Genome-wide association studies (GWASs) have identified over 180 independent schizophrenia risk loci. Nevertheless, how the risk variants in the reported loci confer schizophrenia susceptibility remains largely unknown. Here we systematically investigate the gene regulatory mechanisms underpinning schizophrenia risk through integrating data from functional genomics (including 30 ChIP-Seq experiments) and position weight matrix (PWM). We identify 132 risk single nucleotide polymorphisms (SNPs) that disrupt transcription factor binding and we find that 97 of the 132 TF binding-disrupting SNPs are associated with gene expression in human brain tissues. We validate the regulatory effect of some TF binding-disrupting SNPs with reporter gene assays (9 SNPs) and allele-specific expression analysis (10 SNPs). Our study reveals gene regulatory mechanisms affected by schizophrenia risk SNPs (including widespread disruption of POLR2A and CTCF binding) and identifies target genes for mechanistic studies and drug development. Our results can be accessed and visualized at SZDB database (http://www.szdb.org/).
Schizophrenia (SCZ) is a severe psychiatric disorder characterized by positive symptoms, negative symptoms and cognitive impairments. With high lifetime prevalence (~0.5–1%), substantial morbidity and mortality, SCZ poses a major threat to global health. The pathogenesis of SCZ remains elusive. However, accumulating data suggest that inherited genetic variants play critical roles in SCZ (the heritability of SCZ is estimated around 0.81). To date, genome-wide association studies (GWASs) have identified over 180 loci that show strong association with SCZ2,3,4,5,6,7,8,9,10,11,12,13,14. Nevertheless, for most of the risk loci, the causal variant(s) and the mechanisms by which the risk variants exert their effects on SCZ remain unknown.
Most of the SCZ risk variants identified by GWAS are located in non-coding regions12, implying that these variants exert their effects through altering gene expression. Consistently, recent studies have shown that schizophrenia-associated variants are significantly enriched in regulatory regions15,16, suggesting that disruption of regulatory function may represent a common mechanism that non-coding genetic variants confer risk of SCZ. Though accumulating evidence support the hypothesis that most of the risk variants identified by GWAS contribute to SCZ risk through affecting gene expression rather than protein structure or function, only very limited functional variants have been identified so far17,18,19. Due to the complexity of linkage disequilibrium (LD) and gene regulatory, identifying the functional (or causal) variants (at each reported locus) and elucidating their regulatory mechanisms remain major challenges in psychiatric genetics.
Regulatory elements (REs) (e.g., promoters and enhancers) are non-coding DNA sequences that have a critical role in controlling gene expression. Previous studies have shown that most of associations identified by GWASs were attributable to variants located in REs12,20. In fact, investigating if the risk variants are localized in REs has been proved a useful way to identify causal (or functional) variants for complex diseases21,22. Regulatory elements usually contain multiple binding sites (i.e., DNA motifs that can be recognized by transcription factors (TFs)) for TFs and genetic variations in REs affect gene expression through altering binding affinity of TFs. The architecture and function of REs are variable in different tissues and previous studies have shown that the activity of REs have strong tissue and cellular specificity23,24. Thus, understanding the tissue-specific structure and activity of REs is crucial to elucidate how genetic variants contribute to risk of SCZ through affecting the regulatory function of REs.
Here we perform a systematic and deep analysis to identify the functional variants and to elucidate the gene regulatory mechanisms underlying the genetic associations reported by recent schizophrenia GWASs12,13,14. We identify functional variants at multiple risk loci through integrating a wide range of data from high-throughput functional genomics experiments, including genome-wide binding landscapes (chromatin immunoprecipitation and sequencing (ChIP-Seq)) for 30 TFs and position weight matrices (PWMs). We identify 132 functional single-nucleotide polymorphisms (SNPs) that disrupt TF binding and investigate the gene regulatory mechanisms of these TF binding–disrupting SNPs. We validate the regulatory effect of several identified functional SNPs using reporter gene assays and allele-specific expression analysis. In addition, we identify the potential target genes of the identified regulatory SNPs by using brain expression quantitative loci (eQTL) from three independent eQTL datasets. Finally, we show that nervous system development-related genes are significantly enriched among the target genes of the TF binding–disrupting SNPs, providing further support for the neurodevelopmental hypothesis of schizophrenia. The results reported in this study can be visualized and downloaded at SZDB (http://www.szdb.org/)25.
Prioritization of functional SNPs and experimental validation
Potential causal risk SNPs from three large-scale GWASs12,13,14 were used in this study. The first GWAS was from the schizophrenia working group of the psychiatric genomics consortium (PGC2)12. PGC performed a large-scale GWAS of SCZ (36,989 cases and 113,075 controls) and reported 108 independent risk loci12. The second GWAS was from the study of Li et al.13 which identified 30 new SCZ risk loci recently through combining the association results from the Chinese and PGC2 samples. The third GWAS was from a recent study of Pardinas et al.14 that reported 50 novel risk loci for SCZ. As each risk locus contains hundreds of SNPs that showed similar association significance (due to LD), potential causal SNPs were identified by PGC2 and Pardinas et al.14. PGC2 identified set of SNPs (i.e., potential causal set of SNPs) that were 99% likely to contain the causal variants12. Pardinas et al.14 also identified potential causal SNPs using FINEMAP26. A total of 18,707 potential causal SNPs from PGC2 and 1799 potential causal SNPs (spanning 50 novel risk) from the study of Pardinas et al.14 were used in this study. For the 30 new risk loci reported by Li et al.13, we performed LD analysis and identified 4794 SNPs that were in LD with the index SNPs (r2 > 0.3). The potential causal SNPs (from PGC212 and Pardinas et al.14) and SNPs in LD with the index SNPs (from Li et al.13) are likely to contain the causal variants. In total, 23,400 non-overlapping potential causal SNPs from above three GWASs were included in this study (Fig. 1). To pinpoint the potential causal variant (or variants) at each locus, we systematically annotated the credible causal SNPs through combining bioinformatic and high-throughput functional genomics analyses (Fig. 1). We first annotated the potential causal SNPs with well-characterized functional annotation approaches (CADD27, GWAVA28, Eigen29, RegulomeDB30 and LINSIGHT31) and identified the most possible functional SNPs at each risk locus (Supplementary Data 1 and Supplementary Tables 1 and 2). Of note, two different strategies were used by the functional annotation methods to prioritize the potential functional SNP. For CADD, Eigen, GWAVA and LINSIGHT, the larger the score, the higher probability that the SNP is functional. Therefore, the SNP with the highest score was defined as the top (i.e., the most likely) functional SNP. For RegulomeDB, smaller rating suggests higher probability that the SNP is functional. Thus, the SNP with the smallest rating was defined as the top functional SNP. For CADD, Eigen, GWAVA and LINSIGHT, the SNP with the highest score at each locus was defined as the top functional SNP. For RegulomeDB, the SNP with the smallest rating was defined as the top functional SNP. For each locus, we compared the top functional SNPs identified by different annotation methods and found that 153 loci (PGC212 performed regular LD clumping (implemented in PLINK32) to define the index SNPs (with following parameters: r2 < 0.1, P1 < 5 × 10−8, window size <500 kb) and the genomic region containing all SNPs that were in LD (i.e., r2 > 0.6) with each of the 128 index SNPs was defined as a locus) contained overlapping top functional SNPs prioritized by at least two different annotation methods (i.e., at least two methods annotated the same SNP as the most possible functional or causal SNP) (Supplementary Data 1 and Supplementary Tables 1 and 2), suggesting these SNPs were promising functional SNPs. Most of the prioritized functional SNPs were located in intergenic and intronic regions (Fig. 2a).
To identify the potential target genes regulated by the prioritized top functional SNPs (i.e., top SNPs identified by at least two different annotation approaches), we examined the associations between the prioritized top functional SNPs and gene expression in three brain eQTL databases (including the Lieber Institute for Brain Development (LIBD) eQTL browser33 (dorsolateral prefrontal cortex, N = 412, including 175 patients with schizophrenia and 237 unaffected controls) (http://eqtl.brainseq.org/phase1/eqtl/), the Genotype-Tissue Expression (GTEx)34 (tissues were from 13 brain regions, N ranges from 80 to 154) (Supplementary Table 3) and the CommonMind Consortium (CMC)35 (dorsolateral prefrontal cortex, N = 467). In total, 66 prioritized top functional SNPs showed significant association (default false discovery rates (FDRs) used in the original papers were used in this study, i.e., FDR < 0.05 in CMC, FDR < 0.01 in LIBD). We used P < 0.001 for GTEx) with gene expression in human brain tissues (Supplementary Data 2). We validated the regulatory effects of 10 prioritized top functional SNPs using reporter gene assays (Methods). The selection criteria of top functional SNPs for reporter gene assays were as follows. First, this SNP was prioritized as the top functional SNP (has the highest score or the smallest rating) at least by two different annotation methods simultaneously. Second, this SNP was associated with gene expression in human brains (Supplementary Data 2). We tested 10 SNPs and found that 7 out of 10 prioritized top functional SNPs (including rs11655813, rs9908888, rs17821573, rs301791, rs37718, rs7304782 and rs7752421) showed significant allelic effects in reporter gene assays in HEK 293 cells (i.e., different alleles at these SNPs affected the expression of reporter gene significantly) (P < 0.05, two-tailed Student’s t-test, not corrected for multiple testing) (Fig. 2b). For these 7 significant SNPs, we compared the allelic effects on luciferase activity observed in reporter gene assays with the estimated eQTL effects of the corresponding alleles in CMC dataset. Among these 7 significant SNPs, 5 SNPs (rs11655813, rs9908888, rs17821573, rs301791 and rs7752421) were significantly associated (FDR < 0.01) with gene expression in CMC dataset. For these 5 significant eQTL SNPs, we found that the allelic effects on luciferase activity observed in reporter gene assays are consistent with the estimated eQTL effects of the corresponding alleles in CMC dataset (Supplementary Fig. 1). These results prioritized the most possible functional SNPs at each risk locus and suggested that these functional SNPs may confer risk of schizophrenia through modulating gene expression.
Identification of regulatory risk SNPs using functional genomics
Though promising functional SNPs have been prioritized by the well-characterized annotation approaches (Supplementary Data 1 and Supplementary Tables 1 and 2), there are several limitations for these annotation methods. First, sequence conservation is an important factor for some annotation approaches (including CADD, Eigen and LINSIGHT). However, considering that some of the schizophrenia-associated variants are located in human-specific (or accelerated) region36,37 (e.g., a recent study showed that a human-specific tandem repeat in intronic region of CACNA1C have pivotal role in schizophrenia susceptibility36), it is challenging for these annotation methods to prioritize the potential functional SNPs located in these human-specific regions. Second, despite genomic features such as ChIP-Seq, TF binding sites and eQTL were used by some of these annotation methods, the tissues and cell types used to derive these genomic features were usually not from the brain or neuronal-related tissues. Considering that many of the regulatory variants have strong tissue-specificity, the potential functional SNPs prioritized by these annotation approaches may not be functional in human brains. Third, even the potential functional SNP prioritized by these annotation methods have functional consequences in brain or neuronal-related tissues, and the exact gene regulatory mechanisms (e.g., binding of which transcription factor was disrupted by the potential functional SNPs) of these potential functional SNPs remain unknown.
To further investigate how schizophrenia risk variants affect gene expression and elucidate the regulatory mechanisms of the potential causal variants, we annotated the potential causal SNPs by combining ChIP-Seq and PWM data (Fig. 1), as described previously38. We focused on risk variants that have regulatory effect in human brain tissues (or neuronal cells) as schizophrenia is thought to be a disorder that is mainly originated from dysfunction of brain function. First, most schizophrenia risk genes (including genes involved in neurotransmission (e.g., DRD2, GRM3, GRIN2A, CACNA1C and CACNA1I)) identified by genetic studies play pivotal roles in brain12,14. Second, accumulating evidence supports the neurodevelopmental hypothesis of schizophrenia39,40. Consistently, studies have showed that schizophrenia risk genes (including DISC1, RELN and GLT8D1) have important role in brain development through regulating proliferation and differentiation of neural stem cells41,42,43. More important, a recent study showed that schizophrenia associations were strongly enriched at enhancers active in brain tissues12. These lines of evidence suggest that schizophrenia risk variants exert their effects mainly in brain tissues. Therefore, brain tissues (or neuronal cells) may represent the most relevant tissues for studying the effects of SCZ risk variants. We thus used ChIP-Seq and eQTL data from brain tissues (or neuronal cells) to identify the potential causal SNPs and target genes regulated by the identified TF binding–disrupting SNPs. We downloaded and processed 34 ChIP-Seq experiments (Supplementary Table 4) from ENCODE44. After quality control, ChIP-Seq data of 30 TFs were retained and the genome-wide binding sites of each TF were identified using the ChIP-Seq data. We derived the DNA binding motifs of individual TF using the genomic binding locations from the ChIP-Seq data (Methods)45. DNA binding motifs derived from ChIP-Seq experiments were then compared with PWM data (from PWM databases) (Methods) and the matched PWM was used for further analysis (as EZH2 PWM results derived from ChIP-Seq were inconsistent with the PWM databases, we chose the most significant PWM (i.e., with the smallest E-value) from ChIP-Seq for further analysis). Potential causal SNPs were mapped to the matched PWMs and risk SNPs residing in PWMs were identified. To test if a risk SNP (located in a given PWM) disrupts TF binding, we used FIMO (Find Individual Motif Occurences)46 to analyze the genomic sequences containing two different alleles of the given SNP (Methods). By doing so, we could identify TFs whose binding are disrupted by credible causal risk SNPs at single-base resolution by combining ChIP-Seq and corresponding PWM data.
Through annotating 23,400 potential causal risk SNPs with ChIP-Seq and PWM data, we identified 132 SNPs that disrupted the binding of 21 distinct TFs (Fig. 3a and Supplementary Data 3). Each of these SNPs was located in a TF binding motif that overlapped with a PWM match (P < 0.001, P was converted from log-odds scores, assuming a zero-order background model) on one or both alleles (http://www.szdb.org/)25. These TF binding–disrupting SNPs (which we call regulatory SNPs) are located in DNA binding motifs that have strong nearby ChIP-Seq signals, indicating that corresponding TFs can bind to the genomic regions containing these SNPs in human brain tissues or neuronal cell lines. Over 70% TF binding–disrupting SNPs were located in intronic and intergenic regions (Fig. 3a). To compare the distribution of TF binding–disrupting SNPs identified in this study and random SNPs, we sampled random SNPs and annotated their genomic locations using ANNOVAR47 (see Methods). We found that 56% random SNPs were located in intergenic regions (Supplementary Fig. 2). However, only 21% TF binding–disrupting SNPs were located in intergenic regions. By contrast, 50% TF binding–disrupting SNPs and only 35% random SNPs were located in intronic regions, suggesting that causal risk variants for schizophrenia were enriched in intronic regions. Nevertheless, more work is needed to verify this observation. Among the 132 TF binding–disrupting SNPs, 40 were located in POLR2A (RNA polymerase II subunit A) binding motifs and 38 were located in CTCF binding sites, suggesting widespread disruption of POLR2A and CTCF binding by SCZ risk SNPs (Fig. 3a). We noticed that some regulatory SNPs disrupted binding of two or more TFs simultaneously (Fig. 3b). The binding motif (PWM), ChIP-Seq signal, DNase-Seq signal and histone modification marks for each of the 132 SNPs can be accessed and visualized at SZDB (http://www.szdb.org/).
Disruption of POLR2A binding by regulatory SNPs
Forty SCZ risk SNPs disrupted binding of POLR2A (Fig. 3a), implying disruption of POLR2A binding may represent a common mechanism that schizophrenia risk variants exert their effect. We investigated how a risk SNP (rs1801311) at 22q13.2 disrupted POLR2A binding. Genetic variants at 22q13.2 showed significant association with SCZ in recent GWAS12 (Supplementary Fig. 3). However, due to the complexity of LD, it is challenging to pinpoint the causal (or functional) SNP at this locus. Through integrating ChIP-Seq and PWM data, we identified a functional SNP (rs1801311) at 22q13.2. rs1801311 was located in a well-characterized binding motif for POLR2A (Fig. 4a). Strong POLR2A ChIP-Seq signal clearly showed the binding of POLR2A to the genomic region containing rs1801311 in human brain tissues and neuronal cell lines. Consistently, DNase-Seq and histone modification data indicated that rs1801311 was located in an actively regulatory region (Fig. 4b). We further validated the regulatory effect of rs1801311 using reporter gene assays (Fig. 4c–e). Genomic sequences (638 bp) containing different alleles of rs1801311 were cloned into pGL3-promoter vector to modulate the expression of luciferase reporter gene (Methods). The A allele of rs1801311 conferred a significant higher activity compared with G allele in all three tested cell lines (HEK293, SK-N-SH and SH-SY5Y) (P < 0.001, two-tailed Student’s t-test), supporting the regulatory effect of rs1801311. Collectively, the data from ChIP-Seq, PWM, DNase-Seq, histone modification and reporter gene assays consistently support that rs1801311 may exert its regulatory effect through disrupting POLR2A binding.
Disruption of CTCF binding by regulatory SNPs
In addition to POLR2A, binding of CTCF and other TFs were also frequently disrupted by SCZ risk SNPs (Fig. 3a). CTCF binding was disrupted by 38 SCZ risk SNPs, including rs12912934 (15q25.2), rs16937 (1q32.1) and rs7012106 (8q24.3) (Figs. 5 and 6a). These three regulatory SNPs (i.e., rs12912934, rs16937 and rs7012106) were located in CTCF binding sites and allelic differences at these SNPs disrupted the binding of CTCF. DNase-Seq data showed that these three SNPs were located in transcriptionally active regions. ChIP-Seq data indicated that CTCF could bind to the genomic regions containing these three regulatory SNPs in human brain tissues or neuronal cell lines (Fig. 5). We further verified the regulatory effect of these three SNPs with reporter gene assays. We found that the T allele of rs12912934 conferred a significant higher reporter gene activity compared with C allele in SK-N-SH and SH-SY5Y cells (P < 0.05, two-tailed Student’s t-test) (Fig. 5c, d). For SNP rs16937, the G allele conferred a significant higher expression activity compared with A allele in HEK293 and SH-SY5Y cells (P < 0.001, two-tailed Student’s t-test) (Fig. 5f, h). For rs7012106, the construct containing G allele exhibited significant higher luciferase activity compared with the construct containing the C allele in all three tested cell lines (P < 0.001, two-tailed Student’s t-test) (Fig. 6b–d). The results of reporter gene assays provide further evidence that support the regulatory effect of these three CTCF binding–disrupting SNPs.
Disruption of other TF binding by regulatory SNPs
We demonstrated how a regulatory SNP (rs2270363, located in 16p13.3) disrupted binding of USF1 and MAX1 through integrating data from ChIP-Seq and PWM (Fig. 6e). SNP rs2270363 was located in upstream of NMRAL1 and HMOX2 genes (these two genes have opposite transcription direction). However, as HMOX2 has multiple isoforms, rs2270363 is also located in the intron 1 of the longest transcript of HMOX2. DNase-Seq profiles and histone modification data showed that rs2270363 was located within an active transcription genomic region (Fig. 6e). In addition, ChIP-Seq profiles indicated that USF1 and MAX1 could bind to the region containing rs2270363 in human neuronal cell line. rs2270363 was located in binding motif of USF1 and MAX1, and FIMO analysis showed that rs2270363 disrupted occupied USF1 and MAX1 binding sites. We amplified the DNA fragments containing different alleles of rs2270363 and cloned them into pGL4.11 vector. We then compared the luciferase activity driven by the cloned DNA fragments containing different alleles of rs2270363. The construct containing A allele of rs2270363 exhibited significant higher luciferase activity compared with the construct containing the G allele in all three tested cell lines (P < 0.01, two-tailed Student’s t-test) (Fig. 6f–h). In addition to rs2270363, USF1 binding was disrupted by other regulatory SNPs. For example, SNP rs7014953 also disrupted the binding of USF1 (Fig. 7a). We confirmed the regulatory effect of rs7014953 in SK-N-SH and SH-SY5Y cells (P < 0.001, two-tailed Student’s t-test) (Fig. 7b, c).
In addition to above-mentioned TFs, the identified regulatory SNPs also disrupted bindings of other TFs. As shown in Fig. 7d, TCF12 binding was disrupted by SNP rs6992091. Again, we validated the regulatory effect of rs6992091 (Fig. 7e, f) with reporter gene assays. The construct containing G allele of rs6992091 exhibited a significantly higher luciferase activity compared with the construct containing the A allele in SK-N-SH and SH-SY5Y cells (P < 0.001, two-tailed Student’s t-test). Taken together, these results provide further evidence that supports the identified TF binding–disrupting SNPs are regulatory SNPs.
Regulatory effect of additional TF binding–disrupting SNPs
We identified 132 SCZ-associated regulatory SNPs that disrupted bindings of TFs through annotating potential causal SNPs with ChIP-Seq and PWM data (Supplementary Data 3). These 132 TF binding–disrupting SNPs were from 81 SCZ risk loci (i.e., corresponding to 81 index SNPs). Most of the regulatory SNPs were located in intronic and intergenic regions (Fig. 3a). The wide overlapping of the regulatory SNPs with H3K27ac histone modification (http://www.szdb.org/) suggested that these SNPs were mainly located in enhancer regions. We thus performed reporter gene assays to validate the regulatory effect of some of the identified TF binding–disrupting SNPs. The selection criteria of TF binding–disrupting SNPs for reporter gene assays were as follows. First, this TF binding–disrupting SNP was associated with expression of the same gene simultaneously in at least two independent eQTL datasets. Second, this SNP was located in a genomic region with strong DNase-Seq or Histone modification signal. In addition to the 7 SNPs investigated above (i.e., rs1801311, rs12912934, rs16937, rs7012106, rs2270363, rs7014953 and rs6992019) (Figs. 4–7), regulatory effects of two additional SNPs (rs2535629 and rs2711116) were also tested with reporter gene assays (Supplementary Figs 4 and 5). In total, we studied the regulatory effect of 9 SNPs and found that all of the cloned genomic sequences (containing the tested SNPs) enhanced the activity of luciferase compared with control vector (empty pGL3-promoter) in the tested cell lines (Figs. 4–7, Supplementary Figs 4 and 5), supporting that these SNPs were located in enhancer regions. We also compared the effect of different alleles on luciferase activity and found that all of the tested SNPs showed a significant difference in luciferase activity for the two given alleles in at least one of the tested cells (Figs. 4–7, Supplementary Figs 4 and 5). These allele-specific reporter gene assays indicated that genetic variations (i.e., allelic differences) at the regulatory SNPs influenced the luciferase activity significantly, providing further evidence that supports the regulatory effects of the identified SNPs.
Identification of the target genes of the regulatory SNPs
To further identify the potential target genes regulated by the 132 identified regulatory SNPs, we examined the association between the identified regulatory SNPs and gene expression in human brain tissues in three independent brain eQTL datasets, including CMC35, LIBD eQTL browser33 and GTEx48. Tissues from the prefrontal cortex were used in CMC and LIBD datasets. Tissues from 13 brain regions (sample size range from 80 to 154) (Supplementary Table 3) were included in GTEx. We utilized the default FDR or P thresholds used in the original papers. In CMC dataset, the default FDR threshold is 0.05. In LIBD dataset, the default FDR is 0.01. In GTEx, we used P < 0.001 as the threshold. We found that 97 of the 132 regulatory SNPs were significantly associated with gene expression in human brain (FDR < 0.05 in CMC, FDR < 0.01 in LIBD and P < 0.001 in GTEx) (Supplementary Data 4). Among the 132 regulatory SNPs, 58 showed significant association with the expression of the same gene in at least two independent eQTL datasets (Supplementary Table 5), suggesting these genes are true targets of the identified regulatory SNPs. Nevertheless, further functional assays (e.g., reporter gene assays) are needed to validate if these genes represent true targets of the identified regulatory SNPs. Of note, 29 regulatory SNPs showed significant association with the expression of the same gene in three independent brain eQTL datasets (e.g., rs1801311 is significantly associated with FAM109B expression in all of the three eQTL datasets) (Table 1), strongly suggesting that these genes were regulated by these regulatory SNPs. Interestingly, we noticed that six distinct regulatory SNPs (rs1801311, rs2269524, rs28633410, rs5751195, rs6002621 and rs8135801) showed significant association with the expression of FAM109B gene (Supplementary Table 5 and Table 1), indicating that these SNPs may confer risk of schizophrenia through modulating FAM109B expression. In addition to FAM109B, expression of other genes (including TMEM81, EFTUD1P1, BDH2, RERE, CORO7, NAGA, etc) also showed significant association with different regulatory SNPs. Considering that these regulatory SNPs are located in DNA binding motifs (with corresponding PWM match) and allelic differences at these SNPs disrupt binding sites of TFs, the significant associations between the regulatory SNPs and genes in independent brain eQTL datasets strongly suggest that these genes are true targets for the identified regulatory SNPs. Further functional experiments (such as reporter gene assays and CRISPR/CAS9 (clustered regularly interspaced short palindromic repeats/CRISPR-associated 9) experiments) are needed to verify if these genes are regulated by these regulatory SNPs.
To identify all of the possible target genes of the regulatory SNPs, we performed eQTL annotation (using CMC dataset) to test the associations of the regulatory SNPs with all genes in close physical proximity (e.g., ±2 Mb). For each regulatory SNP (the TF binding–disrupting SNPs are listed in Supplementary Data 3, a total of 132 SNPs), we performed eQTL annotation through using the genotype and expression data from the CMC dataset. The eQTL analysis was conducted with PLINK (v1.9). The associations of the regulatory SNPs with all genes in close physical proximity (e.g., ±2 Mb) are listed in Supplementary Data 5 (Of note, only associations with a P < 0.01 are shown).
To explore if the identified regulatory SNPs were significantly associated with gene expression than random SNPs, we conducted 10,000 simulations (Methods). Compared with the random SNPs, the identified regulatory SNPs showed significant association with gene expression (Z = 14.23, P = 3.09 × 10−46, Methods) (Supplementary Fig. 6), further supporting the potential regulatory effect of the identified TF binding–disrupting SNPs. Collectively, these results identified the potential target genes of the identified TF binding–disrupting SNPs and suggested that these regulatory SNPs may confer schizophrenia risk through affecting the expression of their target genes.
Linkage disequilibrium analysis between the regulatory SNPs
In some cases, we identified several TF binding–disrupting SNPs at a single schizophrenia risk locus. For example, we identified 6 TF binding–disrupting SNPs (rs1801311, rs2269524, rs28633410, rs5751195, rs6002621 and rs8135801) at 22q13.2. To investigate the LD between the 132 TF binding–disrupting SNPs, we performed LD analysis using SNiPA (a tool for annotating and browsing genetic variants)49. We found that 40 TF binding–disrupting SNPs showed LD (r2 > 0.3) with other TF binding–disrupting SNPs in Europeans (Supplementary Table 6). Of note, 8 TF binding–disrupting SNPs (rs10083370, rs2304206, rs3773744, rs4759413, rs60754073, rs76514049, rs78866909 and rs9616378) showed complete LD (i.e., r2 = 1) with other TF binding–disrupting SNPs (Supplementary Table 6). These LD results indicate that some of the TF binding–disrupting were in linkage disequilibrium with each other. However, considering that all of these 132 SNPs disrupt binding of TFs, suggesting that these 132 TF binding–disrupting SNPs may have functional consequences. Thus, more work is needed to investigate if all of the highly linked TF binding–disrupting SNPs or only some of the highly linked TF binding–disrupting SNPs confer risk of schizophrenia through affecting gene expression.
Allele-specific expression of the regulatory SNPs
Our eQTL annotation showed that most of the identified regulatory SNPs were associated with gene expression in brain tissues. To further verify the cis regulatory effects of the identified TF binding–disrupting SNPs, we extracted the allele-specific expression (ASE) results of the identified TF binding–disrupting SNPs from GTEx50. Of note, only very limited regulatory SNPs were suitable for ASE analysis (as ASE analysis requires that the analyzed SNP is heterozygous and expressed in the same individual). We found that 10 TF binding–disrupting SNPs showed significant (P < 0.001, Binomial test) allelic imbalance (i.e., allele-specific expression) in human brain tissues (Fig. 8a–j). For example, the C allele of SNP rs1321 was preferentially expressed compared with the T allele (P = 2.84 × 10−4) (Fig. 8a), and G allele of SNP rs16937 was preferentially expressed compared with A allele (P = 8.19 × 10−5) (Fig. 8b). Of note, reporter gene assays also showed that the G allele of rs16937 conferred a significant higher expression activity compared with A allele in HEK293 and SH-SY5Y cells (P < 0.01). These ASE results provide further evidence that supports the regulatory effects of the identified TF binding–disrupting SNPs.
Pathway analysis of the target genes
To explore if the target genes (Supplementary Data 4) of the regulatory SNPs were enriched in specific pathways, we carried out gene ontology (GO) analysis using DAVID (Database for Annotation, Visualization and Integrated Discovery)51. We found that two categories (including “cell adhesion” and “nervous system development”) were significantly enriched (P < 0.05, corrected by the Benjamini–Hochberg procedure) among the target genes of the regulatory SNPs (Supplementary Table 7). The overrepresentation of nervous system development genes provides further evidence that supports the neurodevelopmental hypothesis of schizophrenia40.
Spatio-temporal expression pattern of target genes
We carried out spatio-temporal expression pattern analysis using expression data from the BrainSpan (http://www.brainspan.org/). Two groups of target genes (i.e., genes listed in Supplementary Data 4 and Supplementary Table 5) were used for spatio-temporal expression pattern analysis. Genes whose expression were associated with regulatory SNPs in any eQTL dataset were listed in Supplementary Data 4. However, genes whose expression are associated with regulatory SNPs in at least two eQTL datasets are listed in Supplementary Table 5. Thus, genes listed in Supplementary Table 5 are a subset of genes listed in Supplementary Data 4. Spatio-temporal expression pattern analysis was carried out as previously described52. We found that the expression level of the target genes in Supplementary Table 5 was significantly higher than the background genes across all developmental stages (P < 1.0 × 10−7, Wilcoxon rank sum test). Similarly, the expression level of the target genes in Supplementary Data 4 was also significantly higher than the background genes across all developmental stages (P < 5.0 × 10−7) (Fig. 8k). In addition, we also found that the expression level of the target genes was higher in prenatal stage compared with postnatal stage (P = 0.001 for gene set in Supplementary Table 5 and P = 0.008 for gene set in Supplementary Data 4) (Fig. 8k), suggesting that the target genes may play a role in brain development.
Cell type-specific expression analysis of target genes
To explore the expression pattern of the target genes of the identified regulatory SNPs in different brain cell types, we extracted the specificity value of each target gene in 24 cell types defined by Skene et al.53. We found that three cell types contained more than 6 target genes at the specificity cutoff of 0.1 (i.e., specificity score >0.1), with pyramidal cells having the most number of target genes (Fig. 8l). This result is consistent with previous findings53 and provides further support for the involvement of pyramidal cells in schizophrenia.
In conclusion, we used two complementary approaches (functional annotation and functional genomics) to systematically annotate the GWAS significant schizophrenia risk loci (Supplementary Fig. 7). The functional annotation prioritized 153 overlapping top functional SNPs and 66 of the 153 prioritized functional SNPs were associated with gene expression in human brains. Reporter gene assays were conducted for 10 prioritized functional SNPs and 7 SNPs showed significant allelic effects on reporter gene activity. In addition, we derived binding motifs of 30 TFs through integrating ChIP-Seq experiments from brain tissues (or neuronal cells) and PWMs. We mapped the potential causal risk SNPs (a total of 23,400) from three schizophrenia GWASs to the derived binding motifs and identified 132 SNPs (from 81 schizophrenia risk loci) that disrupted binding of 21 distinct TFs. We found that 97 out of the 132 TF binding–disrupting SNPs were significantly associated with gene expression in human brain tissues. Finally, regulatory effects of 9 TF binding–disrupting SNPs were validated by reporter gene assays (Supplementary Fig. 7). Our study identified the plausible causal variants for schizophrenia and revealed the gene regulatory mechanisms affected by schizophrenia risk SNPs (including widespread disruption of POLR2A and CTCF binding). In addition, our study also identified the potential target genes of the TF binding–disrupting risk SNPs. It is likely that the identified TF binding–disrupting risk SNPs exert their effects on schizophrenia through modulating the expression level of these target genes.
In the past decade, significant advances have been made in understanding the genetic basis of schizophrenia. Since O’Donovan et al.2 reported the first genome-wide significant risk locus (near ZNF804A) for schizophrenia in 2008, numerous novel risk loci have been identified. Despite the fact that over 180 schizophrenia risk loci have been identified by GWAS12,13,14, pinpointing the causal (or functional) variants at the risk loci and elucidating their roles in schizophrenia susceptibility remain major challenges in psychiatric genetics. In this study, we conducted systematic and deep analyses to identify the potential causal variants and to investigate how these causal variants confer schizophrenia risk. We first prioritized the most possible functional SNP at each risk locus by using the well-characterized functional annotation approaches. We then identified 132 risk SNPs that disrupted binding of 21 distinct TFs through integrating Chip-Seq and PWMs. We validated the regulatory effects of some identified functional SNPs with reporter gene assays and allele-specific expression analysis. We further identified the potential target genes of the regulatory SNPs. Finally, we showed that nervous system development genes were significantly enriched among the target genes of the identified regulatory SNPs.
Our study has important implications for elucidating the genetic mechanisms of schizophrenia. First, through integrating the diverse data sources from functional genomics, we translated the association findings from schizophrenia GWAS into genetic and gene regulatory mechanisms. With the rapid increase in sample size, novel schizophrenia risk variants have been identified at the unprecedented rate. By contrast, identification of causal (or functional) variants and genes lags far behind. Our post-GWAS functional genomics analyses linked the identified risk loci with specific variants and genes, thus providing a starting point for further mechanistic and functional investigation. Second, we systematically identified the causal (or functional) variants and investigated the potential gene regulatory mechanisms at all of the genome-wide significant risk loci. Though previous studies have identified some causal variants (or genes) at several risk loci19,54, large-scale identification of causal variants and characterization of gene regulation at the reported risk loci remain major challenges. Through analyzing the functional genomics data with bioinformatic methods, for the first time, we conducted a systematic and deep analysis to investigate the gene regulatory mechanisms at all of the reported schizophrenia risk loci. Third, our study identified 132 TF binding–disrupting SNPs. These SNPs disrupt binding sites of multiple TFs, thus representing the most plausible causal SNPs. We furthermore verified the regulatory effects of some TF binding–disrupting SNPs using reporter gene assays and allele-specific expression analysis. Fourth, our study revealed new gene regulatory mechanisms affected by schizophrenia risk SNPs, including widespread disruption of POLR2A and CTCF binding. Fifth, we identified the potential target genes of the TF binding–disrupting SNPs through eQTL annotation (boxplots of brain eQTLs results (only SNPs listed in Supplementary Table 5 were plotted) are shown in Supplementary Data 6). It is likely that the TF binding–disrupting SNPs confer schizophrenia risk through modulating the expression of these target genes. Finally, this study provides an example to illuminate the gene regulatory mechanisms underpinning other psychiatric disorders (such as major depressive disorder and bipolar disorder). Most of risk variants identified by GWAS are located in non-coding regions, suggesting the identified risk variants confer schizophrenia risk through modulating gene expression. Currently, pinpointing the causal variant remains a daunting task as each risk locus usually contains multiple variants that show similar association significance (due to LD). By annotating all of the variants at each locus with functional genomics data, our study provides an example for identifying potential causal variants. This method can be applied to other psychiatric disorders.
Of note, we used two complementary methods (i.e., functional annotation and functional genomics, see Fig. 1) to prioritize or identify the potential functional (or causal) variants at the reported schizophrenia risk loci. We compared the potential functional SNPs identified by these two approaches (i.e., functional annotation and functional genomics) and found 6 overlapping functional SNPs (Supplementary Table 8 and Supplementary Fig. 8). The reasons why only 6 overlapping functional SNPs were identified by these two approaches are discussed in the Supplementary Discussion.
We compared the target genes of the identified TF binding–disrupting SNPs with previous findings from Gusev et al.55 and found 44 overlapping genes (Supplementary Table 9 and Supplementary Fig. 9). These overlapping genes may represent promising candidates for schizophrenia as these genes were prioritized by two different methods. In addition, the significant enrichment of nervous system development-related genes among the target genes of the TF binding–disrupting SNPs provides further support for the neurodevelopmental hypothesis of schizophrenia39,40,56. More detailed discussion about the neurodevelopmental hypothesis of schizophrenia is provided in the Supplementary Discussion.
We noticed that CTCF binding was frequently disrupted by the schizophrenia risk SNPs, suggesting that disruption of CTCF binding may represent a common mechanism that schizophrenia risk SNPs exert their effect on schizophrenia. Interestingly, previous genetic studies also suggested that CTCF may have a role in schizophrenia57,58. More detailed information about the potential role of CTCF in SCZ is provided in Supplementary Discussion.
Binding of CTCF and POLR2A were frequently disrupted by schizophrenia risk SNPs. This may be due to the possibility that CTCF and POLR2A have more binding sites (on the genome) than other TFs. To test if disruption of CTCF and POLR2A were random, we conducted additional analyses. We found that the number of POLR2A binding–disrupting SNPs observed in this study were significantly higher than random SNPs (P = 0.013, 1000 simulations, Supplementary Fig. 10a), suggesting that the frequent disruption of POLR2A binding by schizophrenia risk SNPs may not be due to random effect. However, the number of CTCF binding–disrupting SNPs (observed in this study) were not significantly different from random SNPs (P > 0.05, 1000 simulations, Supplementary Fig. 10b), implying that the frequent disruption of CTCF by schizophrenia risk SNPs may be due to random effect.
There are several limitations in this study. First, we only used ChIP-Seq experiments from brain tissues (or neuronal cells) in this study. Considering the fact that most ChIP-Seq experiments in ENCODE were performed in non-brain tissues, only limited TFs (i.e., 34) were included in this study. Therefore, risk SNPs that disrupt binding of other TFs could not be identified in this study. Second, potential target genes of 97 TF binding–disrupting SNPs were identified using eQTL annotation. Nevertheless, in most cases, the identified TF binding–disrupting SNP is associated with the expression of several genes. It remains largely unknown if all of the target genes or only a specific target gene have a role in schizophrenia. Third, considering that the reporter gene assays are relatively labor consuming and time costing, we only tested 19 identified functional SNPs (10 SNPs from functional annotation and 9 SNPs from functional genomics). Thus, only a small proportion of the 132 TF binding–disrupting SNPs were verified with reporter gene assays. Fourth, though we identified several potential causal risk variants in this study, we still do not know how this kind of genetic controls of gene expression confer schizophrenia risk. It is likely these identified risk variants confer schizophrenia risk through affecting gene expression (i.e., these identified SNPs affect the expression level of target genes, and the change of target gene expression may play a pivotal role in schizophrenia pathogenesis). However, more work is needed to further demonstrate how this kind of genetic controls of gene expression confer schizophrenia risk.
In summary, we generated the landscape of the plausible causal variants in schizophrenia for the first time and revealed the gene regulatory mechanisms affected by schizophrenia risk SNPs. Our study provides new insights into the genetic mechanisms of schizophrenia. Further mechanistic investigation and functional characterization of the identified causal variants and genes will help us understand the pathogenesis of schizophrenia.
Schizophrenia GWAS and potential causal SNPs
Genetic associations from three large-scale GWASs12,13,14 were used in this study. The first GWAS was from PGC. PGC performed a large-scale GWAS of schizophrenia (PGC2 release) and identified 128 genome-wide significant (GWS) regions (spanning 108 independent loci)12. For each of the GWS regions, an index SNP was defined (usually the most significant SNP) and a potential causal set of SNPs were identified. There is a 99% possibility that the causal variants were included in the defined potential causal set of SNPs. In addition to the 128 genome-wide significant regions, PGC2 also identified 141 genomic regions that showed suggestive associations (P < 1.0 × 10−6) with schizophrenia. Potential causal SNPs were also identified for these 141 suggestive regions. A total of 20,374 potential causal variants (including SNPs, insertions and deletions) from 125 GWS regions (three GWS regions on X chromosome were not included in this study, as potential causal SNPs were not defined by PGC2 for these three regions) and 141 suggestive risk regions were identified by PGC2. As we focused on SNPs, we excluded insertions and deletions. A total of 18,707 potential causal SNPs from PGC2 were retained for further analysis. More detailed information about the definition and identification of potential causal SNPs can be found in the original paper12. The second GWAS was from a recent study of Li et al.13 Li et al.13 first conducted a GWAS in Chinese population (7699 cases and 18,327 controls). They then carried out a meta-analysis (43,175 cases and 65,166 controls) through combining the associations from Chinese population and PGC2. Finally, they performed replication study using an independent Chinese sample (4384 cases and 5770 controls). Through integrating the results from above three stages, they identified 30 novel schizophrenia risk loci. We extracted the SNPs that were in LD with the index SNPs (r2 > 0.3) using genotype data (379 European individuals) from the 1000 Genomes Project (Phase I data, phase1_v3.20101123). PLINK32 was used to calculate the LD values (r2) between the index SNPs and nearby SNPs with following parameters: –ld-window-kb 1000, –ld-window 100000, –ld-window-r2 0.3. A total of 4794 SNPs (in LD with the 31 index SNPs) were identified. The third GWAS was from the study of Pardinas et al.14 who identified 50 novel schizophrenia risk loci through using 40,675 cases and 64,643 controls. Pardinas et al.14 used FINEMAP26 to identify the potential causal SNPs and they identified 1799 potential causal SNPs for the 50 newly identified risk loci. As some of the potential causal SNPs from above three GWASs were overlapping, we removed the overlapping SNPs (Supplementary Fig. 11). A total of 23,400 non-overlapping SNPs were included in this study. To identify the most possible causal (or functional) SNPs at each of the GWAS risk loci, the potential causal SNPs from above three GWASs were subjected to deep bioinformatic and functional genomics analyses in this study.
Prioritization of functional SNPs using different annotation approaches
To prioritize the most possible functional SNPs at each of the risk loci, we used five well-characterized functional annotation tools, including CADD27, Eigen29, GWAVA28, LINSIGHT31 and RegulomeDB30. CADD uses evolutionary conservation information and data from ENCODE44 to annotate and identify the possible causal or pathogenic variants. The scores of CADD range from 0 to 99. Eigen utilizes an unsupervised spectral approach to score the potential functional variants. The scores of Eigen range from −4.2 to 175.4. GWAVA annotates functional variants through using a wide range of data from genomic and epigenomic annotations, including open chromatin, TF binding, histone modification, conservation CpG islands and so on. The scores of GWAVA range from 0 to 1. LINSIGHT predicts the functional variants through combining functional genomic data with molecular evolution model. The scores of LINSIGHT range from 0 to 1. RegulomeDB annotates functional variants using a variety data from ENCODE, including ChIP-Seq, FAIRE, DNase I hypersensitive sites and eQTL data. The ratings of RegulomeDB range from 1 to 6. For CADD, Eigen, GWAVA and LINSIGHT, the larger the score, the higher probability that the SNP is functional. Therefore, the SNP with the highest score was defined as top functional SNP. For RegulomeDB, smaller rating suggests higher probability that the SNP is functional. Thus, the SNP with the smallest rating was defined as top functional SNP. As two prioritization strategies (CADD, Eigen, GWAVA and LINSIGHT use scores and RegulomeDB uses rating) were used by the functional annotation approaches, we defined the overlapping top functional SNPs as follows: (1) if a SNP has the highest score in at least two scoring annotation methods (CADD, Eigen, GWAVA and LINSIGHT), this SNP was defined as the top functional SNP; (2) assuming a SNP (e.g., SNP X) has the highest score in at least one scoring annotation method (CADD, Eigen, GWAVA and LINSIGHT), if this SNP also has the smallest rating in RegulomeDB, this SNP was defined as overlapping top functional SNP. Of note, as our goal is to identify the most possible functional SNP at each risk locus, we did not compare the scores of the top functional SNPs from different loci. More detailed information about these annotation approaches can be found in previous publications27,28,29,30,31.
Regulatory SNP annotation using functional genomics
We downloaded ChIP-Seq data of 34 TFs from the ENCODE44 (http://www.encodeproject.org). As schizophrenia is a mental disorder that mainly originates from dysfunction of brain, only ChIP-Seq experiments performed in human brain tissues or neuronal cells (including neuronal cell lines) were included. The detailed information about the TFs and ChIP-Seq experiments can be found in the Supplementary Table 4. We annotated regulatory SNPs as previously described38. Briefly, FastQC (http://www.bioinformatics.babraham.ac.uk/projects/fastqc) was used to check the quality of the raw and processed reads. Btrim59 was used for quality control and filtering of the raw reads (with parameters “-a 20 -l 20”). We used cutadapt60 to filter the overrepresented sequences (including adaptors, primers and other sequences). The processed ChIP-Seq reads were then mapped to the human reference genome (GRCh37/hg19, which was used throughout all analyses) and bowtie61 was used to perform alignment (with the parameters “-n 2 -e 70 -m 2 -k 2”). Peak calling was performed using MACS62, with following parameters: “–keep-dup=1 -f BAM -w -S –call-subpeaks -g hs”. For control experiments, if there were biological replicates, we chose the control experiment with the largest size of bam file. For ChIP-Seq experiments, if there were biological replicates, we combined the bam files and conducted peaks calling. The called peaks were then used for PWM identification.
To obtain DNA binding motifs (PWMs) enriched in the genomic sequences surrounding ChIP-Seq peaks, we utilized MEME45 to run motif discovery on the sequences ±20 bp from the top 500 peaks (ranked by peak height), with parameters “-nmotifs 5 -minw 6 -maxw 20”, and the background model was a 0-order Markov model. We compared the peaks with the corresponding control sample and filtered peaks with FDR > 5%. As a result, 30 TFs have peaks with FDR ≤ 5% (CHD2, IRF3, RCOR1 and USF2 were excluded due to limited or no peaks). To model the binding specificity of TFs, Whitington et al.38 compiled a PWMs database that contains 7699 PWMs, including PWMs from the JASPAR, Uniprobe, Hi-SELEX and ChIP-Seq data. We compared the identified DNA binding motifs (PWMs) (derived from the ChIP-Seq experiments) with the PWMs in PWM database38, and the matched PWMs (usually, the MOTIF1) (the most statistically significant, E-value of which is the smallest, motifs with small E-values are very unlikely to be random sequence artifacts) were used to annotate if the potential causal SNPs disrupted binding of TFs.
Potential causal SNPs that resided within ±50 bp of all ChIP-Seq peak summits (with a FDR ≤ 0.05) were identified and FIMO46 was used to scan the occurrences of a given PWM within the genomic sequence overlapping a given SNP (with the parameter “–thresh 0.001”). We extracted the sequence ±20 bp from each potential causal SNP (both or more alleles) and scored every genomic position in which the SNP position overlapped the PWM by at least one base-pair. Both strands (with the reference allele and alternative allele) were considered. If one or more alleles of a SNP had a FIMO LLR (log-likelihood ratio) P < 1 × 10−3, the SNP was defined to disrupt the PWM. More information about FIMO can be found in the original paper46 and FIMO website (http://mccb.umassmed.edu/meme/doc/fimo.html).
DNase-Seq and histone modification data
The DNase-Seq data were downloaded from the UCSC genome browser (http://hgdownload.cse.ucsc.edu/goldenPath/hg19/encodeDCC/wgEncodeUwDnase/). Neuronal cells used for DNase-Seq were BE2C, HAc, SK-N-MC and SK-N-SH. Histone modification data were downloaded from ENCODE. Histone modifications, including H3K4me1, H3K4me3, H3K9ac, H3K9me3, H3K27ac, H3K27me3 and H3K36me3 were from the middle frontal area 46.
Brain eQTL annotation
To identify the potential target genes regulated by the identified regulatory SNPs, we examined three brain eQTL databases, including CMC35, LIBD brain eQTL browser (http://eqtl.brainseq.org/phase1/eqtl/)33 and GTEx34. To identify the genes that were differentially expressed in schizophrenia cases and controls, CMC collected brain tissues (dorsolateral prefrontal cortex (DLPFC)) of 258 schizophrenia cases and 279 controls35. Gene expression was determined using RNA sequencing and genotyping was performed with the Illumina Infinium HumanOmniExpressExome array. After stringent quality control, expression and genotype data from 467 subjects were used to perform eQTL analysis (utilizing an additive linear model implemented in MatrixEQTL). We used the eQTL data from these 467 individuals to explore if the regulatory SNPs were associated with gene expression in human brain. More detailed information about the sample collection, DNA and RNA extraction, gene expression quantification, genotyping, quality control and statistical analyses can be found in previous study35. The GTEx (Genotype-Tissue Expression) collected multiple tissues from healthy subjects. A total of 13 brain tissues (sample size ranges from 80 to 154) were included in the GTEx (Supplementary Table 3). Gene expression was quantified with RNA sequencing and genotyping was performed using Illumina OMNI 5M SNP Array. FastQTL was used to perform the eQTL analysis with following covariates, top 3 genotyping principal components, Genotyping array platform and sex. In addition, covariates identified by the probabilistic estimation of expression residuals (PEER) method were also included. We used brain eQTL data in this study. More information about the GTEx can be found in previous studies34,50 and the GTEx website (https://gtexportal.org/home/). The LIBD eQTL browser (http://eqtl.brainseq.org/phase1/eqtl/)33 contains brain expression data (from the DLPFC, quantified with RNA sequencing) and genotype data of 412 subjects (including 175 schizophrenia cases and 237 controls). Five levels of expression (including gene, exon, junction, transcript and expressed region) were quantified and only gene-level eQTLs were used in this study. The additive genetic effect model was used to test if a SNP was associated with the expression level of a gene, with adjusting for sex, ancestry, and expression heterogeneity.
Distribution of random SNPs
We first downloaded the PGC2 GWAS SNPs (a total of 8,624,491 SNPs with rs ID) from PGC2 website (https://www.med.unc.edu/pgc/results-and-downloads/). We then randomly sampled 186 SNPs from the PGC2 GWAS SNPs each time. We sampled 1000 times in total and SNPs sampled from these 1000 times were used for genomic location annotation. We used ANNOVAR47 to annotate the genomic location of the sampled SNPs.
We performed simulations to test if the 132 TF binding–disrupting SNPs were significantly associated with gene expression in human brain compared with random SNPs. Briefly, we randomly selected 132 SNPs (the number of SNPs equals to the identified TF binding–disrupting SNPs, and the minor allele frequencies of the random SNPs were matched to the 132 TF binding–disrupting SNPs) from PGC2 SNP list (9,444,230 SNPs in total) and calculated the number of the SNPs that showed significant association with gene expression in CMC eQTL results (FDR < 0.05). We conducted 10,000 simulations and calculated the mean and standard deviation of the 10,000 simulations. The significance level of our observation (i.e., 87 out of 132 SNPs were significantly associated with gene expression in CMC (FDR < 0.05)) were measured by Z value as follow: Z = (87–mean of the 10,000 simulations)/standard deviation of the 10,000 simulations. Z value were converted into P value with R command pnorm (-abs(Z)).
LD analysis between the 132 TF binding–disrupting SNPs
LD analysis between the 132 TF binding–disrupting SNPs was performed using SNiPA49. We used default settings of SNiPA (i.e., Genome assembly:GRCh37; variant set:1000 Genome, Phase 3 v5; population: Europeans) to calculate the LD values between the 132 TF binding–disrupting SNPs. More detailed information about SNiPA can be found in the original paper49 and the SNiPA website (http://snipa.helmholtz-muenchen.de/snipa3/).
Validation of the eQTL results with allele-specific expression analysis
We verified the eQTL associations using ASE data from the GTEx (phs000424.v7.p2)50. The GTEx contains genotypes data and expression data (quantified with RNA sequencing) from 714 subjects and 53 tissues. As we focused on brain tissues, we only extracted the ASE results from brain tissues. Binomial tests were used to determine if the ratio of the two alleles was significantly different from the expectation50 and regulatory SNPs with a binomial P < 0.001 were extracted (regulatory SNPs that showed allele-specific expression (or allelic imbalance) were defined at binomial P < 0.001 threshold). More information on ASE analysis can be found in the original paper50 and GTEx website (https://gtexportal.org/home/).
All of the cell lines used in this study were purchased from the Kunming Cell Bank, Chinese Academy of Sciences (these cell lines were originally obtained from the ATCC). HEK293 cells were cultured in high-glucose Dulbecco's Modified Eagle's medium (DMEM; C11995500BT, Gibco) containing 10% fetal bovine serum (FBS; 10091148, Gibco), penicillin and streptomycin (100 U/ml)) (10378016, Gibco). SK-N-SH and SH-SY5Y cells were cultured in high-glucose DMEM (C12430500BT, Gibco) supplemented with 10% FBS, 10 mM sodium pyruvate solution (11360070, Gibco), 1× Minimum Essential Medium non-essential amino acid solution (11140050, Gibco), penicillin and streptomycin (100 U/ml). The antibiotics were withdrawn 48 h before performing assays and all cells were cultured at 37 °C with 5% CO2 and 95% air. No mycoplasma contamination was found for the cell lines used in this study.
The DNA sequence (length ranges from ~300 to 700 bp) containing the test SNP was amplified using primers (Supplementary Table 10) linked with homologous arms (which were identical with the sequence (located at the multiple clone sites) of pGL3-promoter vectors) (Supplementary Fig. 12) and PCR products were purified with DNA Purification Kit (DP209, TIANGEN). We digested pGL3-Promoter vector (E1761, Promega) and pGL4.11 vector (E6661, Promega) with KpnI (FD0524, FastDigest) and XhoI (FD0694, FastDigest), and the digestion products were purified with DNA Purification Kit. Then the purified DNA fragments containing the test SNP were inserted into the pGL3-Promoter vector using the TreliefTM SoSoo Cloning Kit (TSV-S1, TSINGKE). As SNP rs2270363 is located in promoter region, we inserted the DNA fragments containing rs2270363 into the pGL4.11, which is a basic vector with no promoter. The ligated vectors were then used to transform DH5α competent cells (Takara). LB plates (with the selectable marker, ampicillin) were used to select the transformed cells and recombinant plasmids were extracted from the transformed cells grown from single colony. PCR-mediated point mutation technique was used to generate the DNA fragments containing the alternative allele of this test SNP. All sequences of the inserted DNA fragments were verified using Sanger sequencing.
Cell transfection and dual-luciferase reporter gene assays
The constructed vector (contained the test SNP) (150 ng for 96-well plate and 500 ng for 24-well plate) and internal control plasmid pRL-TK (E2241, Promega) (30 ng for 96-well plate and 50 ng for 24-well plate) were co-transfected into the tested cell lines. HEK293 cells were transfected with the PEI method63, and SK-N-SH and SH-SY5Y cells were transfected using the Lipofectamine 3000 (L3000-015, Invitrogen), according to the manufacturer’s instructions. For SK-N-SH and SH-SY5Y cells, dual-Luciferase reporter gene assays were performed in a 96-well white plate containing 150 µl medium at 2 × 105 cells/ml. For HEK293 cells, reporter gene assays were performed in a 24-well white plate containing 500 µl medium at 5 × 105 cells/ml. After 48 h post transfection, Luminoskan Ascent instrument (Thermo Scientific) was used to measure the luciferase activity with the Dual-Luciferase Reporter Assay System (E1960, Promega). All of the experiments were performed according to the instructions recommended by the manufacturer. The luciferase activity data were obtained from at least eight replicate wells. Two-tailed Student’s t-test was used to compare if the difference was significant and the significance threshold was set at P < 0.05.
Gene Ontology analysis
GO analysis was performed using DAVID (v6.8)51. Three GO terms (including biological process (GOTERM_BP_DIRECT), molecular function (GOTERM_MF_DIRECT) and cellular component (GOTERM_CC_DIRECT)) were used to test if specific categories or pathways were enriched among the target genes of the identified regulatory SNPs. The significance (P value) of the overrepresented GO terms was corrected by the Benjamini–Hochberg procedure.
Spatio-temporal expression pattern analysis
Spatio-temporal expression pattern analysis was conducted as previously described52,64. Briefly, expression data from different developmental stages of human brain were downloaded from the BrainSpan (http://www.brainspan.org/). The expression level of each gene was quantified (expressed as RPKM (read per kilobase per million)) with RNA sequencing. For a specific development stage, the median expression level of all genes in a gene set (target genes was treat as a gene set in this study) was used to represent the expression level of the gene set at this stage. Three gene sets (genes in Supplementary Table 5, Supplementary Data 4, and background genes) were used in this study. Background genes were extracted from a previous study65. Wilcoxon rank sum test (implemented in R software (v3.5.0)) was used to compare if the expression level of target genes and background genes was statistically significantly different.
Cell type-specific expression analysis of target genes
Cell type-specific expression data were extracted from the study of Skene et al.53. Skene et al.53 performed cell type-specific expression analysis using single cell sequencing from mouse brain (a total of 9790 cells from different brain regions, including neocortex, striatum, midbrain, hippocampus, etc) and they calculated the specificity (higher specificity of a gene suggests the expression of this gene is enriched in a specific cell type, i.e., this gene is specifically expressed) value of each gene in each cell type. We extracted the specificity value of the target genes of the identified regulatory SNPs and counted the genes with a specificity value >0.10. Detailed information about the single cell sequencing and calculation of the specificity can be found in the study of Skene et al.53.
Comparison of the number of binding sites of TFs
Frequent disruption of CTCF and POLR2A binding (by schizophrenia risk SNPs) was observed in our study. A possible explanation for this observation is that CTCF and POLR2A have more binding sites on the genome than other TFs. Thus, the number of SNPs that disrupt CTCF and POLR2A binding were accordingly larger compared to other TFs. To test if POLR2A and CTCF have more binding sites on the genome, we performed additional analyses. We first identified ChIP-Seq peaks of each TF (as described in previous section). We identified 8447 SNPs that disrupted binding of 30 TFs (these 30 TFs were used in this study) through mapping a total of 968,903 SNPs (from the Illumina HumanOmni1-Quad, only SNPs with rs id were retained) to the identified ChIP-Seq peaks (the identification of TF binding–disrupting SNPs was described in more detail above). We then randomly sampled 132 SNPs (the number of SNPs equals to the identified TF binding–disrupting SNPs in this study) from the 8447 TF binding–disrupting SNPs and counted the number of SNPs that disrupted the binding of each TF. We conducted 1000 simulations and calculated the mean and standard deviation of the 1000 simulations. We plotted the distribution of the number of TF binding–disrupting SNP using ggplot2 package (implemented in R Software). In addition, we also compared the number of motifs (appear on the genome) of the 30 TFs through counting the identified ChIP-Seq peaks of each TF.
For SZDB, see http://www.szdb.org/; for PGC2, see http://www.med.unc.edu/pgc/; for CADD, see http://cadd.gs.washington.edu/; for GWAVA, see https://www.sanger.ac.uk/sanger/StatGen_Gwava; for Eigen, see http://www.columbia.edu/~ii2135/eigen.html; for LINSIGHT, see https://github.com/CshlSiepelLab/LINSIGHT; for RegulomeDB, see http://www.regulomedb.org/; for CMC, see http://www.synapse.org/CMC; for GTEx, see https://gtexportal.org/home/; for LIBD brain eQTL browser, see http://eqtl.brainseq.org/phase1/eqtl/; for ENCODE, see https://www.encodeproject.org/; for BrainSpan, see http://www.brainspan.org/; for MEME, see http://meme-suite.org/tools/meme; for FIMO, see http://meme-suite.org/tools/fimo; for MACS, see http://liulab.dfci.harvard.edu/MACS/; for Bowtie, see http://bowtie-bio.sourceforge.net/index.shtml; for FastQC, see http://www.bioinformatics.babraham.ac.uk/projects/fastqc/; for Cutadapt, see https://cutadapt.readthedocs.io/en/stable/index.html; for The 1000 Genomes Project, see http://www.1000genomes.org/; for PLINK, see http://zzz.bwh.harvard.edu/plink/; for SNiPA, see http://snipa.helmholtz-muenchen.de/snipa3/.
The PWM, ChIP-Seq, DNase-Seq and histone modification data of the 132 TF binding–disrupting SNPs can be accessed and visualized at SZDB database25 (http://www.szdb.org/). The source data underlying Figs. 2b, 4c–e, 5b–d, f–h, 6b–d, f–h, 7b, c, e, f and 8a–j and Supplementary Figs. 4b–d and 5b–d are provided as a Source Data file. The rest of the data (including custom code and plasmids) are available from the corresponding author upon request.
Sullivan, P. F., Kendler, K. S. & Neale, M. C. Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch. Gen. Psychiatry 60, 1187–1192 (2003).
O’Donovan, M. C. et al. Identification of loci associated with schizophrenia by genome-wide association and follow-up. Nat. Genet. 40, 1053–1055 (2008).
Purcell, S. M. et al. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460, 748–752 (2009).
Ripke, S. et al. Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat. Genet. 45, 1150–1159 (2013).
Ikeda, M. et al. Genome-wide association study of schizophrenia in a Japanese population. Biol. Psychiatry 69, 472–478 (2011).
Hamshere, M. L. et al. Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Mol. Psychiatry 18, 708–712 (2013).
Rietschel, M. et al. Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol. Psychiatry 17, 906–917 (2012).
Schizophrenia Psychiatric Genome-Wide Association Study Consortium. Genome-wide association study identifies five new schizophrenia loci. Nat. Genet. 43, 969–976 (2011).
Shi, Y. et al. Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. Nat. Genet. 43, 1224–1227 (2011).
Yue, W. H. et al. Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2. Nat. Genet. 43, 1228–1231 (2011).
Stefansson, H. et al. Common variants conferring risk of schizophrenia. Nature 460, 744–747 (2009).
Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature 511, 421–427 (2014).
Li, Z. et al. Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. Nat. Genet. 49, 1576–1583 (2017).
Pardinas, A. F. et al. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Nat. Genet. 50, 381–389 (2018).
Richards, A. L. et al. Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain. Mol. Psychiatry 17, 193–201 (2012).
Bacanu, S. A. et al. Functional SNPs are enriched for schizophrenia association signals. Mol. Psychiatry 19, 276–277 (2014).
Luo, X. J. et al. Systematic integration of brain eQTL and GWAS identifies ZNF323 as a novel schizophrenia risk gene and suggests recent positive selection based on compensatory advantage on pulmonary function. Schizophr. Bull. 41, 1294–1308 (2015).
Li, M. et al. A human-specific AS3MT isoform and BORCS7 are molecular risk factors in the 10q24.32 schizophrenia-associated locus. Nat. Med. 22, 649–656 (2016).
Sekar, A. et al. Schizophrenia risk from complex variation of complement component 4. Nature 530, 177–183 (2016).
Maurano, M. T. et al. Systematic localization of common disease-associated variation in regulatory DNA. Science 337, 1190–1195 (2012).
Bond, G. L. et al. A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans. Cell 119, 591–602 (2004).
Huang, Q. et al. A prostate cancer susceptibility allele at 6q22 increases RFX6 expression by modulating HOXB13 chromatin binding. Nat. Genet. 46, 126–135 (2014).
Ong, C. T. & Corces, V. G. Enhancer function: new insights into the regulation of tissue-specific gene expression. Nat. Rev. Genet. 12, 283–293 (2011).
Goring, H. H. Tissue specificity of genetic regulation of gene expression. Nat. Genet. 44, 1077–1078 (2012).
Wu, Y., Yao, Y. G. & Luo, X. J. SZDB: a database for schizophrenia genetic research. Schizophr. Bull. 43, 458–471 (2017).
Benner, C. et al. FINEMAP: efficient variable selection using summary data from genome-wide association studies. Bioinformatics 32, 1493–1501 (2016).
Kircher, M. et al. A general framework for estimating the relative pathogenicity of human genetic variants. Nat. Genet. 46, 310–315 (2014).
Ritchie, G. R., Dunham, I., Zeggini, E. & Flicek, P. Functional annotation of noncoding sequence variants. Nat. Methods 11, 294–296 (2014).
Ionita-Laza, I., McCallum, K., Xu, B. & Buxbaum, J. D. A spectral approach integrating functional genomic annotations for coding and noncoding variants. Nat. Genet. 48, 214–220 (2016).
Boyle, A. P. et al. Annotation of functional variation in personal genomes using RegulomeDB. Genome Res. 22, 1790–1797 (2012).
Huang, Y. F., Gulko, B. & Siepel, A. Fast, scalable prediction of deleterious noncoding variants from functional and population genomic data. Nat. Genet. 49, 618–624 (2017).
Purcell, S. et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559–575 (2007).
Jaffe, A. E. et al. Developmental and genetic regulation of the human cortex transcriptome illuminate schizophrenia pathogenesis. Nat. Neurosci. 21, 1117–1125 (2018).
The GTEx Consortium. The Genotype-Tissue Expression (GTEx) project. Nat. Genet. 45, 580–585 (2013).
Fromer, M. et al. Gene expression elucidates functional impact of polygenic risk for schizophrenia. Nat. Neurosci. 19, 1442–1453 (2016).
Song, J. H. T., Lowe, C. B. & Kingsley, D. M. Characterization of a human-specific tandem repeat associated with bipolar disorder and schizophrenia. Am. J. Hum. Genet. 103, 421–430 (2018).
Srinivasan, S. et al. Genetic markers of human evolution are enriched in schizophrenia. Biol. Psychiatry 80, 284–292 (2016).
Whitington, T. et al. Gene regulatory mechanisms underpinning prostate cancer susceptibility. Nat. Genet. 48, 387–397 (2016).
Fatemi, S. H. & Folsom, T. D. The neurodevelopmental hypothesis of schizophrenia, revisited. Schizophr. Bull. 35, 528–548 (2009).
Rapoport, J. L., Giedd, J. N. & Gogtay, N. Neurodevelopmental model of schizophrenia: update 2012. Mol. Psychiatry 17, 1228–1238 (2012).
Mao, Y. et al. Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling. Cell 136, 1017–1031 (2009).
Senturk, A., Pfennig, S., Weiss, A., Burk, K. & Acker-Palmer, A. Ephrin Bs are essential components of the Reelin pathway to regulate neuronal migration. Nature 472, 356–360 (2011).
Yang, C. P. et al. Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes. Nat. Commun. 9, 838 (2018).
The ENCODE Project Consortium. An integrated encyclopedia of DNA elements in the human genome. Nature 489, 57–74 (2012).
Bailey, T. L. & Elkan, C. Fitting a mixture model by expectation maximization to discover motifs in biopolymers. Proc. Int. Conf. Intell. Syst. Mol. Biol. 2, 28–36 (1994).
Grant, C. E., Bailey, T. L. & Noble, W. S. FIMO: scanning for occurrences of a given motif. Bioinformatics 27, 1017–1018 (2011).
Wang, K., Li, M. & Hakonarson, H. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res. 38, e164 (2010).
GTEx Consortium. Genetic effects on gene expression across human tissues. Nature 550, 204–213 (2017).
Arnold, M., Raffler, J., Pfeufer, A., Suhre, K. & Kastenmuller, G. SNiPA: an interactive, genetic variant-centered annotation browser. Bioinformatics 31, 1334–1346 (2014).
The GTEx Consortium. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans. Science 348, 648–660 (2015).
Huang da, W., Sherman, B. T. & Lempicki, R. A. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat. Protoc. 4, 44–57 (2009).
Gilman, S. R. et al. Diverse types of genetic variation converge on functional gene networks involved in schizophrenia. Nat. Neurosci. 15, 1723–1728 (2012).
Skene, N. G. et al. Genetic identification of brain cell types underlying schizophrenia. Nat. Genet. 50, 825–833 (2018).
Roussos, P. et al. A role for noncoding variation in schizophrenia. Cell Rep. 9, 1417–1429 (2014).
Gusev, A. et al. Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights. Nat. Genet. 50, 538–548 (2018).
Owen, M. J., O’Donovan, M. C., Thapar, A. & Craddock, N. Neurodevelopmental hypothesis of schizophrenia. Br. J. Psychiatry 198, 173–175 (2011).
Juraeva, D. et al. Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia. PLoS. Genet. 10, e1004345 (2014).
Baruch, K. et al. Association between golli-MBP and schizophrenia in the Jewish Ashkenazi population: are regulatory regions involved? Int. J. Neuropsychopharmacol. 12, 885–894 (2009).
Kong, Y. Btrim: a fast, lightweight adapter and quality trimming program for next-generation sequencing technologies. Genomics 98, 152–153 (2011).
Martin, M. Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet. J. 17, 10–12 (2011).
Langmead, B., Trapnell, C., Pop, M. & Salzberg, S. L. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 10, R25 (2009).
Zhang, Y. et al. Model-based analysis of ChIP-Seq (MACS). Genome Biol. 9, R137 (2008).
Swiech, K. et al. Transient transfection of serum-free suspension HEK 293 cell culture for efficient production of human rFVIII. BMC Biotechnol. 11, 114 (2011).
Liu, J., Li, M., Luo, X. J. & Su, B. Systems-level analysis of risk genes reveals the modular nature of schizophrenia. Schizophr. Res. 201, 261–269 (2018).
Zhang, Q. et al. Systems-level analysis of human aging genes shed new light on mechanisms of aging. Hum. Mol. Genet. 25, 2934–2947 (2016).
This study was equally supported by the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB13000000) and the National Key Research and Development Program of China (Stem Cell and Translational Research) (2016YFA0100900) (to X.-J.L.). It was also supported by the National Nature Science Foundation of China (31722029 to X.-J.L.) and the Key Research Project of Yunnan Province (2017FA008 to X.-J.L.). We thank Dr. Whitington for sharing the curated PWM data with us. One of the brain eQTL datasets used in this study were generated as part of the CommonMind Consortium supported by funding from Takeda Pharmaceuticals Company Limited, F. Hoffman-La Roche Ltd and NIH grants R01MH085542, R01MH093725, P50MH066392, P50MH080405, R01MH097276, RO1-MH-075916, P50M096891, P50MH084053S1, R37MH057881 and R37MH057881S1, HHSN271201300031C, AG02219, AG05138 and MH06692. Brain tissue for the study was obtained from the following brain bank collections: the Mount Sinai NIH Brain and Tissue Repository, the University of Pennsylvania Alzheimer’s Disease Core Center, the University of Pittsburgh NeuroBioBank and Brain and Tissue Repositories and the NIMH Human Brain Collection Core. CMC Leadership: Pamela Sklar, Joseph Buxbaum (Icahn School of Medicine at Mount Sinai), Bernie Devlin, David Lewis (University of Pittsburgh), Raquel Gur, Chang-Gyu Hahn (University of Pennsylvania), Keisuke Hirai, Hiroyoshi Toyoshiba (Takeda Pharmaceuticals Company Limited), Enrico Domenici, Laurent Essioux (F. Hoffman-La Roche Ltd), Lara Mangravite, Mette Peters (Sage Bionetworks), Thomas Lehner, Barbara Lipska (NIMH). The Genotype-Tissue Expression (GTEx) Project was supported by the Common Fund of the Office of the Director of the National Institutes of Health, and by NCI, NHGRI, NHLBI, NIDA, NIMH and NINDS.
The authors declare no competing interests.
Journal peer review information: Nature Communications thanks Kyoko Watanabe and the other anonymous reviewers for their contribution to the peer review of this work. Peer reviewer reports are available.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Huo, Y., Li, S., Liu, J. et al. Functional genomics reveal gene regulatory mechanisms underlying schizophrenia risk. Nat Commun 10, 670 (2019). https://doi.org/10.1038/s41467-019-08666-4
A Human-Specific Schizophrenia Risk Tandem Repeat Affects Alternative Splicing of a Human-Unique Isoform AS3MTd2d3 and Mushroom Dendritic Spine Density
Schizophrenia Bulletin (2020)
Transcriptomic and epigenomic dynamics associated with development of human iPSC-derived GABAergic interneurons
Human Molecular Genetics (2020)
Frontiers in Genetics (2020)
Identification of a functional human-unique 351-bp Alu insertion polymorphism associated with major depressive disorder in the 1p31.1 GWAS risk loci
Understanding the genetics of neuropsychiatric disorders: the potential role of genomic regulatory blocks
Molecular Psychiatry (2020)