Estado del arte sobre la investigación en identidad organizacional

Working Paper del Departamento de Organización de Empreses de la Universitat Politècnica de Catalunya sobre la investigación en identidad organizacional.El estado del arte es una forma de aludir a lo que se sabe sobre una materia, lo que se ha dicho hasta el momento que ha sido más relevante. En este sentido la pretensión de este documento es situar al lector interesado en cuál es la situación de conocimiento actual sobre la identidad organizacional. Esta materia ha ido tomando relevancia en la investigación científica sobre dirección de empresas en los últimos años. De hecho, la identidad organizacional se ha revelado como un activo intangible de gran influencia en las organizaciones, hasta tal punto que su errónea evaluación o tratamiento puede conllevar graves repercusiones para la organización, incluso su desaparición. La identidad organizacional ha adquirido el interés científico, si bien los investigadores más relevantes en esta materia coinciden en que los trabajos de investigación no han alcanzado su culminación, más bien se encuentran en fases iniciales y animan a continuar investigando en este área de conocimiento.Preprin

Protein coding potential of retroviruses and other transposable elements in vertebrate genomes

We suggest an annotation strategy for genes encoded by retroviruses and transposable elements (RETRA genes) based on a set of marker protein domains. Usually RETRA genes are masked in vertebrate genomes prior to the application of automated gene prediction pipelines under the assumption that they provide no selective advantage to the host. Yet, we show that about 1000 genes in four vertebrate gene sets analyzed contain at least one RETRA gene marker domain. Using the conservation of genomic neighborhood (synteny), we were able to discriminate between RETRA genes with putative functionality in the vertebrates and those that probably function only in the context of mobile elements. We identified 35 such genes in human, along with their corresponding mouse and rat orthologs; which included almost all known human genes with similarity to mobile elements. The results also imply that the vast majority of the remaining RETRA genes in current gene sets are unlikely to encode vertebrate functions. To automatically annotate RETRA genes in other vertebrate genomes, we provide as a tool a set of marker protein domains and a manually refined list of domesticated or ancestral RETRA genes for rescuing genes with vertebrate functions

Triangular Gross-Pitaevskii breathers and Damski-Chandrasekhar shock waves

The recently proposed map [arXiv:2011.01415] between the hydrodynamic equations governing the two-dimensional triangular cold-bosonic breathers [Phys. Rev. X 9, 021035 (2019)] and the high-density zero-temperature triangular free-fermionic clouds, both trapped harmonically, perfectly explains the former phenomenon but leaves uninterpreted the nature of the initial ($t=0$) singularity. This singularity is a density discontinuity that leads, in the bosonic case, to an infinite force at the cloud edge. The map itself becomes invalid at times $t<0$. A similar singularity appears at $t = T/4$, where $T$ is the period of the harmonic trap, with the Fermi-Bose map becoming invalid at $t > T/4$. Here, we first map -- using the scale invariance of the problem -- the trapped motion to an untrapped one. Then we show that in the new representation, the solution [arXiv:2011.01415] becomes, along a ray in the direction normal to one of the three edges of the initial cloud, a freely propagating one-dimensional shock wave of a class proposed by Damski in [Phys. Rev. A 69, 043610 (2004)]. There, for a broad class of initial conditions, the one-dimensional hydrodynamic equations can be mapped to the inviscid Burgers' equation, a nonlinear transport equation. More specifically, under the Damski map, the $t=0$ singularity of the original problem becomes, verbatim, the initial condition for the wave catastrophe solution found by Chandrasekhar in 1943 [Ballistic Research Laboratory Report No. 423 (1943)]. At $t=T/8$, our interpretation ceases to exist: at this instance, all three effectively one-dimensional shock waves emanating from each of the three sides of the initial triangle collide at the origin, and the 2D-1D correspondence between the solution of [arXiv:2011.01415] and the Damski-Chandrasekhar shock wave becomes invalid.Comment: 13 pages, 2 figures. Submission to SciPos

dReDBox: Materializing a full-stack rack-scale system prototype of a next-generation disaggregated datacenter

Current datacenters are based on server machines, whose mainboard and hardware components form the baseline, monolithic building block that the rest of the system software, middleware and application stack are built upon. This leads to the following limitations: (a) resource proportionality of a multi-tray system is bounded by the basic building block (mainboard), (b) resource allocation to processes or virtual machines (VMs) is bounded by the available resources within the boundary of the mainboard, leading to spare resource fragmentation and inefficiencies, and (c) upgrades must be applied to each and every server even when only a specific component needs to be upgraded. The dRedBox project (Disaggregated Recursive Datacentre-in-a-Box) addresses the above limitations, and proposes the next generation, low-power, across form-factor datacenters, departing from the paradigm of the mainboard-as-a-unit and enabling the creation of function-block-as-a-unit. Hardware-level disaggregation and software-defined wiring of resources is supported by a full-fledged Type-1 hypervisor that can execute commodity virtual machines, which communicate over a low-latency and high-throughput software-defined optical network. To evaluate its novel approach, dRedBox will demonstrate application execution in the domains of network functions virtualization, infrastructure analytics, and real-time video surveillance.This work has been supported in part by EU H2020 ICTproject dRedBox, contract #687632.Peer ReviewedPostprint (author's final draft

Implementation of PRRSV status classification system in swine breeding herds from a large integrated group in Spain

Background: Porcine Reproductive and Respiratory Syndrome (PRRS) is an endemic swine disease causing significant productive and economic losses. Knowledge of PRRS epidemiology is crucial to develop control strategies against this disease. In that regard, classifying farms according to PRRS virus (PRRSV) shedding and exposure, and understanding key drivers of change in status over time, provides great applied knowledge for developing disease control programs. In most European countries, PRRSV monitoring is performed most frequently at the individual farm level although criteria selected for monitoring varies among different regions and farms. The aim of this study was to implement a systematic monitoring program for PRRSV in Spanish sow farms. Breeding herds were classified according to a standardized PRRSV infection status using sampling programs and terminology currently adopted in the United States (US), which allowed an evaluation of PRRSV epidemiology in a large integrated Spanish group during a one-year study period (February 2017–March 2018). Results: Fifteen farms achieved a stable PRRSV status after the first 4 consecutive samplings and 20 farms were classified as unstable. One of the farms maintained a stable status throughout the duration of the whole monitoring period. Among the 20 farms classified as unstable at the beginning of the monitoring protocol, 9 farms (45%) never reached the stable status and 11 farms (55%) reached stable status afterwards during the monitoring study period. From PRRSV PCR positive pools, there were 47 different PRRSV nucleotide sequences from 24 different farms. More than one PRRSV sequence was obtained from 15 farms. In the farms with more than one sequence detected, we observed recirculation of the same PRRSV field strain in 7 farms and introduction of a different PRRSV strain in 5 farms and both events in 3 farms. Conclusions: Systematic monitoring for PRRSV in breeding herds established a basis of knowledge of PRRSV epidemiology at the farm level and provided key data to classify farms according to PRRSV exposure and shedding status. These data allow further evaluation of the impact of the PRRSV farm status on production and economic performance in breeding herds and additional investigation of factors related to PRRSV epidemiology

The catalytic subunit of the system L1 amino acid transporter (S<i>lc7a5</i>) facilitates nutrient signalling in mouse skeletal muscle

The System L1-type amino acid transporter mediates transport of large neutral amino acids (LNAA) in many mammalian cell-types. LNAA such as leucine are required for full activation of the mTOR-S6K signalling pathway promoting protein synthesis and cell growth. The SLC7A5 (LAT1) catalytic subunit of high-affinity System L1 functions as a glycoprotein-associated heterodimer with the multifunctional protein SLC3A2 (CD98). We generated a floxed Slc7a5 mouse strain which, when crossed with mice expressing Cre driven by a global promoter, produced Slc7a5 heterozygous knockout (Slc7a5+/-) animals with no overt phenotype, although homozygous global knockout of Slc7a5 was embryonically lethal. Muscle-specific (MCK Cre-mediated) Slc7a5 knockout (MS-Slc7a5-KO) mice were used to study the role of intracellular LNAA delivery by the SLC7A5 transporter for mTOR-S6K pathway activation in skeletal muscle. Activation of muscle mTOR-S6K (Thr389 phosphorylation) in vivo by intraperitoneal leucine injection was blunted in homozygous MS-Slc7a5-KO mice relative to wild-type animals. Dietary intake and growth rate were similar for MS-Slc7a5-KO mice and wild-type littermates fed for 10 weeks (to age 120 days) with diets containing 10%, 20% or 30% of protein. In MS-Slc7a5-KO mice, Leu and Ile concentrations in gastrocnemius muscle were reduced by ∼40% as dietary protein content was reduced from 30 to 10%. These changes were associated with >50% decrease in S6K Thr389 phosphorylation in muscles from MS-Slc7a5-KO mice, indicating reduced mTOR-S6K pathway activation, despite no significant differences in lean tissue mass between groups on the same diet. MS-Slc7a5-KO mice on 30% protein diet exhibited mild insulin resistance (e.g. reduced glucose clearance, larger gonadal adipose depots) relative to control animals. Thus, SLC7A5 modulates LNAA-dependent muscle mTOR-S6K signalling in mice, although it appears non-essential (or is sufficiently compensated by e.g. SLC7A8 (LAT2)) for maintenance of normal muscle mass

Towards Whole Placenta Segmentation At Late Gestation Using Multi-View Ultrasound Images

We propose a method to extract the human placenta at late gestation using multi-view 3D US images. This is the first step towards automatic quantification of placental volume and morphology from US images along the whole pregnancy beyond early stages (where the entire placenta can be captured with a single 3D US image). Our method uses 3D US images from different views acquired with a multi-probe system. A whole placenta segmentation is obtained from these images by using a novel technique based on 3D convolutional neural networks. We demonstrate the performance of our method on 3D US images of the placenta in the last trimester. We achieve a high Dice overlap of up to 0.8 with respect to manual annotations, and the derived placental volumes are comparable to corresponding volumes extracted from MR.Wellcome Trust IEH Award; EPSRC Centre for Medical Engineering; National Institute for Health Research (NIHR); King’s College London; NHS Foundation Trus

CD98hc facilitates B cell proliferation and adaptive humoral immunity.

The proliferation of antigen-specific lymphocytes and resulting clonal expansion are essential for adaptive immunity. We report here that B cell-specific deletion of the heavy chain of CD98 (CD98hc) resulted in lower antibody responses due to total suppression of B cell proliferation and subsequent plasma cell formation. Deletion of CD98hc did not impair early B cell activation but did inhibit later activation of the mitogen-activated protein kinase Erk1/2 and downregulation of the cell cycle inhibitor p27. Reconstitution of CD98hc-deficient B cells with CD98hc mutants showed that the integrin-binding domain of CD98hc was required for B cell proliferation but that the amino acid-transport function of CD98hc was dispensable for this. Thus, CD98hc supports integrin-dependent rapid proliferation of B cells. We propose that the advantage of adaptive immunity favored the appearance of CD98hc in vertebrates