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. 2020 Aug 24;10(1):297.
doi: 10.1038/s41398-020-00966-4.

Integration of postmortem amygdala expression profiling, GWAS, and functional cell culture assays: neuroticism-associated synaptic vesicle glycoprotein 2A (SV2A) gene is regulated by miR-133a and miR-218

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Integration of postmortem amygdala expression profiling, GWAS, and functional cell culture assays: neuroticism-associated synaptic vesicle glycoprotein 2A (SV2A) gene is regulated by miR-133a and miR-218

Magdalena Jurkiewicz et al. Transl Psychiatry. .

Abstract

Recent genome-wide studies have begun to identify gene variants, expression profiles, and regulators associated with neuroticism, anxiety disorders, and depression. We conducted a set of experimental cell culture studies of gene regulation by micro RNAs (miRNAs), based on genome-wide transcriptome, proteome, and miRNA expression data from twenty postmortem samples of lateral amygdala from donors with known neuroticism scores. Using Ingenuity Pathway Analysis and TargetScan, we identified a list of mRNA-protein-miRNA sets whose expression patterns were consistent with miRNA-based translational repression, as a function of trait anxiety. Here, we focused on one gene from that list, which is of particular translational significance in Psychiatry: synaptic vesicle glycoprotein 2A (SV2A) is the binding site of the anticonvulsant drug levetiracetam ((S)-α-Ethyl-2-oxo-1-pyrrolidineacetamide), which has shown promise in anxiety disorder treatments. We confirmed that SV2A is associated with neuroticism or anxiety using an original GWAS of a community cohort (N = 1,706), and cross-referencing a published GWAS of multiple cohorts (Ns ranging from 340,569 to 390,278). Postmortem amygdala expression profiling implicated three putative regulatory miRNAs to target SV2A: miR-133a, miR-138, and miR-218. Moving from association to experimental causal testing in cell culture, we used a luciferase assay to demonstrate that miR-133a and miR-218, but not miR-138, significantly decreased relative luciferase activity from the SV2A dual-luciferase construct. In human neuroblastoma cells, transfection with miR-133a and miR-218 reduced both endogenous SV2A mRNA and protein levels, confirming miRNA targeting of the SV2A gene. This study illustrates the utility of combining postmortem gene expression data with GWAS to guide experimental cell culture assays examining gene regulatory mechanisms that may contribute to complex human traits. Identifying specific molecular mechanisms of gene regulation may be useful for future clinical applications in anxiety disorders or other forms of psychopathology.

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Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1. SV2A protein and mRNA levels in human postmortem lateral amygdala.
a Mean SV2A protein levels of anxious individuals compared to controls. Error bars are standard error of the mean (SEM), t-test p value < 0.05. b Mean SV2A mRNA levels do not differ significantly between controls and anxious individuals. Error bars are SEM, t-test p value = 0.87. c Significantly higher levels of the three miRNAs (miR-133a, miR-138, and miR-218) are found in anxious individuals, compared to controls. Error bars are SEM, *t-test p value < 0.05 for miR-133a and miR-218 expression in anxious individuals versus controls, and + t-test p value = 0.051 for miR-138 expression in anxious individuals versus controls.
Fig. 2
Fig. 2. miR-218 and miR-133a but not miR-138 target the 3′UTR of SV2A.
HEK 293 cells were transfected with the SV2A-3′UTR vector (“SV2A”) or SV2A-3′UTR mutant vector (“SV2Amut”) and respective miRNA mimics and incubated for 24 h. All firefly/renilla ratios are normalized to the SV2A 3′UTR clone. Error bars are SEM, *statistical significance is based on one-way ANOVA with Tukey post-hoc test, p value < 0.05 vs SV2A control.
Fig. 3
Fig. 3. Transfection with miR-133a and miR-218, but not with miR-138, decreases endogenous SV2A mRNA and protein levels in SH-SY5Y cells.
a Cells transfected with miR-133a and miR-218 mimics, but not miR-138 mimics or other controls, showed a significant decrease in SV2A mRNA levels. b Cells transfected with miR-133a and miR-218 mimics, but not miR-138 mimics or other controls, showed a significant decrease in SV2A protein levels. c The blot images are from representative immunoblots. Error bars are SEM, *statistical significance is based on one-way ANOVA with Tukey post-hoc test, p-value < 0.05 vs untreated control condition and mock transfection with negative control mimic.

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