to be (5.2±1.0±0.4)×103(5.2 \pm 1.0 \pm 0.4) \times 10^{-3}.Comment: 6 pages, 5 figures, to be published in Eur.Phys.J.

    Measurement of the chi_{c2} Polarization in psi(2S) to gamma chi_{c2}

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    The polarization of the chi_{c2} produced in psi(2S) decays into gamma chi_{c2} is measured using a sample of 14*10^6 psi(2S) events collected by BESII at the BEPC. A fit to the chi_{c2} production and decay angular distributions in psi(2S) to gamma chi_{c2}, chi_{c2} to pi pi and KK yields values x=A_1/A_0=2.08+/-0.44 and y=A_2/A_0=3.03 +/-0.66, with a correlation rho=0.92 between them, where A_{0,1,2} are the chi_{c2} helicity amplitudes. The measurement agrees with a pure E1 transition, and M2 and E3 contributions do not differ significantly from zero.Comment: 6 pages, 4 figures, 1 tabl

    Search for psi(3770)\ra\rho\pi at the BESII detector at the Beijing Electron-Positron Collider

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    Non-DDˉD\bar{D} decay \psppto \rhopi is searched for using a data sample of (17.3±0.5)pb1(17.3\pm 0.5) pb^{-1} taken at the center-of-mass energy of 3.773 GeV by the BESII detector at the BEPC. No \rhopi signal is observed, and the upper limit of the cross section is measured to be \sigma(\EETO \rhopi)<6.0 pb at 90% C. L. Considering the interference between the continuum amplitude and the \pspp resonance amplitude, the branching fraction of \pspp decays to ρπ\rho\pi is determined to be \BR(\pspp\ra\rho\pi)\in(6.0\times10^{-6}, 2.4\times10^{-3}) at 90% C. L. This is in agreement with the prediction of the SS- and DD-wave mixing scheme of the charmonium states for solving the ``\rhopi puzzle'' between \jpsi and \psp decays.Comment: 15 pages, 5 figure

    Measurement of the branching fractions of psi(2S) -> 3(pi+pi-) and J/psi -> 2(pi+pi-)

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    Using data samples collected at sqrt(s) = 3.686GeV and 3.650GeV by the BESII detector at the BEPC, the branching fraction of psi(2S) -> 3(pi+pi-) is measured to be [4.83 +- 0.38(stat) +- 0.69(syst)] x 10^-4, and the relative branching fraction of J/psi -> 2(pi+pi-) to that of J/psi -> mu+mu- is measured to be [5.86 +- 0.19(stat) +- 0.39(syst)]% via psi(2S) -> (pi+pi-)J/psi, J/psi -> 2(pi+pi-). The electromagnetic form factor of 3(pi+pi-) is determined to be 0.21 +- 0.02 and 0.20 +- 0.01 at sqrt(s) = 3.686GeV and 3.650GeV, respectively.Comment: 17pages, 7 figures, submitted to Phys. Rev.
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