43,491 research outputs found

    Quantitative single-cell splicing analysis reveals an ‘economy of scale’ filter for gene expression

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    In eukaryotic cells, splicing affects the fate of each pre-mRNA transcript, helping to determine whether it is ultimately processed into an mRNA, or degraded. The efficiency of splicing plays a key role in gene expression. However, because it depends on the levels of multiple isoforms at the same transcriptional active site (TAS) in the same cell, splicing efficiency has been challenging to measure. Here, we introduce a quantitative single-molecule FISH-based method that enables determination of the absolute abundances of distinct RNA isoforms at individual TASs. Using this method, we discovered that splicing efficiency behaves in an unexpected ‘economy of scale’ manner, increasing, rather than decreasing, with gene expression levels, opposite to a standard enzymatic process. This behavior could result from an observed correlation between splicing efficiency and spatial proximity to nuclear speckles. Economy of scale splicing represents a non-linear filter that amplifies the expression of genes when they are more strongly transcribed. This method will help to reveal the roles of splicing in the quantitative control of gene expression

    Weight function for the quantum affine algebra Uq(sl^3)U_q(\hat{sl}_3)

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    We give a precise expression for the universal weight function of the quantum affine algebra Uq(sl^3)U_q(\hat{sl}_3). The calculations use the technique of projecting products of Drinfeld currents on the intersections of Borel subalgebras.Comment: 28 page

    Bound States of the Heavy Flavor Vector Mesons and Y(4008) and Z1+(4050)Z^{+}_1(4050)

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    The DDˉD^{*}\bar{D}^{*} and BBˉB^{*}\bar{B}^{*} systems are studied dynamically in the one boson exchange model, where π\pi, η\eta, σ\sigma, ρ\rho and ω\omega exchanges are taken into account. Ten allowed states with low spin parity are considered. We suggest that the 11^{--}, 2++2^{++}, 0++0^{++} and 0+0^{-+} BBˉB^{*}\bar{B}^{*} molecules should exist, and the DDˉD^{*}\bar{D}^{*} bound states with the same quantum numbers very likely exist as well. However, the CP exotic (1+1^{-+}, 2+2^{+-}) BBˉB^{*}\bar{B}^{*} and DDˉD^{*}\bar{D}^{*} states may not be bound by the one boson exchange potential. We find that the I=0 configuration is more deeply bound than the I=1 configuration, hence Z1+(4050)Z^{+}_1(4050) may not be a DDˉD^{*}\bar{D}^{*} molecule. Although Y(4008) is close to the DDˉD^{*}\bar{D}^{*} threshold, the interpretation of Y(4008) as a DDˉD^{*}\bar{D}^{*} molecule is not favored by its huge width. 11^{--} DDˉD^{*}\bar{D}^{*} and BBˉB^{*}\bar{B}^{*} states can be produced copiously in e+ee^{+}e^{-} annihilation, detailed scanning of the e+ee^{+}e^{-} annihilation data near the DDˉD^{*}\bar{D}^{*} and BBˉB^{*}\bar{B}^{*} threshold is an important check to our predictions.Comment: 17 pages,6 figur

    Manin-Olshansky triples for Lie superalgebras

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    Following V. Drinfeld and G. Olshansky, we construct Manin triples (\fg, \fa, \fa^*) such that \fg is different from Drinfeld's doubles of \fa for several series of Lie superalgebras \fa which have no even invariant bilinear form (periplectic, Poisson and contact) and for a remarkable exception. Straightforward superization of suitable Etingof--Kazhdan's results guarantee then the uniqueness of qq-quantization of our Lie bialgebras. Our examples give solutions to the quantum Yang-Baxter equation in the cases when the classical YB equation has no solutions. To find explicit solutions is a separate (open) problem. It is also an open problem to list (\`a la Belavin-Drinfeld) all solutions of the {\it classical} YB equation for the Poisson superalgebras \fpo(0|2n) and the exceptional Lie superalgebra \fk(1|6) which has a Killing-like supersymmetric bilinear form but no Cartan matrix

    Finite-horizon H∞ control for discrete time-varying systems with randomly occurring nonlinearities and fading measurements

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    This technical note deals with the H∞ control problem for a class of discrete time-varying nonlinear systems with both randomly occurring nonlinearities and fading measurements over a finite-horizon. The system measurements are transmitted through fading channels described by a modified stochastic Rice fading model. The purpose of the addressed problem is to design a set of time-varying controllers such that, in the presence of channel fading and randomly occurring nonlinearities, the H∞ performance is guaranteed over a given finite-horizon. The model transformation technique is first employed to simplify the addressed problem, and then the stochastic analysis in combination with the completing squares method are carried out to obtain necessary and sufficient conditions of an auxiliary index which is closely related to the finite-horizon H∞ performance. Moreover, the time-varying controller parameters are characterized via solving coupled backward recursive Riccati difference equations (RDEs). A simulation example is utilized to illustrate the usefulness of the proposed controller design scheme

    Efficient equilibrium sampling of all-atom peptides using library-based Monte Carlo

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    We applied our previously developed library-based Monte Carlo (LBMC) to equilibrium sampling of several implicitly solvated all-atom peptides. LBMC can perform equilibrium sampling of molecules using the pre-calculated statistical libraries of molecular-fragment configurations and energies. For this study, we employed residue-based fragments distributed according to the Boltzmann factor of the OPLS-AA forcefield describing the individual fragments. Two solvent models were employed: a simple uniform dielectric and the Generalized Born/Surface Area (GBSA) model. The efficiency of LBMC was compared to standard Langevin dynamics (LD) using three different statistical tools. The statistical analyses indicate that LBMC is more than 100 times faster than LD not only for the simple solvent model but also for GBSA.Comment: 5 figure
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