The monoamine oxidase A (MAOA) uVNTR (upstream variable number tandem repeat) is one of the most often cited examples of a gene by environment interaction (GxE) in relation to behavioral traits. However, MAOA possesses a second VNTR, 500 bp upstream of the uVNTR, which is termed d- or distal VNTR. Furthermore, genomic analysis indicates that there are a minimum of two transcriptional start sites (TSSs) for MAOA, one of which encompasses the uVNTR within the 5′ untranslated region of one of the isoforms. Through expression analysis in semi-haploid HAP1 cell lines genetically engineered in order to knockout (KO) either the uVNTR, dVNTR, or both VNTRs, we assessed the effect of the two MAOA VNTRs, either alone or in combination, on gene expression directed from the different TSSs. Complementing our functional analysis, we determined the haplotype variation of these VNTRs in the general population. The expression of the two MAOA isoforms was differentially modulated by the two VNTRs located in the promoter region. The most extensively studied uVNTR, previously considered a positive regulator of the MAOA gene, did not modulate the expression of what it is considered the canonical isoform, while we found that the dVNTR positively regulated this isoform in our model. In contrast, both the uVNTR and the dVNTR were found to act as negative regulators of the second less abundant MAOA isoform. The haplotype analysis for these two VNTRs demonstrated a bias against the presence of one of the potential variants. The uVNTR and dVNTR differentially affect expression of distinct MAOA isoforms, and thus, their combined profiling offers new insights into gene-regulation, GxE interaction, and ultimately MAOA-driven behavior.
Monoamine oxidase A (MAOA), a major regulator of monoamine neurotransmitters in the brain, is one of the best characterized and most cited genes in gene × environment interaction (GxE) studies, particularly in relation to central nervous system (CNS) disorders (Nikulina et al. 2012; Philibert et al. 2008; Reif et al. 2014; Samochowiec et al. 2004) and behavioral traits (Aslund et al. 2011; Caspi et al. 2002; Chester et al. 2015; Hill et al. 2013; Pickles et al. 2013). Two coding transcripts for the MAOA gene have been reported, with transcriptional start sites (TSSs) separated by approximately 1.3 kb, resulting in two putative coding isoforms with distinct 5′ untranslated regions (5′ UTRs). These isoforms vary in length and contain alternative exons and distinct start codons which potentially lead to the translation of two protein isoforms (Fig. 1a, b); however, the functional consequences of this have not been discussed in the literature. The regulation of these two TSSs is expected in part to be directed by two distinct variable number tandem repeat (VNTR) domains identified in the MAOA promoter region, which have previously been demonstrated to support gene expression in reporter gene assays (Philibert et al. 2011; Sabol et al. 1998). The first, termed uVNTR, is located 1 kb upstream of the TSS for what we will term the primary MAOA isoform (Fig. 1a; Ensembl isoform 201), which is the most abundant mRNA and the TSS most referred to in previous communications analyzing the function of the uVNTR (Edwards et al. 2010; Lee and Ham 2008; Lung et al. 2011; Reif et al. 2008; Sabol et al. 1998). In this context, the uVNTR is considered a transcriptional regulatory domain upstream of this major TSS. However, in the second isoform, it is transcribed in the 5′UTR (Fig. 1b), which is produced from the more 5′ TSS. The MAOA uVNTR consists of a 30-bp motif that can be repeated 2, 3, 3.5, 4, and 5 times (Sabol et al. 1998). The 2, 3, and 5 repeats are generally defined as low expression variants (MAOA-L), while the 3.5 and 4 repeat VNTRs have been shown to demonstrate a 2- to 10-fold increase in reporter gene expression and considered high expression variants (MAOA-H) (Sabol et al. 1998). We and others have previously reported evidence that specific uVNTR variants act as a moderators of the association observed between certain environmental risk factors and child behavioral problems (Fergusson et al. 2012; Hill et al. 2013; Pickles et al. 2013). However, the majority of the literature refers only to the uVNTR as the major, or sole, mediator of MAOA expression and a possible biomarker for stress-related illnesses, with the different alleles implicated in major depressive disorder, addiction, violent behavior (Fan and Sklar 2005; Frazzetto et al. 2007; Melas et al. 2013; Philibert et al. 2008; Reif et al. 2014), suicide attempts in bipolar females (Ho et al. 2000), and depressed males (Du et al. 2002). The second VNTR, termed dVNTR, is located approximately 500 bp upstream of the uVNTR and is composed of two different decamer repeats CCCCTCCCCG (repeat A) and CTCCTCCCCG (repeat B) (Philibert et al. 2011). Genotypes of 8, 9, 10, 11, and 12 repeats have been documented, with 9R and 10R being the most common. In reporter gene assays, similarly to the uVNTR, the 9R and 10R differ in transcriptional efficiency, where the 9R is stronger than the 10R and the other genotypes are intermediate (Philibert et al. 2011).
Through analysis of the semi-haploid HAP1 cell line (Carette et al. 2011) deleted for either the uVNTR, dVNTR, or both VNTRs, we assessed the effect the two VNTRs, combined and individually, on MAOA expression and specifically on the two distinct TSSs. We also analyzed the variation in the haplotype of the MAOA promoter in the general population to determine common haplotypes that may be used for further stratification of the genetic risk of MAOA polymorphism in psychiatric disorders.
Methods and Materials
The human neuroblastoma cell line SH-SY5Y (ATCC/CRL-2266) which is near diploid (47 chromosomes) (Spengler et al. 2002) was cultured in a 1:1 mix of Dulbecco’s EMEM and Ham’s F12 media supplemented with 10% (v/v) fetal bovine serum, 2 mM l-glutamine, 1 mM sodium pyruvate, and penicillin 100 U/ml/streptomycin 0.1 mg/ml. The HAP1 cell lines (Carette et al. 2011; Essletzbichler et al. 2014) were obtained from Horizon Genomics (Cambridge, UK) and cultured in Iscove’s modified Dulbecco’s medium (GIBCO, Paisley, UK), supplemented with 10% (v/v) fetal bovine serum and 100 U/ml penicillin/0.1 mg/ml streptomycin. Cells were cultured at 37 °C in a humidified 5% CO2 atmosphere to 70–80% confluence with culture media being replaced every other day; reagents unless otherwise stated were from Sigma, Dorset, UK.
Total RNA Preparation and cDNA Synthesis
Total RNA was extracted using Trizol reagent (Invitrogen, Paisley, UK), and 3 μg was reverse-transcribed to cDNA using GoScript® Reverse Transcription System (Promega, Southampton, UK) and random primers following the manufacturers’ instructions.
Genotyping of the MAOA Promoter VNTRs
Genotyping of the MAOA uVNTR was performed as previously described (Pickles et al. 2013). The MAOA dVNTR PCR reactions (20 μl) contained 10 ng genomic DNA template, 5 pmol of each primer (Forward 5′-FAM-GGGTTAAGCGCCTCAGCTTG-3′ and Reverse 5′-CAAGAGTGGACTTAAGGAAGCAG-3′ [Eurofins, Ebersberg, Germany]), 1× GoTaq® flexi buffer, 1 mM MgCl2, 0.1 mM of each dNTP, and 0.625 U of GoTaq® DNA polymerase (Promega, Southampton, UK). 7-DeazaGTP (6.25 μM), 1 M betaine, and 3% (v/v) DMSO were added to the reaction due to the high GC content of the region. PCR cycling conditions included touchdown to the annealing step from 65 to 55 °C over 10 cycles, followed by 35 cycles at the annealing temperature (55 °C). Analyses were by both 2% agarose gel electrophoresis and by capillary electrophoresis ABI 3130 (Life Technologies, Paisley, UK) in which the genotypes were called using Genemapper V4.0 (Life Technologies) or the QIAxcel Advanced System (Qiagen, Manchester, UK). The results from each method were analyzed blind from each other.
Horizon Genomics Generation of HAP1 VNTR KO Cells
The HAP1 clones were generated by Horizon Discovery (https://www.horizondiscovery.com/gene-editing/crispr) using the CRISPR/Cas9 deletion system. The KO cell lines were validated by PCR and Sanger sequencing to confirm the presence of the desired mutation at the genomic level (Supplementary Figs. S1–S2).
mRNA Analysis in the HAP1 Cell Line and KO Derivatives
Reactions containing 10 ng cDNA template, 5 pmol each primer (Eurofins, Ebersberg, Germany), 1× GoTaq® flexi buffer, 1 mM MgCl2, 0.1 mM each dNTP, 1 M betaine, and 0.625 U GoTaq® DNA polymerase (Promega, Southampton, UK) were employed to analyze the levels of distinct isoforms of mRNA produced using the following primer pairs: (a) total MAOA expression (i.e., isoforms 201 and 204 combined) addressed by amplification of MAOA exon III–exon VI fragment Forward 5′-TACGTAGATGTTGGTGGAGCTT-3′, Reverse 5′-AGAATATCCGAGTGGTGCCC-3′; (b) isoform 204 alone MAOA exon I–exon IIA fragment, Forward primer 5′-CGGGTATCAAAAGAAGGATCG-3′, Reverse primer 5′-CCAGGAGCTGCTTTCCTCTGATGC-3′. Cycling conditions were 2 min at 95 °C initial denaturation, followed by 35 cycles of 20 s at 95 °C, 20 s at 61 °C and 30 s 72 °C, and final elongation for 5 min at 72 °C.
Amplicons were analyzed using a QIAxcel Advanced System (Qiagen, Manchester, UK,) with the following parameters: QX DNA screening gel cartridge default 2.0 using the AM420 method. Standard alignment marker of 15–600 bp and QX DNA size marker of 25–500 bp were run simultaneously allowing a fully automated size separation and quantification of each sample. Amplicon properties and concentration were determined by QIAxcel BioCalculator software using a proprietary algorithm supplied by the manufacturer. The clonal cell lines were derived from the same parental background and cultured under identical conditions; thus, MAOA values were normalized only to the housekeeping gene β-actin (Forward primer 5′-CACCTTCTACAATGAGCTGCGTGTG-3′ and Reverse primer 5′-ATAGCACAGCCTGGATAGCAACGTAC-3′) prior to analysis.
Genomic DNA was obtained from saliva of 283 children who participated in the Wirral Child Health and Development Study (WCHADS), a longitudinal Medical Research Council (MRC) funded study of child development. Ethical approval for the study was granted by the Cheshire North and West Research Ethics Committee on the June 27, 2006 (ref: 05/Q1506/107).
In Silico Analysis
The University of California Santa Cruz (UCSC) Genome Browser (http://genome.ucsc.edu) was used for genomic positioning and mapping of the selected markers. Genotyped data were subject to quality control examination and gender check. The data was then formatted into a pedigree format file (.PED). MIDAS (Multiallelic Interallelic Disequilibrium Analysis Software) was employed for the LD analysis and construction of the haplotype blocks of the interallelic linkage disequilibrium. The data for both VNTR loci were analyzed following the instructions given by (Gaunt et al. 2006). Common and rare alleles were then imputed based on the inferred haplotype blocks and analysis conducted separately for males and females.
The relative gene expression data from the different HAP1 cell lines were analyzed with IBM SPSS Statistics software for Windows, version 24 (IBM Corp., Armonk, NY, USA) through a univariate general lineal model followed by a Bonferroni post hoc test. Data were considered significantly different at p < 0.05.
Bioinformatic Analysis of MAOA
Structured searches through accredited publicly available genomic resources, including UCSC (https://genome.ucsc.edu/), AceView (http://www.ncbi.nlm.nih.gov/ieb/research/acembly/), UniProt (http://www.uniprot.org/), and Ensembl (http://www.ensembl.org/) confirmed four mRNA isoforms for the human MAOA gene (201, 202, 203, and 204); two of them (201 and 204) correspond to coding transcripts that predict at least two distinct MAOA protein variants (Fig. 1).
The primary MAOA isoform (Fig. 1a, isoform 201) comprises a 4015-bp transcript and encodes a full-length protein of 527 amino acids. The 5′UTR of this mRNA isoform was found to extend 124 bp upstream from the first ATG codon with the MAOA uVNTR located approximately 1 kb upstream of the TSS used to generate this isoform (Sabol et al. 1998). The second MAOA isoform (Fig. 1b; isoform204) had a longer 5′ UTR (~ 1.3 kb), which encompassed the uVNTR within its sequence. This predicted transcript was actually longer than the primary type (5438 versus 4015 bp) and contained an alternative non-coding exon (here termed exon IIA), which would introduce a premature (TGA) stop codon due to a shift in the reading frame. This, in turn, could result in the translational start site shifting to exon IV where the next in-frame methionine codon (ATG) is located, resulting in an amino-terminal truncated version of the MAOA protein (394 AA), exactly 133 residues shorter than the primary isoform as illustrated in Fig. 1b. De Colibus et al. (2005) identified that the MAOA FAD/NAD binding domain comprised residues 13–88, 220–294, and 400–462 in the primary isoform therefore an N-terminal section of the FAD/NAD binding domain was omitted in this alternative minor isoform, which incidentally largely overlapped with the non-coding isoform 203 (Fig. 1c).
Expression of the Two MAOA Isoforms in SH-SY5Y Cell Line
We used the well-characterized human neuroblastoma female-derived cell line SH-SY5Y which was found to be heterozygous for the uVNTR with three and four copies of the repeat element to address expression of the predicted isoform 204 in extant cells. This allowed identification of allele-specific expression when initiated from the more 5′ TSS that included the uVNTR in the 5′UTR (Fig. 1b, isoform 204). Under basal growth conditions, we detected mRNA corresponding to expression from both alleles using the uVNTR length as the distinguishing feature, thus validating the predicted in silico isoform (Fig. 2a).
HAP 1 Cell Line Characterization
To address the function of the u- and dVNTRs in MAOA gene expression, we utilized CRISPR/Cas9 deletion to produce HAP1cell line clones with selected distinct VNTR haplotypes. As summarized in Fig. 3, four different single KO cell lines were generated from the parental cell line (P) by Horizon Discovery. Two of these had the uVNTR deleted from the MAOA promoter region but still possessed the dVNTR positioned upstream of the gene (clones A and B); similarly, two single KO lines were generated targeting the dVNTR initially (clones C and D). To generate the double VNTR KO clones a second, de novo, CRISPR/Cas9 deletion was performed on single KO clones B or C to either remove the dVNTR (clones E and F) or the uVNTR (clones G and H).
The VNTR deletions were confirmed by PCR, individually targeting MAOA uVNTR and dVNTR, respectively, as shown in the supplementary Fig. S1. The semi-haploid parental cell line (P) contained the alleles 3R and 10R for the uVNTR and dVNTR, respectively.
MAOA Gene Expression in HAP1 Cells
The expression of the combined putative MAOA coding isoforms (i.e., 201 and 204) was assessed using the primer set that amplified the region flanking exon III to exon VI of the MAOA gene (Fig. 1) which reported a significant difference of expression between the groups F(9,27) = 190.2, p < 0.001. Conversely, amplification from exon I to alternative exon IIA allowed us to determine the expression of the less abundant MAOA coding isoform 204 alone, which spans the more upstream TSS and encompassed the uVNTR in its 5′UTR (Fig. 1b), which also reported a significant difference of expression among the groups F(9,27) = 40.4, p < 0.001.
The concentration of each isoform was measured using the QIAxcel system after normalization using the housekeeping gene β-actin. It was found that the total MAOA mRNA (i.e., exon III–exon VI assay) and the alternative isoform 204 alone (i.e., exon I–exon IIA assay) in the parental cell line (P), under basal conditions, had average concentrations of 1.90 and 0.10 ng/μl, respectively (Figs. 4 and 5c, d). This facilitated an estimation of the abundance of the alternative isoform 204 at around 5% of the overall MAOA mRNA produced in the parental cell model. Similarly, when using the uVNTR primer set, we obtained the level of isoform 204 at 8% of the total, with a concentration of 0.13 ng/μl (Fig. 5a, b), consistent with the levels obtained with the exon I–IIA assay (Fig. 5c, d).
Deletion of the uVNTR alone from the MAOA promoter region did not significantly alter the total MAOA expression level when compared to the parental cell line (Fig. 4a, clone B). In contrast, deletion of the dVNTR alone (Fig. 4b, clone C) was sufficient to significantly reduce the expression of total MAOA (multiple comparison of Bonferroni post hoc test ***p < 0.01). The expression directed by the double KO cell lines in both Fig. 4a, b (clones E, F, G, and H) was comparable to that of the single dVNTR KO alone. The expression analysis for each single KO clone for both the uVNTR (clones A and B) and dVNTR (clones C and D), as well as the double KO clones (clones E, F, G and H) are contained in supplementary Figs. S3, S4, and S5, respectively.
We next addressed the regulation of expression of the minor isoform 204 by amplification of exons I–IIA (Fig. 5c, d). The parental cell line (P) expressed only a low level of this isoform (~ 5% of total mRNA); however, in comparison, the clones with single deletions of either the u- (Fig. S6-B, clones A and B) or dVNTR (Fig. S7-B, clones C and D) had higher levels of expression ~ 3-fold increase and ~ 2-fold increase, respectively. Furthermore, the data derived from the double KOs derived from clone C (clones G and H, i.e., –d then –u) (Fig. 5d) was supportive of an additive effect on the expression of this MAOA isoform. Although the same trend was observed for clones derived from clone B (clones E and F, i.e., –u then –d) (Fig. 5c), the increment was not statistically significant compared to their parental clone B. The expression analysis data for this MAOA isoform for the single KO clones for the uVNTR and dVNTR is provided in supplementary Figs. S6 and S7, respectively. These findings were replicated using the primer set targeting the uVNTR (F(9,27) = 66.4, p < 0.001) in the 5′UTR of this isoform (Fig. 5a, b), where a similar pattern to that obtained with the exon I–exon IIA primer set was observed, namely all comparisons of isoform 204 between the double KO clones (E, F, G, and H) and the parental cell line (P) were found to be significant with an increase in expression (Fig. 5a–d).
The Haplotype of Distal and Proximal VNTRs in the Population
As they have different regulatory properties, analyzing the haplotype block containing the d- and uVNTRs may allow for further stratification and consequently improve genetic associations which otherwise would be solely based on the genotype of the uVNTR. The allele frequencies for each VNTR locus are shown in Fig. 6. Further to this and given the multi-allelic nature of these two loci, we tested both markers for Hardy-Weinberg equilibrium (HWE) within the female arm, accounting only for the common alleles in a bi-allelic system (p = 0.82 for dVNTR and p = 0.02 for uVNTR) (HWE test was not conducted for males due to the locus hemizygosity). Next, we employed an analysis tool for the construction of the haplotype blocks of the interallelic linkage disequilibrium that accounted for poly-allelic markers (MIDAS, Multiallelic Interallelic Disequilibrium Analysis Software) (Gaunt et al. 2006). Common and rare alleles were then imputed based on the inferred haplotype blocks, and separate analysis for males and females was conducted. This enabled an assessment of the expected versus the observed frequency of both common and rare VNTR haplotypes assuming independent segregation (Table 1). All the haplotype blocks containing the two common alleles for each locus (i.e., 9R and 10R for dVNTR; and 4R and 3R for uVNTR) significantly deviated from their expected haplotype frequencies, and this was highlighted by the significant adjusted χ2 values observed. This extended previous work by Philibert et al. (2011), demonstrating the existence of significant linkage disequilibrium (LD) between these two loci, suggests a lack of recombination between them, with the alleles likely to segregate as part of the same block. Indeed, only three of the four possible combination haplotypes were commonly observed, with the haplotype containing the 10R dVNTR and 4R uVNTR alleles being very rare. This is consistent with the dVNTR being a more recent polymorphism than the uVNTR and that the minor 10R variant of dVNTR most likely had arose from the same strand containing the minor 3R allele of uVNTR (Supplementary Fig. S8). Therefore, this LD and haplotype analysis allowed us to place the 4R uVNTR with the 9R dVNTR allele and stratify the 3R uVNTR allele with either a 10R, 9R, or, to a lesser extent, the 11R dVNTR. Therefore, in summary, the haplotype comprising both major alleles (9R-4R) was the most common one (59.13% females, 60.29% males), followed by 10R-3R (20.07% females, 18.38% males) and 9R-3R (11.77% females, 9.56% males), with the observed 10R-4R haplotype frequency at around 1% only (against an expected frequency above 10%). The rare 3.5R and 5R uVNTR alleles were both exclusively linked with the common 9R dVNTR, whereas the 11R dVNTR was more often part of the block containing the variant 3R uVNTR. The 8R allele dVNTR was extremely rare in our samples. Our results demonstrated no significant differences in the distribution of haplotypes between males and females (t test p > 0.05).
Transcriptomic mapping using Hg38 and ENCODE data indicated that there are multiple isoforms for the MAOA gene (Fig. 1), which was confirmed by mRNA expression data in this study. These two isoforms could be easily distinguished at several levels. The “canonical” MAOA isoform, which we termed the primary isoform (Fig. 1, isoform 201), comprised 15 exons with a shorter 5′ UTR. Conversely, the alternative isoform (Fig. 1, isoform 204) had 16 exons and a longer 5′ UTR, which contained the commonly reported uVNTR (Sabol et al. 1998). Our in silico analysis suggested that the extra exon present in this latter isoform, here termed exon IIA, would introduce a TGA stop codon, thus potentially causing a shift in the start codon for protein translation to exon IV (Fig. 1b). Our study investigated the role of two VNTRs in the MAOA promoter in directing expression from each of the TSS. To address this, we exploited the near-haploid cell line HAP1, which was engineered to remove either the uVNTR, the dVNTR, or both from the MAOA promoter sequence. This allowed us to assess, separately or in combination, the expression patterns of the distinct MAOA isoforms in the presence or absence of these two elements.
Under basal growth conditions in vitro, deletion of the uVNTR did not significantly modulate expression of total MAOA mRNA (Fig. 4a). Conversely, the dVNTR deletion significantly reduced expression of total MAOA mRNA (Fig. 4b), demonstrating that it was a positive regulator of the primary MAOA isoform, which has not been previously reported. Next, we assessed the impact of the double VNTR KOs and found our results to be in line with the mode of action of the single KOs. Specifically, the expression of the primary MAOA isoform in the double KO cell lines appeared to be significantly lower than the parental cell line (Fig. 4) with the major mediator being the dVNTR. Indeed, when the expression of the double KO clones was compared to the single dVNTR deletion, we did not find any significant differences (Fig. 4b). Our data therefore support a major role for the dVNTR in driving the expression of the primary MAOA isoform, further illustrated by the significant reduction of this isoform seen in the double KOs on the uVNTR KO background (Fig. 4a). In contrast, we demonstrated that deletion of either the d- or u- VNTR resulted in increased expression of the minor alternative isoform 204, which contained the uVNTR within its 5′ UTR (Fig. 5a–d); therefore, both VNTRs individually appeared to act as negative regulators of this isoform. The double VNTR KOs also substantially increased the expression of this transcript in relation to the parental cell line (P) (Fig. 5c, d). These observations were replicated using an independent PCR assay targeting the uVNTR (Fig. 5a, b).
Our data indicated that the haplotype of the d- and uVNTRs could account for significant differential regulation of MAOA expression. This would be consistent with previous data showing that distinct combinations of the d- and uVNTRs (9R:3R and 9R:4R) supported distinct reporter gene expression patterns (Philibert et al. 2011). The DNA sequences of the d-and u-VNTR are quite distinct and are therefore likely to bind a different set of transcription factors and mediate a differential response to the same challenge as we and others have demonstrated for the well-characterized regulatory VNTR elements in the SLC6A4 and SLC6A3 genes (Michelhaugh et al. 2001; Vasiliou et al. 2012). Our data indicated that the uVNTR and dVNTR are parts of the same haplotype block; consequently, several CNS disorders and conditions solely attributed to the uVNTR could in fact be mechanistically associated with the dVNTR. However, confirmation of this hypothesis will require profiling of well-characterized cohorts larger than the WCHADS cohort we used to address the frequency of these VNTRs in the population.
Taken altogether, these results give further insights into the complexity of MAOA regulation, which historically has focused on the uVNTR element to account for variations in the expression of this gene and risk to neuropsychiatric conditions. Here we provide evidence that this is only a partial explanation, the dVNTR plays a significant role in MAOA expression, and our work supports mechanistic interactions between these two elements. Indeed, we have confirmed that deletion of both elements did not preclude expression of the gene itself, although the level of mRNA transcripts was significantly reduced compared to the parental cell line. The dVNTR appeared to be a major positive regulator of the primary transcript isoform, whereas both VNTRs seemed to act in concert to negatively modulate the expression of the minor transcript isoform 204 (Fig. 7). Our data pertains to the HAP1 cell line which was chosen as it expressed both isoforms of MAOA and its haploid karyotype facilitated successful CRISPR deletion of regulatory elements. Expression of MAOA will vary in a tissue specific and stimulus inducible manner and regulation in a neuronal context may differ; however, our model supplies a framework to incorporate both VNTRs in MAOA regulation. Both VNTRs are primate specific, which suggests that there are additional key regulatory domains for MAOA expression in mammals as a whole. Furthermore, the uVNTR could have a dual function in both transcription and post-transcriptional regulations of the MAOA gene as it is contained within the 5′UTR of one of the putative coding isoforms. Such a dual function has been demonstrated for a VNTR in the mir137 gene depending on the mRNA isoform that was expressed (Warburton et al. 2016). In conclusion, we believe that our data provides significant insights into the understanding of the regulation of MAOA expression and its modulation by genetic variants.
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The authors are grateful to the families who participated in the Wirral Child Health and Development Study (WCHADS).Ms. Veridiana Pessoa PhD fees have been supported in part by Francis & Beatrice Anderson Memorial bursary through Dr. Ursula Anderson (USA) and MM fees by IPHS studentship.
This study was funded by a grant from the UK Medical Research Council, G0400577 (JQ, HS, JH, AP, CM) and Wellcome Trust Grant ref. 109095/Z/15/Z (AL).
Ethical approval for the study was granted by the Cheshire North and West Research Ethics Committee on the June 27, 2006 (ref: 05/Q1506/107).
Conflict of Interest
The authors declare that they have no conflict of interest.
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Manca, M., Pessoa, V., Lopez, A.I. et al. The Regulation of Monoamine Oxidase A Gene Expression by Distinct Variable Number Tandem Repeats. J Mol Neurosci 64, 459–470 (2018). https://doi.org/10.1007/s12031-018-1044-z
- Gene expression