253 research outputs found

    Second Language Feedback Abolishes the ā€œHot Handā€ Effect during Even-Probability Gambling

    Get PDF
    Research into languageĆ¢ļæ½ļæ½emotion interactions has revealed intriguing cognitive inhibition effects by emotionally negative words in bilinguals. Here, we turn to the domain of human risk taking and show that the experience of positive recency in games of chanceĆ¢ļæ½ļæ½the Ć¢ļæ½ļæ½hot handĆ¢ļæ½ļæ½ effectĆ¢ļæ½ļæ½is diminished when game outcomes are provided in a second language rather than the native language. We engaged late Chinese-English bilinguals with Ć¢ļæ½ļæ½playĆ¢ļæ½ļæ½ or Ć¢ļæ½ļæ½leaveĆ¢ļæ½ļæ½ decisions upon presentation of equal-odds bets while manipulating language of feedback and outcome value. When positive game outcomes were presented in their second language, English, participants subsequently took significantly fewer gambles and responded slower compared with the trials in which equivalent feedback was provided in Chinese, their native language. Positive feedback was identified as driving the cross-language difference in preference for risk over certainty: feedback for previous winning outcomes presented in Chinese increased subsequent risk taking, whereas in the English context no such effect was observed. Complementing this behavioral effect, event-related brain potentials elicited by feedback words showed an amplified response to Chinese relative to English in the feedback-related negativity window, indicating a stronger impact in the native than in the second language. We also observed a main effect of language on P300 amplitude and found it correlated with the cross-language difference in risk selections, suggesting that the greater the difference in attention between languages, the greater the difference in risk-taking behavior. These results provide evidence that the hot hand effect is at least attenuated when an individual operates in a non-native language

    Changes in ocean vertical heat transport with global warming

    Get PDF
    Heat transport between the surface and deep ocean strongly influences transient climate change. Mechanisms setting this transport are investigated using coupled climate models and by projecting ocean circulation into the temperature-depth diagram. In this diagram, a ā€œcold cellā€ cools the deep ocean through the downwelling of Antarctic waters and upwelling of warmer waters and is balanced by warming due to a ā€œwarm cell,ā€ coincident with the interhemispheric overturning and previously linked to wind and haline forcing. With anthropogenic warming, the cold cell collapses while the warm cell continues to warm the deep ocean. Simulations with increasingly strong warm cells, set by their mean Southern Hemisphere winds, exhibit increasing deep-ocean warming in response to the same anthropogenic forcing. It is argued that the partition between components of the circulation which cool and warm the deep ocean in the preindustrial climate is a key determinant of ocean vertical heat transport with global warming

    EBP1 and DRBP76/NF90 binding proteins are included in the major histocompatibility complex class II RNA operon

    Get PDF
    Major histocompatibility complex class II mRNAs encode heterodimeric proteins involved in the presentation of exogenous antigens during an immune response. Their 3ā€²UTRs bind a protein complex in which we identified two factors: EBP1, an ErbB3 receptor-binding protein and DRBP76, a double-stranded RNA binding nuclear protein, also known as nuclear factor 90 (NF90). Both are well-characterized regulatory factors of several mRNA molecules processing. Using either EBP1 or DRBP76/NF90-specific knockdown experiments, we established that the two proteins play a role in regulating the expression of HLA-DRA, HLA-DRB1 and HLA-DQA1 mRNAs levels. Our study represents the first indication of the existence of a functional unit that includes different transcripts involved in the adaptive immune response. We propose that the concept of ā€˜RNA operonā€™ may be suitable for our system in which MHCII mRNAs are modulated via interaction of their 3ā€²UTR with same proteins

    Overturning in the Subpolar North Atlantic Program: A New International Ocean Observing System

    Get PDF
    For decades oceanographers have understood the Atlantic meridional overturning circulation (AMOC) to be primarily driven by changes in the production of deep-water formation in the subpolar and subarctic North Atlantic. Indeed, current Intergovernmental Panel on Climate Change (IPCC) projections of an AMOC slowdown in the twenty-first century based on climate models are attributed to the inhibition of deep convection in the North Atlantic. However, observational evidence for this linkage has been elusive: there has been no clear demonstration of AMOC variability in response to changes in deep-water formation. The motivation for understanding this linkage is compelling, since the overturning circulation has been shown to sequester heat and anthropogenic carbon in the deep ocean. Furthermore, AMOC variability is expected to impact this sequestration as well as have consequences for regional and global climates through its effect on the poleward transport of warm water. Motivated by the need for a mechanistic understanding of the AMOC, an international community has assembled an observing system, Overturning in the Subpolar North Atlantic Program (OSNAP), to provide a continuous record of the transbasin fluxes of heat, mass, and freshwater, and to link that record to convective activity and water mass transformation at high latitudes. OSNAP, in conjunction with the Rapid Climate Changeā€“Meridional Overturning Circulation and Heatflux Array (RAPIDā€“MOCHA) at 26Ā°N and other observational elements, will provide a comprehensive measure of the three-dimensional AMOC and an understanding of what drives its variability. The OSNAP observing system was fully deployed in the summer of 2014, and the first OSNAP data products are expected in the fall of 2017

    Generation of a genomic tiling array of the human Major Histocompatibility Complex (MHC) and its application for DNA methylation analysis

    Get PDF
    Background: The major histocompatibility complex (MHC) is essential for human immunity and is highly associated with common diseases, including cancer. While the genetics of the MHC has been studied intensively for many decades, very little is known about the epigenetics of this most polymorphic and disease-associated region of the genome.Methods: To facilitate comprehensive epigenetic analyses of this region, we have generated a genomic tiling array of 2 Kb resolution covering the entire 4 Mb MHC region. The array has been designed to be compatible with chromatin immunoprecipitation (ChIP), methylated DNA immunoprecipitation (MeDIP), array comparative genomic hybridization (aCGH) and expression profiling, including of non-coding RNAs. The array comprises 7832 features, consisting of two replicates of both forward and reverse strands of MHC amplicons and appropriate controls.Results: Using MeDIP, we demonstrate the application of the MHC array for DNA methylation profiling and the identification of tissue-specific differentially methylated regions (tDMRs). Based on the analysis of two tissues and two cell types, we identified 90 tDMRs within the MHC and describe their characterisation.Conclusion: A tiling array covering the MHC region was developed and validated. Its successful application for DNA methylation profiling indicates that this array represents a useful tool for molecular analyses of the MHC in the context of medical genomics

    Impaired Chromatin Remodelling at STAT1-Regulated Promoters Leads to Global Unresponsiveness of Toxoplasma gondii-Infected Macrophages to IFN-Ī³

    Get PDF
    Intracellular pathogens including the apicomplexan and opportunistic parasite Toxoplasma gondii profoundly modify their host cells in order to establish infection. We have shown previously that intracellular T. gondii inhibit up-regulation of regulatory and effector functions in murine macrophages (MĪ¦) stimulated with interferon (IFN)-Ī³, which is the cytokine crucial for controlling the parasites' replication. Using genome-wide transcriptome analysis we show herein that infection with T. gondii leads to global unresponsiveness of murine macrophages to IFN-Ī³. More than 61% and 89% of the transcripts, which were induced or repressed by IFN-Ī³ in non-infected MĪ¦, respectively, were not altered after stimulation of T. gondii-infected cells with IFN-Ī³. These genes are involved in a variety of biological processes, which are mostly but not exclusively related to immune responses. Analyses of the underlying mechanisms revealed that IFN-Ī³-triggered nuclear translocation of STAT1 still occurred in Toxoplasma-infected MĪ¦. However, STAT1 bound aberrantly to oligonucleotides containing the IFN-Ī³-responsive gamma-activated site (GAS) consensus sequence. Conversely, IFN-Ī³ did not induce formation of active GAS-STAT1 complexes in nuclear extracts from infected MĪ¦. Mass spectrometry of protein complexes bound to GAS oligonucleotides showed that T. gondii-infected MĪ¦ are unable to recruit non-muscle actin to IFN-Ī³-responsive DNA sequences, which appeared to be independent of stimulation with IFN-Ī³ and of STAT1 binding. IFN-Ī³-induced recruitment of BRG-1 and acetylation of core histones at the IFN-Ī³-regulated CIITA promoter IV, but not Ī²-actin was diminished by >90% in Toxoplasma-infected MĪ¦ as compared to non-infected control cells. Remarkably, treatment with histone deacetylase inhibitors restored the ability of infected macrophages to express the IFN-Ī³ regulated genes H2-A/E and CIITA. Taken together, these results indicate that Toxoplasma-infected MĪ¦ are unable to respond to IFN-Ī³ due to disturbed chromatin remodelling, but can be rescued using histone deacetylase inhibitors
    • ā€¦
    corecore