Mutation screening of melatonin-related genes in patients with autism spectrum disorders
© Jonsson et al; licensee BioMed Central Ltd. 2010
Received: 2 December 2009
Accepted: 8 April 2010
Published: 8 April 2010
One consistent finding in autism spectrum disorders (ASD) is a decreased level of the pineal gland hormone melatonin and it has recently been demonstrated that this decrease to a large extent is due to low activity of the acetylserotonin O-methyltransferase (ASMT), the last enzyme in the melatonin synthesis pathway. Moreover, mutations in the ASMT gene have been identified, including a splice site mutation, that were associated with low ASMT activity and melatonin secretion, suggesting that the low ASMT activity observed in autism is, at least partly, due to variation within the ASMT gene.
In the present study, we have investigated all the genes involved in the melatonin pathway by mutation screening of AA-NAT (arylalkylamine N-acetyltransferase), ASMT, MTNR1A, MTNR1B (melatonin receptor 1A and 1B) and GPR50 (G protein-coupled receptor 50), encoding both synthesis enzymes and the three main receptors of melatonin, in 109 patients with autism spectrum disorders (ASD). A cohort of 188 subjects from the general population was used as a comparison group and was genotyped for the variants identified in the patient sample.
Several rare variants were identified in patients with ASD, including the previously reported splice site mutation in ASMT (IVS5+2T>C). Of the variants affecting protein sequence, only the V124I in the MTNR1B gene was absent in our comparison group. However, mutations were found in upstream regulatory regions in three of the genes investigated, ASMT, MTNR1A, and MTNR1B.
Our report of another ASD patient carrying the splice site mutation IVS5+2T>C, in ASMT further supports an involvement of this gene in autism. Moreover, our results also suggest that other melatonin related genes might be interesting candidates for further investigation in the search for genes involved in autism spectrum disorders and related neurobehavioral phenotypes. However, further studies of the novel variants identified in this study are warranted to shed light on their potential role in the pathophysiology of these disorders.
Autism spectrum disorders (ASDs) are pervasive developmental disorders that include Autistic disorder, Asperger syndrome, and pervasive developmental disorder-not otherwise specified (PDD-NOS). These conditions are complex, behaviorally-defined syndromes with variable severity and highly diverse symptomatology and etiologies, characterized by impairments in social interaction and communication and patients often display repetitive behaviors, abnormal movements, and sensory dysfunction . Moreover, the severity of mental retardation (MR) is highly variable among cases with ASD .
Twin studies have demonstrated a much higher concordance for ASD in monozygotic (>70%) than in dizygotic twins (0-10%), suggesting genetic factors to play a major role in the etiology [3, 4]. However, although the high heritability of autism is well established and inherited forms of the disorder have been demonstrated, most autism cases seem to occur as sporadic cases . Moreover, several monogenic disorders, such as fragile X syndrome, Rett syndrome and tuberous sclerosis, are well known causes of autism like behavior patterns, and recently, rare mutations and copy number variations have been found to be causative or contributory factors for autism spectrum disorders [6–9]. These observations, together with the early age of onset, indicate that rare, high impact, genetic variants may play an important role in the etiology of ASD .
Sleep disturbances are often reported in patients with ASD , suggesting that neuroendocrine functions involved in the circadian sleep-wake cycle may be altered in these disorders. Moreover, it is well established that mutations altering the biological clock can cause severe sleep problems by modifying sleep phase or duration . Melatonin, a hormone secreted by the pineal gland in the brain, serves as the body's signal for darkness and is involved in various physiologic functions, including sleep induction, circadian rhythm regulation, and immune response . Melatonin as a medication has been shown to improve the sleep of patients with ASD [13, 14], suggesting that the endogenous level of this hormone may not be sufficient to adequately set the clock in these patients. Indeed, one consistent biological finding in autism is low levels of melatonin [15–18], and in a recent study, it could be demonstrated that this decrease of melatonin seems to be due to low activity of the acetylserotonin O-methyltransferase (ASMT), the last enzyme in the melatonin synthesis .
In the same study, several mutations in the ASMT gene were identified, including a splice site mutation, IVS5+2T>C, that were associated with low ASMT activity and melatonin secretion, suggesting that the low ASMT activity in autism is, at least partly, due to variation within the ASMT gene. In a replication study investigating almost 400 ASD patients from Italy, Finland, and the UK, several mutations in the ASMT gene were identified, including the previously reported splice site mutation and a novel stop-mutation (R319X) .
Recently, further support for an involvement of the ASMT gene in ASD was presented in a Multiplex Ligation-dependent Probe Amplification (MLPA) study showing that a duplication in the ASMT gene was significantly more common in ASD, as compared to controls , suggesting that the expression of the ASMT protein may be altered in ASD patients. In addition, other genes implicated in circadian rhythm regulation and central effects of melatonin, i.e., the clock genes, have also been found to be associated with autism [21, 22]. Taken together, previous data suggest that the ASMT gene and the melatonin signaling pathway may play an important role in the etiology of autism spectrum disorders.
The aim of the present study was to search for mutations in genes involved in the melatonin pathway in cases of ASD. To this end, we performed mutation screening of all the genes of the melatonin pathway, i.e., AA-NAT, ASMT, MTNR1A, MTNR1B and GPR50, in 109 subjects with ASD. Hence, the focus of this study was on identifying rare variants within these genes, rather than on common polymorphisms.
Patient recruitment and clinical assessment
In total, 109 patients with ASD from two different populations were included in this study. In the first population, 65 patients (39 males and 26 females) were recruited at a tertiary neuropsychiatric outpatient unit at Mölndals Hospital, Göteborg, Sweden. Thirty-two of these patients met the criteria for autistic disorder and 33 patients were considered to have pervasive developmental disorder not otherwise specified (PDD-NOS); 24 and 28 of the patients were also diagnosed with moderate and severe mental retardation, respectively. The second patient cohort consisted of 44 ASD patients (30 males and 14 females), recruited from several child and psychiatric outpatient clinics in Stockholm county as well as from the neuropediatric department in Astrid Lindgrens hospital and the neuropediatric department at Sachsska childrens hospital, Stockholm, Sweden. In the second cohort, 26 of the patients met the criteria for autistic disorder, 13 of the patients were considered to have pervasive developmental disorder not otherwise specified (PDD-NOS), 5 met the criteria for Asperger's syndrome, and 21 of the 44 patients had a mental retardation ranging from mild to moderate. All patients from both populations were diagnosed based on clinical evaluation by experienced clinicians using DSM-IV criteria, and the Autism Diagnostic Interview-Revised (ADI-R), and patients diagnosed with medical conditions related to autism and mental retardation, including major chromosomal abnormalities, fragile X syndrome, and tuberous sclerosis, were excluded from the study. The vast majority of included patients were of Swedish origin and the control sample used in this study consisted of 188 (94 male and 94 female) Swedish subjects recruited from the general population in Gothenburg, Sweden . The control group in this study served only to investigate if mutations identified in patients were present also in the general population, hence, the control group was not matched to the patient group with respect to age and gender.
The study was conducted in accordance with the declaration of Helsinki and approved by the local Research Ethics Boards. Written informed consent was obtained from parents or legal guardians, and, if possible (i.e. if the patient did not have severe MR) from patients, as well as from controls.
Mutation screening was performed by direct sequencing of the exons, the exon-intron boundaries, the 5' UTR and the proximal promoter of AA-NAT, ASMT, MTNR1A, MTNR1B, and GPR50. Genotyping of healthy controls for rare variants identified by mutation screening was performed using direct sequencing, pyrosequencing technology (Pyrosequencing AB, Uppsala, Sweden) or RFLP, restriction fragment length polymorphism, (the MTNR1B c.-39G, C>A, A) using Cfr3I (Sau96I). Primer sequences and PCR-conditions are summarized in additional file 1 and 2: supplemental table S1 and S2. The ClustalW alignment program http://www.ebi.ac.uk/clustalw/ was used to study conservation of the mutation sites among different species. The possible functional impact of amino acid changes was predicted by the PolyPhen (Polymorphism Phenotyping) program http://coot.embl.de/PolyPhen/) which makes predictions based on sequence annotation and alignment as well as structural information and SIFT (Sorting Intolerant From Tolerant) http://blocks.fhcrc.org/sift/SIFT.html), which use sequence homology for prediction. Identification of putative binding sites for transcription factors was performed using TFsitescan http://www.ifti.org/cgi-bin/ifti/Tfsitescan.pl and the TRANSFAC database .
The goal of this study was to search for mutations in genes involved in the melatonin pathway in cases of ASD. To this end, we performed mutation screening of all the genes of the melatonin pathway (AA-NAT, ASMT, MTNR1A, MTNR1B and GPR50) by direct sequencing. Identified variants were analyzed using different bioinformatic tools (above), however, we did not have the possibility to perform functional analyses in our laboratory. Moreover, to assess if identified variants were present also in the general population, we genotyped a reference group of subjects recruited from the general population in the same geographical area as the patients. However, since our main goal was to study rare variants, rather than common polymorphisms, and since our samples are too small for meaningful statistical comparisons, we did not perform any case-control association studies using the genotype data of common polymorphisms identified in the mutation screening.
Sequence variants identified in ASMT, MTNR1A, MTNR1B in patients with ASD.
Amino acid change
(n = 109)
(n = 188)
The splice site mutation, IVS5+2T>C, and the 5'UTR variant in ASMT were identified in patients with autistic disorder and PDD-NOS, respectively. The promoter variant in MTNR1A was identified in a patient with PDD-NOS and the two MTNR1B mutations were identified in one patient with PDD-NOS (c.-39GC>AA) and one patient with autistic disorder (V124I). Interestingly, of the patients carrying variants that were not present in the unaffected group, only those with the splice site mutation in ASMT, and the non-synonymous V124I in MTNR1B met the diagnostic criteria for autistic disorder [additional file 3: Supplemental Table S3]. Moreover, four of the five patients carrying variants not present in controls have had seizures and/or diagnosed epilepsy and four of the five patients also displayed moderate to severe MR. For more detailed clinical information on the patients carrying the identified mutations, see additional file 3: Supplemental Table S3.
Common, previously reported, SNPs were identified at frequencies comparable to those found in the databases (data not shown). The two non-synonymous SNPs rs61747139 (K243R) in MTNR1B, and rs62620754 (S493N) in GPR50 were also genotyped in our reference group and the rare alleles of these polymorphisms were found to have similar frequencies in our non-patient cohort. Moreover, none of these variants were predicted to have any major effect on the encoded protein, according to computer based prediction.
In the present study, several rare variants were found in melatonin related genes in patients with ASD. Most importantly, the previously reported [15, 19] splice site mutation, IVS5+2T>C, in ASMT was once again found in a patient with autistic disorder. To our knowledge, this mutation has now been found in six patients with ASD, two parents and only one control. Moreover, this variant has been shown to have a dramatic effect on melatonin synthesis, both in cultured cell lines and in vivo . The other two variants identified in ASMT in our study were situated in upstream regulatory regions of the gene, and might therefore affect the expression of the ASMT-protein. This finding is in line with a recent study by Cai and coworkers , who found that a duplication in the ASMT gene was significantly more common in ASD, as compared to controls , thus suggesting that the expression of the ASMT protein may be altered in ASD patients. Moreover, three different transcripts of the ASMT gene have been identified
The identification of mutations in the genes encoding melatonin receptors suggests that also variants in other melatonin related genes might be implicated in the abnormal melatonin metabolism observed in ASD. Although the functional effects of the novel mutations were not assessed by laboratory assays in our study, bioinformatics analyses suggest that some of the variants identified indeed may influence the encoded protein. First, one of the novel variants identified, the V124I in the in the third transmembrane domain of the MTNR1B protein, is conserved through all vertebrates and among the three melatonin receptors, including GPR50 (figure 1). The most interesting of the identified variants were identified in patients for which we did not have access to DNA from parents and/or other relatives, hence, we do not know how these alleles are transmitted or whether they have appeared de novo in the patients. Further studies that screen ASD-patients for genetic variants in melatonin-related genes thus are highly warranted.
In summary, our identification of the functional splice site mutation in ASMT in yet another patient with autistic disorder support the notion that melatonin may be involved in the psychopathology of autism. Since melatonin regulates the rhythmic expression of clock genes in the hypothalamus , our results also indirectly support previous studies implicating clock genes in autism . Although only one of the six mutations identified in our screen was present also in controls, our study sample is too small to conclude that mutations in melatonin related genes are enriched in patients with ASD. However, it cannot be excluded that some of the mutations found in melatonin related genes may infer an increased risk for circadian rhythm dysfunction in a subgroup of ASD patients. Moreover, the presence of seizures and moderate to severe MR in four of the five patients with the observed variants may suggest a broader role for melatonin related genes in neurodevelopmental disorders.
Our findings suggest that melatonin related genes in general and ASMT in particular may be important candidates for further investigation in the search for genes involved in autism spectrum disorders and related neurobehavioral phenotypes. However, further studies of the novel variants identified in this study are warranted to shed light on their potential role in the pathophysiology of these disorders.
We are grateful to the patients and their relatives who have made this study possible. Technicians Gunilla Bourghardt and Inger Oscarsson and nurse Carina Algede are warmly thanked for their skilful assistance, and professor Göran Holm for collecting and characterizing the control samples. This work has been supported by the Swedish Research Council (2004-6588), the Wilhelm and Martina Lundgren Foundation, the Magnus Bergvall Foundation, the Åhlens Foundation, the Frimurarna Barnhuset Foundation and the Linnea and Josef Carlsson Foundation. We also would like to thank the SWEGENE Göteborg Genomics Core Facility platform, funded by a grant from the Knut and Alice Wallenberg Foundation.
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