3,226 research outputs found
p120 catenin is required for the stress response in Drosophila
p120ctn is a ubiquitously expressed core component of cadherin junctions and essential for vertebrate development. Surprisingly, Drosophila p120ctn (dp120ctn) is dispensable for adherens junctions and development, which has discouraged Drosophila researchers from further pursuing the biological role of dp120ctn. Here we demonstrate that dp120ctn loss results in increased heat shock sensitivity and reduced animal lifespan, which are completely rescued by ectopic expression of a dp120ctn-GFP transgene. Transcriptomic analysis revealed multiple relish/NF-κB target genes differentially expressed upon loss of dp120ctn. Importantly, this aberrant gene expression was rescued by overexpression of dp120ctn-GFP or heterozygosity for relish. Our results uncover a novel role for dp120ctn in the regulation of animal stress response and immune signalling. This may represent an ancient role of p120ctn and can influence further studies in Drosophila and mammals
On the Singular Scheme of Split Foliations
We prove that the tangent sheaf of a codimension one locally free
distribution splits as a sum of line bundles if and only if its singular scheme
is arithmetically Cohen-Macaulay. In addition, we show that a foliation by
curves is given by an intersection of generically transversal holomorphic
distributions of codimension one if and only if its singular scheme is
arithmetically Buchsbaum. Finally, we establish that these foliations are
determined by their singular schemes, and deduce that the Hilbert scheme of
certain arithmetically Buchsbaum schemes of codimension is birational to a
Grassmannian.Comment: 21 page
Comparison of the AQO and the QAOA for the vertex coloring problem
Treballs Finals de Grau de Física, Facultat de Física, Universitat de Barcelona, Curs: 2023, Tutors: Marta P. Estarellas, Jordi Riu, Lluís GarridoWe benchmark the time resources needed to execute the adiabatic quantum optimization (AQO), and to run the Quantum Approximate Optimization Algorithm (QAOA), for the vertex coloring problem. This is done via a numerical simulation of 20 Erd˝os-R´eny random graphs for different cases ranging from 8 to 21 qubits. With this comparison, we explore two of the most important algorithms of the analog and gate-based quantum computing paradigms, respectively. We apply the canonical implementation for both algorithms, so their initial Hamiltonian is the same, the one with the typical sum of Pauli-X matrices. In this line, we consider linear scheduling time for the AQO. For final adiabatic time T = 100 ns, the AQO achieves an overlap with the degenerate solutions over 0.9 in all cases. Meanwhile, the QAOA using the Powell classical optimizer, 5 layers and thousands of iterations has an overlap around 0.5 for the 8 qubits case and below 0.25 for the other cases. So, our results for the given task and idealized conditions indicate that the AQO significantly outperforms
the QAOA in terms of time and success probabilit
Brain network alterations in Attention-Deficit and Hyperactivity Disorder: towards an integrative perspective based on systems neuroscience
Mención Internacional en el título de doctorAttention-Deficit and Hyperactivity Disorder (ADHD) is one of the most common
neurodevelopmental disorders, affecting mainly the school-age population but also having
a moderate prevalence rate into adulthood. It is characterized by symptoms of inattention,
impulsivity, and hyperactivity improper for the patient’s age. However, this agedependent
characterization of ADHD makes the diagnosis such a problematic issue: the
maturation rate is different for each child, making the evaluation of what is age-proper a
subjective and difficult question. All of this leads to the ubiquitous question of ADHD,
namely, whether there is overdiagnosis of the disease or if it even exists. That is why
studying the brain is crucial in ADHD, because finding effective biomarkers able to characterize
the disease will allow us to diagnose it more accurately.
Magnetic Resonance Imaging (MRI) is one of the most powerful and versatile tools for
studying the brain, providing information about both its structure and activity. Traditional
MRI studies have focused on analyzing properties of specific brain regions in terms of
their shape (e.g., the volume of a structure) or their relation with a cognitive function
(e.g., if a structure activates during object recognition), finding multiple alterations in
ADHD [8]. However, these widespread regions that present abnormalities are connected
between them and with other areas forming the brain network, and their alterations may
indeed represent different parts of a more global phenomenon [8, 9].
There are four main neurobiological models that explain ADHD: the maturational lag
hypothesis, the dual-pathway model, the Default Mode Network (DMN) interference hypothesis,
and multinetwork models. The maturational lag hypothesis is based on ADHD
diagnostic criteria and posits that the brain of people with this condition will resemble
a younger one [10]. The dual-pathway model proposes two different processing streams
for the main symptoms of ADHD: inattention is related to alterations in the corticostriatal
executive circuits, while impulsivity/hyperactivity is associated with abnormalities in
emotional processing [11, 12]. The DMN interference hypothesis posits that this functional
network is not properly suppressed during goal-directed tasks, which is translated
into intrusion of inner mental activity [13]. Finally, multinetwork models approach the
neurobiology of people with ADHD as an alteration of multiple functional networks [14,
15].
All of these models have received substantial support from neuroimaging studies,
which suggests that all of them are correct but incomplete descriptions of the brain profile
of people with ADHD. The present dissertation aims to determine whether there is an
alteration of the global brain organization in people with ADHD that may underlie the features
that characterize the different neurobiological models of the disorder. For that, we
will apply two different graph-theory methods based on systems science to the restingstate functional Magnetic Resonance Imaging data of adults and children with ADHD.
The two proposed metrics are Stepwise Functional Connectivity (SFC) and Local and
Distant Functional Connectivity (LFC and DFC). The first one measures the integration
of information from sensory cortices to areas related to high-order cognitive functions,
and in Study 1 [16], it will be applied to a sample of medication-naïve adults with ADHD.
LFC and DFC study topological properties with physical distance restrictions, that is, the
level of connectivity of each voxel with those around it or those far away. This method
will be applied to a sample of children with ADHD in Study 2 [17] and the same sample
of adults used in Study 1 in Study 3 [18].
Our results consist of alterations in widespread regions that overlap with most functional
networks [19]. Specifically, in adults with ADHD, we observed a decrease in integration
in the DMN that locally affects the Posterior Cingulate Cortex and its functional
connectivity with the medial Prefrontal Cortex. Additionally, the integration of sensory
information in these areas was also found to be reduced in the same sample. The integration
of the DMN and its development into cortical hubs is a crucial process in the
maturation of the brain [20], which relates this finding with a maturational lag. In both
children and adults with ADHD, we also observed a lack of segregation between the
DMN, the Ventral Attentional Network, and the Frontoparietal Network in a frontal area
of the brain. The developmental trajectory of this area consists of the differentiation of
three regions, each of them pertaining to one of these networks [21], and thus, it is a
sign of brain immaturity. Also, overconnectivity (lack of segregation) between these networks
underlies the DMN interference hypothesis and is indeed a multinetwork alteration
[14, 22]. We also found abnormalities in the Visual Network in the form of increased
integration of information in these areas while decreased local functional integration of
the region, which reflects a behavior more typical of associative than sensory cortices
[23, 24]. Finally, local connectivity of sensorimotor cortices presents different maturation
trends between ADHD and controls while predicting ADHD symptomatology in all of
them.
In conclusion, our results suggest that for understanding ADHD, we cannot focus
just on a few areas related to high-order cognitive functions, but the whole brain functional
network is compromised. This goes in line with a recent meta-analysis [8] that was
unable to find convergence in specific regions abnormalities and proposed an analysis
based on network interactions. Altogether, this dissertation reflects the need to approach
ADHD from a systems neuroscience perspective that encompasses all the currently available
models instead of proposing alternative reductionist ones.Programa de Doctorado en Ciencia y Tecnología Biomédica por la Universidad Carlos III de MadridPresidente: Juan Domingo Gispert López.- Secretario: Carles Soriano Mas.- Vocal: Óscar Esteban Sanz-Drangue
Transformed epithelia trigger non-tissue-autonomous tumor suppressor response by adipocytes via activation of toll and Eiger/TNF signaling
High tumor burden is associated with increased levels of circulating inflammatory cytokines that influence the pathophysiology of the tumor and its environment. The cellular and molecular events mediating the organismal response to a growing tumor are poorly understood. Here, we report a bidirectional crosstalk between epithelial tumors and the fat body—a peripheral immune tissue—in Drosophila. Tumors trigger a systemic immune response through activation of Eiger/TNF signaling, which leads to Toll pathway upregulation in adipocytes. Reciprocally, Toll elicits a non-tissue-autonomous program in adipocytes, which drives tumor cell death. Hemocytes play a critical role in this system by producing the ligands Spätzle and Eiger, which are required for Toll activation in the fat body and tumor cell death. Altogether, our results provide a paradigm for a long-range tumor suppression function of adipocytes in Drosophila, which may represent an evolutionarily conserved mechanism in the organismal response to solid tumors
Strong superadditivity and monogamy of the Renyi measure of entanglement
Employing the quantum R\'enyi -entropies as a measure of
entanglement, we numerically find the violation of the strong superadditivity
inequality for a system composed of four qubits and . This violation
gets smaller as and vanishes for when the
measure corresponds to the Entanglement of Formation (EoF). We show that the
R\'enyi measure aways satisfies the standard monogamy of entanglement for
, and only violates a high order monogamy inequality, in the rare
cases in which the strong superadditivity is also violated. The sates
numerically found where the violation occurs have special symmetries where both
inequalities are equivalent. We also show that every measure satisfing monogamy
for high dimensional systems also satisfies the strong superadditivity
inequality. For the case of R\'enyi measure, we provide strong numerical
evidences that these two properties are equivalent.Comment: replaced with final published versio
On The Singular Scheme Of Split Foliations
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)We prove that the tangent sheaf of a codimension-one locally free distribution splits as a sum of line bundles if and only if its singular scheme is arithmetically Cohen-Macaulay. In addition, we show that a foliation by curves is given by an intersection of generically transversal holomorphic distributions of codimension one if and only if its singular scheme is arithmetically Buchsbaum. Finally, we establish that these foliations are determined by their singular schemes, and deduce that the Hilbert scheme of certain arithmetically Buchsbaum schemes of codimension 2 is birational to a Grassmannian.64513591381Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)CNPq [302477/2010-1]FAPESP [2014/14743-8
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