7,448 research outputs found
A New Scintillator Tile/Fiber Preshower Detector for the CDF Central Calorimeter
A detector designed to measure early particle showers has been installed in
front of the central CDF calorimeter at the Tevatron. This new preshower
detector is based on scintillator tiles coupled to wavelength-shifting fibers
read out by multi-anode photomultipliers and has a total of 3,072 readout
channels. The replacement of the old gas detector was required due to an
expected increase in instantaneous luminosity of the Tevatron collider in the
next few years. Calorimeter coverage, jet energy resolution, and electron and
photon identification are among the expected improvements. The final detector
design, together with the R&D studies that led to the choice of scintillator
and fiber, mechanical assembly, and quality control are presented. The detector
was installed in the fall 2004 Tevatron shutdown and started collecting
colliding beam data by the end of the same year. First measurements indicate a
light yield of 12 photoelectrons/MIP, a more than two-fold increase over the
design goals.Comment: 5 pages, 10 figures (changes are minor; this is the final version
published in IEEE-Trans.Nucl.Sci.
HMGA1 Modulates Gene Transcription Sustaining a Tumor Signalling Pathway Acting on the Epigenetic Status of Triple-Negative Breast Cancer Cells
Chromatin accessibility plays a critical factor in regulating gene expression in cancer cells. Several factors, including the High Mobility Group A (HMGA) family members, are known to participate directly in chromatin relaxation and transcriptional activation. The HMGA1 oncogene encodes an architectural chromatin transcription factor that alters DNA structure and interacts with transcription factors favouring their landing onto transcription regulatory sequences. Here, we provide evidence of an additional mechanism exploited by HMGA1 to modulate transcription. We demonstrate that, in a triple-negative breast cancer cellular model, HMGA1 sustains the action of epigenetic modifiers and in particular it positively influences both histone H3S10 phosphorylation by ribosomal protein S6 kinase alpha-3 (RSK2) and histone H2BK5 acetylation by CREB-binding protein (CBP). HMGA1, RSK2, and CBP control the expression of a set of genes involved in tumor progression and epithelial to mesenchymal transition. These results suggest that HMGA1 has an effect on the epigenetic status of cancer cells and that it could be exploited as a responsiveness predictor for epigenetic therapies in triple-negative breast cancers
Three-Body Dynamics and Self-Powering of an Electrodynamic Tether in a Plasmasphere
The dynamics of an electrodynamic tether in a three-body gravitational environment are investigated. In the classical two-body scenario the extraction of power is at the expense of orbital kinetic energy. As a result of power extraction, an electrodynamic tether satellite system loses altitude and deorbits. This concept has been proposed and well investigated in the past, for example for orbital debris mitigation and spent stages reentry. On the other hand, in the three-body scenario an electrodynamic tether can be placed in an equilibrium position fixed with respect to the two primary bodies without deorbiting, and at the same time generate power for onboard use. The appearance of new equilibrium positions in the perturbed three-body problem allow this to happen as the electrical power is extracted at the expenses of the plasma corotating with the primary body. Fundamental differences between the classical twobody dynamics and the new phenomena appearing in the circular restricted three-body problem perturbed by the electrodynamic force of the electrodynamic tether are shown in the paper. An interesting application of an electrodynamic tether placed in the Jupiter plasma torus is then considered, in which the electrodynamic tether generates useful electrical power of about 1 kW with a 20-km-long electrodynamic tether from the environmental plasma without losing orbital energy
The High Mobility Group A1 (HMGA1) Chromatin Architectural Factor Modulates Nuclear Stiffness in Breast Cancer Cells
13siPlasticity is an essential condition for cancer cells to invade surrounding tissues. The nucleus is the most rigid cellular organelle and it undergoes substantial deformations to get through environmental constrictions. Nuclear stiffness mostly depends on the nuclear lamina and chromatin, which in turn might be affected by nuclear architectural proteins. Among these is the HMGA1 (High Mobility Group A1) protein, a factor that plays a causal role in neoplastic transformation and that is able to disentangle heterochromatic domains by H1 displacement. Here we made use of atomic force microscopy to analyze the stiffness of breast cancer cellular models in which we modulated HMGA1 expression to investigate its role in regulating nuclear plasticity. Since histone H1 is the main modulator of chromatin structure and HMGA1 is a well-established histone H1 competitor, we correlated HMGA1 expression and cellular stiffness with histone H1 expression level, post-translational modifications, and nuclear distribution. Our results showed that HMGA1 expression level correlates with nuclear stiffness, is associated to histone H1 phosphorylation status, and alters both histone H1 chromatin distribution and expression. These data suggest that HMGA1 might promote chromatin relaxation through a histone H1-mediated mechanism strongly impacting on the invasiveness of cancer cells-openopenSenigagliesi B, Penzo C, Severino LU, Maraspini R, Petrosino S, Morales-Navarrete H, Pobega E, Ambrosetti E, Parisse P, Pegoraro S, Manfioletti G, Casalis L, Sgarra RSenigagliesi, Beatrice; Penzo, C; Severino, Lu; Maraspini, R; Petrosino, Sara; Morales-Navarrete, H; Pobega, E; Ambrosetti, E; Parisse, P; Pegoraro, S; Manfioletti, G; Casalis, L; Sgarra,
Forward Neutron Production at the Fermilab Main Injector
We have measured cross sections for forward neutron production from a variety
of targets using proton beams from the Fermilab Main Injector. Measurements
were performed for proton beam momenta of 58 GeV/c, 84 GeV/c, and 120 GeV/c.
The cross section dependence on the atomic weight (A) of the targets was found
to vary as where is for a beam momentum of
58 GeV/c and 0.540.05 for 120 GeV/c. The cross sections show reasonable
agreement with FLUKA and DPMJET Monte Carlos. Comparisons have also been made
with the LAQGSM Monte Carlo.Comment: Accepted for publication in Physical Review D. This version
incorporates small changes suggested by referee and small corrections in the
neutron production cross sections predicted by FLUK
Human dyskerin binds to cytoplasmic H/ACA-box-containing transcripts affecting nuclear hormone receptor dependence
Background Dyskerin is a nuclear protein involved in H/ACA box snoRNA-guided uridine modification of RNA. In humans, its defective function is associated with cancer development and induces specific post-transcriptional alterations of gene expression. In this study, we seek to unbiasedly identify mRNAs regulated by dyskerin in human breast cancer-derived cells. Results We find that dyskerin depletion affects the expression and the association with polysomes of selected mRNA isoforms characterized by the retention of H/ACA box snoRNA-containing introns. These snoRNA retaining transcripts (snoRTs) are bound by dyskerin in the cytoplasm in the form of shorter 3 ' snoRT fragments. We then characterize the whole cytoplasmic dyskerin RNA interactome and find both H/ACA box snoRTs and protein-coding transcripts which may be targeted by the snoRTs' guide properties. Since a fraction of these protein-coding transcripts is involved in the nuclear hormone receptor binding, we test to see if this specific activity is affected by dyskerin. Obtained results indicate that dyskerin dysregulation may alter the dependence on nuclear hormone receptor ligands in breast cancer cells. These results are paralleled by consistent observations on the outcome of primary breast cancer patients stratified according to their tumor hormonal status. Accordingly, experiments in nude mice show that the reduction of dyskerin levels in estrogen-dependent cells favors xenograft development in the absence of estrogen supplementation. Conclusions Our work suggests a cytoplasmic function for dyskerin which could affect mRNA post-transcriptional networks relevant for nuclear hormone receptor functions
Measurement of Charged Pion Production Yields off the NuMI Target
The fixed-target MIPP experiment, Fermilab E907, was designed to measure the
production of hadrons from the collisions of hadrons of momenta ranging from 5
to 120 GeV/c on a variety of nuclei. These data will generally improve the
simulation of particle detectors and predictions of particle beam fluxes at
accelerators. The spectrometer momentum resolution is between 3 and 4%, and
particle identification is performed for particles ranging between 0.3 and 80
GeV/c using , time-of-flight and Cherenkov radiation measurements. MIPP
collected events of 120 GeV Main Injector protons striking a
target used in the NuMI facility at Fermilab. The data have been analyzed and
we present here charged pion yields per proton-on-target determined in bins of
longitudinal and transverse momentum between 0.5 and 80 GeV/c, with combined
statistical and systematic relative uncertainties between 5 and 10%.Comment: 15 pages, 13 figure
Spin-Splitter Studies: Polarization Stability Measurements at IUCF
This research was sponsored by the National Science Foundation Grant NSF PHY-931478
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