Skip to main content
Top
Published in: Molecular Autism 1/2011

Open Access 01-12-2011 | Research

A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders

Authors: Soo-Jeong Kim, Raquel M Silva, Cindi G Flores, Suma Jacob, Stephen Guter, Gregory Valcante, Annette M Zaytoun, Edwin H Cook, Judith A Badner

Published in: Molecular Autism | Issue 1/2011

Login to get access

Abstract

Background

SLC25A12 was previously identified by a linkage-directed association analysis in autism. In this study, we investigated the relationship between three SLC25A12 single nucleotide polymorphisms (SNPs) (rs2056202, rs908670 and rs2292813) and restricted repetitive behavior (RRB) traits in autism spectrum disorders (ASDs), based on a positive correlation between the G allele of rs2056202 and an RRB subdomain score on the Autism Diagnostic Interview-Revised (ADI-R).

Methods

We used the Repetitive Behavior Scale-Revised (RBS-R) as a quantitative RRB measure, and conducted linear regression analyses for individual SNPs and a previously identified haplotype (rs2056202-rs2292813). We examined associations in our University of Illinois at Chicago-University of Florida (UIC-UF) sample (179 unrelated individuals with an ASD), and then attempted to replicate our findings in the Simons Simplex Collection (SSC) sample (720 ASD families).

Results

In the UIC-UF sample, three RBS-R scores (ritualistic, sameness, sum) had positive associations with the A allele of rs2292813 (p = 0.006-0.012) and with the rs2056202-rs2292813 haplotype (omnibus test, p = 0.025-0.040). The SSC sample had positive associations between the A allele of rs2056202 and four RBS-R scores (stereotyped, sameness, restricted, sum) (p = 0.006-0.010), between the A allele of rs908670 and three RBS-R scores (stereotyped, self-injurious, sum) (p = 0.003-0.015), and between the rs2056202-rs2292813 haplotype and six RBS-R scores (stereotyped, self-injurious, compulsive, sameness, restricted, sum)(omnibus test, p = 0.002-0.028). Taken together, the A alleles of rs2056202 and rs2292813 were consistently and positively associated with RRB traits in both the UIC-UF and SSC samples, but the most significant SNP with phenotype association varied in each dataset.

Conclusions

This study confirmed an association between SLC25A12 and RRB traits in ASDs, but the direction of the association was different from that in the initial study. This could be due to the examined SLC25A12 SNPs being in linkage disequilibrium with another risk allele, and/or genetic/phenotypic heterogeneity of the ASD samples across studies.
Literature
1.
go back to reference APA: Diagnostic and Statistical Manual of Mental Disorders, Text Revision (DSM-IV-TR). 2000, Washington, DC: American Psychiatric Publishing, 4 APA: Diagnostic and Statistical Manual of Mental Disorders, Text Revision (DSM-IV-TR). 2000, Washington, DC: American Psychiatric Publishing, 4
2.
go back to reference Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E, Rutter M: Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med. 1995, 25: 63-77. 10.1017/S0033291700028099.CrossRefPubMed Bailey A, Le Couteur A, Gottesman I, Bolton P, Simonoff E, Yuzda E, Rutter M: Autism as a strongly genetic disorder: evidence from a British twin study. Psychol Med. 1995, 25: 63-77. 10.1017/S0033291700028099.CrossRefPubMed
3.
go back to reference Folstein SE, Rosen-Sheidley B: Genetics of autism: complex aetiology for a heterogeneous disorder. Nat Rev Genet. 2001, 2: 943-955. 10.1038/35103559.CrossRefPubMed Folstein SE, Rosen-Sheidley B: Genetics of autism: complex aetiology for a heterogeneous disorder. Nat Rev Genet. 2001, 2: 943-955. 10.1038/35103559.CrossRefPubMed
4.
go back to reference Jorde LB, Hasstedt SJ, Ritvo ER, Mason-Brothers A, Freeman BJ, Pingree C, McMahon WM, Petersen B, Jenson WR, Mo A: Complex segregation analysis of autism. Am J Hum Genet. 1991, 49: 932-938.PubMedCentralPubMed Jorde LB, Hasstedt SJ, Ritvo ER, Mason-Brothers A, Freeman BJ, Pingree C, McMahon WM, Petersen B, Jenson WR, Mo A: Complex segregation analysis of autism. Am J Hum Genet. 1991, 49: 932-938.PubMedCentralPubMed
5.
go back to reference Pickles A, Bolton P, Macdonald H, Bailey A, Le Couteur A, Sim CH, Rutter M: Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism. Am J Hum Genet. 1995, 57: 717-726.PubMedCentralPubMed Pickles A, Bolton P, Macdonald H, Bailey A, Le Couteur A, Sim CH, Rutter M: Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism. Am J Hum Genet. 1995, 57: 717-726.PubMedCentralPubMed
6.
go back to reference Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T: A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet. 1999, 65: 493-507. 10.1086/302497.PubMedCentralCrossRefPubMed Risch N, Spiker D, Lotspeich L, Nouri N, Hinds D, Hallmayer J, Kalaydjieva L, McCague P, Dimiceli S, Pitts T: A genomic screen of autism: evidence for a multilocus etiology. Am J Hum Genet. 1999, 65: 493-507. 10.1086/302497.PubMedCentralCrossRefPubMed
7.
go back to reference Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg IC, Jakobsson G, Bohman M: A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry. 1989, 30: 405-416. 10.1111/j.1469-7610.1989.tb00254.x.CrossRefPubMed Steffenburg S, Gillberg C, Hellgren L, Andersson L, Gillberg IC, Jakobsson G, Bohman M: A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J Child Psychol Psychiatry. 1989, 30: 405-416. 10.1111/j.1469-7610.1989.tb00254.x.CrossRefPubMed
8.
go back to reference Veenstra-VanderWeele J, Cook EH: Molecular genetics of autism spectrum disorder. Mol Psychiatry. 2004, 9: 819-832. 10.1038/sj.mp.4001505.CrossRefPubMed Veenstra-VanderWeele J, Cook EH: Molecular genetics of autism spectrum disorder. Mol Psychiatry. 2004, 9: 819-832. 10.1038/sj.mp.4001505.CrossRefPubMed
9.
go back to reference Geschwind D: Autism: searching for coherence. Biol Psychiatry. 2007, 62: 949-950. 10.1016/j.biopsych.2007.09.001.CrossRefPubMed Geschwind D: Autism: searching for coherence. Biol Psychiatry. 2007, 62: 949-950. 10.1016/j.biopsych.2007.09.001.CrossRefPubMed
10.
go back to reference Veenstra-Vanderweele J, Christian SL, Cook EH: Autism as a paradigmatic complex genetic disorder. Annu Rev Genomics Hum Genet. 2004, 5: 379-405. 10.1146/annurev.genom.5.061903.180050.CrossRefPubMed Veenstra-Vanderweele J, Christian SL, Cook EH: Autism as a paradigmatic complex genetic disorder. Annu Rev Genomics Hum Genet. 2004, 5: 379-405. 10.1146/annurev.genom.5.061903.180050.CrossRefPubMed
11.
go back to reference Ramoz N, Cai G, Reichert JG, Silverman JM, Buxbaum JD: An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene. Am J Med Genet B Neuropsychiatr Genet. 2008, 1152-1158. 147B Ramoz N, Cai G, Reichert JG, Silverman JM, Buxbaum JD: An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene. Am J Med Genet B Neuropsychiatr Genet. 2008, 1152-1158. 147B
12.
go back to reference Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL, Buxbaum JD: Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism. Am J Psychiatry. 2004, 161: 662-669. 10.1176/appi.ajp.161.4.662.CrossRefPubMed Ramoz N, Reichert JG, Smith CJ, Silverman JM, Bespalova IN, Davis KL, Buxbaum JD: Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism. Am J Psychiatry. 2004, 161: 662-669. 10.1176/appi.ajp.161.4.662.CrossRefPubMed
13.
go back to reference Segurado R, Conroy J, Meally E, Fitzgerald M, Gill M, Gallagher L: Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31. Am J Psychiatry. 2005, 162: 2182-2184. 10.1176/appi.ajp.162.11.2182.CrossRefPubMed Segurado R, Conroy J, Meally E, Fitzgerald M, Gill M, Gallagher L: Confirmation of association between autism and the mitochondrial aspartate/glutamate carrier SLC25A12 gene on chromosome 2q31. Am J Psychiatry. 2005, 162: 2182-2184. 10.1176/appi.ajp.162.11.2182.CrossRefPubMed
14.
go back to reference Turunen JA, Rehnstrom K, Kilpinen H, Kuokkanen M, Kempas E, Ylisaukko-Oja T: Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism. Autism Res. 2008, 1: 189-192. 10.1002/aur.25.CrossRefPubMed Turunen JA, Rehnstrom K, Kilpinen H, Kuokkanen M, Kempas E, Ylisaukko-Oja T: Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism. Autism Res. 2008, 1: 189-192. 10.1002/aur.25.CrossRefPubMed
15.
go back to reference Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT: A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet. 2010, 19: 4072-4082. 10.1093/hmg/ddq307.PubMedCentralCrossRefPubMed Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT: A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet. 2010, 19: 4072-4082. 10.1093/hmg/ddq307.PubMedCentralCrossRefPubMed
16.
go back to reference Correia C, Coutinho AM, Diogo L, Grazina M, Marques C, Miguel T, Ataide A, Almeida J, Borges L, Oliveira C: Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene. J Autism Dev Disord. 2006, 36: 1137-1140. 10.1007/s10803-006-0138-6.CrossRefPubMed Correia C, Coutinho AM, Diogo L, Grazina M, Marques C, Miguel T, Ataide A, Almeida J, Borges L, Oliveira C: Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene. J Autism Dev Disord. 2006, 36: 1137-1140. 10.1007/s10803-006-0138-6.CrossRefPubMed
17.
go back to reference Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH: Lack of association between autism and SLC25A12. Am J Psychiatry. 2006, 163: 929-931. 10.1176/appi.ajp.163.5.929.PubMed Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH: Lack of association between autism and SLC25A12. Am J Psychiatry. 2006, 163: 929-931. 10.1176/appi.ajp.163.5.929.PubMed
18.
go back to reference Blasi F, Bacchelli E, Carone S, Toma C, Monaco AP, Bailey AJ, Maestrini E: SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. Eur J Hum Genet. 2006, 14: 123-126.PubMed Blasi F, Bacchelli E, Carone S, Toma C, Monaco AP, Bailey AJ, Maestrini E: SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. Eur J Hum Genet. 2006, 14: 123-126.PubMed
19.
go back to reference Chien WH, Wu YY, Gau SS, Huang YS, Soong WT, Chiu YN, Chen CH: Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan. Prog Neuropsychopharmacol Biol Psychiatry. 2010, 34: 189-192. 10.1016/j.pnpbp.2009.11.004.CrossRefPubMed Chien WH, Wu YY, Gau SS, Huang YS, Soong WT, Chiu YN, Chen CH: Association study of the SLC25A12 gene and autism in Han Chinese in Taiwan. Prog Neuropsychopharmacol Biol Psychiatry. 2010, 34: 189-192. 10.1016/j.pnpbp.2009.11.004.CrossRefPubMed
20.
go back to reference Silverman JM, Buxbaum JD, Ramoz N, Schmeidler J, Reichenberg A, Hollander E, Angelo G, Smith CJ, Kryzak LA: Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism. Am J Med Genet B Neuropsychiatr Genet. 2008, 147: 408-410.CrossRefPubMed Silverman JM, Buxbaum JD, Ramoz N, Schmeidler J, Reichenberg A, Hollander E, Angelo G, Smith CJ, Kryzak LA: Autism-related routines and rituals associated with a mitochondrial aspartate/glutamate carrier SLC25A12 polymorphism. Am J Med Genet B Neuropsychiatr Genet. 2008, 147: 408-410.CrossRefPubMed
21.
go back to reference Lord C, Rutter M, Le Couteur A: Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord. 1994, 24: 659-685. 10.1007/BF02172145.CrossRefPubMed Lord C, Rutter M, Le Couteur A: Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord. 1994, 24: 659-685. 10.1007/BF02172145.CrossRefPubMed
22.
go back to reference Lord C, Risi S, Lambrecht L, Cook EH, Leventhal BL, DiLavore PC, Pickles A, Rutter M: The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord. 2000, 30: 205-223. 10.1023/A:1005592401947.CrossRefPubMed Lord C, Risi S, Lambrecht L, Cook EH, Leventhal BL, DiLavore PC, Pickles A, Rutter M: The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord. 2000, 30: 205-223. 10.1023/A:1005592401947.CrossRefPubMed
23.
go back to reference Berument SK, Rutter M, Lord C, Pickles A, Bailey A: Autism screening questionnaire: diagnostic validity. Br J Psychiatry. 1999, 175: 444-451. 10.1192/bjp.175.5.444.CrossRefPubMed Berument SK, Rutter M, Lord C, Pickles A, Bailey A: Autism screening questionnaire: diagnostic validity. Br J Psychiatry. 1999, 175: 444-451. 10.1192/bjp.175.5.444.CrossRefPubMed
24.
go back to reference Rutter M, Bailey A, Lord C: Social Communication Questionnaire (SCQ). 2001, Los Angeles, CA: Western Psychological Services Rutter M, Bailey A, Lord C: Social Communication Questionnaire (SCQ). 2001, Los Angeles, CA: Western Psychological Services
25.
go back to reference Fischbach GD, Lord C: The Simons Simplex Collection: a resource for identification of autism genetic risk factors. Neuron. 2010, 68: 192-195. 10.1016/j.neuron.2010.10.006.CrossRefPubMed Fischbach GD, Lord C: The Simons Simplex Collection: a resource for identification of autism genetic risk factors. Neuron. 2010, 68: 192-195. 10.1016/j.neuron.2010.10.006.CrossRefPubMed
26.
go back to reference Bodfish JW, Symons FJ, Lewis MH: The Repetitive Behavior Scales (RBS). Western Carolina Center Research Reports. 1999 Bodfish JW, Symons FJ, Lewis MH: The Repetitive Behavior Scales (RBS). Western Carolina Center Research Reports. 1999
27.
go back to reference Bodfish JW, Symons FJ, Parker DE, Lewis MH: Varieties of repetitive behavior in autism: comparisons to mental retardation. J Autism Dev Disord. 2000, 30: 237-243. 10.1023/A:1005596502855.CrossRefPubMed Bodfish JW, Symons FJ, Parker DE, Lewis MH: Varieties of repetitive behavior in autism: comparisons to mental retardation. J Autism Dev Disord. 2000, 30: 237-243. 10.1023/A:1005596502855.CrossRefPubMed
28.
go back to reference Lam KS, Aman MG: The Repetitive Behavior Scale-Revised: independent validation in individuals with autism spectrum disorders. J Autism Dev Disord. 2007, 37: 855-866. 10.1007/s10803-006-0213-z.CrossRefPubMed Lam KS, Aman MG: The Repetitive Behavior Scale-Revised: independent validation in individuals with autism spectrum disorders. J Autism Dev Disord. 2007, 37: 855-866. 10.1007/s10803-006-0213-z.CrossRefPubMed
29.
go back to reference Sparrow SS, Cicchetti DV: Diagnostic uses of the Vineland Adaptive Behavior Scales. J Pediatr Psychol. 1985, 10: 215-225. 10.1093/jpepsy/10.2.215.CrossRefPubMed Sparrow SS, Cicchetti DV: Diagnostic uses of the Vineland Adaptive Behavior Scales. J Pediatr Psychol. 1985, 10: 215-225. 10.1093/jpepsy/10.2.215.CrossRefPubMed
30.
go back to reference Aman MG, Singh NN, Stewart AW, Field CJ: The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects. Am J Ment Defic. 1985, 89: 485-491.PubMed Aman MG, Singh NN, Stewart AW, Field CJ: The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects. Am J Ment Defic. 1985, 89: 485-491.PubMed
32.
go back to reference Lepagnol-Bestel AM, Maussion G, Boda B, Cardona A, Iwayama Y, Delezoide AL, Moalic JM, Muller D, Dean B, Yoshikawa T: SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects. Mol Psychiatry. 2008, 13: 385-397. 10.1038/sj.mp.4002120.CrossRefPubMed Lepagnol-Bestel AM, Maussion G, Boda B, Cardona A, Iwayama Y, Delezoide AL, Moalic JM, Muller D, Dean B, Yoshikawa T: SLC25A12 expression is associated with neurite outgrowth and is upregulated in the prefrontal cortex of autistic subjects. Mol Psychiatry. 2008, 13: 385-397. 10.1038/sj.mp.4002120.CrossRefPubMed
33.
go back to reference Sakurai T, Ramoz N, Barreto M, Gazdoiu M, Takahashi N, Gertner M, Dorr N, Gama Sosa MA, De Gasperi R, Perez G: Slc25a12 disruption alters myelination and neurofilaments: a model for a hypomyelination syndrome and childhood neurodevelopmental disorders. Biol Psychiatry. 2010, 67: 887-894. 10.1016/j.biopsych.2009.08.042.PubMedCentralCrossRefPubMed Sakurai T, Ramoz N, Barreto M, Gazdoiu M, Takahashi N, Gertner M, Dorr N, Gama Sosa MA, De Gasperi R, Perez G: Slc25a12 disruption alters myelination and neurofilaments: a model for a hypomyelination syndrome and childhood neurodevelopmental disorders. Biol Psychiatry. 2010, 67: 887-894. 10.1016/j.biopsych.2009.08.042.PubMedCentralCrossRefPubMed
34.
go back to reference Wibom R, Lasorsa FM, Tohonen V, Barbaro M, Sterky FH, Kucinski T, Naess K, Jonsson M, Pierri CL, Palmieri F, Wedell A: AGC1 deficiency associated with global cerebral hypomyelination. N Engl J Med. 2009, 361: 489-495. 10.1056/NEJMoa0900591.CrossRefPubMed Wibom R, Lasorsa FM, Tohonen V, Barbaro M, Sterky FH, Kucinski T, Naess K, Jonsson M, Pierri CL, Palmieri F, Wedell A: AGC1 deficiency associated with global cerebral hypomyelination. N Engl J Med. 2009, 361: 489-495. 10.1056/NEJMoa0900591.CrossRefPubMed
35.
go back to reference Jalil MA, Begum L, Contreras L, Pardo B, Iijima M, Li MX, Ramos M, Marmol P, Horiuchi M, Shimotsu K: Reduced N-acetylaspartate levels in mice lacking aralar, a brain- and muscle-type mitochondrial aspartate-glutamate carrier. J Biol Chem. 2005, 280: 31333-31339. 10.1074/jbc.M505286200.CrossRefPubMed Jalil MA, Begum L, Contreras L, Pardo B, Iijima M, Li MX, Ramos M, Marmol P, Horiuchi M, Shimotsu K: Reduced N-acetylaspartate levels in mice lacking aralar, a brain- and muscle-type mitochondrial aspartate-glutamate carrier. J Biol Chem. 2005, 280: 31333-31339. 10.1074/jbc.M505286200.CrossRefPubMed
36.
37.
go back to reference Greene CS, Penrod NM, Williams SM, Moore JH: Failure to replicate a genetic association may provide important clues about genetic architecture. PLoS One. 2009, 4: e5639-10.1371/journal.pone.0005639.PubMedCentralCrossRefPubMed Greene CS, Penrod NM, Williams SM, Moore JH: Failure to replicate a genetic association may provide important clues about genetic architecture. PLoS One. 2009, 4: e5639-10.1371/journal.pone.0005639.PubMedCentralCrossRefPubMed
38.
39.
go back to reference Turner M: Annotation: Repetitive behaviour in autism: a review of psychological research. J Child Psychol Psychiatry. 1999, 40: 839-849. 10.1111/1469-7610.00502.CrossRefPubMed Turner M: Annotation: Repetitive behaviour in autism: a review of psychological research. J Child Psychol Psychiatry. 1999, 40: 839-849. 10.1111/1469-7610.00502.CrossRefPubMed
40.
go back to reference Mooney EL, Gray KM, Tonge BJ: Early features of autism: Repetitive behaviours in young children. Eur Child Adolesc Psychiatry. 2006, 15: 12-18. 10.1007/s00787-006-0499-6.CrossRefPubMed Mooney EL, Gray KM, Tonge BJ: Early features of autism: Repetitive behaviours in young children. Eur Child Adolesc Psychiatry. 2006, 15: 12-18. 10.1007/s00787-006-0499-6.CrossRefPubMed
Metadata
Title
A quantitative association study of SLC25A12 and restricted repetitive behavior traits in autism spectrum disorders
Authors
Soo-Jeong Kim
Raquel M Silva
Cindi G Flores
Suma Jacob
Stephen Guter
Gregory Valcante
Annette M Zaytoun
Edwin H Cook
Judith A Badner
Publication date
01-12-2011
Publisher
BioMed Central
Published in
Molecular Autism / Issue 1/2011
Electronic ISSN: 2040-2392
DOI
https://doi.org/10.1186/2040-2392-2-8

Other articles of this Issue 1/2011

Molecular Autism 1/2011 Go to the issue