Summary: A new study reports on the role a microRNA plays in major depressive disorder.
Source: University of Alabama at Birmingham.
A UAB study that is the first of its kind found that a tiny RNA — miR-124-3p — appears to play a role in producing major depression.
A tiny RNA appears to play a role in producing major depression, the mental disorder that affects as many as 250 million people a year worldwide.
Major depression, formally known as major depressive disorder, or MDD, brings increased risk of suicide and is reported to cause the second-most years of disability after low-back pain.
University of Alabama at Birmingham researchers have found that amounts of this microRNA are significantly elevated in the brains of experimental rats with induced depression from corticosterone treatment, in the post-death brains of humans diagnosed with MDD and in peripheral blood serum from living patients with MDD, according to a study by led by Yogesh Dwivedi, Ph.D., the Elesabeth Ridgely Shook Endowed Professor and director of Translational Research, UAB Mood Disorders Program, Department of Psychiatry.
This microRNA — miR-124-3p — is thus a potential therapeutic target for novel drug development, and it can serve as a putative biomarker for MDD pathogenesis.
Micro RNAs, or miRNAs, interact with messenger RNA after the miRNA is exported from the cell nucleus and processed by a team of enzymes. MiRNAs are robust players of gene regulation in cells, and there are more than 1,300 different miRNAs at work in the brain.
In previous work, Dwivedi and colleagues had seen that a set of miRNAs were coordinately regulated in the prefrontal cortex of the brains of MDD subjects. The prefrontal cortex, known for controlling the executive function of the brain, is critically involved in the response to stress, by regulating the endocrine glands known as the hypothalamic-pituitary-adrenal axis. The adrenal gland produces the stress hormone cortisol in humans and corticosterone in rodents.
To see if stress plays a role in the coordinated regulation of prefrontal cortex miRNAs, the UAB researchers then turned to a rat depression model. They found that rats treated with corticosterone to induce depression-like behavior showed coordinated dysregulation of miRNAs in the prefrontal cortex, and the most significantly affected miRNA was miR-124-3p.
Their current paper, previewed in the journal Neuropsychopharmacology, examined the relevance of miR-124-3p in MDD pathogenesis.
Using computer analysis of genome sequences, the researchers:
- Identified eight highly potential target genes for binding by miR-124-3p, genes whose function is also reported to be critical in brain physiology during stress and MDD pathogenesis. Four of these potential target genes were significantly down-regulated in the prefrontal cortex of corticosterone-treated rats, and this down-regulation inversely correlated with miR-124-3p levels.
- Showed that the four genes that were significantly down-regulated have evolutionarily conserved miR-124-3p binding sites across a wide range of higher vertebrate species.
In neuroblastoma cells grown in culture:
- Overexpression of miR-124-3p caused significant down-regulation for two of the potential target genes.
In prefrontal cortex neurons from depression-model rats treated with corticosterone:
- Significant binding by miR-124-3p to two of the potential target genes was seen, as measured from immunoprecipitated RNA-induced silencing complexes.
- The locus-specific origin of for mature miR-124-3p was identified at a site on chromosome 3, out of three possible chromosomal sites, and two CpG “islands” that can act as sites from epigenetic modification by DNA methylation were identified near the miR-124 gene promoter on chromosome 3.
- This miR-124-3 promoter was found to be hypo-methylated in the corticosterone-treated rats, and the gene expression of one DNA methyltransferase — Dnmt3a — was significantly repressed.
- In post-mortem brains of 15 controls and 15 MDD subjects, the MDD group showed significant increase in the expression of miR-124-3p, and expression of three of the potential target genes was significantly lower.
- The level of miR-124-3p was significantly higher in the serum of 18 antidepressant-free MDD patients, as compared with 17 healthy controls.
“Altogether,” the UAB researchers conclude, “this is the first comprehensive and mechanistic study at in-vitro and in-vivo levels which demonstrates that, not only are there consistent depression-associated changes in the expression of miR-124-3p across different species, but also the genes that are targets of this miRNA are highly dysregulated, showing altered response at functional level.”
Besides Dwivedi, authors of the paper, “Identification of microRNA-124-3p as a Putative Epigenetic Signature of Major Depressive Disorder,” are Bhaskar Roy, Ph.D., Michael Dunbar, and Richard C. Shelton, M.D., all of the UAB Department of Psychiatry and Behavioral Neurobiology. Shelton holds the Charles Byron Ireland Chair of Psychiatric Research at UAB.
Funding: The research was supported by National Institute of Mental Health grants MH082802, MH081099, MH101890, MH100616 and MH107183; and an American Foundation for Suicide Prevention grant, SRG-XXXX-001778-1209.
Source: Jeff Hansen – University of Alabama at Birmingham
Image Source: This NeuroscienceNews.com image is adapted from the University of Alabama at Birmingham press release.
Original Research: Abstract for “Identification of microRNA-124-3p as a Putative Epigenetic Signature of Major Depressive Disorder” by Bhaskar Roy, Michael Dunbar, Richard C Shelton and Yogesh Dwivedi in Neuropsychopharmacology. Published online August 31 2016 doi:10.1038/npp.2016.175
Identification of microRNA-124-3p as a Putative Epigenetic Signature of Major Depressive Disorder
Major depressive disorder (MDD) is predicted to be the 2nd leading cause of global disease burden by 2030. A large number of MDD patients do not respond to the currently available medication because of its poorly understood etiology. Recently, studies of microRNAs (miRNAs), which act as a molecular switch of gene expression, have shown promise in identifying molecular network that could provide significant clues to various psychiatric illnesses. Using an in vitro system, a rodent depression model, and human postmortem brain, we investigated the role of a brain enriched, neuron specific miRNA, miR-124-3p, whose expression is highly dysregulated in stressed rodents, and identified a set of target genes involved in stress response and neural plasticity. We also found that miR-124-3p is epigenetically regulated and its interaction with RNA induced silencing complex (RISC) is compromised in MDD. Using blood serum, we found similar dysregulation of miR-124-3p in antidepressant free MDD subjects. Altogether, our study demonstrates potential contribution of miR-124-3p in the pathophysiology of MDD and suggests that this miRNA may serve as a novel target for drug development and a biomarker for MDD pathogenesis.
“Identification of microRNA-124-3p as a Putative Epigenetic Signature of Major Depressive Disorder” by Bhaskar Roy, Michael Dunbar, Richard C Shelton and Yogesh Dwivedi in Neuropsychopharmacology. Published online August 31 2016 doi:10.1038/npp.2016.175