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. Author manuscript; available in PMC: 2012 Aug 1.
Published in final edited form as: Psychiatr Genet. 2011 Aug;21(4):212–213. doi: 10.1097/YPG.0b013e328341a323

Family-based association testing of glutamate transporter genes in autism

Suma Jacob 1, Camille W Brune 1, Judith A Badner 2, Katherine Ernstrom 1, Eric Courchesne 3, Catherine Lord 4,5, Bennett L Leventhal 1,6,7, Edwin H Cook 1, Soo-Jeong Kim 8
PMCID: PMC3210568  NIHMSID: NIHMS332203  PMID: 21085054

SUMMARY

Glutamate transporters are critical for signaling and excitotoxicity because they regulate extracellular glutamate in the synapse. Four glutamate transporter genes, SLC1A1, SLC1A2, SLC1A3, and SLC1A6, are positional and functional candidates for autism. Studies have implicated SLC1A1 in obsessive compulsive disorder (Arnold et al. 2006) and autism spectrum disorder (ASD) (Brune et al. 2008). Up-regulation of SLC1A2 and SLC1A3 has been reported in brains of individuals with autism (Purcell et al. 2001). SLC1A2 is under the highest linkage peak in the Autism Genome Project scan (Szatmari et al. 2007). Both SLC1A3 and SLC1A6 are most abundantly expressed in cerebellum (Bridges and Esslinger 2005) where structural and functional deficits occur in autism. Based on these lines of evidence, we hypothesized that variations in these four glutamate transporter genes confer risk for autism susceptibility.

Previously we tested the association between autism and SLC1A1 in a strictly defined sample (N=85) and a found nominally significant association with a SLC1A1 SNP (rs301979) (Brune et al. 2008). Subsequently, we recruited additional families (N= 68) with either “strict autism” (N=39) or “broad ASD” (N=29). “Strict” autism was defined as a proband with Autism Diagnostic Interview-Revised (ADI-R) and Autism Diagnostic Observation Schedule (ADOS) autism plus a best estimate diagnosis of autism by a clinical psychologist and/or child psychiatrist. The “broad ASD” probands had a best estimate diagnosis of any ASD (autism, Asperger’s disorder or PDD-NOS) plus combinations of ADI-R/ADOS criteria of Autism/ASD, ASD/Autism, or ASD/ASD. Altogether, 14 SNPs were genotyped in 153 trio families using TaqMan® SNP genotyping assay, including four SLC1A1 SNPs (rs301430, rs301979, rs301434, rs301443), three SLC1A2 SNPs (rs3088168, rs911562, rs1923291), three SLC1A3 SNPs (rs13173144, rs2269271, rs2301066), three SLC1A6 SNPs (rs10414225, rs873599, rs2285980), and one C9ORF68 (gene overlapping SLC1A1) SNP (rs384535).

We dropped rs13173144 (SLC1A3, p=0.014) and rs384535 (C9ORF68, p=0.024) due to deviation from Hardy-Weinberg Equilibrium in founders; dropped four trio families because of Mendelian errors in remaining SNPs. Family-Based Association Test (FBAT) was performed on the new sample (N=68), strict combined sample (N=124) and overall combined sample (N=153) for both additive and recessive models. Only p < 0.05 uncorrected for multiple testing are reported. Association between rs301979 (SLC1A1) and autism was observed in the new samples (recessive model, Z=−2.778, p=0.005) as well as in the overall combined samples (additive, Z=−2.137, p=0.033; recessive, Z=−2.424, p=0.015). One SLC1A2 SNP (rs3088168) was nominally significant in the new sample under a recessive model (Z=−2.178, p=0.029), but not in the overall combined sample. Exploratory haplotype analyses revealed nominally significant associations between five SNP pairs including rs301979-rs301434 (p=0.04), rs301979-rs1923291 (p=0.02), rs1923291-rs911562 (p=0.03), rs911562-rs10414225 (p=0.01), rs301443-rs2285980 (p=0.01) under a recessive model.

In summary, this study supported the previous association between SLC1A1 and autism, but failed to provide additional evidence for associations with three other glutamate transporter genes. However, given the small sample size and power, these genes require further investigation with denser markers and exploration of copy number variations in a larger sample set.

Acknowledgments

SJ is supported in part by the NIH K23MH082121. EC is supported in part by an NIMH Autism Center of Excellence award P50 MH081755. SJK is an Advanced Postgraduate Program in Clinical Investigation (APPCI) fellow at the University of Florida and supported in part by a 2007 NARSAD young investigator award, the 2008 PWSA (USA) Research Award, the NIH R03MH083673 and K23MH082883 awards. This work was supported in part by an NIH Autism Center of Excellence award P50 HD055751 (EHC) and Children’s Brain Research Foundation (BLL).

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