269 research outputs found
Generic scale of the "scale-free" growing networks
We show that the connectivity distributions of scale-free growing
networks ( is the network size) have the generic scale -- the cut-off at
. The scaling exponent is related to the exponent
of the connectivity distribution, . We propose the
simplest model of scale-free growing networks and obtain the exact form of its
connectivity distribution for any size of the network. We demonstrate that the
trace of the initial conditions -- a hump at --
may be found for any network size. We also show that there exists a natural
boundary for the observation of the scale-free networks and explain why so few
scale-free networks are observed in Nature.Comment: 4 pages revtex, 3 figure
Hypothalamic S1p/s1pr1 axis controls energy homeostasis
Sphingosine 1-phosphate receptor 1 (S1PR1) is a G-protein-coupled receptor for sphingosine-1-phosphate (S1P) that has a role in many physiological and pathophysiological processes. Here we show that the S1P/S1PR1 signalling pathway in hypothalamic neurons regulates energy homeostasis in rodents. We demonstrate that S1PR1 protein is highly enriched in hypothalamic POMC neurons of rats. Intracerebroventricular injections of the bioactive lipid, S1P, reduce food consumption and increase rat energy expenditure through persistent activation of STAT3 and the melanocortin system. Similarly, the selective disruption of hypothalamic S1PR1 increases food intake and reduces the respiratory exchange ratio. We further show that STAT3 controls S1PR1 expression in neurons via a positive feedback mechanism. Interestingly, several models of obesity and cancer anorexia display an imbalance of hypothalamic S1P/S1PR1/STAT3 axis, whereas pharmacological intervention ameliorates these phenotypes. Taken together, our data demonstrate that the neuronal S1P/S1PR1/STAT3 signalling axis plays a critical role in the control of energy homeostasis in rats.Sphingosine 1-phosphate receptor 1 (S1PR1) is a G-protein-coupled receptor for sphingosine-1-phosphate (S1P) that has a role in many physiological and pathophysiological processes. Here we show that the S1P/S1PR1 signalling pathway in hypothalamic neurons regulates energy homeostasis in rodents. We demonstrate that S1PR1 protein is highly enriched in hypothalamic POMC neurons of rats. Intracerebroventricular injections of the bioactive lipid, S1P, reduce food consumption and increase rat energy expenditure through persistent activation of STAT3 and the melanocortin system. Similarly, the selective disruption of hypothalamic S1PR1 increases food intake and reduces the respiratory exchange ratio. We further show that STAT3 controls S1PR1 expression in neurons via a positive feedback mechanism. Interestingly, several models of obesity and cancer anorexia display an imbalance of hypothalamic S1P/S1PR1/STAT3 axis, whereas pharmacological intervention ameliorates these phenotypes. Taken together, our data demonstrate that the neuronal S1P/S1PR1/STAT3 signalling axis plays a critical role in the control of energy homeostasis in rats5485
Fine-Tuning Solution for Hybrid Inflation in Dissipative Chaotic Dynamics
We study the presence of chaotic behavior in phase space in the
pre-inflationary stage of hybrid inflation models. This is closely related to
the problem of initial conditions associated to these inflationary type of
models. We then show how an expected dissipative dynamics of fields just before
the onset of inflation can solve or ease considerably the problem of initial
conditions, driving naturally the system towards inflation. The chaotic
behavior of the corresponding dynamical system is studied by the computation of
the fractal dimension of the boundary, in phase space, separating inflationary
from non-inflationary trajectories. The fractal dimension for this boundary is
determined as a function of the dissipation coefficients appearing in the
effective equations of motion for the fields.Comment: 10 pages, 4 eps figures (uses epsf), Revtex. Replaced with version to
match one in press Physical Review
Anatomical and histological characteristics of teeth in agouti (Dasyprocta prymnolopha Wagler, 1831)
tartan underlies the evolution of male Drosophila genital morphology
Male genital structures are among the most rapidly evolving morphological traits and are often the only features that can distinguish closely related species. This process is thought to be driven by sexual selection and may reinforce species separation. However, while the genetic bases of many phenotypic differences have been identified, we still lack knowledge about the genes underlying evolutionary differences in male genital organs and organ size more generally. The claspers (surstyli) are periphallic structures that play an important role in copulation in insects. Here, we show that divergence in clasper size and bristle number between Drosophila mauritiana and Drosophila simulans is caused by evolutionary changes in tartan (trn), which encodes a transmembrane leucine-rich repeat domain protein that mediates cell–cell interactions and affinity. There are no fixed amino acid differences in trn between D. mauritiana and D. simulans, but differences in the expression of this gene in developing genitalia suggest that cis-regulatory changes in trn underlie the evolution of clasper morphology in these species. Finally, analyses of reciprocal hemizygotes that are genetically identical, except for the species from which the functional allele of trn originates, determined that the trn allele of D. mauritiana specifies larger claspers with more bristles than the allele of D. simulans. Therefore, we have identified a gene underlying evolutionary change in the size of a male genital organ, which will help to better understand not only the rapid diversification of these structures, but also the regulation and evolution of organ size more broadly
Unravelling the genetic basis for the rapid diversification of male genitalia between Drosophila species
In the last 240,000 years, males of the Drosophila simulans species clade have evolved striking differences in the morphology of their epandrial posterior lobes and claspers (surstyli). These appendages are used for grasping the female during mating and so their divergence is most likely driven by sexual selection. Mapping studies indicate a highly polygenic and generally additive genetic basis for these morphological differences. However, we have limited understanding of the gene regulatory networks that control the development of genital structures and how they evolved to result in this rapid phenotypic diversification. Here, we used new D. simulans/D. mauritiana introgression lines on chromosome 3L to generate higher resolution maps of posterior lobe and clasper differences between these species. We then carried out RNA-seq on the developing genitalia of both species to identify the expressed genes and those that are differentially expressed between the two species. This allowed us to test the function of expressed positional candidates during genital development in D. melanogaster. We identified several new genes involved in the development and possibly the evolution of these genital structures, including the transcription factors Hairy and Grunge. Furthermore, we discovered that during clasper development Hairy negatively regulates tartan (trn), a gene known to contribute to divergence in clasper morphology. Taken together, our results provide new insights into the regulation of genital development and how this has evolved between species
Computer Simulations of Hippocampal Mossy Fiber Cleft Zinc Movements
Zinc ions have key regulatory, structural, and catalytic functions and mediate a variety of intra- and intercellular processes. The hippocampal mossy fiber boutons contain large amounts of free or loosely bound vesicular zinc, which can be co-released with glutamate. Zinc can interact with a variety of ionic channels (N-VDCCs, L-VDCCs, KATP), glutamate receptors (AMPA, KA, NMDA 2A, 2B), glutamate transporters (GLAST, EAAT4), and molecules (ATP). The dynamic properties of cleft free, complexed, and total zinc were addressed, considering the known concentration and affinity of various cleft zinc sensitive sites, mainly in the postsynaptic area and in glial cells. The computer model included three different zinc release processes, with short, medium, and long duration, described, like the uptake ones, by alpha functions. The results suggest that, depending on the amount of release, zinc clearance is largely due, either, to zinc binding to NMDA 2A receptor sites or to glial GLAST transporters
Can we live in a self-tuning universe?
The self-tuning brane scenario is an attempt to solve the cosmological
constant problem in the context of extra dimensions. Rather than making the
vacuum energy small, this approach proceeds by removing the gravitational
effect of vacuum energy on the expansion of the universe. Such behavior is only
possible through changing the Friedmann equation of conventional cosmology, and
we discuss difficulties in obtaining cosmological evolution compatible with
observation in this context. Specific models considered include a bulk scalar
field coupling to the brane via a conformal transformation of the brane metric,
and via a rescaling of the brane volume element
Exploring interactions of plant microbiomes
A plethora of microbial cells is present in every gram of soil, and microbes are found extensively in plant and animal tissues. The mechanisms governed by microorganisms in the regulation of physiological processes of their hosts have been extensively studied in the light of recent findings on microbiomes. In plants, the components of these microbiomes may form distinct communities, such as those inhabiting the plant rhizosphere, the endosphere and the phyllosphere. In each of these niches, the "microbial tissue" is established by, and responds to, specific selective pressures. Although there is no clear picture of the overall role of the plant microbiome, there is substantial evidence that these communities are involved in disease control, enhance nutrient acquisition, and affect stress tolerance. In this review, we first summarize features of microbial communities that compose the plant microbiome and further present a series of studies describing the underpinning factors that shape the phylogenetic and functional plant-associated communities. We advocate the idea that understanding the mechanisms by which plants select and interact with their microbiomes may have a direct effect on plant development and health, and further lead to the establishment of novel microbiome-driven strategies, that can cope with the development of a more sustainable agriculture
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