Abstract

BackgroundRecent studies suggest that alterations in expression of genes, including those which regulate neural and structural plasticity, may be crucial in the pathogenesis of depression. MicroRNAs (miRNAs) are newly discovered regulators of gene expression that have recently been implicated in a variety of human diseases, including neuropsychiatric diseases.Methodology/Principal FindingsThe present study was undertaken to examine whether the miRNA network is altered in the brain of depressed suicide subjects. Expression of miRNAs was measured in prefrontal cortex (Brodmann Area 9) of antidepressant-free depressed suicide (n = 18) and well-matched non-psychiatric control subjects (n = 17) using multiplex RT-PCR plates. We found that overall miRNA expression was significantly and globally down-regulated in prefrontal cortex of depressed suicide subjects. Using individual tests of statistical significance, 21 miRNAs were significantly decreased at p = 0.05 or better. Many of the down-regulated miRNAs were encoded at nearby chromosomal loci, shared motifs within the 5′-seeds, and shared putative mRNA targets, several of which have been implicated in depression. In addition, a set of 29 miRNAs, whose expression was not pairwise correlated in the normal controls, showed a high degree of co-regulation across individuals in the depressed suicide group.Conclusions/SignificanceThe findings show widespread changes in miRNA expression that are likely to participate in pathogenesis of major depression and/or suicide. Further studies are needed to identify whether the miRNA changes lead to altered expression of prefrontal cortex mRNAs, either directly (by acting as miRNA targets) or indirectly (e.g., by affecting transcription factors).

Highlights

  • Depression is a major public health concern

  • This study was designed to examine whether miRNA expression is altered in postmortem prefrontal cortex of depressed suicide subjects compared to matched control subjects who died from natural or accidental causes

  • We observed that miRNA expression was globally down-regulated in depressed suicide subjects, by 17% on average, a finding that has extremely high statistical significance

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Summary

Introduction

Depression is a major public health concern. Despite many years of research, the molecular and cellular mechanisms associated with depression are not clear. In the past few years, it has become clear that besides the traditional transcriptional mechanisms (e.g., by transcription factors and alternative splicing), gene expression is regulated by a variety of noncoding RNA transcripts that generate antisense RNAs, microRNAs (miRNAs), and other small RNAs, which are linked to several posttranscriptional and epigenetic mechanisms. In PLoS ONE | www.plosone.org miRNA and Depression length, which, together with eIF2c and other associated proteins such as FMRP, comprises the so-called RISC complex. Recent studies suggest that alterations in expression of genes, including those which regulate neural and structural plasticity, may be crucial in the pathogenesis of depression. MicroRNAs (miRNAs) are newly discovered regulators of gene expression that have recently been implicated in a variety of human diseases, including neuropsychiatric diseases

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