TeV-Scale Horizontal Symmetry and the Slepton Mass Problem of Anomaly Mediation

We propose a new scenario for solving the tachyonic slepton mass problem of anomaly mediated supersymmetry breaking models with a non-Abelian horizontal gauge symmetry broken at the TeV scale. A specific model based on SU(3)_{H} horizontal symmetry is presented wherein the sleptons receive positive mass-squared from the asymptotically free SU(3)_{H} gauge sector. Approximate global symmetries present in the model strongly suppress flavor changing processes induced by the horizontal vector gauge bosons. The model predicts m_{h} < 120 GeV for the lightest Higgs boson mass, tan{beta} nearly equal to 4, and M_V = 1-4 TeV for the SU(3)_{H} gauge boson masses. The lightest SUSY particle is found to be the neutral Wino, which is a candidate for cold dark matter.Comment: 25 pages in LaTeX, 2 eps figure

Constraining Z' From Supersymmetry Breaking

We suggest and analyze a class of supersymmetric Z' models based on the gauge symmetry U(1)_x = x Y - (B-L), where Y is the Standard Model hypercharge. For 1 < x < 2, the U(1)_x D-term generates positive contributions to the slepton masses, which is shown to solve the tachyonic slepton problem of anomaly mediated supersymmetry breaking (AMSB). The resulting models are very predictive, both in the SUSY breaking sector and in the Z' sector. We find M_Z' = (2-4) TeV and the Z-Z' mixing angle \xi = 0.001. Consistency with symmetry breaking and AMSB phenomenology renders the Z' "leptophobic", with Br(Z' -> e^+ e^-) = (1-1.6)% and Br(Z' -> q q-bar) = 44%. The lightest SUSY particle is either the neutral Wino or the sneutrino in these models.Comment: 34 pages in LaTe

Berry Curvature in Graphene: A New Approach

In the present paper we have directly computed the Berry curvature terms relevant for Graphene in the presence of an \textit{inhomogeneous} lattice distortion. We have employed the generalized Foldy Wouthuysen framework, developed by some of us \cite{ber0,ber1,ber2}. We show that a non-constant lattice distortion leads to a valley-orbit coupling which is responsible to a valley-Hall effect. This is similar to the valley-Hall effect induced by an electric field proposed in \cite{niu2} and is the analogue of the spin-Hall effect in semiconductors \cite{MURAKAMI, SINOVA}. Our general expressions for Berry curvature, for the special case of homogeneous distortion, reduce to the previously obtained results \cite{niu2}. We also discuss the Berry phase in the quantization of cyclotron motion.Comment: Slightly modified version, to appear in EPJ

Anomalous U(1) symmetry and lepton flavor violation

We show that in a large class of models based on anomalous U(1) symmetry which addresses the fermion mass hierarchy problem, leptonic flavor changing processes are induced that are in the experimentally interesting range. The flavor violation occurs through the renormalization group evolution of the soft SUSY breaking parameters between the string scale and the U(1)_A breaking scale. We derive general expressions for the evolution of these parameters in the presence of higher dimensional operators. Several sources for the flavor violation are identified: flavor-dependent contributions to the soft masses from the U(1)_A gaugino, scalar mass corrections proportional to the trace of U(1)_A charge, non-proportional A-terms from vertex corrections, and the U(1)_A D-term. Quantitative estimates for the decays \mu -> e \gamma and \tau -> \mu \gamma are presented in supergravity models which accommodate the relic abundance of neutralino dark matter.Comment: References added, typos corrected, 28 pages LaTeX, includes 14 eps figure

Salerno's model of DNA reanalysed: could solitons have biological significance?

We investigate the sequence-dependent behaviour of localised excitations in a toy, nonlinear model of DNA base-pair opening originally proposed by Salerno. Specifically we ask whether ``breather'' solitons could play a role in the facilitated location of promoters by RNA polymerase. In an effective potential formalism, we find excellent correlation between potential minima and {\em Escherichia coli} promoter recognition sites in the T7 bacteriophage genome. Evidence for a similar relationship between phage promoters and downstream coding regions is found and alternative reasons for links between AT richness and transcriptionally-significant sites are discussed. Consideration of the soliton energy of translocation provides a novel dynamical picture of sliding: steep potential gradients correspond to deterministic motion, while ``flat'' regions, corresponding to homogeneous AT or GC content, are governed by random, thermal motion. Finally we demonstrate an interesting equivalence between planar, breather solitons and the helical motion of a sliding protein ``particle'' about a bent DNA axis.Comment: Latex file 20 pages, 5 figures. Manuscript of paper to appear in J. Biol. Phys., accepted 02/09/0

Determination of |Vcb| using the semileptonic decay \bar{B}^0 --> D^{*+}e^-\bar{\nu}

We present a measurement of the Cabibbo-Kobayashi-Maskawa (CKM) matrix element |Vcb| using a 10.2 fb^{-1} data sample recorded at the \Upsilon(4S) resonance with the Belle detector at the KEKB asymmetric e^+e^- storage ring. By extrapolating the differential decay width of the \bar{B}^0 --> D^{*+}e^-\bar{\nu} decay to the kinematic limit at which the D^{*+} is at rest with respect to the \bar{B}^0, we extract the product of |Vcb| with the normalization of the decay form factor F(1), |Vcb |F(1)= (3.54+/-0.19+/-0.18)x10^{-2}, where the first error is statistical and the second is systematic. A value of |Vcb| = (3.88+/-0.21+/-0.20+/-0.19)x10^{-2} is obtained using a theoretical calculation of F(1), where the third error is due to the theoretical uncertainty in the value of F(1). The branching fraction B(\bar{B}^0 --> D^{*+}e^-\bar{\nu}) is measured to be (4.59+/-0.23+/-0.40)x10^{-2}.Comment: 20 pages, 6 figures, elsart.cls, submitted to PL

Molecular basis of microhomology-mediated end-joining by purified full-length Polθ

DNA polymerase θ (Polθ) is a unique polymerase-helicase fusion protein that promotes microhomology-mediated end-joining (MMEJ) of DNA double-strand breaks (DSBs). How full-length human Polθ performs MMEJ at the molecular level remains unknown. Using a biochemical approach, we find that the helicase is essential for Polθ MMEJ of long ssDNA overhangs which model resected DSBs. Remarkably, Polθ MMEJ of ssDNA overhangs requires polymerase-helicase attachment, but not the disordered central domain, and occurs independently of helicase ATPase activity. Using single-particle microscopy and biophysical methods, we find that polymerase-helicase attachment promotes multimeric gel-like Polθ complexes that facilitate DNA accumulation, DNA synapsis, and MMEJ. We further find that the central domain regulates Polθ multimerization and governs its DNA substrate requirements for MMEJ. These studies identify unexpected functions for the helicase and central domain and demonstrate the importance of polymerase-helicase tethering in MMEJ and the structural organization of Polθ