118 research outputs found

    “Hot” executive functions are comparable across monolingual and bilingual elementary school children: Results from a study with the Iowa Gambling Task

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    Past research found performance differences between monolingual and bilingual children in the domain of executive functions (EF). Furthermore, recent studies have reported advantages in processing efficiency or mental effort in bilingual adults and children. These studies mostly focused on the investigation of “cold” EF tasks. Studies including measures of “hot” EF, i.e., tasks operating in an emotionally significant setting, are limited and hence results are inconclusive. In the present study, we extend previous research by investigating performance in a task of the “hot” EF domain by both behavioral data and mental effort via pupillary changes during task performance. Seventy-three monolingual and bilingual school children (mean age = 107.23 months, SD = 10.26) solved the Iowa Gambling Task in two different conditions. In the standard task, characterized by constant gains and occasional losses, children did not learn to improve their decision-making behavior. In a reversed task version, characterized by constant losses and occasional gains, both monolinguals and bilinguals learned to improve their decision-making behavior over the course of the task. In both versions of the task, children switched choices more often after losses than after gains. Bilinguals switched their choices less often than monolinguals in the reversed task, indicating a slightly more mature decision-making strategy. Mental effort did not differ between monolinguals and bilinguals. Conclusions of these findings for the bilingual advantage assumption will be discussed

    Adaptive remodeling of the bacterial proteome by specific ribosomal modification regulates Pseudomonas infection and niche colonisation

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    Post-transcriptional control of protein abundance is a highly important, underexplored regulatory process by which organisms respond to their environments. Here we describe an important and previously unidentified regulatory pathway involving the ribosomal modification protein RimK, its regulator proteins RimA and RimB, and the widespread bacterial second messenger cyclic-di-GMP (cdG). Disruption of rimK affects motility and surface attachment in pathogenic and commensal Pseudomonas species, with rimK deletion significantly compromising rhizosphere colonisation by the commensal soil bacterium P. fluorescens, and plant infection by the pathogens P. syringae and P. aeruginosa. RimK functions as an ATP-dependent glutamyl ligase, adding glutamate residues to the C-terminus of ribosomal protein RpsF and inducing specific effects on both ribosome protein complement and function. Deletion of rimK in P. fluorescens leads to markedly reduced levels of multiple ribosomal proteins, and also of the key translational regulator Hfq. In turn, reduced Hfq levels induce specific downstream proteomic changes, with significant increases in multiple ABC transporters, stress response proteins and non-ribosomal peptide synthetases seen for both ΔrimK and Δhfq mutants. The activity of RimK is itself controlled by interactions with RimA, RimB and cdG. We propose that control of RimK activity represents a novel regulatory mechanism that dynamically influences interactions between bacteria and their hosts; translating environmental pressures into dynamic ribosomal changes, and consequently to an adaptive remodeling of the bacterial proteome

    Analysis of the modes of energy consumption of the complex of an incoherent scattering of the institute of ionosphere of national academy of sciences and the ministry of education and science of Ukraine

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    ĐŁ ĐŽĐ°ĐœŃ–Đč статті прДЎстаĐČĐ»Đ”ĐœŃ– Ń€Đ”Đ·ŃƒĐ»ŃŒŃ‚Đ°Ń‚Đž Đ°ĐœĐ°Đ»Ń–Đ·Ńƒ Ń€Đ”Đ¶ĐžĐŒŃ–ĐČ Đ”ĐœĐ”Ń€ĐłĐŸŃĐżĐŸĐ¶ĐžĐČĐ°ĐœĐœŃ ĐșĐŸĐŒĐżĐ»Đ”Đșсу ĐœĐ”ĐșĐŸĐłĐ”Ń€Đ”ĐœŃ‚ĐœĐŸĐłĐŸ Ń€ĐŸĐ·ŃŃ–ŃĐœĐœŃ Đ†ĐœŃŃ‚ĐžŃ‚ŃƒŃ‚Ńƒ Ń–ĐŸĐœĐŸŃŃ„Đ”Ń€Đž НАН і МОН ĐŁĐșŃ€Đ°Ń—ĐœĐž Đ· ĐŒĐ”Ń‚ĐŸŃŽ ĐČĐžŃ€Ń–ŃˆĐ”ĐœĐœŃ ĐżŃ€ĐŸĐ±Đ»Đ”ĐŒĐž піЮĐČĐžŃ‰Đ”ĐœĐœŃ Đ”ĐœĐ”Ń€ĐłĐŸĐ”Ń„Đ”ĐșтоĐČĐœĐŸŃŃ‚Ń– ĐœĐ°ŃƒĐșĐŸĐČĐŸ-ĐŽĐŸŃĐ»Ń–ĐŽĐœĐŸĐłĐŸ ĐșĐŸĐŒĐżĐ»Đ”Đșсу та стĐČĐŸŃ€Đ”ĐœĐœŃ Đ”ĐœĐ”Ń€ĐłĐŸĐ”Ń„Đ”ĐșтоĐČĐœĐŸŃ— ŃĐžŃŃ‚Đ”ĐŒĐž ДлДĐșŃ‚Ń€ĐŸĐżĐŸŃŃ‚Đ°Ń‡Đ°ĐœĐœŃ, яĐșĐ° Đ·Đ°Đ±Đ”Đ·ĐżĐ”Ń‡ĐžŃ‚ŃŒ стіĐčĐșу Ń€ĐŸĐ±ĐŸŃ‚Ńƒ ĐœĐ°ŃƒĐșĐŸĐČĐŸĐłĐŸ ĐŸĐ±Đ»Đ°ĐŽĐœĐ°ĐœĐœŃ ĐŽĐ»Ń ĐČĐžĐșĐŸĐœĐ°ĐœĐœŃ ĐŽĐŸŃĐ»Ń–ĐŽĐœĐžŃ†ŃŒĐșох ĐżŃ€ĐŸĐłŃ€Đ°ĐŒ НАН ĐŁĐșŃ€Đ°Ń—ĐœĐž. ĐžĐżĐžŃĐ°ĐœĐ° ŃĐžŃŃ‚Đ”ĐŒĐ° ДлДĐșŃ‚Ń€ĐŸĐ¶ĐžĐČĐ»Đ”ĐœĐœŃ ĐșĐŸĐŒĐżĐ»Đ”Đșсу та Ń€Đ”Đ¶ĐžĐŒĐž Đ”ĐœĐ”Ń€ĐłĐŸŃĐżĐŸĐ¶ĐžĐČĐ°ĐœĐœŃ ĐșĐŸĐŒĐżĐ»Đ”Đșсу. ĐžĐżĐžŃĐ°ĐœĐŸ ĐżŃ€ĐžŃŃ‚Ń€ĐŸŃ— Ń€Đ°ĐŽĐ°Ń€ĐœĐŸŃ— ŃĐžŃŃ‚Đ”ĐŒĐž, Đ° таĐșĐŸĐ¶ ĐœĐ°ĐčĐ±Ń–Đ»ŃŒŃˆ ĐżĐŸŃ‚ŃƒĐ¶ĐœŃ– ŃĐżĐŸĐ¶ĐžĐČачі ДлДĐșŃ‚Ń€ĐŸĐ”ĐœĐ”Ń€ĐłŃ–Ń—, яĐșі ŃĐżĐŸĐ¶ĐžĐČають ДлДĐșŃ‚Ń€ĐŸĐ”ĐœĐ”Ń€ĐłŃ–ŃŽ ĐœĐ° Đ”ĐșŃĐżĐ”Ń€ĐžĐŒĐ”ĐœŃ‚Đ°Đ»ŃŒĐœŃ– і ĐłĐŸŃĐżĐŸĐŽĐ°Ń€ŃŃŒĐșі ĐżĐŸŃ‚Ń€Đ”Đ±Đž. ĐŸŃ€ĐŸĐ°ĐœĐ°Đ»Ń–Đ·ĐŸĐČĐ°ĐœĐŸ Đ”ĐœĐ”Ń€ĐłĐŸŃĐżĐŸĐ¶ĐžĐČĐ°ĐœĐœŃ ĐșĐŸĐŒĐżĐ»Đ”Đșсу ĐœĐ”ĐșĐŸĐłĐ”Ń€Đ”ĐœŃ‚ĐœĐŸĐłĐŸ Ń€ĐŸĐ·ŃŃ–ŃĐœĐœŃ Đ·Đ° 2013 р. ĐžŃ‚Ń€ĐžĐŒĐ°ĐœĐŸ і прДЎстаĐČĐ»Đ”ĐœĐŸ графіĐșĐž ŃĐ”Ń€Đ”ĐŽĐœŃŒĐŸŃ— ŃĐżĐŸĐ¶ĐžĐČĐ°ĐœĐŸŃ— ĐżĐŸŃ‚ŃƒĐ¶ĐœĐŸŃŃ‚Ń– (ŃĐ”Ń€Đ”ĐŽĐœŃŒĐŸĐŽĐŸĐ±ĐŸĐČĐžĐč ĐżĐŸĐșĐ°Đ·ĐœĐžĐș) і ŃĐ”Ń€Đ”ĐŽĐœŃŒĐŸŃ— ŃĐżĐŸĐ¶ĐžĐČĐ°ĐœĐŸŃ— ĐżĐŸŃ‚ŃƒĐ¶ĐœĐŸŃŃ‚Ń– ĐČ Ń€Đ”Đ¶ĐžĐŒŃ– ĐČĐžĐŒŃ–Ń€ŃŽĐČĐ°ĐœŃŒ. ĐžĐżĐžŃĐ°ĐœĐ° ĐŽĐŸŃ†Ń–Đ»ŃŒĐœŃ–ŃŃ‚ŃŒ ĐżŃ€ĐŸĐČĐ”ĐŽĐ”ĐœĐœŃ Ń€ĐŸĐ±Ń–Ń‚ Đ· ĐŸĐżŃ‚ĐžĐŒŃ–Đ·Đ°Ń†Ń–Ń— Đ”ĐœĐ”Ń€ĐłĐŸĐżĐŸŃŃ‚Đ°Ń‡Đ°ĐœĐœŃ ĐœĐ°ŃƒĐșĐŸĐČĐŸ-ĐŽĐŸŃĐ»Ń–ĐŽĐœĐŸĐłĐŸ ĐșĐŸĐŒĐżĐ»Đ”Đșсу Đ†ĐœŃŃ‚ĐžŃ‚ŃƒŃ‚Ńƒ Ń–ĐŸĐœĐŸŃŃ„Đ”Ń€Đž. Đ—Đ°ĐżŃ€ĐŸĐżĐŸĐœĐŸĐČĐ°ĐœĐŸ ĐŒĐŸĐ¶Đ»ĐžĐČі Đ·Đ°Ń…ĐŸĐŽĐž ĐŽĐ»Ń Đ·ĐœĐžĐ¶Đ”ĐœĐœŃ Đ”ĐșĐŸĐœĐŸĐŒŃ–Ń‡ĐœĐŸŃ— ĐČĐ°Ń€Ń‚ĐŸŃŃ‚Ń– ĐżŃ€ĐŸĐČĐ”ĐŽĐ”ĐœĐœŃ Đ”ĐșŃĐżĐ”Ń€ĐžĐŒĐ”ĐœŃ‚Ń–ĐČ Đ· ĐŽĐŸŃĐ»Ń–ĐŽĐ¶Đ”ĐœĐœŃ Ń–ĐŸĐœĐŸŃŃ„Đ”Ń€Đž ĐœĐ°ŃƒĐșĐŸĐČĐŸ-ĐŽĐŸŃĐ»Ń–ĐŽĐœĐŸĐłĐŸ ĐșĐŸĐŒĐżĐ»Đ”Đșсу ĐœĐ”ĐșĐŸĐłĐ”Ń€Đ”ĐœŃ‚ĐœĐŸĐłĐŸ Ń€ĐŸĐ·ŃŃ–ŃĐœĐœŃ. ĐŸŃ€ĐŸĐČĐ”ĐŽĐ”ĐœĐŸ Đ°ĐœĐ°Đ»Ń–Đ· Ń€ĐŸĐ±Ń–Ń‚ ŃŃƒŃ‡Đ°ŃĐœĐžŃ… Đ°ĐČŃ‚ĐŸŃ€Ń–ĐČ Đ· ĐŒĐ”Ń‚ĐŸŃŽ ĐżĐŸĐșĐ°Đ·Đ°Ń‚Đž, Ń‰ĐŸ піЮĐČĐžŃ‰Đ”ĐœĐœŃ ДфДĐșтоĐČĐœĐŸŃŃ‚Ń– Ń„ŃƒĐœĐșŃ†Ń–ĐŸĐœŃƒĐČĐ°ĐœĐœŃ ŃĐžŃŃ‚Đ”ĐŒ ДлДĐșŃ‚Ń€ĐŸĐżĐŸŃŃ‚Đ°Ń‡Đ°ĐœĐœŃ є Đ°ĐșŃ‚ŃƒĐ°Đ»ŃŒĐœĐŸŃŽ ĐżŃ€ĐŸĐ±Đ»Đ”ĐŒĐŸŃŽ ŃŃƒŃ‡Đ°ŃĐœĐžŃ… ĐŽĐŸŃĐ»Ń–ĐŽĐ¶Đ”ĐœŃŒ.This article presents the results of the analysis of the energy consumption modes of the incoherent scattering complex of the Institute of Ionosphere of the National Academy of Sciences and the Ministry of Education and Science of Ukraine to solve the problem of increasing the energy efficiency of a research complex and creating an energy efficient power supply system that will ensure the sustainability of scientific equipment for research programs of the National Academy of Sciences of Ukraine. The system of power supply of the complex and modes of power consumption of the complex are described. The devices of the radar system are described, as well as the most powerful consumers of electricity, which consume electricity for experimental and economic needs. The energy consumption of the incoherent scattering complex in 2013 is analyzed. Graphs of the average power consumption (daily average) and average power consumption in measurement modes were obtained and presented. The feasibility of work to optimize the energy supply of the research complex of the institute of the ionosphere is described. Possible measures are proposed to reduce the economic cost of conducting experiments on the study of the ionosphere of an incoherent scattering research complex. The analysis of the works of modern authors i s carried out in order to show that increasing the efficiency of the power supply systems is an actual problem of modern research

    Plasmids manipulate bacterial behaviour through translational regulatory crosstalk

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    Beyond their role in horizontal gene transfer, conjugative plasmids commonly encode homologues of bacterial regulators. Known plasmid regulator homologues have highly targeted effects upon the transcription of specific bacterial traits. Here, we characterise a plasmid translational regulator, RsmQ, capable of taking global regulatory control in Pseudomonas fluorescens and causing a behavioural switch from motile to sessile lifestyle. RsmQ acts as a global regulator, controlling the host proteome through direct interaction with host mRNAs and interference with the host’s translational regulatory network. This mRNA interference leads to large-scale proteomic changes in metabolic genes, key regulators, and genes involved in chemotaxis, thus controlling bacterial metabolism and motility. Moreover, comparative analyses found RsmQ to be encoded on a large number of divergent plasmids isolated from multiple bacterial host taxa, suggesting the widespread importance of RsmQ for manipulating bacterial behaviour across clinical, environmental, and agricultural niches. RsmQ is a widespread plasmid global translational regulator primarily evolved for host chromosomal control to manipulate bacterial behaviour and lifestyle

    The Maltase Involved in Starch Metabolism in Barley Endosperm Is Encoded by a Single Gene

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    During germination and early seedling growth of barley (Hordeum vulgare), maltase is responsible for the conversion of maltose produced by starch degradation in the endosperm to glucose for seedling growth. Despite the potential relevance of this enzyme for malting and the production of alcoholic beverages, neither the nature nor the role of maltase is fully understood. Although only one gene encoding maltase has been identified with certainty, there is evidence for the existence of other genes and for multiple forms of the enzyme. It has been proposed that maltase may be involved directly in starch granule degradation as well as in maltose hydrolysis. The aim of our work was to discover the nature of maltase in barley endosperm. We used ion exchange chromatography to fractionate maltase activity from endosperm of young seedlings, and we partially purified activity for protein identification. We compared maltase activity in wild-type barley and transgenic lines with reduced expression of the previously-characterised maltase gene Agl97, and we used genomic and transcriptomic information to search for further maltase genes. We show that all of the maltase activity in the barley endosperm can be accounted for by a single gene, Agl97. Multiple forms of the enzyme most likely arise from proteolysis and other post-translational modifications

    Pseudomonas aeruginosa PilY1 Binds Integrin in an RGD- and Calcium-Dependent Manner

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    PilY1 is a type IV pilus (tfp)-associated protein from the opportunistic pathogen Pseudomonas aeruginosa that shares functional similarity with related proteins in infectious Neisseria and Kingella species. Previous data have shown that PilY1 acts as a calcium-dependent pilus biogenesis factor necessary for twitching motility with a specific calcium binding site located at amino acids 850–859 in the 1,163 residue protein. In addition to motility, PilY1 is also thought to play an important role in the adhesion of P. aeruginosa tfp to host epithelial cells. Here, we show that PilY1 contains an integrin binding arginine-glycine-aspartic acid (RGD) motif located at residues 619–621 in the PilY1 from the PAK strain of P. aeruginosa; this motif is conserved in the PilY1s from the other P. aeruginosa strains of known sequence. We demonstrate that purified PilY1 binds integrin in vitro in an RGD-dependent manner. Furthermore, we identify a second calcium binding site (amino acids 600–608) located ten residues upstream of the RGD. Eliminating calcium binding from this site using a D608A mutation abolished integrin binding; in contrast, a calcium binding mimic (D608K) preserved integrin binding. Finally, we show that the previously established PilY1 calcium binding site at 851–859 also impacts the protein's association with integrin. Taken together, these data indicate that PilY1 binds to integrin in an RGD- and calcium-dependent manner in vitro. As such, P. aeruginosa may employ these interactions to mediate host epithelial cell binding in vivo

    Microarray Analyses of Inflammation Response of Human Dermal Fibroblasts to Different Strains of Borrelia burgdorferi Sensu Stricto

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    In Lyme borreliosis, the skin is the key site of bacterial inoculation by the infected tick, and of cutaneous manifestations, erythema migrans and acrodermatitis chronica atrophicans. We explored the role of fibroblasts, the resident cells of the dermis, in the development of the disease. Using microarray experiments, we compared the inflammation of fibroblasts induced by three strains of Borrelia burgdorferi sensu stricto isolated from different environments and stages of Lyme disease: N40 (tick), Pbre (erythema migrans) and 1408 (acrodermatitis chronica atrophicans). The three strains exhibited a similar profile of inflammation with strong induction of chemokines (CXCL1 and IL-8) and IL-6 cytokine mainly involved in the chemoattraction of immune cells. Molecules such as TNF-alpha and NF-ÎșB factors, metalloproteinases (MMP-1, -3 and -12) and superoxide dismutase (SOD2), also described in inflammatory and cellular events, were up-regulated. In addition, we showed that tick salivary gland extracts induce a cytotoxic effect on fibroblasts and that OspC, essential in the transmission of Borrelia to the vertebrate host, was not responsible for the secretion of inflammatory molecules by fibroblasts. Tick saliva components could facilitate the early transmission of the disease to the site of injury creating a feeding pit. Later in the development of the disease, Borrelia would intensively multiply in the skin and further disseminate to distant organs

    Isolation and Characterization of Intestinal Epithelial Cells from Normal and SIV-Infected Rhesus Macaques

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    Impairment of intestinal epithelial barriers contributes to the progression of HIV/SIV infection and leads to generalized HIV-induced immune-cell activation during chronic infection. Rhesus macaques are the major animal model for studying HIV pathogenesis. However, detailed characterization of isolated rhesus epithelial cells (ECs) from intestinal tissues is not well defined. It is also not well documented whether isolated ECs had any other cell contaminants from intestinal tissues during the time of processing that might hamper interpretation of EC preparations or cultures. In this study, we identify and characterize ECs based on flow cytometry and immunohistochemistry methods using various enzymatic and mechanical isolation techniques to enrich ECs from intestinal tissues. This study shows that normal healthy ECs differentially express HLA-DR, CD23, CD27, CD90, CD95 and IL-10R markers. Early apoptosis and upregulation of ICAM-1 and HLA-DR in intestinal ECs are thought to be the key features in SIV mediated enteropathy. The data suggest that intestinal ECs might be playing an important role in mucosal immune responses by regulating the expression of different important regulatory and adhesion molecules and their function

    Molecular mechanisms of vaspin action: from adipose tissue to skin and bone, from blood  vessels to the brain 

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    Visceral adipose tissue derived serine protease inhibitor (vaspin) or SERPINA12 according to the serpin nomenclature was identified together with other genes and gene products that  were specifically expressed or overexpressed in the intra abdominal or visceral adipose tissue  (AT) of the Otsuka Long-Evans Tokushima fatty rat. These rats spontaneously develop visceral  obesity, insulin resistance, hyperinsulinemia and ‐glycemia, as well as hypertension and thus represent a well suited animal model of obesity and related metabolic disorders such as type  2 diabetes.  The follow-up study reporting the cloning, expression and functional characterization of  vaspin suggested the great and promising potential of this molecule to counteract obesity induced insulin resistance and inflammation and has since initiated over 300 publications, clinical and experimental, that have contributed to uncover the multifaceted functions and molecular mechanisms of vaspin action not only in the adipose, but in many different cells, tissues and organs. This review will give an update on mechanistic and structural aspects of vaspin with a focus on its serpin function, the physiology and regulation of vaspin expression, and will summarize the latest on vaspin function in various tissues such as the different adipose tissue depots as well as the vasculature, skin, bone and the brain

    Serologic and immunohistochemical prognostic biomarkers of cutaneous malignancies

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    Biomarkers are important tools in clinical diagnosis and prognostic classification of various cutaneous malignancies. Besides clinical and histopathological aspects (e.g. anatomic site and type of the primary tumour, tumour size and invasion depth, ulceration, vascular invasion), an increasing variety of molecular markers have been identified, providing the possibility of a more detailed diagnostic and prognostic subgrouping of tumour entities, up to even changing existing classification systems. Recently published gene expression or proteomic profiling data relate to new marker molecules involved in skin cancer pathogenesis, which may, after validation by suitable studies, represent future prognostic or predictive biomarkers in cutaneous malignancies. We, here, give an overview on currently known serologic and newer immunohistochemical biomarker molecules in the most common cutaneous malignancies, malignant melanoma, squamous cell carcinoma and cutaneous lymphoma, particularly emphasizing their prognostic and predictive significance
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