378 research outputs found

    Geweldstructuur in 40 ontwikkelingslanden in de periode 1950—1967

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    In this article an attempt is made to give a classification of internal violence, occurring in 40 developing countries, in order to provide a ’structure of violence’ for each country in the period 1950-1967, and to correlate this structure to the changes in the real per capita income of these countries. For the collection of the various items of internal violence, Keesings Historical Archives (Dutch version) was used. They were classified as follows: I Diffuse socio-political unrest (strikes, demonstrations, riots etc., in which people were wounded, killed and/or property was destroyed). II Coup d’état-like activities. III Small guerrilla’s in the countryside and clusters of (anticolonial) violent actions in the towns. IV Limited civil or anticolonial war. V ’Endemic’ guerrillas. VI Situation of serious anarchy. VII ’Political’ pogroms and total civil or anticolonial war. Thus a ’profile of violence’ for each country was constructed. It appeared that in the Latin American countries coup d’état activities prevailed; that in several African countries these activities became numerous some years after independence was obtained; that in the Middle East countries all types of violence occurred and that in the ethnically complicated Asian countries, small and endemic guerrillas frequently arose. A relation between types and extent of internal violence, and level of national income and its yearly per capita growth (obtained from the O.E.C.D. publication: National Accounts of Less Developed Countries, 1967) could not be proved. The material suggests that national income and changes therein as such, may not be very interesting variables. Distribution of income and changes therein might be more relevant. The difficulty, however, is to obtain hard and fast data on these variables. The following suggestions are made: 1. To collect more detailed information from different sources on the various violent conflicts occurring within a number of selected countries, in order to obtain complete data on internal violence. 2. Redefinition or refining of the typology of violence, in order to make it less ambigious. 3. The selection of the countries could be determined by: a. the possibility of obtaining data on distribution of income and changes therein; b. the possibility of differentiating between ethnic homogeneous and non-homogenous countries; c. the possibility of differentiating between countries receives relatively much or little foreign aid

    Probabilistic sequential matrix factorization

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    We introduce the probabilistic sequential matrix factorization (PSMF) method for factorizing time-varying and non-stationary datasets consisting of high-dimensional time-series. In particular, we consider nonlinear Gaussian state-space models where sequential approximate inference results in the factorization of a data matrix into a dictionary and time-varying coefficients with potentially nonlinear Markovian dependencies. The assumed Markovian structure on the coefficients enables us to encode temporal dependencies into a low-dimensional feature space. The proposed inference method is solely based on an approximate extended Kalman filtering scheme, which makes the resulting method particularly efficient. PSMF can account for temporal nonlinearities and, more importantly, can be used to calibrate and estimate generic differentiable nonlinear subspace models. We also introduce a robust version of PSMF, called rPSMF, which uses Student-t filters to handle model misspecification. We show that PSMF can be used in multiple contexts: modeling time series with a periodic subspace, robustifying changepoint detection methods, and imputing missing data in several high-dimensional time-series, such as measurements of pollutants across London.Comment: Accepted for publication at AISTATS 202

    Wnt target genes identified by DNA microarrays in immature CD34+ thymocytes regulate proliferation and cell adhesion

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    The thymus is seeded by very small numbers of progenitor cells that undergo massive proliferation before differentiation and rearrangement of TCR genes occurs. Various signals mediate proliferation and differentiation of these cells, including Wnt signals. Wnt signals induce the interaction of the cytoplasmic cofactor beta-catenin with nuclear T cell factor (TCF) transcription factors. We identified target genes of the Wnt/beta-catenin/TCF pathway in the most immature (CD4-CD8-CD34+) thymocytes using Affymetrix DNA microarrays in combination with three different functional assays for in vitro induction of Wnt signaling. A relatively small number (approximately 30) of genes changed expression, including several proliferation-inducing transcription factors such as c-fos and c-jun, protein phosphatases, and adhesion molecules, but no genes involved in differentiation to mature T cell stages. The adhesion molecules likely confine the proliferating immature thymocytes to the appropriate anatomical sites in the thymus. For several of these target genes, we validated that they are true Wnt/beta-catenin/TCF target genes using real-time quantitative PCR and reporter gene assays. The same core set of genes was repressed in Tcf-1-null mice, explaining the block in early thymocyte development in these mice. In conclusion, Wnt signals mediate proliferation and cell adhesion, but not differentiation of the immature thymic progenitor pool

    Specific members of the TOPLESS family are susceptibility genes for Fusarium wilt in tomato and Arabidopsis

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    Vascular wilt diseases caused by Fusarium oxysporum are a major threat to many agriculturally important crops. Genetic resistance is rare and inevitably overcome by the emergence of new races. To identify potentially durable and non-race-specific genetic resistance against Fusarium wilt diseases, we set out to identify effector targets in tomato that mediate susceptibility to the fungus. For this purpose, we used the SIX8 effector protein, an important and conserved virulence factor present in many pathogenic F. oxysporum isolates. Using protein pull-downs and yeast two-hybrid assays, SIX8 was found to interact specifically with two members of the tomato TOPLESS family: TPL1 and TPL2. Loss-of-function mutations in TPL1 strongly reduced disease susceptibility to Fusarium wilt and a tpl1;tpl2 double mutant exerted an even higher level of resistance. Similarly, Arabidopsis tpl;tpr1 mutants became significantly less diseased upon F. oxysporum inoculation as compared to wildtype plants. We conclude that TPLs encode susceptibility genes whose mutation can confer resistance to F. oxysporum

    Probabilistic sequential matrix factorization

    Get PDF
    We introduce the probabilistic sequential matrix factorization (PSMF) method for factorizing time-varying and non-stationary datasets consisting of high-dimensional time-series. In particular, we consider nonlinear Gaussian state-space models where sequential approximate inference results in the factorization of a data matrix into a dictionary and time-varying coefficients with potentially nonlinear Markovian dependencies. The assumed Markovian structure on the coefficients enables us to encode temporal dependencies into a low-dimensional feature space. The proposed inference method is solely based on an approximate extended Kalman filtering scheme, which makes the resulting method particularly efficient. PSMF can account for temporal nonlinearities and, more importantly, can be used to calibrate and estimate generic differentiable nonlinear subspace models. We also introduce a robust version of PSMF, called rPSMF, which uses Student-t filters to handle model misspecification. We show that PSMF can be used in multiple contexts: modeling time series with a periodic subspace, robustifying changepoint detection methods, and imputing missing data in several high-dimensional time-series, such as measurements of pollutants across London

    Synergistic interaction between the type III secretion system of the endophytic bacterium <i>Pantoea agglomerans</i> DAPP-PG 734 and the virulence of the causal agent of olive knot <i>Pseudomonas savastanoi pv. savastanoi</i> DAPP-PG 722

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    The endophytic bacterium Pantoea agglomerans DAPP-PG 734 was previously isolated from olive knots caused by infection with Pseudomonas savastanoi pv. savastanoi DAPP-PG 722. Whole-genome analysis of this P. agglomerans strain revealed the presence of a Hypersensitive response and pathogenicity (Hrp) type III secretion system (T3SS). To assess the role of the P. agglomerans T3SS in the interaction with P. savastanoi pv. savastanoi, we generated independent knockout mutants in three Hrp genes of the P. agglomerans DAPP-PG 734 T3SS (hrpJ, hrpN, and hrpY). In contrast to the wildtype control, all three mutants failed to cause a hypersensitive response when infiltrated in tobacco leaves, suggesting that P. agglomerans T3SS is functional and injects effector proteins in plant cells. In contrast to P. savastanoi pv. savastanoi DAPP-PG 722, the wildtype strain P. agglomerans DAPP-PG 734 and its Hrp T3SS mutants did not cause olive knot disease in 1-year-old olive plants. Coinoculation of P. savastanoi pv. savastanoi with P. agglomerans wildtype strains did not significantly change the knot size, while the DAPP-PG 734 hrpY mutant induced a significant decrease in knot size, which could be complemented by providing hrpY on a plasmid. By epifluorescence microscopy and confocal laser scanning microscopy, we found that the localization patterns in knots were nonoverlapping for P. savastanoi pv. savastanoi and P. agglomerans when coinoculated. Our results suggest that suppression of olive plant defences mediated by the Hrp T3SS of P. agglomerans DAPP-PG 734 positively impacts the virulence of P. savastanoi pv. savastanoi DAPP-PG 722

    In the light of directed evolution: Pathways of adaptive protein evolution

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    Directed evolution is a widely-used engineering strategy for improving the stabilities or biochemical functions of proteins by repeated rounds of mutation and selection. These experiments offer empirical lessons about how proteins evolve in the face of clearly-defined laboratory selection pressures. Directed evolution has revealed that single amino acid mutations can enhance properties such as catalytic activity or stability and that adaptation can often occur through pathways consisting of sequential beneficial mutations. When there are no single mutations that improve a particular protein property experiments always find a wealth of mutations that are neutral with respect to the laboratory-defined measure of fitness. These neutral mutations can open new adaptive pathways by at least 2 different mechanisms. Functionally-neutral mutations can enhance a protein's stability, thereby increasing its tolerance for subsequent functionally beneficial but destabilizing mutations. They can also lead to changes in “promiscuous” functions that are not currently under selective pressure, but can subsequently become the starting points for the adaptive evolution of new functions. These lessons about the coupling between adaptive and neutral protein evolution in the laboratory offer insight into the evolution of proteins in nature
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