Genomic structure and expression of the human serotonin 2A receptor gene (HTR2A) locus: identification of novel HTR2A and antisense (HTR2A-AS1) exons
© Ruble et al. 2016
Received: 9 September 2015
Accepted: 22 December 2015
Published: 6 January 2016
The serotonin 2A receptor is widely implicated in genetic association studies and remains an important drug target for psychiatric, neurological, and cardiovascular conditions. RNA sequencing redefined the architecture of the serotonin 2A receptor gene (HTR2A), revealing novel mRNA transcript isoforms utilizing unannotated untranslated regions of the gene. Expression of these untranslated regions is modulated by common single nucleotide polymorphisms (SNPs), namely rs6311. Previous studies did not fully capture the complexity of the sense- and antisense-encoded transcripts with respect to novel exons in the HTR2A gene locus. Here, we comprehensively catalogued exons and RNA isoforms for both HTR2A and HTR2A-AS1 using RNA-Seq from human prefrontal cortex and multiple mouse tissues. We subsequently tested associations between expression of newfound gene features and common SNPs in humans.
We find that the human HTR2A gene spans ~66 kilobases and consists of 7, rather than 4 exons. Furthermore, the revised human HTR2A-AS1 gene spans ~474 kilobases and consists of 18, rather than 3 exons. Three HTR2A exons directly overlap with HTR2A-AS1 exons, suggesting potential for complementary nucleotide interactions. The repertoire of possible mouse Htr2a splice isoforms is remarkably similar to humans and we also find evidence for overlapping sense-antisense transcripts in the same relative positions as the human transcripts. rs6311 and SNPs in high linkage disequilibrium are associated with HTR2A-AS1 expression, in addition to previously described associations with expression of the extended 5’ untranslated region of HTR2A.
Our proposed HTR2A and HTR2A-AS1 gene structures dramatically differ from current annotations, now including overlapping exons on the sense and anti-sense strands. We also find orthologous transcript isoforms expressed in mice, providing opportunities to elucidate the biological roles of the human isoforms using a model system. Associations between rs6311 and expression of HTR2A and HTR2A-AS1 suggest this polymorphism is capable of modulating the expression of the sense or antisense transcripts. Still unclear is whether these SNPs act directly on the expression of the sense or antisense transcripts and whether overlapping exons are capable of interacting through complimentary base-pairing. Additional studies are necessary to determine the extent and nature of interactions between the SNPs and the transcripts prior to interpreting these findings in the context of phenotypes associated with HTR2A.
KeywordsSerotonin HTR2A Alternative splicing Antisense RNA mRNA expression Regulatory polymorphism Allelic expression Comparative genomics Long non-coding RNA 5-HT2A
The serotonin 2A receptor (5-HT2A) is a G protein-coupled receptor (GPCR) that serves as a primary target for serotonin signaling and is expressed on many cell types in the brain and periphery. 5-HT2A remains of great scientific interest due to its many roles in normal biological functions, which include cerebral cortex excitability , platelet aggregation , smooth muscle contraction , vasoconstriction and dilation , inflammatory processes , and hormone signaling . Among the many tissues expressing 5-HT2A, it is especially prevalent in the cerebral cortex, enriched at the apical dendrites of pyramidal neurons [7, 8]. Commensurate with its broad biological influence, studies examining single nucleotide polymorphisms (SNPs) in the gene encoding 5-HT2A (HTR2A) have identified more than 100 genotypic associations with a wide range of phenotypes, especially brain-related disorders . Drugs that directly or indirectly modulate serotonergic signaling through 5-HT2A receptors are used to treat neuropsychiatric, neurologic, and cardiovascular conditions, and 5-HT2A is an emerging drug target for a variety of other indications [10–13].
Transcriptome profiling in human tissues has greatly increased our appreciation for RNA isoform diversity, revealing pervasive alternative splicing and transcription start and termination sites for nearly all multi-exon genes [14, 15]. Consequently, we can utilize this information to better understand disease states and tailor therapeutics , but this requires in-depth characterization of RNA expression for important targets, such as HTR2A. Knowledge of the different exons and mRNAs for HTR2A has evolved over the past 20 years. Human HTR2A complementary DNA (cDNA) was first cloned in 1991 (GenBank X57830.1) , followed in 1992 by a genomic structure consisting of 3 exons spanning 20kB . The original Reference Sequence (RefSeq) mRNA annotation (NM_000621.1) reflects these findings. Since this first annotation, HTR2A has undergone three revisions, which removed cloning sites and altered alleles at polymorphic sites (NM_000621.2), added a 5’ exon (NM_000621.3), and extended the 3’ untranslated region (UTR), adding a consensus polyadenylation signal (NM_000621.4). The current gene model consists of 4 exons, spanning more than 65kB, and also includes evidence for alternative splicing of exon 2 (NM_001165947). Based on length, these two RefSeq annotations (NM_000621.4 and NM_001165947.2) likely reflect the transcripts detected by Northern blot in 1990 . There are additional HTR2A splice variants described in the literature that are not yet annotated in RefSeq. This includes an RNA isoform containing a novel 118-bp exon residing in intron 3 of the current annotation  and four additional exon boundary changes resulting in novel RNA isoforms: a truncated exon 2, a retained intron between exons 1 and 2, a 5’ extension of exon 1, and a 3’ extension of exon 4 .
The HTR2A locus also hosts a long non-coding RNA (lncRNA) gene on the antisense strand, annotated as HTR2A-AS1 in RefSeq, and encoding two alternatively spliced isoforms (NR_103752 and NR_046612). Four Expressed Sequence Tags (ESTs) (AI076014.1, AI216351.1, AI914390.1, and AW469493.1) suggest the existence of at least three different splice variants, some of which are detectable following PCR amplification of cDNA synthesized from human brain and testes [21, 22]. Furthermore, HTR2A-AS1 expression is readily detectable in human testes according to RNA-Seq data from the Genotype-Tissue Expression (GTEx) project . However, expression is sparse in other GTEx-investigated tissues, including the cerebral cortex (www.GTExportal.org).
The 5-HT2A gene in mice spans approximately 66kB on chromosome 14 and contains 3 exons. The mouse gene shares many similarities with the human gene. For example, the relative genomic spacing of the protein-coding exons and the use of constitutive splice sites is conserved, such that the mouse exon 1/human exon 2 both encode the first 138 amino acids of 5-HT2A, followed by a relatively short intron (2.6kB in mouse, 2.9kB in human). Mouse exon 2/human exon 3 both encode the subsequent 67 amino acids, followed by a relatively large intron (60.4kB in mouse, 56.8kB in humans). Mouse exon 3/human exon 4 both encode the remaining 266 amino acids. However, mouse Htr2a currently lacks in-depth analysis of RNA isoform expression to delineate alternative transcripts, as previously performed on human HTR2A. Therefore, it is unclear how well the mouse recapitulates the molecular biology of human HTR2A splice variants, limiting its capacity as a model organism for understanding HTR2A expression.
At the crux of the many genotype-phenotype associations involving HTR2A is whether the implicated genetic variants have functional consequences. The most frequently cited SNPs in studies concerning HTR2A are rs6311 and rs6313. rs6311 and rs6313 are in near-perfect linkage disequilibrium (LD) , located 1538 bases apart on chromosome 13, and neither alter the encoded protein. rs6311 (also known as -1438G > A and A-1438G) is historically described as being located in the upstream or promoter region of HTR2A. However, rs6311 is transcribed in minor isoforms of HTR2A mRNA expressed in the brain, perhaps through the use of an alternative transcription start site that results in an extended 5’ UTR . The variant “A” allele of rs6311 is associated with reduced expression of isoforms containing this 5’ UTR extension. rs6311 has also been correlated with total HTR2A mRNA and protein expression [25, 26], although multiple studies failed to find an allele-specific effect of rs6311 on the most abundant primary transcript isoform [21, 27, 28]. rs6313 (also known as T102C) is a synonymous SNP residing in exon two. Because rs6313 lacks strong functional evidence and is in high LD with rs6311, genetic associations with rs6313 are often attributed to the functional consequences of rs6311.
Understanding the functional consequences of SNPs is a critical first step towards appreciating their roles in disease. To date, only a single study has examined HTR2A SNPs and the expression of the extended 5’ UTR isoform in affected tissues, finding no difference between post-mortem brain tissue from autistic individuals and controls . To better understand the role of HTR2A in human disease, here we have comprehensively catalogued the transcripts expressed from the HTR2A gene locus in the dorsolateral prefrontal cortex (DLPFC) from unaffected controls and schizophrenia patients. We also characterized Htr2a locus expression in the mouse, contrasting it with our human findings to determine where mice could provide models for studying human 5-HT2A function. Following, we asked whether rs6311 and rs6313 are associated with sense or antisense transcript expression.
HTR2A exons defined by splice junction analysis
Described in Smith et al., 2013
Described in Smith et al., 2013
As annotated in RefSeq
As annotated in RefSeq
Described in Smith et al., 2013
As annotated in RefSeq
Described in Guest et al., 2000
As annotated in RefSeq
Partially described in Smith et al., 2013
HTR2A Splice Junctions
Total Junction Countsa
1 or 1ext
1 or 1ext
1 or 1ext
1 or 1ext
2 or 1int
2 or 1int
4 or 4ext
4 or 4ext
Exons 1, 1int, 1ext, and 0 do not have exon-exon junctions defining their 5’ boundaries and are therefore considered as transcription initiation sites. The parsimonious interpretation based on RNA-Seq coverage in this area supports the existence of two transcription start sites. Transcripts containing exons 0, 1ext, and at least some of 1int likely use a transcription initiation site upstream of the annotated exon 1, consistent with previous reports . However, the majority of transcripts likely utilize the transcription initiation site beginning with exon 1, given the large increase in read depth at this exon (Additional file 3: Figure S3). Exons 3b and 4 do not have exon-exon junctions defining their 3’ boundaries. Exon 4 contains a canonical poly-adenylation (poly-A) signal (AATAAA) at position chr13:47405698-47405703, after which the number of mapped reads drops off precipitously, signaling the termination of the major transcript isoform(s) (Additional file 4: Figure S4). Consistent with previous findings, we observed a continuation of the 3’ UTR that extends beyond the canonical poly-A signal , continuing 5.6kB distally from the annotated 3’ UTR to a cluster of four canonical poly-A signals within a stretch of 88 nucleotides (chr13:47400058-47400144; Additional file 4: Figure S4). The lack of an exon-exon junction read to define the 3’ boundary of exon 3b suggests that it is unlikely to be spliced into transcripts containing exon 4 and could represent a terminal exon. Reduced read coverage following a cluster of canonical and non-canonical poly-A signals supports the interpretation that exon 3b is a terminal exon (Additional file 5: Figure S5).
Transcript assembly for HTR2A
Putative Transcript Assembly for HTR2A
mRNA Exons Utilized
# of Predicted TM Domains
HTR2A-AS1 exons defined by splice junction analysis
Predicted TSSb (hg19)
As annotated in RefSeq
As annotated in RefSeq; No junction reads observed
As annotated in RefSeq; No junction reads observed
Overlaps HTR2A exon 3
Overlaps HTR2A exon 3
Overlaps HTR2A exon 2
Overlaps HTR2A exon 1ext
Overlaps HTR2A exon 1ext
Contains canonical polyA signal
Transcript assembly for HTR2A-AS1
From the 22 different HTR2A-AS1 exons we found to be expressed in the DLPFC, we inferred the transcript isoforms by examining the number of incoming junction reads spliced from upstream exons versus the outgoing junction reads going to downstream exons. Furthermore, we grouped junctions according to how often they were observed (number of samples, number of junction reads) into rare, low, medium, and high frequency groups, to aid our inference of transcript isoforms (Additional file 6: Table S2). Rare classification required only a single junction read in a single sample. Low, medium, and high classifications required a minimum of 2 reads in 2 samples, 25 reads in 25 samples, and 100 reads in 100 samples, respectively. Next, we exhaustively assembled 57 models of possible HTR2A-AS1 RNA isoforms, which begin at transcription start sites, allow for only a single low coverage exon junction, and terminate at exons 17 or 18 (Additional file 7: Table S3 and HTR2A-AS1.FASTA). While we find it unlikely that 57 different transcripts are expressed from the HTR2A-AS1 locus, we used permissive criteria for assembly to next test for protein-coding potential of any possible antisense transcript. The transcript isoform models range in size from 248 to 626 nt. From all possible transcripts, the longest predicted open reading frame (ATG-to-stop) is only 31 amino acids long and is not supported as coding using the tcode program in EMBOSS . Therefore, we find it likely that HTR2A-AS1 represents an lncRNA.
Mouse Htr2a and Htr2a-AS1 alignments
Using publically available RNA-Seq data generated from a variety of mouse tissues (Gene Expression Omnibus; GEO Accessions GSE36025, GSE52564, and GSE27243) [34–36], we analyzed mouse Htr2a and Htr2a-AS1 expression in a manner similar to the human brain tissues. The majority of reads mapped to the three annotated exons for Htr2a. However, we also found evidence for seven additional alternative sense-encoded exons (Additional file 8: Table S4). In the mouse, Htr2a exons 1 and 2 can be alternatively spliced to form low-abundance isoforms orthologous to human transcripts (Additional file 9: Figure S6). Of particular note, the highly-expressed archetype mouse isoform is orthologous to the human isoform that retains intron 1. The mouse also expresses an orthologue to the human isoform in which exon 2 is spliced out. This is predicted to translate a protein that lacks the first two transmembrane domains, consistent with the human isoform lacking exon 2. We also observed infrequent utilization of the splice acceptor site equivalent to the human exon 2 truncation (E2tr) that truncates the N-terminus of 5-HT2A, resulting in a 6TM isoform. However, the splice donor site in mouse differs from that in humans, resulting in a predicted protein that includes all seven transmembrane domains, but lacks 71 of 75 amino acids constituting the N-terminus. Finally, much like human HTR2A, the mouse gene has a well-expressed extended 3’ UTR, approximately 2.6kB longer than the current annotation, terminating at a canonical poly-A site (Additional file 10: Figure S7). The lack of a poly-A site (canonical or non-canonical) at the end of the current annotation and the contiguous high expression into the extended 3’ UTR argues for revised annotation. As noted in Additional file 8: Table S4 and Additional file 9: Figure S6, we also see alternative splicing of the 3’ UTR, which is predicted to shorten the protein by a single amino acid and change three terminal amino acids (…NEKVSCV vs. …NEKMPF). This alternative isoform also excludes a large portion of the 3’ UTR, the significance of which is unknown. Unlike human HTR2A, we do not see strong evidence for an extended 5’ UTR in the mouse.
Genetic influence of HTR2A and HTR2A-AS1 expression
Significant Allelic Expression Imbalance at rs6313
Binom Dist p-val
Associations Between rs6311 or rs6313 and RNA Expression
HTR2A-AS1 Unique Readsb
HTR2A Unique Readsc
HTR2A, AS1 Overlapping Readsd
HTR2A-AS1 Exon 14 Readse
HTR2A-AS1 Exon 17.1 Readsf
HTR2A-AS1 Exon 14 to 17.1 Readsg
Our analysis of RNA expression from the HTR2A gene locus provides us with valuable insight into the sense- and antisense-encoded genes of this region, and delineates the use of known and novel exons. Of note, we see evidence for expression of up to 10 distinct sense-encoded human HTR2A exons generated through the use of alternative transcription start sites, alternative splicing (intron retention, alternative donor site), and the infrequent use of novel splice donor/acceptor sites. On the antisense strand, we observed an abundance of novel HTR2A-AS1 exons. Including the previously-described HTR2A-AS1 exons, our splice junction analysis provides evidence for up to 22 unique antisense exons, 5 of which overlap with sense-encoded HTR2A exons (Fig. 3a). Furthermore, we found evidence that the common SNPs rs6311 and rs6313 are associated with expression of the HTR2A transcripts with the extended 5’ UTR and HTR2A-AS1 exon 14. Finally, we demonstrated that the expression of Htr2a and Htr2a-AS1 in the mouse parallels expression in humans, suggesting that the mouse is suitable for studying specific sense and antisense isoforms.
Consequences of HTR2A alternative splicing
The genomics era, ushered in by massively-parallel DNA sequencing, has rapidly expanded our knowledge of gene architecture. At one time, nearly all GPCRs were considered to be without introns in their open reading frames (ORFs) . While GPCRs are enriched for intronless ORFs relative to other protein classes, up to 42 % of rhodopsin family GPCR genes have multiple exons that undergo alternative splicing . Here, we found that HTR2A undergoes a variety of different splicing events, including utilization of alternative splice acceptor sites, exon skipping, rare exon usage, and intron retention, similar to previously described GPCR splicing patterns .
Inferred from splice junction reads, the majority of HTR2A transcripts encode for the full-length 7TM receptor (Table 3). However, some of the transcripts likely encode receptor proteins lacking the N-terminus and varying stretches of transmembrane domains; particularly the isoforms with junctions shared between exon 0 and 3 and those utilizing exon 2tr. The previously described 6TM form resulting from usage of exon 2tr  bears resemblance to other GPCRs reported to have truncated or “headless” forms: CALCR , CNR1 , CCKBR , OPRL1 , OPRM1 , and SSTR5 . While a headless form of 5-HT2A would not necessarily disrupt the binding site for serotonin, it could abate membrane expression due to the deletion of N-glycosylation sites . A comparison across species at the nucleotide level reveals strong conservation beginning specifically at the splice acceptor site for exon 2tr and a relative lack of amino acid conservation in the N-terminus across species (Additional file 12: Figure S8). In our analysis of mouse Htr2a, we observed usage of the exon 2tr splice site, which is predicted to result in a 7TM receptor that lacks almost the entire N-terminus. The N-glycosylation sites critical for 5-HT2A membrane expression are conserved in mice, and are deleted by the use of the orthologous exon 2tr splice site. Consequently, we speculate that membrane expression for the truncated receptor would be reduced in mice and humans.
It is not known whether the alternatively spliced mRNAs are translated into truncated 5-HT2A protein isoforms in vivo, or subsequently capable of signaling from the cytoplasm. Assuming translation occurs, there are two observations arguing for the plausibility of intracellular 5-HT2A signaling. First, serotonin that enters cells via the serotonin transporter is biologically active and involved in “serotonylation” of proteins . Second, GPCRs in the cytoplasm, internalized via the endosome, can continue to signal through G protein-dependent and independent mechanisms . Further studies characterizing the cell type-specific and developmental expression patterns of this truncated isoform could lend insights into the biological relevance of this, and perhaps other, headless GPCRs.
HTR2A-AS1, a lncRNA
Long non-coding RNAs are stringently defined by their length (>200 nt), lack of protein-coding potential, use of independent transcriptional units, presence of canonical splice site signals, and ability to undergo alternative splicing . Some lncRNAs can have over 100 exons (SNURF-SNRPN)  and many are species-specific [51, 52]. With the additional exons and junctions we uncovered here, we reassessed classification of HTR2A-AS1, firmly concluding that it meets criteria as an lncRNA.
The question of HTR2A-AS1 function remains. lncRNAs have diverse roles, but most characterized up to this point influence transcription and processing of RNAs from nearby genes, sometimes by direct RNA-RNA interactions, and other times through epigenetic modifications . The fact that HTR2A-AS1 has exons directly overlapping with HTR2A transcripts (Fig. 3a), a feature which is also apparent in the mouse (Fig. 3b), argues strongly for the possibility of direct interaction through complementary nucleotide base-pairing, assuming the sense- and antisense-encoded transcripts are expressed at the same time and location. Direct RNA-RNA interactions could influence RNA processing, protein translation, or both. The relatively low abundance of the antisense transcripts relative to the sense isoforms and their apparent isoform diversity argues against a role in translation of the major HTR2A protein isoform, as these transcripts would have to exit the nucleus, find their respective targets, and impact the function of the translating ribosome.
Instead, we speculate that HTR2A-AS1 is more likely to have roles in HTR2A mRNA expression or processing. The variable use of 5’ exons in HTR2A-AS1 and Htr2a-AS1, coupled with their conserved overlap with alternatively-spliced HTR2A exons 1 and 2 (Fig. 3), could allow HTR2A-AS1 to participate in the alternative splicing of HTR2A through direct RNA-RNA interactions. Additionally, the associations between the ancestral “G” allele of rs6311, greater expression of HTR2A exon 1ext, and decreased expression of the seemingly constitutive HTR2A-AS1 exon 14 suggests a possible role in transcription start site usage or epigenetic modifications, perhaps through RNA-DNA interactions. In this case, we would presume that expression of the lncRNA is inversely associated with usage of the transcription start site that results in longer 5’ UTR HTR2A transcripts. It is also possible that HTR2A-AS1 transcripts impact HTR2A expression at multiple levels and in a species-specific manner. While molecular data showing an interaction of any kind between HTR2A-AS1 and HTR2A is lacking, our study provides critical information for testing these hypotheses, including evidence that an orthologous lncRNA is expressed in mice.
HTR2A and HTR2A-AS1 genetics: rs6311 and rs6313
HTR2A demonstrates many genotype-phentoype associations. A cursory analysis of the HuGE Navigator Genopedia shows 201 disease terms where HTR2A was investigated in 540 publications . To put this into perspective, of the 12,488 genes listed in the HuGE Navigator, HTR2A ranks 58th with respect to the number of associated disease terms. Of the 540 HTR2A publications listed, 333 specifically mention rs6311 or rs6313 (or some variation of the nomenclature; e.g. -1438 A/G, T102C, etc.) in their abstract or title, highlighting the interest in understanding disease associations conferred by these SNPs. While contradictory findings for any one phenotype-genotype association exist, overwhelming evidence implicates HTR2A, and specifically rs6311 or rs6313, in a variety of phenotypes.
Because rs6311 and rs6313 are in near perfect LD, genetic association studies have the liberty of using either SNP to obtain similar results. However, each SNP must be considered separately when attempting to elucidate their biological functions and contributions to disease. To date, the most compelling evidence for modulating biological function supports a role for rs6311 in the expression of HTR2A mRNAs with the extended 5’ UTR [21, 29], while no apparent role has been identified for rs6313. The allelic expression analysis of rs6311 in our current study supports the conclusion that rs6311 modulates expression of the extended 5’ UTR. Aside from the infrequent allelic expression imbalances noted for rs6313, we find little evidence that expression of the highly-expressed primary HTR2A transcript not containing the extended 5’ UTR is modulated by these common SNPs.
Regarding the transcription factors binding to the region of DNA harboring rs6311 to exert an allelic effect, the question remains open. An interesting candidate that unites genetic findings in schizophrenia is Early Growth Response 3 (EGR3). Polymorphisms in the promoter of the gene encoding EGR3 are implicated in schizophrenia . Multiple studies have now demonstrated a link between EGR3, 5-HT2A receptor expression, and schizophrenia-like behaviors in transgenic animals [56, 57]. The consensus binding site for EGR3 does align, although imperfectly, at the rs6311 region and the minor allele for rs6311 impacts this alignment (Additional file 13: Figure S9). Other transcription factors predicted to bind at the rs6311 locus in silico include the nuclear factor 1 family (NFIA/B/C), the Thing1/e47 heterodimer, and SMAD3 (Additional file 13: Figure S9). However, molecular evidence and additional bioinformatic studies are required to test such relationships, given the imprecision of transcription factor binding site tools in predicting relationships in vivo.
Changes in expression conferred by rs6311 or rs6313 could also result from other RNA processing events, such as alternative splicing. Considering the extent of alternative splicing on both the sense and antisense strands adjacent to rs6313, and the proximity of this SNP to alternative exons, we find it possible that this SNP could impact splicing. In silico analysis of splicing factors using a number of tools suggest this SNP can impact their binding (Additional file 14: Table S6). However, the aggregated results do not demonstrate a clear consensus for any single splicing factor being impacted by rs6313.
Future studies of HTR2A-AS1 expression should consider regulation by rs6311 or rs6313, as we found some evidence suggesting differential expression across genotype. However, the low read coverage across the entire HTR2A-AS1 transcript leads us to interpret these findings with caution. Both SNPs sit in intronic regions of HTR2A-AS1; rs6313 is 61 nucleotides downstream of exon 8 and rs6311 is 100 nucleotides downstream of exon 9. Both exons 8 and 9 share a relatively high number of splice junctions with the antisense exon 14 that exhibits genotype-expression associations. Our analyses are unable to isolate the individual contributions of either SNP due to high LD. Until stronger evidence delineates specific roles for each SNP, it remains equally plausible that either could modulate HTR2A-AS1 expression.
We examined HTR2A and HTR2A-AS1 gene structure by mapping RNA-Seq junction reads from human prefrontal cortex, utilizing conventional definitions for exon structure independent of established gene annotations. This approach revealed two novel exons in HTR2A and showed the extent to which all exons are included in the mature mRNA transcripts. While the majority of transcripts consist of the previously-annotated exons that encode for the full-length 7TM protein, we also found evidence supporting the use of unannotated but previously-described exons that likely form truncated protein isoforms of 5-HT2A. In contrast, HTR2A-AS1 has numerous novel exons, some of which overlap with annotated HTR2A exons. The biological significance of HTR2A-AS1 transcripts is yet to be revealed, but the current findings enable studies to directly test if they regulate HTR2A expression. To that end, we conclude that the mouse could serve as a suitable model organism for studying whether sense-antisense interactions occur in Htr2a, as it also expresses many orthologous sense and antisense transcripts, and the overlapping features between the transcripts are spatially similar. Finally, we found evidence that the common genetic variant rs6311 regulates expression of HTR2A transcripts containing the extended 5’ UTR, consistent with previous studies. We also found associations between rs6311, rs6313, and expression of HTR2A-AS1. Guided by these findings, we can begin to examine variable transcript expression in the HTR2A gene locus, especially focusing on diseases where it is implicated.
Human Tissue Demographics
Schizophrenia (n = 105)
Control (n = 106)
74.3 % (n = 78)
74.5 % (n = 79)
25.7 % (n = 27)
25.5 % (n = 27)
60.0 % (n = 63)
59.4 % (n = 63)
40.0 % (n = 42)
40.6 % (n = 43)
Age at Death
45.6 ± 13.8 years
45.9 ± 13.8 years
Manner of Death
59.0 % (n = 62)
82.1 % (n = 87)
13.3 % (n = 14)
8.5 % (n = 9)
26.7 % (n = 28)
0.0 % (n = 0)
1.0 % (n = 1)
0.9 % (n = 1)
0.0 % (n = 0)
0.9 % (n = 1)
0.0 % (n = 0)
7.5 % (n = 8)
Smoking Status at Time of Death
70.5 % (n = 74)
26.4 % (n = 28)
21.0 % (n = 22)
70.8 % (n = 75)
8.6 % (n = 9)
2.8 % (n = 3)
6.46 ± 0.24
6.56 ± 0.26
40.3 ± 26.6 hours
29.4 ± 14.1 hours
RNA Integrity Number
8.0 ± 0.91
8.3 ± 0.75
Genotyping, illumina chips
Genomic DNA was extracted from cerebellar tissues (Qiagen, Valencia CA, USA) and genotyped with HumanHap650Y_v3 or Human 1 M-Duo_v3 Illumina BeadChips (Illumina, San Diego, CA, USA) according to the manufacturer’s instructions. Genotypes were called using the Illumina GenomeStudio v2010.1 software using the default settings and the chip-specific cluster files supplied by Illumina. For data analysis, SNPs had an overall missing rate <0.02 %, CAUC and AA Hardy-Weinberg Equilibrium (HWE) p-values each > = 0.001, and minor allele frequencies (MAF) > = 0.01.
RNA extraction and quality assessment
Tissue from DLPFC was pulverized and stored at -80 °C. Total RNA was extracted from 100 mg of tissue with TRIzol Reagent (Life Technologies, Grand Island, New York). The yield of total RNA was determined by spectrophotometry by measuring absorbance at 260 nm. RNA quality was assessed with high-resolution capillary electrophoresis on an Agilent Bioanalyzer 2100 (Agilent Technologies, Palo Alto, California), yielding an RNA Integrity Number (RIN; scale 1–10, with 1 being the lowest and 10 being the highest RNA quality).
RNA-Seq library construction
RNA-seq libraries were constructed using Illumina TruSeq RNA sample Prep Kit, following the manufacturer’s protocol. The poly-A containing mRNA molecules were purified from ~ 800 ng DNAse treated total RNA. Following poly-A purification, the mRNA was fragmented into small pieces using divalent cations under elevated temperature (94°) for 2 min. Under this condition, fragment lengths range from 130 to 290 bp with a median length of 185 bp. Fragmented RNA was reverse transcribed into a first strand cDNA-RNA hybrid using random hexamers. Following, DNA Polymerase I and RNaseH were used to generate the complementary second strand cDNA. These double-stranded cDNA fragments then underwent end repair using T4 DNA polymerase, T4 PNK and Klenow DNA polymerase. Illumina PE barcoded adapters were ligated using T4 DNA Ligase following the addition of a single ‘A’ base using Klenow exo (3’ to 5’ exo minus). These products were then purified and PCR-enriched to create the final cDNA library for high through put DNA sequencing using a Highseq2000. The concentrations of RNA-seq libraries were measured by Qubit (Invitrogen, CA). The quality of each RNA-seq library was measured by LabChipGX (Caliper, MA) using HT DNA 1 K/12 K/HiSens Labchip.
Mouse tissues and sequencing
All mouse data was obtained from public sources. Mouse tissues collection, RNA isolation, library preparation, and RNA-Seq were performed as described in their original publications [34–36]. Collected animal data conformed to local institutional review boards, as described in their original publications [34–36]. Raw BAM files from each of the three studies (Series Numbers GSE27243, GSE52564, and GSE36025) were downloaded from GEO (http://www.ncbi.nlm.nih.gov/geo/) and aligned with GSNAP as described below to Mus musculus reference genome mm10.
RNA sequence mapping
Demultiplexing was performed with CASAVA v1.8.2 (http://support.illumina.com/sequencing/sequencing_software/casava.ilmn). Alignments were first performed with Tophat v2.0.4  using the reference genome: Illumina UCSC hg19; and gene annotations: Ensembl GRCh37.67. An example command is: tophat –p 4 –r 160 –G Homo_sapiens.GRCh37.67.gtf –o Sample_out. Reads over the HTR2A region were extracted post processing with samtools v0.1.18  with the following example command: samtools view –h Sample_RNA/accepted_hits.bam chr13:47357513-47521169 > HTR2A_regions/Sample_RNA/accepted_hits.sam. The extracted reads for each of the 211 samples were subsequently re-aligned to the human genome reference with GSNAP  which allows for gapped alignments, including intron-spanning alignments. Descriptive and statistical analyses were performed using this subsequent alignment.
Alignment to the HTR2A locus
On average, we generated 114 million reads per sample, 82 % of which mapped to the reference genome (mapping statistics in Additional file 15: Table S1). HTR2A is on the reverse strand of chromosome 13. Consequently, we defined canonical splice junctions with respect to transcription on the reverse strand and subsequently mapped junction reads across putative exons in order to define exon boundaries. In order for reads at novel junctions to be attributed to HTR2A, they must follow canonical splicing rules such that the nucleotides comprising the presumptive splice donor and acceptor sites are GU and AG, respectively. Adherence to this rule establishes the genomic DNA strand from which transcription occurred, eliminating ambiguity when assigning junction reads to HTR2A versus the overlapping HTR2A-AS1. This resulted in an average of 7248 aligned reads per sample over the HTR2A locus. Observational analysis, for the purpose of correcting for obvious bias in HTR2A mapping, revealed no overt differences across diagnosis or sex with respect to HTR2A expression.
Gene expression was quantified using the total number of reads for each sample that uniquely aligned to the reference. The read depth of each gene was computed based on the coordinates of mapped reads and newly annotated exons in the reference genome. Visualization of the mapping was carried out using publicly available software, primarily the Integrated Genomic Viewer (IGV) (http://www.broadinstitute.org/software/igv/).
Allelic expression imbalance
Allele-specific expression was assessed for those samples that were heterozygous over rs6311 and rs6313. For measuring quality base counts, we used the following command, varying the region and sample: samtools mpileup -uD -r chr13:47357513-47521169 -f ref_genome.fa R3924_*.bam | bcftools view -cg - | grep 47469940. Read counts from the DP4 field was used in a binomial statistical test with a 5 % multiple test corrected significance cut-off.
In silico splicing and transcription factor binding analysis
Sequences 100 bp upstream and downstream of exons was downloaded from UCSC Genome Browser and submitted to the Human Splice Finder v2.4.1 in silico webserver (http://www.umd.be/HSF/), which scores splicing characteristics (splice donor site, acceptor site, branch point) . For the branch point analysis, the highest scoring motif between positions -50 and -17 relative to the exon start site was considered for analysis. Positions -40 to -5 were analyzed for polypyrimidine frequency, expressed as a percentage.
Splicing characteristics were also scored using the Alternative Splice Site Predictor . For this analysis, sequence for the entire HTR2A region was downloaded via the UCSC Genome Browser and submitted to the webserver (http://wangcomputing.com/assp/index.html) for scoring. We compared the average of scores obtained for annotated RefSeq exons vs. newly-discovered exons vs. all other predicted splice donor/acceptor sites using independent sample t-tests. In-depth analysis of splicing events for rs6313 alleles used multiple in silico tools for predicting putative splicing-related proteins [63–67].
A natural choice to model read counts is the Poisson distribution. However, it has been shown that Poisson distribution does not capture biological variation in read counts [69–71]. To account for the extra variation found in biological replicates, the Poisson distribution can be extended through the negative binomial distribution, which has been used extensively to model RNA-Seq data [72, 73]. Thus, a generalized linear model (GLM) with logit link function using the negative binomial distribution was used to analyze read counts. The genotypic model was log(UniquelyMappedReads*ExpressionRate) = Covariates + SNP. The best set of covariates was chosen using the model that minimized the Bayesian Information Criterion. Covariates considered were age, race, gender, diagnosis, alcohol use, smoking status, PMI, brain pH, RIN, and suicide. The brain pH and RIN were the main covariates explaining significant amounts of read count variability and were included in most models. Multiplicity correction was performed using a Bonferroni adjustment for the number of endpoints tested times the effective number of independent SNPs tested , to control type I error at an experiment-wise alpha level of 0.2.
Availability of supporting data
Human DLPFC RNA-Seq and genotyping data will be available for download in early 2016 according to the data sharing policy described Schubert et al. (2015) . Mouse data used in this study can be downloaded from GEO at http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE27243 , http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE52564 , and http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE36025 . Mapping software used in the current study includes CASAVA 1.8.2 (http://support.illumina.com/sequencing/sequencing_software/casava.ilmn), TopHat 2.0.4 (https://ccb.jhu.edu/software/tophat/index.shtml) , samtools v0.1.18 (http://samtools.sourceforge.net/) , and GSNAP (http://research-pub.gene.com/gmap/) . Aligned .BAM files were viewed using IGV (https://www.broadinstitute.org/igv/). Splicing analyses were performed using Human Splice Finder v2.4.1 (http://www.umd.be/HSF/) , Alternative Splice Site Predictor (http://wangcomputing.com/assp/index.html) , SpliceAid2 (http://www.introni.it/splicing.html) , Rescue-ESE (http://genes.mit.edu/burgelab/rescue-ese/) , FAS-ESS (http://genes.mit.edu/fas-ess/) , SFmap (http://sfmap.technion.ac.il) , ACEScan (http://genes.mit.edu/acescan2/) . Transcription factor analysis was performed using MatInspector (http://www.genomatix.de/matinspector) .
This study was funded by Eli Lilly and Company.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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