33 research outputs found

    Transcriptome Sequencing Revealed Significant Alteration of Cortical Promoter Usage and Splicing in Schizophrenia

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    While hybridization based analysis of the cortical transcriptome has provided important insight into the neuropathology of schizophrenia, it represents a restricted view of disease-associated gene activity based on predetermined probes. By contrast, sequencing technology can provide un-biased analysis of transcription at nucleotide resolution. Here we use this approach to investigate schizophrenia-associated cortical gene expression.The data was generated from 76 bp reads of RNA-Seq, aligned to the reference genome and assembled into transcripts for quantification of exons, splice variants and alternative promoters in postmortem superior temporal gyrus (STG/BA22) from 9 male subjects with schizophrenia and 9 matched non-psychiatric controls. Differentially expressed genes were then subjected to further sequence and functional group analysis. The output, amounting to more than 38 Gb of sequence, revealed significant alteration of gene expression including many previously shown to be associated with schizophrenia. Gene ontology enrichment analysis followed by functional map construction identified three functional clusters highly relevant to schizophrenia including neurotransmission related functions, synaptic vesicle trafficking, and neural development. Significantly, more than 2000 genes displayed schizophrenia-associated alternative promoter usage and more than 1000 genes showed differential splicing (FDR<0.05). Both types of transcriptional isoforms were exemplified by reads aligned to the neurodevelopmentally significant doublecortin-like kinase 1 (DCLK1) gene.This study provided the first deep and un-biased analysis of schizophrenia-associated transcriptional diversity within the STG, and revealed variants with important implications for the complex pathophysiology of schizophrenia

    Social anxiety, fear of negative evaluation and the detection of negative emotion in others.

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    The present study sought to investigate whether social anxiety is associated with enhanced ability to detect negative emotion in others. Subjects scoring high and low on Fear of Negative Evaluation (FNE) performed two tasks before and after a social threat induction. The first task involved identifying the affect (negative vs neutral) in briefly presented (60 msec) slides of faces. The second involved rating the overall emotion conveyed in brief video clips of an actor and detecting discrepancies in the affect conveyed by the visual and auditory channels of the video. Overall the results suggest that high social anxiety subjects have a bias towards identifying others' emotional expressions as negative in the absence of an enhanced ability to discriminate between different emotional states in others. Implications and limitations of the results are discussed
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