Next Article in Journal
Transcriptomic Changes Following Partial Depletion of CENP-E in Normal Human Fibroblasts
Previous Article in Journal
Evolution, Expression and Meiotic Behavior of Genes Involved in Chromosome Segregation of Monotremes
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Genes
Volume 12
Issue 9
10.3390/genes12091321
genes-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome—Where Are We?

by
Amanda M. Levy
1,
Peristera Paschou
2,3 and
Zeynep Tümer
1,4,*
1
Kennedy Center, Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, 2600 Glostrup, Denmark
2
Department of Molecular Biology and Genetics, Democritus University of Thrace, 68100 Alexandroupolis, Greece
3
Department of Biological Sciences, Purdue University, West Lafayette, IN 47907, USA
4
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, 2200 Copenhagen, Denmark
*
Author to whom correspondence should be addressed.
Genes 2021, 12(9), 1321; https://doi.org/10.3390/genes12091321
Submission received: 14 May 2021 / Revised: 5 August 2021 / Accepted: 25 August 2021 / Published: 26 August 2021
(This article belongs to the Section Human Genomics and Genetic Diseases)
Browse Figures
Review Reports Versions Notes

Abstract

:
Gilles de la Tourette syndrome (GTS) is a childhood-onset neurodevelopmental and -psychiatric tic-disorder of complex etiology which is often comorbid with obsessive-compulsive disorder (OCD) and/or attention deficit hyperactivity disorder (ADHD). Twin and family studies of GTS individuals have shown a high level of heritability suggesting, that genetic risk factors play an important role in disease etiology. However, the identification of major GTS susceptibility genes has been challenging, presumably due to the complex interplay between several genetic factors and environmental influences, low penetrance of each individual factor, genetic diversity in populations, and the presence of comorbid disorders. To understand the genetic components of GTS etiopathology, we conducted an extensive review of the literature, compiling the candidate susceptibility genes identified through various genetic approaches. Even though several strong candidate genes have hitherto been identified, none of these have turned out to be major susceptibility genes yet.

1. Introduction

Gilles de la Tourette syndrome (GTS) is a complex early-onset neurodevelopmental/-psychiatric disorder with a prevalence between 0.52% and 0.77% in children [1,2]. GTS is one of the four tic disorders included in the fifth edition of the American Diagnostic and Statistical Manual of Mental Disorders (DSM-5): GTS, persistent (chronic) tic disorder (CTD), provisional tic disorder, and other specified and unspecified tic disorders. Diagnostic criteria for GTS are the presence of multiple motor tics and at least one vocal tic persisting for at least one year with onset of the first tic before age 18 [3]. Diagnostic criteria for CTD includes all of these criteria that exception that an individual has either motor or vocal tics, but not both. Provisional tic disorder meets all of the criteria for GTS except for the fact that tics do not last longer than 12 months. Finally, it is categorized as other specified and unspecified tic disorder when none of the above criteria are met [3]. Recently, the term “tic spectrum disorders” was suggested to replace the GTS and CTD diagnoses [4]. In addition to tics, most GTS individuals present a variety of symptoms due to comorbidities, the most common of which are obsessive-compulsive disorder (OCD) and/or attention deficit hyperactivity disorder (ADHD), and to a lesser extent autism spectrum disorder (ASD), migraine, anxiety, depression, sleep disorders, and rage attacks, implying an overlapping etiology [5,6,7,8,9,10]. Several neurotransmitter systems have been implicated in disease pathogenesis and amongst these, the dopaminergic and the serotonergic pathways are the most widely studied.
GTS is a complex disorder, where several environmental factors (such as streptococcus infections, birth complications and maternal smoking) are thought to interact with multiple genes in yet undiscovered ways [11]. Altered immune regulation is also suggested to predispose to inflammation and infection, thereby triggering GTS [11], and there is growing evidence for dysregulation of the brain’s resident immune cells, the microglia [12]. Several lines of evidence suggest that GTS has a strong genetic component [13], and it has been suggested as one of the non-Mendelian neuropsychiatric disorders with the highest heritability [9]. However, the identification of susceptibility genes has been challenging, which is likely due to the complex and heterogeneous genetic architecture of GTS, wherein common and rare variants in several different genes and biological pathways are involved. Even though neurophysiology and neuroimaging studies suggest that GTS is associated with altered synaptic neurotransmission, the pathophysiology is far from understood, which also hampers the identification of possible associated genetic factors. The overall results of the hitherto genetic studies suggest that in lieu of one or more major susceptibility loci, several rare and low-penetrance variants account for the genetic risk factors in GTS etiology.
We have performed an extensive review of the literature to compile the candidate GTS susceptibility genes identified through a candidate gene approach or data-driven studies such as GWAS or linkage analyses (Supplementary Table S1). In this review, we will highlight some of the most recent and notable studies in tic genetics, genes of historical significance in tic research, and studies focusing on candidate biological systems, such as the dopaminergic and serotonergic neurotransmission pathways.

2. Candidate Gene and Pathway Studies

Most of the studies utilizing a candidate gene/pathway approach have focused on the genes encoding the proteins of the neurotransmitter pathways of the cortico–basal ganglia–thalamo–cortical (CBGTC) loops. The CBGTC loops are the primary neural circuits associated with GTS pathogenesis, and they are altered in both structure and activity in GTS individuals [14,15,16]. The CBGTC loops connect specific regions of the cerebral cortex, the thalamus, and the basal ganglia, which is associated with several movement disorders [17]; and notably, GTS is also categorized as a movement disorder. Multiple neurotransmission systems present within the CBGTC loops, including dopaminergic, serotonergic, glutamatergic, and γ-aminobutyric acid (GABA)ergic systems, have been the target for GTS candidate gene studies.

2.1. The Dopaminergic Pathway

The most extensively studied neurotransmission system in GTS is the dopaminergic pathway (Figure 1). Upon the excitation of the dopaminergic neurons, dopamine is released from the synaptic vesicles of the presynaptic neurons into the synaptic cleft, where it is either transported back to the cytosol facilitated by the dopamine transporter DAT1 (encoded by SLC6A3) or interacts with post- or presynaptic dopamine receptors [18]. Dopamine receptors are categorized in two classes; D1-like receptors (D1 and D5 are encoded by DRD1 and DRD5, respectively) and D2-like receptors (D2, D3, and D4 are encoded by DRD2, DRD3, and DRD4, respectively) coupled to excitatory and inhibitory G proteins, respectively [19]. Other players of the dopaminergic pathway include monoamine oxidase A (encoded by MAOA) and catechol O-methyltransferase (encoded by COMT), which metabolize unbound cytosolic dopamine, and dopamine β-hydroxylase (encoded by DBH), which catalyzes the conversion of dopamine to norepinephrine [18].
Aberrant regulation of dopamine uptake and release [20,21] and increased levels of dopaminergic innervation of the striatum (a component of the basal ganglia) have been reported in GTS individuals [22], and dopamine receptor blockers have successfully been used for the treatment of tics in GTS [21]. Dopamine receptors are also common drug targets in the treatment of other neuropsychiatric disorders such as schizophrenia and Parkinson’s disease and, to a lesser extent, ADHD [19].
Genes encoding the proteins of the dopaminergic system have thus been investigated extensively as candidate GTS susceptibility genes. The first association and linkage studies were conducted at the end of the previous century, where Comings et al. showed association between GTS and the DRD2, DRD3, SLC6A3, and DBH polymorphisms [23,24,25]. Subsequently, several other studies investigated the involvement of the dopaminergic pathway genes in GTS etiology [26,27,28,29]. In 2004, Díaz-Anzaldúa et al. [30] investigated 110 French Canadian trios and provided support for DRD4 and MAOA as GTS susceptibility genes, but not for DRD2, DRD3, or SLC6A3. However, these results could not be replicated in other studies [31,32,33], with the exception of a single publication suggesting the involvement of DRD4 in GTS etiology, particularly in Asian populations [34].
Later studies, however, reported an association between GTS and DRD2, especially the downstream Taq1A polymorphism (rs1800497): A meta-analysis including a total of 523 GTS individuals and 564 controls together with 87 GTS probands and 152 relatives from five studies concluded that Taq1A polymorphism might confer an increased risk of developing GTS, particularly in Caucasian populations [35]. The Taq1A polymorphism was later shown to be located within the coding region of the previously unknown ANKK1 gene (the locus now called ANKK1/DRD2) which encodes a receptor interacting protein kinase. ANKK1 may also be associated with the dopaminergic system in the brain, as ANKK1 expression is affected by activation of dopamine receptors [36,37], but additional functional studies are needed to determine its role in GTS pathogenesis.
In a more recent study including 51 GTS individuals and 51 controls, the hypermethylation of DRD2 was correlated to GTS and tic severity, and significant hypomethylation of SLC6A3 was observed in GTS individuals with severe symptoms [38]. These results suggest that the altered epigenetic regulation of dopamine-related genes may play a role in GTS etiology, but this finding should be replicated in larger cohorts.
In conclusion, the above-mentioned studies have been conducted in small cohorts with limited statistical power and an unequivocal conclusion regarding the involvement of the dopaminergic pathway genes in GTS etiology cannot be drawn. Similarly, none of the later GTS GWASs identified any significant association, altogether suggesting that the genes of the dopaminergic pathway do not markedly contribute to GTS pathogenesis.

2.2. The Serotonergic Pathway

The serotonergic pathway, which is closely linked to the dopaminergic pathway, has also been studied in GTS, especially in OCD etiology [39]. Similar to dopamine, serotonin (5-hydroxytryptamine, 5-HT) is released from a presynaptic neuron into the synaptic cleft and is transported back to the cytosol by the serotonin transporter SERT (encoded by SLC6A4) or is bound to serotonin receptors. There are at least 14 different classes of serotonin receptors on the post- or presynaptic membranes [40]. Serotonin metabolism involves tryptophan 5-hydroxylase 2 (encoded by TPH2) which is responsible for the biosynthesis of serotonin from L-tryptophan; as for dopamine, MAOA is responsible for the degradation of serotonin to 5-hydroxyindole acetic acid (5-HIAA).
Interest in the serotonergic pathway in GTS etiology began when decreased levels of serotonin and 5-HIAA were detected in the cerebrospinal fluid and subcortical brain regions of GTS individuals [41,42,43], although these results could not be replicated in a later study [44]. In addition, serotonin reuptake inhibitors were also found to have an, albeit modest, effect on tic treatment [45,46].
Several serotonin receptors, including 5-HT1A, 5-HT1B, 5-HT2A, 5-HT2C, 5-HT3, and 5-HT4, are capable of facilitating and inhibiting dopamine activity in addition to that of serotonin [47,48,49], just as SERT can act both as a serotonin and dopamine transporter [50]. This has collectively led to the speculation that these two neurotransmitter pathways might be involved in various neuropsychiatric disorders in a combined manner. However, while the genes encoding the proteins of the dopaminergic pathway have been extensively studied in GTS, similar studies for the serotonergic pathway are scarce.
In 2010, common polymorphisms in several serotonin receptors (HTR1A, HTR2A, and HTR2C) were investigated in 87 Caucasian GTS individuals and 311 controls, and only the HTR2C polymorphisms Cys759Thr and Gly697Cys showed a nominally significant association with GTS [51]. These results could not be replicated in a Han Chinese cohort of 110 GTS individuals and 440 controls [52]. Similarly, polymorphisms of the serotonin receptors HTR3A and HTR3B could not be linked to GTS [53].
SLC6A4 encoding SERT has repeatedly been investigated in GTS cohorts focusing particularly on the SERT-linked polymorphic region (5-HTTLPR) in the promoter region of SLC6A4. The 5-HTTLPR is a 43bp insertion/deletion giving rise to a long (L) allele and a short (S) allele (Figure 2). The LAC haplotype, which is a combination of the L allele and the major alleles of the rs25531 (A/G) and rs25532 (C/T) SNPs and which is associated with the highest rate of SLC6A4 mRNA expression (Figure 2), was found to be more prevalent in 151 GTS individuals compared to 858 controls [54]. Recently, SLC6A4 promoter variants and mRNA levels were investigated in a Danish cohort comprising 72 GTS individuals and 87 controls. SLC6A4 mRNA expression levels were found to be higher in GTS individuals, particularly when only considering the individuals with the LAC/LAC genotype [55]. In earlier studies, an association between GTS and the 5-HTTLPR variants was not detected [51,56,57]. These contradictory results may be due to the previously unnoticed effect of the rs25531 (A/G) and rs25532 (C/T) SNPs on SLC6A4 mRNA expression, as it is likely that higher expression of SLC6A4 mRNA is associated with the 5-HTTLPR/rs25531 LA allele but not with the LG and S alleles [58] (Figure 2). Most recently, the exome sequencing of 13 multiplex GTS families suggested SLC6A4 as a high confidence GTS risk gene [59].
TPH2 has also been the focus of several candidate gene studies. The C/C genotype and the C allele of rs4565946 (C/T) were associated with GTS in a German cohort comprising 98 GTS individuals and 178 ancestry-matched controls [60]. In a Han Chinese cohort comprising 149 children with tic disorders and 125 controls, the T allele was linked to tic disorders suggesting an ancestry-dependent association [61]. Subsequently, a large association study including 412 North American, European, and South Korean GTS/CTD trios and quartets and a replication cohort consisting of 1285 GTS individuals and 4964 controls found a nominally significant association of rs4565946 to GTS/CTD, though it ceased to be significant after correction for multiple testing [62].
The data regarding the role of the serotonergic pathway in GTS etiology are limited and again, individual studies have been of limited statistical power due to their low sample size. However, when studies of the dopaminergic system are taken into consideration, it is plausible to hypothesize that the serotonergic system may play a complex role in GTS etiology that is directly and/or indirectly in combination with or through modulating dopaminergic neurotransmission. Additional neurotransmitter pathways (e.g., glutamatergic and GABAergic) may also be involved in the pathology of GTS, as the dysfunction of one pathway may affect others due to interaction or self-regulation among them.

3. Linkage Analyses, GWAS & Other Studies

Besides the hypothesis-driven approach, several data-driven genetic studies such as linkage analyses and GWASs have been conducted to elucidate the underlying genetic risk factors for GTS. In this review, we will highlight SLITRK1 and IMMPL2 due to their historical significance, as well as candidate susceptibility genes such as HDC, CELSR3, FN1, ASH1L, FLT3, NRXN1, and CNTN6, which have been identified in independent studies. All of the other studies are described very briefly in Supplementary Table S1.

3.1. SLITRK1

SLITRK1 (Slit and Trk-like 1) is the most investigated GTS candidate gene, since one of the breakpoints of a de novo inversion of chromosome 13 in a child with GTS was mapped within its proximity [63]. Functional studies showed that neurite outgrowth was affected by a truncating SLITRK1 variant (varCDf) identified in a GTS individual, and a missense variant (var321) in the 3′ untranslated region (3′-UTR) of the gene altered a microRNA binding site leading to decreased mRNA expression [63].
However, several subsequent association studies, predominantly in European populations, could not detect an association between GTS and var321 or other SLITRK1 variants [64,65,66,67,68]. A cohort study comprising 114 Costa Rican and 193 Ashkenazi Jewish GTS probands and their parents suggested population stratification rather than an association between var321 and GTS, as the variant was found in several of the Ashkenazi parents and one of the Ashkenazi controls [65]. A later study did not find any evidence for a var321 founder allele amongst Ashkenazi Jews but showed an association between var321 and GTS [69].
Other studies demonstrated an association between other SLITRK1 variants and GTS individuals from European (n = 447 total), Canadian (n = 231 total), and East Asian populations (n = 252 total) [70,71,72,73,74,75]. A total of four of the variants (c.1061G > C, c.1158G > T, c.892C > T, and c.1252A > T) were concluded to be rare but deleterious variants [70].
The first two GTS GWASs were conducted on 1285 GTS individuals (4964 controls) and 2723 individuals with GTS and/or OCD (5667 controls) [76,77] and more recently, a GWAS meta-analysis with a larger sample size (4819 GTS individuals and 9488 controls) was conducted [78]. All of the cases and the controls of these three studies were of European ancestry, and none of the studies identified an association between GTS and SLITRK1. In the GWAS conducted by Scharf et al., the SNP rs7336083 residing in the intergenic region between SLITRK1 and SLITRK6 was one of the highest-ranking loci, but it did not reach the threshold of genome-wide significance [76]. However, in a cohort comprising 399 Han Chinese trios, an association between SLITRK6 and GTS could not be detected [79]. Similarly, SLITRK5, which has been associated with OCD and is within the same cluster as SLITRK1 and SLITRK6, could not be linked to GTS [80,81], although a de novo SLITRK5 missense mutation was recently identified in a proband with GTS and ASD [82].
SLITRK1 promotes neurite outgrowth and SLITRK1 is predominantly expressed in the brain, including in the CBGTC circuits [83]. In addition, the six proteins belonging to the SLITRK family play important roles in the development of the central nervous system and neuronal processes and have been implicated in several other neurodevelopmental and -psychiatric disorders [84]. The SLITRK-genes have therefore been attractive candidates in the search for the genes involved in GTS etiology. However, it is likely that these genes, especially SLITRK1, do not play a major role in GTS etiology.

3.2. IMMPL2

Similar to SLITRK1, IMMPL2 (inner mitochondrial membrane peptidase, subunit 2) was suggested as a candidate GTS gene by the finding of a chromosome aberration in a GTS individual, where the gene was disrupted by a 7q31 breakpoint [85], a region previously linked to GTS [86]. The role of IMMPL2 and the 7q31 region in GTS etiology was further supported by the finding of another Caucasian individual with tics and a disruption of IMMP2L [87] and a family based association study (86 French Canadian GTS trios) suggesting an association between GTS and several 7q31 markers, including a tendency of association with an intragenic IMMP2L marker [88].
Even though deleterious IMMPL2 variants could not be detected in 39 European GTS individuals [89], a chromosome microarray study of a Danish cohort (188 GTS individuals and 316 controls) showed a significantly increased number of intragenic IMMPL2 deletions in GTS individuals, and some of these deletions affected an alternatively spliced isoform [90]. As IMMP2L functions in the mitochondria and as mitochondrial dysfunction is linked to movement disorders, fibroblasts from the Danish GTS individuals and controls, both with or without deletions, were assessed on various parameters relating to mitochondrial dysfunction, without detecting a significant disruption in mitochondrial function [91]. Finally, a recent meta-analysis of previously reported GTS candidate genes in European GTS individuals and controls detected an association between GTS and IMMPL2 [92], further implicating IMMPL2 in GTS etiology. However, how a defective IMMP2L function may be involved in GTS pathogenesis is still unknown.

3.3. HDC

HDC encodes the histidine decarboxylase enzyme essential for histamine synthesis and hence for histaminergic neurotransmission, and the striatum has a high density of histamine receptors which modulate both dopaminergic and serotonergic neurotransmission [93]. HDC was first implicated as a candidate GTS susceptibility gene by the identification of a nonsense truncating variant (Trp317Ter) segregating with the disorder in a Caucasian, nonconsanguineous two-generation family (eight siblings and their parents) with an extremely high prevalence of GTS, as only a single family member was unaffected [94]. This variant was not present in 3000 Caucasian controls, in a replication cohort of 720 GTS individuals, nor in 360 controls not screened for psychiatric disorders. These results suggested the Trp317Ter variant is a very rare genetic GTS risk factor with high penetrance. This study implicated disrupted histamine production in GTS etiology and raised the histaminergic hypothesis. Since then, several studies have found an association between GTS and HDC variants in populations of European ancestry [70,72,95], and HDC knockout mice exhibited tic-like stereotypies [96]. A genome-wide analysis of de novo copy number variations (CNVs) in 460 Caucasian GTS individuals (including 148 trios) and 1131 ancestry-matched controls showed enrichment of genes within the histamine receptor (H1R and H2R) signaling pathways in GTS individuals, further supporting the histaminergic hypothesis [97]. However, two studies among Han Chinese GTS individuals, one with a case-control approach (120 cases and 240 controls) [98] and the other with a family-based approach (241 nuclear family trios) [99], did not detect an association between HDC and GTS. Taken together, this could indicate that a causal role for HDC in GTS etiology primarily applies to individuals of European ancestry, in which case it has the potential to be an important candidate gene with high penetrance in very rare cases, an uncommon feature in complex disorders such as GTS.

3.4. CELSR3, WWC1, FN1, and NIPBL

In 2017, exome sequencing of 511 GTS trios with various ancestries suggested that de novo damaging variants in approximately 400 genes contributed to the genetic risk load in 12% of the individuals [100]. In addition, four likely susceptibility genes with multiple de novo damaging variants were identified in unrelated GTS individuals: CELSR3 (cadherin EGF LAG seven-pass G-type receptor 3), WWC1 (WW and C2 domain containing 1), FN1 (Fibronectin 1), and NIPBL (Nipped-B-like) [100]. In a follow-up study, additional variants of these four genes were identified [101]. All of these variants were either absent or present in very low frequency in the gnomAD database, which comprised about 250,000 individuals [102]. The two former genes were suggested as high confidence GTS risk genes and the two latter were suggested as probable GTS risk genes. FN1, which encodes a cell adhesion protein, was further implicated in GTS etiology by the finding of a de novo missense variant in a GTS/ASD proband [82]. Similarly, variants of CELSR3, which encodes a non-classic cadherin transmembrane receptor, were identified in two European [72] and one Chinese GTS individual [103].

3.5. ASH1L

One of the most recent and quite notable additions to the list of potential GTS candidate genes is ASH1L (ASH1-like histone lysine methyltransferase), identified through the exome sequencing of 100 GTS trios [104]. ASH1L was suggested to be associated with GTS based on a transmission disequilibrium test (TDT) as well as a finding of de novo variants. Of the nineteen reported damaging ASH1L variants, five were present in very low frequency in the gnomAD database. The association was replicated through targeted sequencing of 524 GTS samples (and 2822 East Asian ExAC controls). Some of the variants altered the methyltransferase activity of the protein, and Ash1l+/− transgenic mice manifested compulsive and tic-like behaviors that could be rescued by a tic-relieving drug. The disruption of Ash1l also affected dopaminergic modulation in the dorsal striatum in the basal ganglia [104], altogether indicating a role of ASH1L in GTS physiopathology.

3.6. FLT3

Recently, in a GWAS with a cohort comprising 4819 GTS individuals and 9488 controls, Yu et al. reported a single genome-wide significant SNP (rs2504235) within FLT3, encoding FMS-like tyrosine kinase 3 [78]. rs2504235 is in strong linkage disequilibrium with the common FLT3 missense variant rs1933437 (p.Thr227Met), which in the same study had a p-value of 8.2 × 10−8 [78]. This latter variant drove the association between GTS and a lymphocytic gene set in a recent large pathway analysis based on genome-wide genotypic data from 3581 GTS individuals and 7682 controls [105]. The association between lymphocytic genes, FLT3, and GTS not only provides further support for a role of FLT3 in GTS, but also suggests an involvement of a neuroinflammatory element in disease pathogenesis. In addition, the pathway analysis also implicated ligand-gated ion channel signaling and cell adhesion and transsynaptic signaling processes [105].

3.7. NRXN1 and CNTN6

Rare CNVs are known to be associated with a number of neuropsychiatric disorders [106], including GTS [97]. The investigation of rare CNVs in a large cohort (2434 GTS individuals and 4093 controls) of European ancestry showed an increased global burden of CNVs in the GTS sample [107]. Notably, NRXN1 deletions and CNTN6 duplications were present in 1% of the GTS individuals and survived genome-wide correction for multiple testing and were suggested as definitive GTS susceptibility loci. CNTN6 encodes a cell adhesion molecule, contactin-6, and has been implicated in ASD and intellectual disability [108,109]. NRXN1 encodes the presynaptic cell adhesion molecule neurexin 1 which is involved in glutamatergic and GABAergic neurotransmission and synaptogenesis [110]. NRXN1 deletions have previously been associated with GTS, although the sample sizes have been considerably smaller (111 Caucasian GTS individuals with 73 ancestry-matched controls and 263 Latin American GTS individuals with 285 ancestry-matched controls, respectively) [111,112]. Furthermore, NRXN1 deletions have been implicated in other neurodevelopmental and -psychiatric disorders, including ASD and schizophrenia [113,114,115]. The two susceptibility loci are important additions to the list of candidate GTS susceptibility loci and demonstrate the importance of rare structural variations in GTS etiology.

4. Discussion—Future Opportunities and Challenges

GTS is a disorder with complex and heterogeneous genetic architecture, seemingly due to a combination of rare genetic risk factors, either de novo or inherited, and an inter-individual variation in polygenic burden. Several lines of evidence point towards neurotransmitter mediated involvement of the CBGTC circuits in GTS pathology. We hypothesize that a link between the dopaminergic and serotonergic pathways may involve MAOA, which is responsible for the degradation of both cytosolic dopamine and serotonin in presynaptic neurons, and potential feedback mechanisms regulating MAOA levels or activity. If this is the case, an overexpression of a neurotransmitter transporter such as SERT as reported by Hildonen et al. [55] might result in an upregulation of MAOA due to increased levels of cytosolic serotonin. This could potentially have a more global effect, leading to increased degradation of both serotonin and dopamine.
To identify GTS susceptibility genes within neurotransmission pathways, early studies applied the candidate gene approach in relatively small cohorts, investigating a few polymorphisms at a time. Today, technological advances allow for larger and hypothesis-free studies such as GWAS, exome sequencing, and whole genome sequencing (WGS). The rationale behind GWAS is the common disease-common variant hypothesis and requires very large cohorts when studying highly complex diseases, where rare variants often play a more considerable role. The first GWAS in GTS was conductedin a relatively small cohort, which likely explains why none of the individual SNP signals reached a genome-wide level of significance [76]. The more recent GWAS conductedin a cohort that was nearly four times larger, identified a single SNP within FLT3 reaching genome-wide significance [78], consistent with the call for large sample sizes in these studies. Due to the fall in the running costs, exome and genome sequencing are now attractive alternative methods for detecting novel and rare variants, and exome sequencing in particular has been utilized in several recent GTS studies [100,101,104,116,117]. Through pathway analyses, Tsetsos et al. identified three significant gene sets that may be involved in GTS pathogenesis, demonstrating yet another useful approach in the search for candidate GTS susceptibility genes [105]. Meta-analyses and replication studies of the most significant hits from all of these screening studies, in combination with functional analyses such as investigation of mRNA expression, methylation patterns or the more cumbersome cellular studies, would be future approaches for a better understanding of the underlying genetic risk factors in GTS.
Genetic variation due to ancestry and clinical heterogeneity, including the presence of comorbidities, are confounding factors hampering the identification of susceptibility genes in complex disorders. GTS has been reported to occur less frequently among individuals of African descent compared to Caucasian Europeans [118], although it is not clear whether this is due to decreased awareness of the disorder in specific populations. As accounted for throughout this review, there also appears to be some general distribution differences of genetic susceptibility factors between populations of different ancestry. This potential confounding effect of a hidden population substructure further challenges approaches searching for common, and more notably, rare variants that are associated with the disorder. Furthermore, there is a risk of stratification on genetic ancestry, particularly in GWAS [119], which should be taken into consideration in the search for potential candidate GTS genes.
The presence of comorbidities likewise impedes the identification of GTS susceptibility genes, comparison between studies, and meta-analyses introducing additional levels of heterogeneity. In several GTS studies, CTD and other tic disorders are also included and the presence of comorbidities, occasionally apart from OCD, are not taken into consideration. Furthermore, in some studies, not all GTS individuals are diagnosed using clinically validated instruments, and some are noted as self-reported. Diagnosis of GTS is further challenged by the suggestion that there may be more than one GTS phenotype [120]. Cross-disorder studies have suggested a significant proportion of GTS heritability to be shared with OCD, ADHD, major depression disorder, and migraine [121,122], and heritable cross-disorder endophenotypes of GTS and OCD have been identified [123]. A recent cross-disorder study reported 11 previously unidentified regions likely associated with GTS, ADHD, and ASD as well as two separate pleiotropic regions associated with both GTS and OCD, indicating that the genetic etiology shared between GTS and OCD might differ from that shared between GTS, ADHD and ASD [124]. On the other hand, another cross-disorder GWAS investigating the genetic architecture behind OCD and GTS suggested that the susceptibility genes behind OCD with comorbid GTS might differ from those involved in OCD alone [77]. Similarly, individuals with pure GTS (without comorbidities) were shown to have no family history of OCD [125], altogether indicating the presence of distinct genetic components of GTS.

5. Conclusions

The collaborative research conducted over the last few years and the investigation of large cohorts to identify the genetic susceptibility factors involved in GTS etiology are beginning to bear fruit. The employment of uniform methodology and clinically homogeneous cohorts taking comorbidities and ancestry into consideration are crucial in achieving more consistent and comparable results in future studies. Furthermore, functional analyses and cross-disorder studies might offer novel insights into the etiology and pathophysiology of GTS and overlapping neurodevelopmental, -psychiatric, and movement disorders. A better understanding of the complex etiology of GTS and new insights into the pathophysiology of GTS, which is far from being fully understood, are crucial in new treatment strategies for this disorder.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/genes12091321/s1, Table S1: Gilles de la Tourette Syndrome Candidate Genes and Regions.

Funding

This research was funded by Lundbeck Fonden, grant number R100-2011-9332.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Knight, T.; Steeves, T.; Day, L.; Lowerison, M.; Jette, N.; Pringsheim, T. Prevalence of Tic Disorders: A Systematic Review and Meta-Analysis. Pediatr. Neurol. 2012, 47, 77–90. [Google Scholar] [CrossRef]
  2. Scharf, J.M.; Miller, L.L.; Bs, C.A.G.; Ma, J.A.; Mathews, C.A.; Ben-Shlomo, Y. Population prevalence of Tourette syndrome: A systematic review and meta-analysis. Mov. Disord. 2014, 30, 221–228. [Google Scholar] [CrossRef] [PubMed]
  3. American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 5th ed.; American Psychiatric Association: Arlington, VA, USA, 2013. [Google Scholar]
  4. Müller-Vahl, K.R.; Sambrani, T.; Jakubovski, E. Tic disorders revisited: Introduction of the term “tic spectrum disorders”. Eur. Child Adolesc. Psychiatry 2019, 28, 1129–1135. [Google Scholar] [CrossRef] [Green Version]
  5. Conte, G.; Valente, F.; Fioriello, F.; Cardona, F. Rage attacks in Tourette Syndrome and Chronic Tic Disorder: A systematic review. Neurosci. Biobehav. Rev. 2020, 119, 21–36. [Google Scholar] [CrossRef] [PubMed]
  6. Darrow, S.M.; Grados, M.; Sandor, P.; Hirschtritt, M.E.; Illmann, C.; Osiecki, L.; Dion, Y.; King, R.; Pauls, D.; Budman, C.L.; et al. Autism Spectrum Symptoms in a Tourette’s Disorder Sample. J. Am. Acad. Child Adolesc. Psychiatry 2017, 56, 610–617.e1. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  7. Huisman-van Dijk, H.M.; van de Schoot, R.; Rijkeboer, M.M.; Mathews, C.A.; Cath, D.C. The relationship between tics, OC, ADHD and autism symptoms: A cross- disorder symptom analysis in Gilles de la Tourette syndrome patients and family-members. Psychiatry Res. 2016, 237, 138–146. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Jiménez-Jiménez, F.J.; Alonso-Navarro, H.; García-Martín, E.; Agundez, J. Sleep disorders in tourette syndrome. Sleep Med. Rev. 2020, 53, 101335. [Google Scholar] [CrossRef] [PubMed]
  9. Robertson, M.M.; Eapen, V.; Singer, H.S.; Martino, D.; Scharf, J.M.; Paschou, P.; Roessner, V.; Woods, D.W.; Hariz, M.; Mathews, C.A.; et al. Gilles de la Tourette syndrome. Nat. Rev. Dis. Prim. 2017, 3, 16097. [Google Scholar] [CrossRef]
  10. Vermilion, J.; Pedraza, C.; Augustine, E.F.; Adams, H.R.; Vierhile, A.; Lewin, A.B.; Collins, A.T.; McDermott, M.P.; O’Connor, T.; Kurlan, R.; et al. Anxiety Symptoms Differ in Youth With and Without Tic Disorders. Child Psychiatry Hum. Dev. 2021, 52, 301–310. [Google Scholar] [CrossRef] [PubMed]
  11. Hoekstra, P.J.; Dietrich, A.; Edwards, M.J.; Elamin, I.; Martino, D. Environmental factors in Tourette syndrome. Neurosci. Biobehav. Rev. 2013, 37, 1040–1049. [Google Scholar] [CrossRef] [PubMed]
  12. Frick, L.; Pittenger, C. Microglial Dysregulation in OCD, Tourette Syndrome, and PANDAS. J. Immunol. Res. 2016, 2016, 1–8. [Google Scholar] [CrossRef] [PubMed]
  13. Paschou, P. The genetic basis of Gilles de la Tourette Syndrome. Neurosci. Biobehav. Rev. 2013, 37, 1026–1039. [Google Scholar] [CrossRef]
  14. Draganski, B.; Martino, D.; Cavanna, A.E.; Hutton, C.; Orth, M.; Robertson, M.M.; Critchley, H.D.; Frackowiak, R.S. Multispectral brain morphometry in Tourette syndrome persisting into adulthood. Brain 2010, 133, 3661–3675. [Google Scholar] [CrossRef] [Green Version]
  15. Peterson, B.S.; Thomas, P.; Kane, M.J.; Scahill, L.; Zhang, H.; Bronen, R.; King, R.A.; Leckman, J.F.; Staib, L. Basal Ganglia Volumes in Patients With Gilles de la Tourette Syndrome. Arch. Gen. Psychiatry 2003, 60, 415–424. [Google Scholar] [CrossRef] [Green Version]
  16. Wang, Z.; Maia, T.; Marsh, R.; Colibazzi, T.; Gerber, A.; Peterson, B.S. The Neural Circuits That Generate Tics in Tourette’s Syndrome. Am. J. Psychiatry 2011, 168, 1326–1337. [Google Scholar] [CrossRef] [PubMed]
  17. Neuner, I.; Schneider, F.; Shah, N.J. Functional Neuroanatomy of Tics. In International Review of Neurobiology; Harris, R.A., Jenner, P., Eds.; Elsevier Inc.: Amsterdam, The Netherlands, 2013; pp. 35–71. [Google Scholar] [CrossRef]
  18. Cumming, P. The life history of dopamine. In Imaging Dopamine; Cambridge University Press: Cambridge, UK, 2009; pp. 5–18. [Google Scholar]
  19. Beaulieu, J.-M.; Gainetdinov, R. The Physiology, Signaling, and Pharmacology of Dopamine Receptors. Pharmacol. Rev. 2011, 63, 182–217. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Ernst, M.; Zametkin, A.J.; Jons, P.H.; Matochik, J.A.; Pascualvaca, D.; Cohen, R.M. High Presynaptic Dopaminergic Activity in Children With Tourette’s Disorder. J. Am. Acad. Child Adolesc. Psychiatry 1999, 38, 86–94. [Google Scholar] [CrossRef] [PubMed]
  21. Lavenstein, B.L. Treatment approaches for children with Tourette’s syndrome. Curr. Neurol. Neurosci. Rep. 2003, 3, 143–148. [Google Scholar] [CrossRef]
  22. Swain, J.; Scahill, L.; Lombroso, P.J.; King, R.A.; Leckman, J.F. Tourette Syndrome and Tic Disorders: A Decade of Progress. J. Am. Acad. Child Adolesc. Psychiatry 2007, 46, 947–968. [Google Scholar] [CrossRef] [Green Version]
  23. Comings, D.E.; Comings, B.G.; Muhleman, D.; Dietz, G.; Shahbahrami, B.; Tast, D.; Knell, E.; Kocsis, P.; Baumgarten, R.; Kovacs, B.W.; et al. The Dopamine D2 Receptor Locus as a Modifying Gene in Neuropsychiatric Disorders. JAMA 1991, 266, 1793–1800. [Google Scholar] [CrossRef]
  24. Comings, D.; Muhleman, D.; Dietz, G.; Dino, M.; Legro, R.; Gade, R. Association between Tourette’s syndrome and homozygosity at the dopamine D3 receptor gene. Lancet 1993, 341, 906. [Google Scholar] [CrossRef]
  25. Comings, D.E.; Wu, S.; Chiu, C.; Ring, R.; Gade, R.; Ahn, C.; MacMurray, J.P.; Dietz, G.; Muhleman, D. Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: The additive and subtractive effect of the three dopaminergic genes—DRD2, DβH, and DAT1. Am. J. Med. Genet. 1996, 67, 264–288. [Google Scholar] [CrossRef]
  26. Cruz, C.; Camarena, B.; King, N.; Páez, F.; Sidenberg, D.; De La Fuente, J.R.; Nicolini, H. Increased prevalence of the seven-repeat variant of the dopamine D4 receptor gene in patients with obsessive-compulsive disorder with tics. Neurosci. Lett. 1997, 231, 1–4. [Google Scholar] [CrossRef]
  27. Gade, R.; Muhleman, D.; Blake, H.; MacMurray, J.; Johnson, P.; Verde, R.; Saucier, G.; Comings, D.E. Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse. Mol. Psychiatry 1998, 3, 50–60. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  28. Grice, D.E.; Leckman, J.F.; Pauls, D.L.; Kurlan, R.; Kidd, K.K.; Pakstis, A.J.; Chang, F.M.; Buxbaum, J.; Cohen, D.J.; Gelernter, J. Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test. Am. J. Hum. Genet. 1996, 59, 644–652. [Google Scholar] [PubMed]
  29. Rowe, D.C.; Stever, C.; Gard, J.M.C.; Cleveland, H.H.; Sanders, M.L.; Abramowitz, A.; Kozol, S.T.; Mohr, J.H.; Sherman, S.L.; Waldman, I.D. The relation of the dopamine transporter gene (DAT1) to symptoms of internalizing disorders in children. Behav. Genet. 1998, 28, 215–225. [Google Scholar] [CrossRef]
  30. Díaz-Anzaldúa, A.; Joober, R.; Rivière, J.B.; Dion, Y.; Lespérance, P.; Richer, F.; Chouinard, S.; Rouleau, G.A. Tourette syndrome and dopaminergic genes: A family-based association study in the French Canadian founder population. Mol. Psychiatry 2004, 9, 272–277. [Google Scholar] [CrossRef] [Green Version]
  31. Huertas-Fernández, I.; Gómez-Garre, P.; Madruga-Garrido, M.; Bernal, I.; Bonilla-Toribio, M.; Martín-Rodríguez, J.F.; Cáceres-Redondo, M.T.; Vargas-González, L.; Carrillo, F.; Pascual, A.; et al. GDNF gene is associated with tourette syndrome in a family study. Mov. Disord. 2015, 30, 1115–1120. [Google Scholar] [CrossRef] [Green Version]
  32. Tárnok, Z.; Rónai, Z.; Gervai, J.; Kereszturi, E.; Gadoros, J.; Sasvari-Szekely, M.; Nemoda, Z. Dopaminergic candidate genes in Tourette syndrome: Association between tic severity and 3′ UTR polymorphism of the dopamine transporter gene. Am. J. Med. Genet. Part B Neuropsychiatr. Genet. 2007, 144B, 900–905. [Google Scholar] [CrossRef]
  33. Yoon, D.Y.; Rippel, C.A.; Kobets, A.J.; Morris, C.M.; Lee, J.E.; Williams, P.N.; Bridges, D.D.; Vandenbergh, D.; Shugart, Y.Y.; Singer, H.S. Dopaminergic polymorphisms in Tourette syndrome: Association with the DAT gene (SLC6A3). Am. J. Med. Genet. Part B Neuropsychiatr. Genet. 2007, 144B, 605–610. [Google Scholar] [CrossRef]
  34. Liu, S.; Cui, J.; Zhang, X.; Wu, W.; Niu, H.; Ma, X.; Xu, H.; Yi, M. Variable number tandem repeats in dopamine receptor D4 in Tourette’s syndrome. Mov. Disord. 2014, 29, 1687–1691. [Google Scholar] [CrossRef] [PubMed]
  35. Yuan, A.; Su, L.; Yu, S.; Li, C.; Yu, T.; Sun, J. Association between DRD2/ANKK1 TaqIA Polymorphism and Susceptibility with Tourette Syndrome: A Meta-Analysis. PLoS ONE 2015, 10, e0131060. [Google Scholar] [CrossRef] [PubMed]
  36. Ponce, G.; Lombraña, A.Q.; Martín-Palanco, N.G.; Rubio-Solsona, E.; Jimenez-Arriero, M.A.; Palomo, T.; Hoenicka, J. The Addiction-Related Gene Ankk1 is Oppositely Regulated by D1R- and D2R-Like Dopamine Receptors. Neurotox. Res. 2015, 29, 345–350. [Google Scholar] [CrossRef] [PubMed]
  37. Ponce, G.; Pérez-González, R.; Aragüés, M.; Palomo, T.; Rodríguez-Jiménez, R.; Jiménez-Arriero, M.A.; Hoenicka, J. The ANKK1 Kinase Gene and Psychiatric Disorders. Neurotox. Res. 2009, 16, 50–59. [Google Scholar] [CrossRef] [PubMed]
  38. Müller-Vahl, K.R.; Loeber, G.; Kotsiari, A.; Müller-Engling, L.; Frieling, H. Gilles de la Tourette syndrome is associated with hypermethylation of the dopamine D2 receptor gene. J. Psychiatr. Res. 2017, 86, 1–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. Sinopoli, V.M.; Burton, C.; Kronenberg, S.; Arnold, P.D. A review of the role of serotonin system genes in obsessive-compulsive disorder. Neurosci. Biobehav. Rev. 2017, 80, 372–381. [Google Scholar] [CrossRef] [PubMed]
  40. Olivier, B. Serotonin: A never-ending story. Eur. J. Pharmacol. 2015, 753, 2–18. [Google Scholar] [CrossRef] [Green Version]
  41. Anderson, G.M.; Pollak, E.S.; Chatterjee, D.; Leckman, J.F.; Riddle, M.A.; Cohen, D.J. Brain Monoamines and Amino Acids in Gilles de la Tourette’s Syndrome: A Preliminary Study of Subcortical Regions. Arch. Gen. Psychiatry 1992, 49, 584–586. [Google Scholar] [CrossRef]
  42. Butler, I.J.; Koslow, S.H.; Seifert, W.E.; Caprioli, R.M.; Singer, H.S. Biogenic amine metabolism in tourette syndrome. Ann. Neurol. 1979, 6, 37–39. [Google Scholar] [CrossRef]
  43. Leckman, J.F.; Anderson, G.M.; Cohen, D.J.; Ort, S.; Harcherik, D.F.; Hoder, E.; Shaywitz, B.A. Whole blood serotonin and tryptophan levels in Tourette’s disorder: Effects of acute and chronic clonidine treatment. Life Sci. 1984, 35, 2497–2503. [Google Scholar] [CrossRef]
  44. Leckman, J.F.; Goodman, W.K.; Anderson, G.M.; Riddle, M.A.; Chappell, P.B.; McSwiggan-Hardin, M.T.; McDougle, C.J.; Scahill, L.D.; Ort, S.I.; Pauls, D.L.; et al. Cerebrospinal Fluid Biogenic Amines in Obsessive Compulsive Disorder, Tourette’s Syndrome, and Healthy Controls. Neuropsychopharmacology 1995, 12, 73–86. [Google Scholar] [CrossRef] [Green Version]
  45. Müller-Vahl, K.R.; Meyer, G.J.; Knapp, W.H.; Emrich, H.M.; Gielow, P.; Brücke, T.; Berding, G. Serotonin transporter binding in Tourette Syndrome. Neurosci. Lett. 2005, 385, 120–125. [Google Scholar] [CrossRef]
  46. Steeves, T.D.; Fox, S.H. Neurobiological Basis of Serotonin-Dopamine Antagonists in the Treatment of Gilles de La Tourette Syndrome. Prog. Brain Res. 2008, 172, 495–513. [Google Scholar] [PubMed]
  47. Bortolozzi, A.; Diaz-Mataix, L.; Scorza, M.C.; Celada, P.; Artigas, F. The activation of 5-HT2A receptors in prefrontal cortex enhances dopaminergic activity. J. Neurochem. 2005, 95, 1597–1607. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. De Deurwaerdère, P.; Navailles, S.; Berg, K.A.; Clarke, W.P.; Spampinato, U. Constitutive Activity of the Serotonin2C Receptor Inhibits In Vivo Dopamine Release in the Rat Striatum and Nucleus Accumbens. J. Neurosci. 2004, 24, 3235–3241. [Google Scholar] [CrossRef] [PubMed]
  49. Esposito, E.; Di Matteo, V.; Di Giovanni, G. Serotonin–dopamine interaction: An overview. Prog. Brain Res. 2008, 172, 3–6. [Google Scholar] [CrossRef] [Green Version]
  50. Larsen, M.B.; Sonders, M.S.; Mortensen, O.V.; Larson, G.A.; Zahniser, N.R.; Amara, S.G. Dopamine Transport by the Serotonin Transporter: A Mechanistically Distinct Mode of Substrate Translocation. J. Neurosci. 2011, 31, 6605–6615. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  51. Dehning, S.; Müller, N.; Matz, J.; Bender, A.; Kerle, I.; Benninghoff, J.; Musil, R.; Spellmann, I.; Bondy, B.; Möller, H.-J.; et al. A genetic variant of HTR2C may play a role in the manifestation of Tourette syndrome. Psychiatr. Genet. 2010, 20, 35–38. [Google Scholar] [CrossRef] [PubMed]
  52. Guo, Y.; Su, L.; Zhang, J.; Lei, J.; Deng, X.; Xu, H.; Yang, Z.; Kuang, S.; Tang, J.; Luo, Z.; et al. Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome. Psychiatr. Genet. 2012, 22, 300–303. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Niesler, B.; Frank, B.; Hebebrand, J.; Rappold, G. Serotonin receptor genes HTR3A and HTR3B are not involved in Gilles de la Tourette syndrome. Psychiatr. Genet. 2005, 15, 303–304. [Google Scholar] [CrossRef]
  54. Moya, P.; Wendland, J.R.; Rubenstein, L.M.; Timpano, K.; Heiman, G.; Tischfield, J.; King, R.A.; Andrews, A.; Ramamoorthy, S.; McMahon, F.; et al. Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette’s disorder. Mov. Disord. 2013, 28, 1263–1270. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Hildonen, M.; Levy, A.M.; Dahl, C.; Bjerregaard, V.A.; Møller, L.B.; Guldberg, P.; Debes, N.M.; Tümer, Z. Elevated Expression of SLC6A4 Encoding the Serotonin Transporter (SERT) in Gilles de la Tourette Syndrome. Genes 2021, 12, 86. [Google Scholar] [CrossRef] [PubMed]
  56. Cavallini, M.C.; Di Bella, D.; Catalano, M.; Bellodi, L. An association study between 5-HTTLPR polymorphism, COMT polymorphism, and Tourette’s syndrome. Psychiatry Res. 2000, 97, 93–100. [Google Scholar] [CrossRef]
  57. Liu, S.; Zhang, X.; Yin, Y.; Wang, M.; Che, F.; Ma, X. An Association Analysis between 5-HTTLPR Polymorphism and Obsessive-Compulsive Disorder, Tourette Syndrome in a Chinese Han Population. CNS Neurosci. Ther. 2011, 17, 793–795. [Google Scholar] [CrossRef] [PubMed]
  58. Hu, X.-Z.; Lipsky, R.; Zhu, G.; Akhtar, L.A.; Taubman, J.; Greenberg, B.D.; Xu, K.; Arnold, P.D.; Richter, M.A.; Kennedy, J.L.; et al. Serotonin Transporter Promoter Gain-of-Function Genotypes Are Linked to Obsessive-Compulsive Disorder. Am. J. Hum. Genet. 2006, 78, 815–826. [Google Scholar] [CrossRef] [Green Version]
  59. Cao, X.; Zhang, Y.; Abdulkadir, M.; Deng, L.; Fernandez, T.V.; Julie, B.G.; Pieter, H.; Robert, J.H.; Justin, A.K.; Kuperman, S.; et al. Whole-exome sequencing identifies genes associated with Tourette’s disorder in multiplex families. Mol. Psychiatry 2021, 1–15. [Google Scholar] [CrossRef]
  60. Mössner, R.; Müller-Vahl, K.; Döring, N.; Stuhrmann, M. Role of the novel tryptophan hydroxylase-2 gene in Tourette syndrome. Mol. Psychiatry 2007, 12, 617–619. [Google Scholar] [CrossRef] [Green Version]
  61. Zheng, P.; Li, E.; Wang, J.; Cui, X.; Wang, L. Involvement of tryptophan hydroxylase 2 gene polymorphisms in susceptibility to tic disorder in Chinese Han population. Behav. Brain Funct. 2013, 9, 6. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Abdulkadir, M.; Londono, D.; Gordon, D.; Fernandez, T.V.; Brown, L.W.; Cheon, K.-A.; Coffey, B.J.; Elzerman, L.; Fremer, C.; Fründt, O.; et al. Investigation of previously implicated genetic variants in chronic tic disorders: A transmission disequilibrium test approach. Eur. Arch. Psychiatry Clin. Neurosci. 2017, 268, 301–316. [Google Scholar] [CrossRef] [Green Version]
  63. Abelson, J.F.; Kwan, K.Y.; O’Roak, B.J.; Baek, D.Y.; Stillman, A.A.; Morgan, T.M.; Mathews, C.A.; Pauls, D.L.; Rašin, M.-R.; Gunel, M.; et al. Sequence Variants in SLITRK1 Are Associated with Tourette’s Syndrome. Science 2005, 310, 317–320. [Google Scholar] [CrossRef] [Green Version]
  64. Deng, H.; Le, W.D.; Xie, W.J.; Jankovic, J. Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome. Acta Neurol. Scand. 2006, 114, 400–402. [Google Scholar] [CrossRef]
  65. Keen-Kim, D.; Mathews, C.A.; Reus, V.I.; Lowe, T.L.; Herrera, L.D.; Budman, C.L.; Gross-Tsur, V.; Pulver, A.E.; Bruun, R.D.; Erenberg, G.; et al. Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. Hum. Mol. Genet. 2006, 15, 3324–3328. [Google Scholar] [CrossRef] [Green Version]
  66. Scharf, J.M.; Moorjani, P.; Fagerness, J.; Platko, J.V.; Illmann, C.; Galloway, B.; Jenike, E.; Stewart, S.E.; Pauls, D.L.; Cath, D.; et al. Lack of Association Between Slitrk1var321 and Tourette Syndrome in a Large Family-Based Sample. Neurology 2008, 70, 1495–1496. [Google Scholar] [CrossRef] [Green Version]
  67. Yasmeen, S.; Melchior, L.; Bertelsen, B.; Skov, L.; Debes, N.; Tümer, Z. Sequence analysis of SLITRK1 for var321 in Danish patients with Tourette syndrome and review of the literature. Psychiatr. Genet. 2013, 23, 130–133. [Google Scholar] [CrossRef]
  68. Zimprich, A.; Hatala, K.; Riederer, F.; Stogmann, E.; Aschauer, H.N.; Stamenkovic, M. Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette’s disorder. Psychiatr. Genet. 2008, 18, 308–309. [Google Scholar] [CrossRef]
  69. O’Roak, B.J.; Morgan, T.M.; Fishman, D.O.; Saus, E.; Alonso, P.; Gratacòs, M.; Estivill, X.; Teltsh, O.; Kohn, Y.; Kidd, K.K.; et al. Additional support for the association of SLITRK1 var321 and Tourette syndrome. Mol. Psychiatry 2010, 15, 447–450. [Google Scholar] [CrossRef] [PubMed]
  70. Alexander, J.; Potamianou, H.; Xing, J.; Deng, L.; Karagiannidis, I.; Tsetsos, F.; Drineas, P.; Tarnok, Z.; Rizzo, R.; Wolanczyk, T.; et al. Targeted Re-Sequencing Approach of Candidate Genes Implicates Rare Potentially Functional Variants in Tourette Syndrome Etiology. Front. Neurosci. 2016, 10, 428. [Google Scholar] [CrossRef] [PubMed]
  71. Chou, I.-C.; Wan, L.; Liu, S.-C.; Tsai, C.-H.; Tsai, F.-J. Association of the Slit and Trk-like 1 Gene in Taiwanese Patients With Tourette Syndrome. Pediatr. Neurol. 2007, 37, 404–406. [Google Scholar] [CrossRef] [PubMed]
  72. Depienne, C.; Ciura, S.; Trouillard, O.; Bouteiller, D.; Leitão, E.; Nava, C.; Keren, B.; Marie, Y.; Guegan, J.; Forlani, S.; et al. Association of Rare Genetic Variants in Opioid Receptors with Tourette Syndrome. Tremor Other Hyperkinet. Mov. (N. Y.) 2019, 9. [Google Scholar] [CrossRef]
  73. Inai, A.; Tochigi, M.; Kuwabara, H.; Nishimura, F.; Kato, K.; Eriguchi, Y.; Shimada, T.; Furukawa, M.; Kawamura, Y.; Sasaki, T.; et al. Analysis of SLITRK1 in Japanese patients with Tourette syndrome using a next-generation sequencer. Psychiatr. Genet. 2015, 25, 256–258. [Google Scholar] [CrossRef] [PubMed]
  74. Karagiannidis, I.; Rizzo, R.; Tarnok, Z.; Wolanczyk, T.; Hebebrand, J.; Nöthen, M.M.; Lehmkuhl, G.; Farkas, L.; Nagy, P.; Barta, C.; et al. Replication of association between a SLITRK1 haplotype and Tourette Syndrome in a large sample of families. Mol. Psychiatry 2012, 17, 665–668. [Google Scholar] [CrossRef] [Green Version]
  75. Miranda, D.M.; Wigg, K.; Kabia, E.M.; Feng, Y.; Sandor, P.; Barr, C.L. Association ofSLITRK1to Gilles de la Tourette Syndrome. Am. J. Med. Genet. Part B Neuropsychiatr. Genet. 2009, 150B, 483–486. [Google Scholar] [CrossRef] [PubMed]
  76. Scharf, J.M.; Yu, D.; Mathews, C.A.; Neale, B.M.; Stewart, S.E.; Fagerness, J.A.; Evans, P.; Gamazon, E.; Edlund, C.K.; Service, S.K.; et al. Genome-wide association study of Tourette’s syndrome. Mol. Psychiatry 2013, 18, 721–728. [Google Scholar] [CrossRef] [Green Version]
  77. Yu, D.; Mathews, C.A.; Scharf, J.M.; Neale, B.M.; Davis, L.K.; Gamazon, E.R.; Derks, E.; Evans, P.; Edlund, C.K.; Crane, J.; et al. Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette’s Syndrome and OCD. Am. J. Psychiatry 2015, 172, 82–93. [Google Scholar] [CrossRef] [PubMed]
  78. Yu, D.; Sul, J.H.; Tsetsos, F.; Nawaz, M.S.; Huang, A.Y.; Zelaya, I.; Illmann, C.; Osiecki, L.; Darrow, S.M.; Hirschtritt, M.E.; et al. Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. Am. J. Psychiatry 2019, 176, 217–227. [Google Scholar] [CrossRef]
  79. Liu, W.; Zhang, X.; Deng, Z.; Li, G.; Zhang, R.; Yang, Z.; Che, F.; Liu, S.; Li, H. The role of SLITRK6 in the pathogenesis of Tourette syndrome: From the conclusion of a family-based study in the Chinese Han population. J. Gene Med. 2020, 22, e3173. [Google Scholar] [CrossRef] [PubMed]
  80. Song, M.; Mathews, C.A.; Stewart, S.E.; Shmelkov, S.V.; Mezey, J.G.; Rodriguez-Flores, J.L.; Rasmussen, S.A.; Britton, J.C.; Oh, Y.-S.; Walkup, J.T.; et al. Rare Synaptogenesis-Impairing Mutations in SLITRK5 Are Associated with Obsessive Compulsive Disorder. PLoS ONE 2017, 12, e0169994. [Google Scholar] [CrossRef] [Green Version]
  81. Zhang, K.; Feng, Y.; Wigg, K.G.; Sandor, P.; Barr, C. Association study of the SLITRK5 gene and Tourette syndrome. Psychiatr. Genet. 2015, 25, 31–34. [Google Scholar] [CrossRef]
  82. Carias, K.V.; Wevrick, R. Clinical and genetic analysis of children with a dual diagnosis of Tourette syndrome and autism spectrum disorder. J. Psychiatr. Res. 2019, 111, 145–153. [Google Scholar] [CrossRef] [PubMed]
  83. Stillman, A.A.; Krsnik, Ž.; Sun, J.; Rašin, M.-R.; State, M.W.; Şestan, N.; Louvi, A. Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome. J. Comp. Neurol. 2009, 513, 21–37. [Google Scholar] [CrossRef] [Green Version]
  84. Proenca, C.C.; Gao, K.P.; Shmelkov, S.V.; Rafii, S.; Lee, F.S. Slitrks as emerging candidate genes involved in neuropsychiatric disorders. Trends Neurosci. 2011, 34, 143–153. [Google Scholar] [CrossRef] [Green Version]
  85. Petek, E.; Windpassinger, C.; Vincent, J.B.; Cheung, J.; Boright, A.P.; Scherer, S.; Kroisel, P.M.; Wagner, K. Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome. Am. J. Hum. Genet. 2001, 68, 848–858. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  86. Boghosian-Sell, L.; Comings, D.E.; Overhauser, J. Tourette syndrome in a pedigree with a 7;18 translocation: Identification of a YAC spanning the translocation breakpoint at 18q22.3. Am. J. Hum. Genet. 1996, 59, 999–1005. [Google Scholar] [PubMed]
  87. Patel, C.J.; Cooper-Charles, L.; McMullan, D.J.; Walker, J.M.; Davison, V.; Morton, J.E. Translocation breakpoint at 7q31 associated with tics: Further evidence for IMMP2L as a candidate gene for Tourette syndrome. Eur. J. Hum. Genet. 2011, 19, 634–639. [Google Scholar] [CrossRef] [PubMed]
  88. Díaz-Anzaldúa, A.; Joober, R.; Rivière, J.-B.; Dion, Y.; Lespérance, P.; Chouinard, S.; Richer, F.; Rouleau, G.A. Association between 7q31 markers and tourette syndrome. Am. J. Med. Genet. Part A 2004, 127A, 17–20. [Google Scholar] [CrossRef]
  89. Petek, E.; Schwarzbraun, T.; Noor, A.; Patel, M.; Nakabayashi, K.; Choufani, S.; Windpassinger, C.; Stamenkovic, M.; Robertson, M.M.; Aschauer, H.N.; et al. Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome. Mol. Genet. Genom. 2006, 277, 71–81. [Google Scholar] [CrossRef] [PubMed]
  90. Bertelsen, B.; Melchior, L.; Jensen, L.R.; Groth, C.; Glenthøj, B.; Rizzo, R.; Debes, N.M.; Skov, L.; Brøndum-Nielsen, K.; Paschou, P.; et al. Intragenic deletions affecting two alternative transcripts of the IMMP2L gene in patients with Tourette syndrome. Eur. J. Hum. Genet. 2014, 22, 1283–1289. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  91. Bjerregaard, V.A.; Schönewolf-Greulich, B.; Rasmussen, L.J.; Desler, C.; Tümer, Z. Mitochondrial Function in Gilles de la Tourette Syndrome Patients With and Without Intragenic IMMP2L Deletions. Front. Neurol. 2020, 11, 163. [Google Scholar] [CrossRef] [Green Version]
  92. Pagliaroli, L.; Vereczkei, A.; Padmanabhuni, S.S.; Tarnok, Z.; Farkas, L.; Nagy, P.; Rizzo, R.; Wolanczyk, T.; Szymanska, U.; Kapisyzi, M.; et al. Association of Genetic Variation in the 3′UTR of LHX6, IMMP2L, and AADAC With Tourette Syndrome. Front. Neurol. 2020, 11, 803. [Google Scholar] [CrossRef]
  93. Haas, H.L.; Sergeeva, O.A.; Selbach, O. Histamine in the Nervous System. Physiol. Rev. 2008, 88, 1183–1241. [Google Scholar] [CrossRef]
  94. Ercan-Sencicek, A.G.; Stillman, A.A.; Ghosh, A.K.; Bilguvar, K.; O’Roak, B.J.; Mason, C.E.; Abbott, T.; Gupta, A.; King, R.A.; Pauls, D.L.; et al. L-Histidine Decarboxylase and Tourette’s Syndrome. N. Engl. J. Med. 2010, 362, 1901–1908. [Google Scholar] [CrossRef] [Green Version]
  95. Karagiannidis, I.; Dehning, S.; Sandor, P.; Tarnok, Z.; Rizzo, R.; Wolanczyk, T.; Madruga-Garrido, M.; Hebebrand, J.; Nöthen, M.; Lehmkuhl, G.; et al. Support of the histaminergic hypothesis in Tourette Syndrome: Association of the histamine decarboxylase gene in a large sample of families. J. Med. Genet. 2013, 50, 760–764. [Google Scholar] [CrossRef] [Green Version]
  96. Baldan, L.C.; Williams, K.A.; Gallezot, J.-D.; Pogorelov, V.; Rapanelli, M.; Crowley, M.; Anderson, G.M.; Loring, E.; Gorczyca, R.; Billingslea, E.; et al. Histidine Decarboxylase Deficiency Causes Tourette Syndrome: Parallel Findings in Humans and Mice. Neuron 2014, 81, 77–90. [Google Scholar] [CrossRef] [Green Version]
  97. Fernandez, T.V.; Sanders, S.; Yurkiewicz, I.R.; Ercan-Sencicek, A.G.; Kim, Y.-S.; Fishman, D.O.; Raubeson, M.J.; Song, Y.; Yasuno, K.; Ho, W.S.; et al. Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism. Biol. Psychiatry 2012, 71, 392–402. [Google Scholar] [CrossRef] [Green Version]
  98. Lei, J.; Deng, X.; Zhang, J.; Su, L.; Xu, H.; Liang, H.; Huang, X.; Song, Z.; Deng, H. Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome. Am. J. Med. Genet. Part B Neuropsychiatr. Genet. 2011, 159B, 72–76. [Google Scholar] [CrossRef]
  99. Dong, H.; Liu, W.; Liu, M.; Xu, L.; Li, Q.; Zhang, R.; Zhang, X.; Liu, S. Investigation of a Possible Role for the Histidine Decarboxylase Gene in Tourette Syndrome in the Chinese Han Population: A Family-Based Study. PLoS ONE 2016, 11, e0160265. [Google Scholar] [CrossRef] [PubMed]
  100. Willsey, A.J.; Fernandez, T.V.; Yu, D.; King, R.A.; Dietrich, A.; Xing, J.; Sanders, S.J.; Mandell, J.D.; Huang, A.Y.; Richer, P.; et al. De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron 2017, 94, 486–499.e9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  101. Wang, S.; Mandell, J.D.; Kumar, Y.; Sun, N.; Morris, M.T.; Arbelaez, J.; Nasello, C.; Dong, S.; Duhn, C.; Zhao, X.; et al. De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Rep. 2018, 24, 3441–3454.e12. [Google Scholar] [CrossRef] [Green Version]
  102. gnomAD. Genome Aggregation Database. Available online: https://gnomad.broadinstitute.org/ (accessed on 19 February 2021).
  103. Zhao, X.; Wang, S.; Hao, J.; Zhu, P.; Zhang, X.; Wu, M. A Whole-Exome Sequencing Study of Tourette Disorder in a Chinese Population. DNA Cell Biol. 2020, 39, 63–68. [Google Scholar] [CrossRef] [PubMed]
  104. Liu, S.; Tian, M.; He, F.; Li, J.; Xie, H.; Liu, W.; Zhang, Y.; Zhang, R.; Yi, M.; Che, F.; et al. Mutations in ASH1L confer susceptibility to Tourette syndrome. Mol. Psychiatry 2020, 25, 476–490. [Google Scholar] [CrossRef]
  105. Tsetsos, F.; Yu, D.; Sul, J.H.; Huang, A.Y.; Illmann, C.; Osiecki, L.; Darrow, S.M.; Hirschtritt, M.E.; Greenberg, E.; Muller-Vahl, K.R.; et al. Synaptic processes and immune-related pathways implicated in Tourette syndrome. Transl. Psychiatry 2021, 11, 1–12. [Google Scholar] [CrossRef]
  106. Malhotra, D.; Sebat, J. CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics. Cell 2012, 148, 1223–1241. [Google Scholar] [CrossRef] [Green Version]
  107. Huang, A.Y.; Yu, D.; Davis, L.K.; Sul, J.H.; Tsetsos, F.; Ramensky, V.; Zelaya, I.; Ramos, E.M.; Osiecki, L.; Chen, J.A.; et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron 2017, 94, 1101–1111.e7. [Google Scholar] [CrossRef] [Green Version]
  108. Mercati, O.; Huguet, G.; Danckaert, A.; André-Leroux, G.; Maruani, A.; Bellinzoni, M.; Rolland, T.; Gouder, L.; Mathieu, A.; Buratti, J.; et al. CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders. Mol. Psychiatry 2017, 22, 625–633. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  109. Kashevarova, A.A.; Nazarenko, L.P.; Schultz-Pedersen, S.; Skryabin, N.A.; Salyukova, O.A.; Chechetkina, N.N.; Tolmacheva, E.N.; Rudko, A.A.; Magini, P.; Graziano, C.; et al. Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability. Mol. Cytogenet. 2014, 7, 97. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  110. Pak, C.; Danko, T.; Zhang, Y.; Aoto, J.; Anderson, G.; Maxeiner, S.; Yi, F.; Wernig, M.; Südhof, T.C. Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1. Cell Stem Cell 2015, 17, 316–328. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  111. Sundaram, S.K.; Huq, A.M.; Wilson, B.J.; Chugani, H.T. Tourette syndrome is associated with recurrent exonic copy number variants. Neurology 2010, 74, 1583–1590. [Google Scholar] [CrossRef] [Green Version]
  112. Nag, A.; Bochukova, E.; Kremeyer, B.; Campbell, D.; Muller, H.; Valencia-Duarte, A.V.; Cardona, J.; Rivas, I.C.; Mesa, S.C.; Cuartas, M.; et al. CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1. PLoS ONE 2013, 8, e59061. [Google Scholar] [CrossRef] [Green Version]
  113. Glessner, J.T.; Wang, K.; Cai, G.; Korvatska, O.; Kim, C.E.; Wood, S.; Zhang, H.; Estes, A.; Brune, C.W.; Bradfield, J.P.; et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 2009, 459, 569–573. [Google Scholar] [CrossRef] [PubMed]
  114. Ching, M.; Shen, Y.; Tan, W.-H.; Jeste, S.; Morrow, E.; Chen, X.; Mukaddes, N.M.; Yoo, S.-Y.; Hanson, E.; Hundley, R.; et al. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. Am. J. Med. Genet. Part B Neuropsychiatr. Genet. 2010, 153B, 937–947. [Google Scholar] [CrossRef]
  115. Kirov, G.; Gumus, D.; Chen, W.; Norton, N.; Georgieva, L.; Sari, M.; O’Donovan, M.C.; Erdogan, F.; Owen, M.J.; Ropers, H.-H.; et al. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Hum. Mol. Genet. 2007, 17, 458–465. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  116. Eriguchi, Y.; Kuwabara, H.; Inai, A.; Kawakubo, Y.; Nishimura, F.; Kakiuchi, C.; Tochigi, M.; Ohashi, J.; Aoki, N.; Kato, K.; et al. Identification of candidate genes involved in the etiology of sporadic Tourette syndrome by exome sequencing. Am. J. Med. Genet. Part B Neuropsychiatr. Genet. 2017, 174, 712–723. [Google Scholar] [CrossRef] [PubMed]
  117. Sun, N.; Nasello, C.; Deng, L.; Wang, N.; Zhang, Y.; Xu, Z.; Song, Z.; Kwan, K.; King, R.A.; Pang, Z.P.; et al. The PNKD gene is associated with Tourette Disorder or Tic disorder in a multiplex family. Mol. Psychiatry 2017, 23, 1487–1495. [Google Scholar] [CrossRef] [Green Version]
  118. Robertson, M.M. The Prevalence and Epidemiology of Gilles de La Tourette Syndrome. Part 1: The Epidemiological and Prevalence Studies. J. Psychosom. Res. 2008, 65, 461–472. [Google Scholar] [CrossRef]
  119. Carlson, C.S.; Matise, T.C.; North, K.E.; Haiman, C.A.; Fesinmeyer, M.; Buyske, S.; Schumacher, F.; Peters, U.; Franceschini, N.; Ritchie, M.D.; et al. Generalization and Dilution of Association Results from European GWAS in Populations of Non-European Ancestry: The PAGE Study. PLoS Biol. 2013, 11, e1001661. [Google Scholar] [CrossRef]
  120. Cavanna, A.E.; Rickards, H. The psychopathological spectrum of Gilles de la Tourette syndrome. Neurosci. Biobehav. Rev. 2013, 37, 1008–1015. [Google Scholar] [CrossRef]
  121. Anttila, V.; Bulik-Sullivan, B.; Finucane, H.K.; Walters, R.K.; Bras, J.; Duncan, L.; Escott-Price, V.; Falcone, G.J.; Gormley, P.; Malik, R.; et al. Analysis of shared heritability in common disorders of the brain. Science 2018, 360, eaap8757. [Google Scholar] [CrossRef] [Green Version]
  122. Lee, P.H.; Anttila, V.; Won, H.; Feng, Y.-C.A.; Rosenthal, J.; Zhu, Z.; Tucker-Drob, E.M.; Nivard, M.; Grotzinger, A.D.; Posthuma, D.; et al. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Cell 2019, 179, 1469–1482.e11. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  123. Mathews, C.; Darrow, S.; Hirschtritt, M.; Yu, N.; Davis, L.; Scharf, J. Symmetry and Disinhibition are Heritable Endophenotypes For Tourette Syndrome. Eur. Neuropsychopharmacol. 2019, 29, S738. [Google Scholar] [CrossRef]
  124. Yang, Z.; Wu, H.; Lee, P.H.; Tsetsos, F.; Davis, L.K.; Yu, D.; Lee, S.H.; Dalsgaard, S.; Haavik, J.; Barta, C.; et al. Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum. Biol. Psychiatry 2021, 90, 317–327. [Google Scholar] [CrossRef]
  125. Eapen, V.; Robertson, M. Are there distinct subtypes in Tourette syndrome? Pure-Tourette syndrome versus Tourette syndrome-plus, and simple versus complex tics. Neuropsychiatr. Dis. Treat. 2015, 11, 1431–1436. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Genes 12 01321 g001 550
Figure 1. Visualization of dopaminergic neurotransmission in the synaptic cleft. Dopamine is released from the vesicles in the presynaptic neuron into the synaptic cleft, where it binds to either presynaptic or postsynaptic dopamine receptors or is transported back to the cytosol of the presynaptic neuron by dopamine transporters.
Figure 1. Visualization of dopaminergic neurotransmission in the synaptic cleft. Dopamine is released from the vesicles in the presynaptic neuron into the synaptic cleft, where it binds to either presynaptic or postsynaptic dopamine receptors or is transported back to the cytosol of the presynaptic neuron by dopamine transporters.
Genes 12 01321 g001
Genes 12 01321 g002 550
Figure 2. SLC6A4 and serotonergic neurotransmission. SLC6A4 gene, exon numbers, and the polymorphisms 5-HTTLPR, rs25531, rs25532, STin2, and Ile425Val in the top part of the figure. The different 5-HTTLPR/rs25531/rs25532 three-locus haplotypes (bottom middle) are likely to affect SLC6A4 mRNA expression (bottom middle). It is hypothesized that S and LG haplotypes result in low SLC6A4 mRNA expression (bottom left), while the LAC haplotype results in SLC6A4 overexpression, leading to increased SERT in the presynaptic neuron followed by increased serotonin clearance from the synaptic cleft (bottom right). 5-HTTLPR: SERT-linked polymorphic region; S: short allele of 5-HTTLPR; LG: long allele of 5-HTTLPR and minor allele of rs25531; LAT and LAC: 5-HTTLPR/rs25531/rs25532 three-locus haplotypes, differing in rs25532 alleles.
Figure 2. SLC6A4 and serotonergic neurotransmission. SLC6A4 gene, exon numbers, and the polymorphisms 5-HTTLPR, rs25531, rs25532, STin2, and Ile425Val in the top part of the figure. The different 5-HTTLPR/rs25531/rs25532 three-locus haplotypes (bottom middle) are likely to affect SLC6A4 mRNA expression (bottom middle). It is hypothesized that S and LG haplotypes result in low SLC6A4 mRNA expression (bottom left), while the LAC haplotype results in SLC6A4 overexpression, leading to increased SERT in the presynaptic neuron followed by increased serotonin clearance from the synaptic cleft (bottom right). 5-HTTLPR: SERT-linked polymorphic region; S: short allele of 5-HTTLPR; LG: long allele of 5-HTTLPR and minor allele of rs25531; LAT and LAC: 5-HTTLPR/rs25531/rs25532 three-locus haplotypes, differing in rs25532 alleles.
Genes 12 01321 g002
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Levy, A.M.; Paschou, P.; Tümer, Z. Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome—Where Are We? Genes 2021, 12, 1321. https://doi.org/10.3390/genes12091321

AMA Style

Levy AM, Paschou P, Tümer Z. Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome—Where Are We? Genes. 2021; 12(9):1321. https://doi.org/10.3390/genes12091321

Chicago/Turabian Style

Levy, Amanda M., Peristera Paschou, and Zeynep Tümer. 2021. "Candidate Genes and Pathways Associated with Gilles de la Tourette Syndrome—Where Are We?" Genes 12, no. 9: 1321. https://doi.org/10.3390/genes12091321

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop