Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents

Abstract

Despite the recognition that cortical thickness is heritable and correlates with intellectual ability in children and adolescents, the genes contributing to individual differences in these traits remain unknown. We conducted a large-scale association study in 1583 adolescents to identify genes affecting cortical thickness. Single-nucleotide polymorphisms (SNPs; n=54 837) within genes whose expression changed between stages of growth and differentiation of a human neural stem cell line were selected for association analyses with average cortical thickness. We identified a variant, rs7171755, associating with thinner cortex in the left hemisphere (P=1.12 × 107), particularly in the frontal and temporal lobes. Localized effects of this SNP on cortical thickness differently affected verbal and nonverbal intellectual abilities. The rs7171755 polymorphism acted in cis to affect expression in the human brain of the synaptic cell adhesion glycoprotein-encoding gene NPTN. We also found that cortical thickness and NPTN expression were on average higher in the right hemisphere, suggesting that asymmetric NPTN expression may render the left hemisphere more sensitive to the effects of NPTN mutations, accounting for the lateralized effect of rs7171755 found in our study. Altogether, our findings support a potential role for regional synaptic dysfunctions in forms of intellectual deficits.

Introduction

Genetic factors have a significant contribution in defining brain structure and cognition. In particular, cortical thickness is heritable, with the strongest genetic influences (heritability range, 0.50–0.90) showing region- and age-specific variations1 that seem to follow patterns of brain maturation from childhood to early adulthood. Cortical thickness also closely correlates with intellectual ability in normally developing children and adolescents.2,3 Yet, little is known about the genetic factors accounting for interindividual differences in both of these traits.

Advances in neuroimaging studies have enabled the demonstration of spatiotemporal alterations in brain structure and function that occur over a lifetime. This plasticity is particularly important during adolescence, when both hormonal and social environments change dramatically. Whereas white matter increases linearly during this period,4 regional changes in cortical gray matter are nonlinear.5 Localized, region-specific brain gray matter maturation progresses in patterns that appear to follow cognitive and functional maturation.6 Roughly, areas involved in spatial orientation (parietal lobes) and more advanced functions (frontal lobe) mature around adolescence, after areas of the brain associated with more basic functions (occipital lobe) and before the temporal cortex. Measures of cortical thickness revealed asymmetrical changes in the brain of normally developing children and adolescents. Of notable significance, changes in cortical thickness in the left hemisphere have been found to correlate with performance of children on a test of general verbal intellectual functioning.2 This plasticity appears to be important in shaping behaviors and cognitive processes that contribute to normal development into adulthood.

Twin studies have demonstrated that brain structure is under significant genetic influence,7 with cortical thickness showing high heritability in children1,8 and adults.9,10 Differences in heritability are nonetheless notable. First, comparison of estimates of genetic effects in the left and right hemispheres indicate that these values are higher for the left hemisphere, suggesting that the language-dominant left cerebral cortex may be under stronger genetic control than the right cortex.8 Second, age-related differences in the heritability of cortical thickness in children and adolescents have been reported: although regions of primary sensory and motor cortex, which develop earlier, show relatively greater genetic effects in childhood than in adolescence, regions within the frontal cortex, parietal and temporal lobes, associated with complex cognitive processes, such as language executive function and social cognition, show relatively greater genetic effects in adolescence.1 Thus, as suggested by these studies, it would seem necessary to consider both region-specific effects and developmental stage (that is, age) of individuals while investigating links between genes, cortical thickness and behavior.

At the cellular level, changes in cortical thickness during adolescence are consistent with known cellular maturational alterations, such as the changes in synaptic density11 and intracortical myelination12 occurring during this developmental stage. Thus, the age-related changes in heritability noted above may be linked to the timing of the expression of given set of genes involved in specific stages of neural development. It has been postulated that cortical thickness is determined by the number of neurons within radial units of the cortex, and that a diminished ability of the neurogenic progenitors contained in these units to proliferate or to generate neurons will result in a thinner cortex.13,14 According to this, genes involved in neural progenitor cell division and/or differentiation are expected to influence cortical thickness. Yet, although cortical thickness is heritable and closely correlates with cognitive ability in children and adolescents,3 the genes influencing these traits remain to be identified.

Therefore, aiming at identifying genes influencing cortical thickness, we decided to focus our analysis on genes relevant for neural progenitor cell proliferation and differentiation. For this purpose, we selected genes whose expression changed between various stages of growth and differentiation of a human neural progenitor cell line. We then conducted association analyses of genetic variations at the selected gene loci and cortical thickness at each hemisphere. Using this approach, we uncovered a gene linking cortical thickness to cognition.

Materials and methods

Participants

Data analyzed in this study were obtained from 1583 14-year-old adolescents, participants of the IMAGEN project, for which magnetic resonance images passing quality control procedures were available. Recruitment procedures have been described previously,15 and written informed consent was obtained from all participants and their legal guardians. Individuals completed an extensive battery of neuropsychological, clinical, personality and drug use assessments online and at the testing centers. Participants were excluded if they had contraindications for magnetic resonance imaging (for example, metal implants and claustrophobia). Some individuals were only included in part of the analyses, depending on availability of the genotype, imaging and cognitive data for each participant. The characteristics of this sample are described in Table 1.

Table 1 Characteristics of study participants

Cognitive assessment

The Block Design and Matrix Reasoning subtests of the Wechsler Intelligence Scale for Children-Fourth Edition16 were computed to generate a Perceptual Reasoning Index and assess nonverbal intelligence (nonverbal intelligence quotient (IQ)). The Similarities and Vocabulary subtests were computed to generate a Verbal Comprehension Index measuring verbal concept formation, that is, the subjects’ ability to verbally reason (referred to as verbal IQ). For this, single test scores were converted to more precise age-equivalent scores values. Score values of the relevant subtests were summed to generate indices for Perceptual Reasoning or Verbal Comprehension. To control for differences in developmental status between participants, pubertal status of the sample was assessed using the Puberty Development Scale,17 which provides an eight-item self-report measure of physical development based on the Tanner stages.

SNP genotyping and quality control

DNA purification and genotyping were performed by the Centre National de Génotypage in Paris. DNA was purified from whole-blood samples (~10 ml) preserved in BD Vacutainer EDTA tubes (Becton, Dickinson and Company, Oxford, UK) using the Gentra Puregene Blood Kit (Qiagen, Manchester, UK) according to the manufacturer’s instructions. A total of 705 and 1382 individuals were genotyped with the Illumina (Little Chesterford, UK) Human610-Quad Beadchip and Illumina Human660-Quad Beadchip, respectively. For each genotyping platform the following quality control was performed separately. Single-nucleotide polymorphisms (SNPs) with call rates <95%, minor allele frequency <5%, deviation from the Hardy–Weinberg equilibrium (P1 × 103) and nonautosomal SNPs were excluded from the analyses. Individuals with excessive missing genotypes (failure rate >5%) were also excluded. Population homogeneity was examined with the Structure software using HapMap populations as reference groups.18 Individuals with divergent ancestry (from Utah residents with ancestry from northern and western Europe) were excluded. Identity-by-state clustering and multidimentional scaling were used to estimate cryptic relatedness for each pair of individuals using the PLINK software19 and closely related individuals were eliminated from the subsequent analysis. We applied principal component analysis to remove remaining outliers,20 defined as individuals located at more than four s.d. of the mean principal component analysis scores on one of the first 20 dimensions. Finally, the integrated genotypes from both Illumina Human610 Quad BeadChip and Human660-Quad BeadChip were combined and platform- specific SNPs were removed. After the quality control measures, we obtained a total of 466 125 SNPs in 1834 individuals.

Magnetic resonance imaging

Full details of the magnetic resonance imaging acquisition protocols and quality checks have been described previously.21 Brain images were segmented with the FreeSurfer software package (http://surfer.nmr.mgh.harvard.edu/) and the entire cortex of each individual was inspected for inaccuracies. Individuals with major malformations of the cerebral cortex were excluded from further analysis. Out of 1909 images, 1584 passed these quality control checks. In addition to global mean thickness of the left and right cerebral hemispheres, neuroimaging measures included cortical thickness for 33 individual regions per hemisphere. These were combined to produce weighted average thickness (weighted for surface at each region) for the four cerebral lobes (that is, frontal, temporal, parietal and occipital). The effect of magnetic resonance imaging site was controlled by adding it as a nuisance covariate in all statistical analyses.

Human neural stem cell culture

The human neural stem cell line SPC-04 was generated from 10-week-old human fetal spinal cord22 and was cultured mainly as previously described.23 In brief, cells were plated on tissue culture flasks that had been freshly coated with laminin (20 μg ml−1 in Dulbecco’s modified Eagle’s medium:F12 for 3 h at 37 °C), at a density of 20 000 cells cm2 and routinely grown into a reduced minimum media formulation consisting of Dulbecco’s modified Eagle’s medium:F12 with 0.03% human serum albumin, 100 μg ml−1 human Apo-transferrin, 16.2 μg ml−1 putrescine dihydrochloride, 5 μg ml−1 human insulin, 60 ng ml−1 progesterone, 2 mM L- glutamine and 40 ng ml−1 sodium selenite. This reduced minimum medium was also supplemented with growth factors (10 ng ml−1 basic fibroblast growth factor and 20 ng ml−1 epidermal growh factor) and 100 nM 4-hydroxy-tamoxifen. Cell differentiation was triggered when cells reached about 80% confluence by depleting the medium of growth factors and 4-hydroxy-tamoxifen. This was achieved in two steps. First, the growth factor- and 4-hydroxy-tamoxifen-depleted medium was supplemented with 10 μM of the γ-secretase inhibitor N-[N-(3,5-difluorophenacetyl)-L-alanyl]-S-phenylglycine t-butyl ester and 100 nM all-trans-retinoic acid for 48 h. We referred to this stage as ‘pre-differentiation’. Afterward, differentiation was achieved by maintaining the cells in reduced minimum media without any supplements for up to 7 days, with media change every 2 days.

RNA extraction and microarray analyses and SNP selection

RNA was extracted from triplicate SPC04 differentiation experiments using the RNeasy Mini Kit (Qiagen), according to the manufacturer’s instructions. Total RNA samples were processed using the TargetAmp-Nano Labeling Kit (Cambio, Cambridge, UK) and hybridized to Illumina HumanHT-12 v4 Expression BeadChips according to the manufacturers’ instructions at the Biomedical Genomics microarray core facility of the University of California, San Diego, CA, USA. Raw data were extracted by the Illumina BeadStudio software and further processed in R statistical environment (http://www.r-project.org) using the lumi24 and limma25 Bioconductor packages. Raw expression data were log2 transformed and normalized by quantile normalization. Differential expression between each differentiated versus undifferentiated conditions was assessed using the linear model for microarray analyses package. P-values were adjusted for multiple testing according to the false discovery rate procedure of Benjamini and Hochberg, and differentially expressed genes were selected at false discovery rate <5%. See Supplementary Table 1 for the list of differentially expressed genes. The functional annotation clustering tool, part of the Database for Annotation, Visualisation and Integrated Discovery26 was used to determine enrichment of functional groups in genes’ list generated from the microarray analyses. SNPs (n=59 643) lying within ±10 kB of each differentially expressed autosomal genes were selected for genetic association studies; of these, n=54 837 passed genetic quality controls and were used in further association analyses.

Genetic associations

Linear regression analyses were performed in PLINK19 using average cortical thickness of the left or right hemisphere as a dependent variable and the additive dosage of each SNP as an independent variable of interest, controlling for covariates of age, sex, puberty and the first four principal components from multidimentional scaling analysis. Dummy covariates were also used to control for different scanning sites. Genome-wide complex trait analysis27 was used to estimate the proportion of phenotypic variance in left cortical thickness explained by all genotyped SNPs and SNPs selected from our differential gene expression analyses. The genome-wide complex trait analysis was fitted using a restricted maximum likelihood method. The Broad Institute’s SNAP online plotting tool28 was used to generate the regional association and recombination rate plots.

The same conditions were used when investigating the association between rs7171755 and IQ except that ethnicity was also included as a nuisance covariate. Given correlations between brain volume (that is, the sum of all cortical and subcortical gray and white matter, excluding ventricle and cerebrospinal fluid), cortical thickness, cortical surface area and IQ, left surface area was also included as a covariate when using brain volume or IQ as a variable. For the associations of rs7171755 with brain volume, linear regression analyses were performed using site, sex, left surface area and four multidimentional scaling components as covariates. Handedness influenced none of the above associations and was not included as a covariate in our analyses. Mediation analyses between SNP × left (average or frontal) cortical thickness × non verbal IQ were performed in SPSS (version 20.0) using the PROCESS boostrapping procedure29 with 1000 boostrap samples used to calculate 95% confidence interval estimates of indirect effects.

Bonferroni corrections adjusting for the total number of tests in each analysis were performed to control for multiple testing. For the genotypes × cortical thickness association analyses with the selected 54 837 SNPs, on the left and right hemispheres, the corresponding significance threshold was P=4.56 × 107.

Meta-analytic association of rs7171755 with brain volumes in ENIGMA

We have used the ENIGMA data set, the largest meta-analysis of gene × neuroimaging phenotypes, to investigate association of rs7171755 with total brain volume, the brain phenotype most closely related to cortical thickness available in this data set. Association of rs7171755 with brain volume was performed using the online tool EnigmaVis,30 generating an interactive association plot. Only the healthy subsample (N=5775) of ENIGMA, for which this brain volume was available, were included in the meta-analysis.

Bootstraping procedure

To provide bias-reduced estimates of the associations reported above, we used a bootstrap resampling approach31 for linear regression models in the following way: first, subjects were resampled with replacement from the subjects passing quality controls criteria, here referred to as the bootstrap sample. Second, the coefficient βSNP for the SNP of interest from the bootstrap sample was calculated. We shuffled the SNP column of the bootstrap sample 100 000 times and recalculated the βSNP, generating a NULL distribution of βSNP for the bootstrap sample, denoted as βNULL. Third, the Pemp (empirical P-value) of the bootstrap sample was determined as the portion of βNULL greater than βSNP. We repeated this bootstrap procedure 10 000 times to obtain an empirical distribution of the P-values for each variable of interest.

Least square kernel machine association tests for candidate genes

As genetic association testing based on single SNPs might suffer from low power, we have also used a more sophisticated lease square kernel machine (LSKM) procedure that we have recently developed to analyze joint effects of several SNPs with imaging traits32 to detect possible genetic influences on cortical thickness. In short, this procedure compares individuals’ allele profiles, composes a similarity matrix (Kernel Matrix), and then determines to what extent the similarity matrix explains variations in the phenotype. A summary statistics is used to evaluate the significance under null hypothesis. We considered SNPs within ±10 kb of a gene’s transcript region as ‘belonging to’ the corresponding gene. In the current analysis, a gene-wide identity-by-state matrix was used as the similarity matrix. After quality control, 2659 out of the ~3540 genes differentially expressed in our microarray analyses were retained and subjected to the LSKM analysis. As for the single SNP association analyses, recruitment site, gender, age, puberty, ethnicity and the four first multidimentional scaling components were used as covariates in the LSKM analyses.

NPTN expression on mouse brain samples

RNA samples extracted from CD1 mouse brains at embryonic day 10 (E10), E14, E18 and at postnatal (P) stages 1 week, 1 month or 6 months were obtained from AMS Biotechnology (Abingdon-on-Thames, UK). Whole-brain mouse RNAs extracted from pools of five and three embryos were used for the E10 and E14 stages, respectively. RNAs extracted from the frontal cortex were used for later developmental stages (that is, E18–P6 months). In this case, triplicate samples from independent brains were analyzed for each stage, except for the P6 month stage for which data were derived from a single mouse brain. Complementary DNAs obtained by reverse transcription using the SuperScript III First-Strand Synthesis System (Invitrogen, Paisley, UK) following the manufacturer’s instructions were amplified by PCR with GAPDH as an internal control, using the following forward and reverse primers: GAPDH-F 5′-IndexTermTGTTCCTACCCCCAATGTGT-3′; GAPDH-R 5′- IndexTermCCTGCTTCACCACCTTCTTG-3′; NPTN-F 5′-IndexTermGCCTTTCTTGGGAATTCTGGC-3′; NPTN-R 5′- IndexTermAGAGTTGGTTTTCATTGGTCCAG-3′. PCRs were run in triplicate in the Applied Biosystems real-time PCR device (7900HT Fast Real-Time PCR system) in 20 μl reactions containing 4 μl complementary DNA, 0.5 μM of each forward and reverse primers and 1 × Power SYBR Green Mix (Applied Biosystems, Paisley, UK) using the following cycles: 95 °C for 15 min and 40 cycles at 95 °C for 30 s and 59 °C for 30 s. The PCR reaction products were evaluated by a melting curve analysis. Relative quantification of the PCR products was performed using the SDS software (Applied Biosystems) comparing threshold cycles (Ct). NPTN mRNA levels were first normalized to that of GAPDH (ΔCt=CtNPTN−CtGAPDH) at each developmental stage, and changes in expression relative to E10 were calculated as 2−(ΔCt−ΔCtE10). Statistical analysis (one-way analysis of variance, followed by Bonferroni-based post hoc analysis with α=0.05, two sided) was performed comparing expression of triplicates at the E18, P1 week and P1 month stages to that at E10.

NPTN expression in human brain samples

Expression of NPTN in the human brain was investigated using two databases. To study effects of rs7171755 on NPTN expression (probe 33624, targeting NM_001161363 and NM_012428), we used the publicly available BrainCloud database (http://BrainCloud.jhmi.edu/), which includes data on gene expression and genotypes from post-mortem dorsolateral prefrontal cortex samples collected from 272 subjects across the lifetime. In this database, transcript expression levels were measured on Illumina Oligoset array of 49 152 probes, and genotyping was performed using Illumina Infinium II or HD Gemini 1M Duo BeadChips.33 The genetic data sets were obtained from dbGaP at http://www.ncbi.nlm.nih.gov/gap through dbGaP accession number phs000417.v1.p1. Submission of the data phs000417.v1.p1 to dbGaP was provided by Drs Barbara Lipska and Joel Kleinman. Data collection was through a collaborative study sponsored by the National Institute of Mental Health Intramural Research Program. Initial report on this data set is from Colantuoni et al.33 For this study, we considered only samples with good RNA quality (RNA integrity number8). Statistical analyses measuring effects of rs7171755 on the postnatal expression of NPTN were performed on 147 samples (individuals0.5 year old) by general linear models controlling for age, ethnicity and RNA quality.

To investigate possible differences in NPTN expression between brain hemispheres, we analyzed a database (GEO series GSE25219) containing genome-wide gene expression data from 16 brain regions on both hemispheres, collected from 57 subjects across the lifetime (N=1340 post-mortem brain samples).34 Paired sample t-tests were performed comparing expression of NPTN on the right and the left hemisphere for each sample, controlling for the developmental stage and RNA integrity factor.

Results

Selection of genes involved in neural progenitor function

We first selected genes differentially expressed at any stage of proliferation and differentiation of a human neural stem cell line, SPC04. These cells proliferated readily in undifferentiated conditions and acquired a typical neural morphology, with well-developed neurites as early as 3 days after induction of differentiation (Figure 1a). Microarray analyses, comparing gene expression profiles of undifferentiated cells with pre-differentiated cells, or cells that have been induced to differentiate for 3 or 7 days, led to identification of ~3540 genes that were differentially expressed between these stages, with most of the changes in gene expression occurring 7 days after differentiation (Figure 1b). Gene ontology clustering analyses indicated enrichment of genes downregulated (n=1605) at differentiation day 7 for genes involved in cell cycle (enrichment score: 44.57) and DNA metabolic processes (enrichment score: 16.92). Upregulated genes (n=1675) were mainly enriched for genes involved in cell adhesion (enrichment score: 7.97), synaptic transmission (enrichment score: 5.83), neuron morphogenesis and differentiation (enrichment score: 5.46) and synapse formation and organization (enrichment score: 4.43). SNPs (n=59 643) located within ±10 kb of differentially expressed autosomal genes were selected for association with cortical thickness.

Figure 1
figure1

Differentiation of SPC04 neural progenitor cells in culture. (a) Changes that accompany differentiation are evident when comparing morphology of undifferentiated, proliferating cells (A) or pre-differentiated cells (B) with that of cells that have been induced to differentiate for 3 days (C) or 7 days (D). (b) Venn diagram representing number of genes differentially expressed between undifferentiated cells and each of the three stages of differentiation and their intersection. und, undifferentiated; pre, pre-differentiated; 3 d, differentiated for 3 days; 7 d, differentiated for 7 days. Scale bars represent 100 μm.

PowerPoint slide

Large-scale association studies with cortical thickness in adolescents

Given that left-right asymmetry of the brain is a well-known phenomenon35,36 that may be triggered by left-right differential gene expression,37,38 we analyzed each hemisphere separately. Highest associations with left cortical thickness were found for SNPs on chromosome 15 (Figure 2a, Table 2 and Supplementary Figure 1), with one SNP, rs7171755 (β=−0.01973; P=1.12 × 107), passing the threshold of Bonferroni-corrected significance (the Bonferroni-adjusted significance threshold for association with the selected 54 837 SNPs, on the left and right hemispheres, was P=4.56 × 10−7). In the right hemisphere, highest associations with cortical thickness were found on chromosome 11 (Supplementary Figure 2); however, none remained significant after Bonferroni correction for multiple testing. rs7171755 was associated with right cortical thickness at P=3.22 × 104 (β=−0.0134; Table 2). Neither handedness nor ethnicity influenced this association. It is worth pointing out that our gene selection procedure resulted in significant gene enrichment: estimation of the variance explained by the SNPs using Genome-wide Complex Trait Analysis27 indicated that the 59 643 selected SNPs explain 13.3% (s.e.=0.093, P=0.02) of the total variance in left cortical thickness, a fivefold enrichment relative to the 22.2% (s.e.=0.195, P=0.03) variance explained by considering all 506 932 genotyped SNPs simultaneously.

Figure 2
figure2

Genetic associations with cortical thickness on the left hemisphere. (a) Manhattan plots of single SNPs associations. SNP markers are plotted according to chromosomal location on the x axis, whereas the y axis −log10 (P-values) indicate the significance of the additive effect of the number of minor alleles of each SNP on average cortical thickness for the left hemisphere. A conservative Bonferroni-corrected P-value threshold (red horizontal line) for significance was set to P=8.4 × 107. (b) Manhattan plots of least square kernel machine (LSKM) gene-wide associations. Each dot represents a gene (SNPs set), plotted according to chromosomal location on the x axis. The NPTN gene, which is most significantly associated with left cortical thickness, is indicated by an arrow.

PowerPoint slide

Table 2 Top 20 SNPs associating with left cortical thickness

The number of minor alleles at rs7171755 was inversely correlated with average cortical thickness. In the left hemisphere, we observed a decrease of 0.0189 mm (that is, 0.7% of the average left cortical thickness) per risk allele, explaining 2% of variance. To investigate whether effects of rs7171755 on cortical thickness differed across brain regions, we processed the segmented left and right cortical lobes (frontal, temporal, parietal and occipital) into 66 cortical subregions39 and performed linear regressions, analyzing associations of rs7171755 with cortical thickness within each region. Region-specific effects of rs7171755 on cortical thickness were observed, with most significant overall influences on the cortical thickness in the left temporal (β=−0.0275; P=1.23 × 107), frontal (β=−0.0212; P=6.98 × 107) and parietal (β=−0.0170; P=1.684 × 104) lobes. In the right hemisphere, associations were significant only for the frontal and temporal lobes (β=−0.0169; P=8.91 × 105 and β=−0.0165; P=1.667 × 103, respectively). A further refined neuroanatomical segmentation revealed that these asymmetric associations occurred throughout the left frontal cortex, including the lateral orbitofrontal, the caudal middle frontal and the superior frontal cortex, the para- and pre-central region and the pars orbitalis. Other significant associations were observed in the left superior and middle temporal cortices and in the left supramarginal region (Table 3).

Table 3 Associations of rs7171755 across brain regions

The SNP rs7171755 is located less than 2 kb downstream of the NPTN gene and is in high linkage disequilibrium with other SNPs within the NPTN locus. Regional association analysis for SNPs around rs7171755 clearly show that NPTN is the candidate gene associated with this signal: the SNPs with the smallest P-values, all in high linkage disequilibrium with rs7171755, are located across this gene (Figure 3).

Figure 3
figure3

SNPs within the NPTN locus are associated with cortical thickness in the left hemisphere. Regional association and recombination rate plots for SNPs around rs7171755, genotyped in our sample. The SNP with the most significant association is denoted with a red diamond. The left y axis represents −log10 P-values for association with cortical thickness in the left hemisphere, the right y axis represents the recombination rate and the x axis represents base pair positions along the chromosome (human genome Build 36).

PowerPoint slide

To confirm our finding and to test for a possible significance of joint contribution of multiple SNPs within the NPTN locus to left cerebral cortex thickness, we performed gene-wide SNP-sets analyses using the LSKM approach.32,40,41 The results indicate that, in addition to rs7171755, eight SNPs: rs7176637, rs11854138, rs8028749, rs12185108, rs1564492, rs899981, rs7178269 and rs4075802, in the NPTN locus, jointly show significant association with average left cortical thickness (P=1.264 × 108; Figure 2b). As for the single SNP analyses, the most significant associations were observed, in decreasing order, in the left temporal (P=1.97 × 1010), left frontal (P=1.87 × 108), left parietal (P=4.59 × 105) and right frontal (P=6 × 104) lobes. More refined region-specific analyses confirmed the single SNP associations described above (Supplementary Table 2). To demonstrate the stability of the above associations and obtain unbiased estimation of the genetic effects, we used a bootstrapping resampling procedure.31,42 Effects of rs7171755 on left cortical thickness were confirmed, with a decrease of 0.0196 mm per risk allele. Effects of this variant were also confirmed for the hemispheric lobes (left frontal lobe: β=−0.022, Pemp=1 × 106; left temporal lobe: β=−0.027, Pemp=1 × 106; left parietal lobe: β=−0.017, Pemp=7.1 × 105; right frontal lobe: β=−0.017, P=3.3 × 105 and right temporal lobe: β=−0.017, P=6.64 × 104) and individual region of interests (Table 3 and Supplementary Figure 3).

In order to have sufficient power to unambiguously reject an observed association, a sample size larger than that of the original study is required.43 However, a replication sample larger than the IMAGEN sample, with comparable phenotypic characteristics, including assessment of cortical thickness during adolescence is not yet available. We have nonetheless attempted to overcome these limitations by further testing rs7171755 in the ENIGMA data set, a meta-analysis of gene × neuroimaging phenotypes, where we analyzed its association with brain volume. As cortical thickness measures were not available in the ENIGMA samples, brain volume was the most closely related brain phenotype available.44 The correlation between brain volume and cortical thickness on the left hemisphere in the IMAGEN sample was high (r(1188)=0.491; P=4.29 × 1073). Upon measuring association of rs7171755 with brain volume, we found in the IMAGEN sample, an association of rs7171755 with significant decrease of brain volume of 3080 mm3 (β=−3080, P=0.0457) per risk allele. We have replicated this finding in the subsample of healthy individuals (n=5775) of ENIGMA, using the EnigmaVis tool,30 confirming the negative effects of the risk allele on brain volume (decrease of 5945.91 mm3 per risk allele: β=−5945.91, P=0.00327; Supplementary Figure 4). Altogether, these results further support a role for NPTN-related genotypes in influencing brain structure.

Association of rs7171755 with adolescents’ intellectual ability

The results presented above, along with previous findings showing relationships between intellectual ability and cortical thickness in healthy subjects, predominantly in frontal and temporal cortical regions,2,3 suggest that rs7171755 might influence cognitive ability. To test this, and assess gene–brain–behavior relationships, we estimated Pearson’s correlations between indices of intellectual ability and cortical thickness in our sample and found significant positive correlations between average cortical thickness and nonverbal IQ, which were more pronounced in the left hemisphere (r(1168)=0.074; P=0.012 and r(1168)=0.06; P=0.041, in the left and right hemisphere, respectively; see Supplementary Table 3). A positive correlation between left cortical thickness and school performance was also observed (r(1168)=0.062; P=0.033). Correlations with verbal IQ were not significant at an unadjusted P<0.05. In the regions of the left cerebral cortex most significantly affected by rs7171755, that is, the left temporal and frontal cortices, correlations were also significant for nonverbal IQ (r(1170)=0.061; P=0.036; and r(1170)=0.075; P=0.011, respectively); there was also borderline significance for correlations with verbal IQ (in the temporal lobe only (r(1170)=0.059; P=0.044)).

These results suggested that, by affecting cortical thickness, rs7171755 might influence IQ. Mediation analyses performed to test this hypothesis indicated that the minor A-allele at rs7171755 associates with lower scores for nonverbal IQ (β=−1.239; P=0.0219). This association was mediated by significant indirect effects (that is, via left frontal lobe thickness) of this SNP on nonverbal IQ (β=−0.1851; 95% confidence interval (−0.391; −0.046)), whereas direct effects of the SNP on nonverbal IQ were not significant (95% confidence interval (−2.12; 0.023)). Surprisingly, rs7171755 also associated with verbal IQ (β=−1.5048; P=0.0076), an association that was not mediated by indirect effects on mean or temporal thickness. This suggested that more localized effects of rs7171755 on brain structure might underlie this association. To test this, we investigated correlations between verbal IQ and cortical thickness in language-related region of interests in the left frontal and temporal lobes where effects of rs7171755 on cortical thickness were strongest (see Table 3): the pars orbitalis and the middle temporal and superior temporal regions. Positive correlations between verbal IQ and cortical thickness were found in the pars orbitalis (r(1170)=0.080; P=0.006), while a trend was also found in the middle temporal gyrus (r(1170)=0.055; P=0.060). No correlation was observed with thickness in the superior temporal gyrus. Mediation analyses indicated that indirect effects (β=−0.1486; 95% confidence interval (−0.3347; −0.0376)) of rs7171755 on left pars orbitalis thickness partially contributed to its association with verbal IQ, with other factors accounting for the remaining effects (β=−1.3562; P=0.0165).

Boostrapping analysis revealed similarly negative effect of rs717175 on IQ with a decrease in intelligence by about 1.81 points and 1.41 points per allele for verbal and nonverbal IQ, respectively (β=−1.808, P=0.002 and β=−1.407, P=0.008; for verbal and nonverbal IQ, respectively; Supplementary Figure 3), accounting for 0.7 and 0.5% of the total variance in IQ, respectively. Altogether, these analyses indicate that the minor allele at rs7171755, via its effects on cortical thickness, particularly in the left frontal lobe, negatively has an impact on intellectual abilities.

Effects of rs7171755 on NPTN expression

NPTN, a gene selected for our analyses because of its increased expression in differentiating human neural progenitor cells (1.5-fold increase at differentiation day 7 compared with undifferentiated cells; false discovery rate <0.05) encodes splice isoforms of neuroplastin, a synaptic cell adhesion glycoprotein.45 This induction of NPTN occurs at a time when neurites are well developed, and appears to coincide with induction of genes involved in cell adhesion and synaptic transmission (see above). To confirm this, we investigated patterns of NPTN expression in the brain. First, we investigated changes in NPTN expression in the mouse brain during stages of embryonic and postnatal development. One-way analysis of variance indicated that, although levels of NPTN mRNA are low in the mouse neocortex during embryonic development, expression of this gene is markedly increased in the first week after birth, reaching maximum levels 1 month after birth (F(3, 8)=53.83; P=1.2 × 105), a time period that corresponds to adolescence in mice (Figure 4a). To confirm relevance of our findings to human brain development, we interrogated the BrainCloud database, which contains genome-wide expression data of the prefrontal cortex of 272 individuals across the lifespan as well as their genotype information.33 Investigations of changes in NPTN expression in the human prefrontal cortex across lifetime confirmed the expression patterns observed in the mouse brain. Although levels of NPTN (isoforms NM_001161363 and NM_012428) were low during early fetal development, its expression increased at later stages of development to reach maximum levels in childhood through early adulthood, after which expression declines (Figure 4b). To gain functional insight into these changing expression patterns, we searched for genes whose expression correlated with that of NPTN in the human prefrontal cortex across the lifespan and examined their enrichment for functional gene groups. Expression of NPTN positively correlated with a cluster of 721 genes (r>0.6) enriched for genes involved in energy metabolism (n=36 (7%), P=1.08 × 1011), synaptic transmission (n=27 (5%), P=7.98 × 107) as well as learning and memory (n=14 (3%), P=2.3 × 105). Lists of correlated genes and their grouping into functional clusters are contained in Supplementary Tables 4 and 5, respectively.

Figure 4
figure4

Developmental stage- and genotype-specific expression of NPTN in the cerebral cortex. (a) Highest expression of Nptn in the adolescent mouse brain. Nptn mRNA levels in the whole-mouse brain at embryonic day 14 (E14), and in the frontal cortex at E18 or 1 week, 1 month and 6 months postnatally (P) were calculated relative to expression in the brain at E10. Statistical analysis compared expression at E10, E18, P1 week and P1 month. ***P<5 × 104. (b) Changes in expression of NPTN across lifespan in the dorsolateral prefrontal cortex of individuals stratified by rs7171755 genotypes. Each subject is colored to indicate its rs7171755 genotype, with the thick dotted curves representing an estimate of the local mean (loess) of NPTN expression for each genotype as it varies across age. Only samples with RNA quality RNA integrity number (RIN)8 are displayed. (c) Statistical analysis of a subset of the data displayed in b, visualizing differences in NPTN expression between rs7171755 genotypes in the postnatal brain (age0.5 year). The y axis represents NPTN expression after controlling for age, ethnicity and RNA quality (RIN). The x axis represents genotype groups. For b and c, rs7171755 genotypes: dark blue, AA; light blue, AG; pink, GG.

PowerPoint slide

We then investigated possible cis-effects of rs7171755 on NPTN expression, by testing whether rs7171755 genotypes correlated with differences in NPTN expression. We found that expression of NPTN differed by genotypes; individuals homozygotic for the minor A-allele at rs7171755 had lower expression of this gene (P=0.009; Figure 4c). Remarkably, this difference was most notable from adolescence to early adulthood (late 20 s; Figure 4b), suggesting age-dependent effects of rs7171755.

The results presented above point to a lateralized effect of rs7171755, associated with cortical thickness predominantly in the left hemisphere. We analyzed this further, investigating possible asymmetries in cortical thickness and NPTN expression. For this purpose, we performed paired samples t-tests that indicated that, although cortical thickness correlated well between hemispheres (r(1583)=0.864) in our sample, the cortex was on average 0.012 mm thicker on the right hemisphere (t(1582)=9.818, P=3.977 × 1022). To test for asymmetric expression of NPTN in the human brain, we analyzed a database (GEO series GSE25219) containing gene expression data from 16 brain regions on both hemispheres (n=1340 post-mortem brain samples).34 Paired samples t-tests comparing expression on NPTN in the right vs the left hemisphere indicated that RNA levels of this gene were higher in the right hemisphere than in the left (NPTN left−NPTN right=−0.0377, t(523)=−2.703, P=0.007). These results illustrate asymmetries in the human brain, with both cortical thickness and NPTN expression being more pronounced in the right hemisphere. The observed asymmetry in NPTN expression may render the left hemisphere more sensitive to the effects of NPTN mutations, accounting for the lateralized effects of rs7171755 found in our study.

Discussion

In this study, we have used a large sample of healthy adolescents to investigate the genetic basis of interindividual variations in cortical thickness and relevant cognitive phenotypes. We performed transcriptional profiling of human neural progenitor cells for neural gene enrichment to allow targeted SNP selection for association analyses with structural neuroimaging and cognitive phenotypes. Using this combined, hypothesis driven, approach we were able to identify the NPTN locus as contributing to individual differences in brain structure and cognition. The SNPs within NPTN associate with cortical thickness in the left hemisphere, most significantly in areas associated with higher cognitive functions including regions throughout the left frontal and temporal cortices and the left supramarginal area. The minor allele at rs7171755, which associates with lower cortical thickness at those regions and decreased performance of adolescents on tests of intellectual ability, also associates with lower expression of NPTN in the human prefrontal cortex. We have provided additional corroborative evidence from the ENIGMA study, the largest gene × neuroimaging meta-analysis study to date by demonstrating the association of NPTN rs7171755 with brain volume, a measure of brain structure related to cortical thickness. We also provide evidence for asymmetries in the human brain and propose that asymmetry in NPTN expression may render the left hemisphere more sensitive to the effects of NPTN mutations, accounting for the lateralized effects of rs7171755 found in our study.

In keeping with our data, asymmetric genetic influences on brain structure have previously been reported, specifically in the frontal and language-related left temporal cortices, where cortical gray matter distribution displays high heritability.7 Our study, on a cohort very homogenous for age (that is, 14 year), yielded results consistent with a previous report,3 which described positive correlations, peaking in late childhood/early adolescence, between cortical thickness and levels of intelligence, particularly in the prefrontal cortex. This age homogeneity is a critical characteristic of our sample, given the reported changes in correlations between intelligence and cortical thickness from childhood to early adulthood.3 Our data also support the notion that cortical thickness differentially has an impact on verbal and nonverbal abilities. Although average thickness, particularly in the prefrontal cortex, influenced nonverbal cognitive abilities, more regionally restricted structural effects may control verbal abilities. In this context, our identification of the pars orbitalis as a region mediating such effects is notable, as this is a part of the Broca language area selectively involved in processing the semantic aspects of sentences.46 Regionally specific cortical thinning in the pars orbitalis has been documented in individuals with DiGeorge, velocardiofacial syndrome,47 whose cognitive deficits include language and speech delays.48

In line with the proposed role of NPTN in neurite outgrowth, we found that induction of this gene in cultured neural progenitor cells occurs at a time when neurites are well developed, coinciding with induction of genes involved in cell adhesion and synaptic transmission. We also found that NPTN is expressed in the brain at periods of intense neuronal activation and synaptic activity, which fits well with the emerging role of this gene as encoding a cell adhesion protein regulating neuritogenesis and synaptic plasticity.49, 50, 51 Our results also indicate that expression of NPTN in the cerebral cortex is highest around adolescence, a period that in humans is accompanied by decrease in gray matter in frontal, parietal and temporal areas.5 This and the proposed role of NPTN in neurite outgrowth and synaptic plasticity suggest that, at the cellular level, synaptic architecture of the cerebral cortex underlie the observed differences in cortical thickness and cognitive abilities.

A role for deregulation of NPTN in disorders of the nervous system is also emerging. NPTN and other genes involved in neurite outgrowth have recently been identified as direct targets of FOXP2,52 a transcription factor that when mutated causes a monogenic speech and language disorder in humans53 and the reduced dosage of which impairs synaptic plasticity, motor-skill learning and ultrasonic vocalizations in mice,54,55 and disrupts vocal learning in songbirds.56 In agreement with our data, this suggests that similar to FOXP2, NPTN may be involved in learning vocal and nonvocal skills. Furthermore, functional polymorphisms in the NPTN promoter that may confer susceptibility to schizophrenia have been identified.57 Analyzing data from the 1000 Genomes Project, we found substantial linkage disequilibrium (D′=1, r2=0.502; data not shown) between rs7171755 and rs3743500, one of these promoter polymorphisms associated with schizophrenia. Taken together, these data highlight a potential role for NPTN and, more generally, synaptic dysfunctions in forms of intellectual deficits.

Such aspects of neural development have long been thought to underlie formation of higher-order cortical functions. The synaptic architecture of the cortex has been proposed to define the extent of intellectual capacity: changes in dendritic arborization and spine structure are commonly observed in brain tissue of patients with various types of intellectual disabilities,58,59 and mutations are found in many different types of cognitive disorders, including intellectual disability, schizophrenia and autism spectrum disorders, which affect synaptic morphology and plasticity.60, 61, 62 The most recent observations using animal models of intellectual disability/autism spectrum disorder indicate that the pace of maturation of dentritic spine synapses in early postnatal life is vital for normal intellectual development.63 It is of interest that those dendritic spines that become larger and functionally stronger (that is, more stable synapses) too early in development trigger subsequent cognitive deficits.63

It should be noted that the effect sizes observed in our experiments are small, as might be expected from mutations in human genes that regulate late events in neural differentiation. Such mutations may not cause gross cortical malformations, but rather more subtle cognitive and behavioral defects. Given this and the age specificity of our observations, a major challenge remains to generate additional studies to replicate our findings. Nonetheless, we have partly overcome these limitations, further testing the relevance of NPTN genotypes for interindividual variations in brain structure in our sample and in the ENIGMA consortium for meta-analysis of large neuroimaging and genetics data set, and demonstrated the negative association of the rs7171755 risk allele with brain volume, further supporting a role for NPTN in influencing brain structure. There still is a need to directly replicate our findings. Even more thrilling is the prospect of applying our approach to the longitudinal study of normal as well as learning disabled and psychiatric samples to investigate spatiotemporal alterations in the genetic influences reported here.

References

  1. 1

    Lenroot RK, Schmitt JE, Ordaz SJ, Wallace GL, Neale MC, Lerch JP et al. Differences in genetic and environmental influences on the human cerebral cortex associated with development during childhood and adolescence. Hum Brain Mapp 2009; 30: 163–174.

  2. 2

    Sowell ER, Thompson PM, Leonard CM, Welcome SE, Kan E, Toga AW . Longitudinal mapping of cortical thickness and brain growth in normal children. J Neurosci 2004; 24: 8223–8231.

  3. 3

    Shaw P, Greenstein D, Lerch J, Clasen L, Lenroot R, Gogtay N et al. Intellectual ability and cortical development in children and adolescents. Nature 2006; 440: 676–679.

  4. 4

    Perrin JS, Herve PY, Leonard G, Perron M, Pike GB, Pitiot A et al. Growth of white matter in the adolescent brain: role of testosterone and androgen receptor. J Neurosci 2008; 28: 9519–9524.

  5. 5

    Giedd JN, Blumenthal J, Jeffries NO, Castellanos FX, Liu H, Zijdenbos A et al. Brain development during childhood and adolescence: a longitudinal MRI study. Nat Neurosci 1999; 2: 861–863.

  6. 6

    Gogtay N, Giedd JN, Lusk L, Hayashi KM, Greenstein D, Vaituzis AC et al. Dynamic mapping of human cortical development during childhood through early adulthood. Proc Natl Acad Sci USA 2004; 101: 8174–8179.

  7. 7

    Thompson PM, Cannon TD, Narr KL, van Erp T, Poutanen VP, Huttunen M et al. Genetic influences on brain structure. Nat Neurosci 2001; 4: 1253–1258.

  8. 8

    Yoon U, Fahim C, Perusse D, Evans AC . Lateralized genetic and environmental influences on human brain morphology of 8-year-old twins. Neuroimage 2010; 53: 1117–1125.

  9. 9

    Joshi AA, Lepore N, Joshi SH, Lee AD, Barysheva M, Stein JL et al. The contribution of genes to cortical thickness and volume. Neuroreport 2011; 22: 101–105.

  10. 10

    Panizzon MS, Fennema-Notestine C, Eyler LT, Jernigan TL, Prom-Wormley E, Neale M et al. Distinct genetic influences on cortical surface area and cortical thickness. Cereb Cortex 2009; 19: 2728–2735.

  11. 11

    Huttenlocher PR . Synaptic density in human frontal cortex-developmental changes and effects of aging. Brain Res 1979; 163: 195–205.

  12. 12

    Yakovlev PI, Lecours AR . The myelogenetic cycles of regional maturation of the brain. In: Minkowski A (ed). Regional Development of the Brain in Early Life. Blackwell Scientific Boston: MA, USA, 1967, pp 3–70.

  13. 13

    Rakic P . Specification of cerebral cortical areas. Science 1988; 241: 170–176.

  14. 14

    Pontious A, Kowalczyk T, Englund C, Hevner RF . Role of intermediate progenitor cells in cerebral cortex development. Dev Neurosci 2008; 30: 24–32.

  15. 15

    Schumann G, Loth E, Banaschewski T, Barbot A, Barker G, Buchel C et al. The IMAGEN study: reinforcement-related behaviour in normal brain function and psychopathology. Mol Psychiatry 2010; 15: 1128–1139.

  16. 16

    Wechsler D . The Wechsler Intelligence Scale for Children—Fourth Edition. Technical and Interpretive Manual. Psychological Association: San Antonio, TX, USA, 2003.

  17. 17

    Petersen AC, Crockett L, Richards M, Boxer A . A self-report measure of pubertal status: reliability, validity, and initial norms. J Youth Adolesc 1988; 17: 117–133.

  18. 18

    Pritchard JK, Stephens M, Donnelly P . Inference of population structure using multilocus genotype data. Genetics 2000; 155: 945–959.

  19. 19

    Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, Bender D et al. PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 2007; 81: 559–575.

  20. 20

    Price AL, Patterson NJ, Plenge RM, Weinblatt ME, Shadick NA, Reich D . Principal components analysis corrects for stratification in genome-wide association studies. Nat Genet 2006; 38: 904–909.

  21. 21

    Schilling C, Kuhn S, Paus T, Romanowski A, Banaschewski T, Barbot A et al. Cortical thickness of superior frontal cortex predicts impulsiveness and perceptual reasoning in adolescence. Mol Psychiatry 2012; 18: 624–630.

  22. 22

    Cocks G, Romanyuk N, Amemori T, Jendelova P, Forostyak O, Jeffries AR et al. Conditionally immortalized stem cell lines from human spinal cord retain regional identity and generate functional V2a interneurons and motorneurons. Stem Cell Res Ther 2013; 4: 69.

  23. 23

    Pollock K, Stroemer P, Patel S, Stevanato L, Hope A, Miljan E et al. A conditionally immortal clonal stem cell line from human cortical neuroepithelium for the treatment of ischemic stroke. Exp Neurol 2006; 199: 143–155.

  24. 24

    Du P, Kibbe WA, Lin SM . lumi: a pipeline for processing Illumina microarray. Bioinformatics 2008; 24: 1547–1548.

  25. 25

    Smyth GK . Limma: linear models for microarray data. In: Gentleman R, Carey V, Dudoit S, Irizarry R, Huber W (eds). Bioinformatics and Computational Biology Solutions using R and Bioconductor. Springer: New York, 2005, pp 397–420.

  26. 26

    Huang DW, Sherman BT, Lempicki RA . Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc 2009; 4: 44–57.

  27. 27

    Yang J, Lee SH, Goddard ME, Visscher PM . GCTA: a tool for genome-wide complex trait analysis. Am J Hum Genet 2011; 88: 76–82.

  28. 28

    Johnson AD, Handsaker RE, Pulit SL, Nizzari MM, O'Donnell CJ, de Bakker PI . SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 2008; 24: 2938–2939.

  29. 29

    Hayes AF . Introduction to Mediation, Moderation, and Conditional Process Analysis: A Regression-Based Approach. 1st edn. The Guilford Press: New York, NY, USA, 2013.

  30. 30

    Novak NM, Stein JL, Medland SE, Hibar DP, Thompson PM, Toga AW . EnigmaVis: online interactive visualization of genome-wide association studies of the Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) consortium. Twin Res Hum Genet 2012; 15: 414–418.

  31. 31

    Sun L, Bull SB . Reduction of selection bias in genomewide studies by resampling. Genet Epidemiol 2005; 28: 352–367.

  32. 32

    Ge T, Feng J, Hibar DP, Thompson PM, Nichols TE . Increasing power for voxel- wise genome-wide association studies: the random field theory, least square kernel machines and fast permutation procedures. Neuroimage 2012; 63: 858–873.

  33. 33

    Colantuoni C, Lipska BK, Ye T, Hyde TM, Tao R, Leek JT et al. Temporal dynamics and genetic control of transcription in the human prefrontal cortex. Nature 2011; 478: 519–523.

  34. 34

    Kang HJ, Kawasawa YI, Cheng F, Zhu Y, Xu X, Li M et al. Spatio-temporal transcriptome of the human brain. Nature 2011; 478: 483–489.

  35. 35

    Galaburda AM, LeMay M, Kemper TL, Geschwind N . Right-left asymmetrics in the brain. Science 1978; 199: 852–856.

  36. 36

    Toga AW, Thompson PM . Mapping brain asymmetry. Nat Rev Neurosci 2003; 4: 37–48.

  37. 37

    Sun T, Patoine C, Abu-Khalil A, Visvader J, Sum E, Cherry TJ et al. Early asymmetry of gene transcription in embryonic human left and right cerebral cortex. Science 2005; 308: 1794–1798.

  38. 38

    Chang S, Johnston RJ Jr, Hobert O . A transcriptional regulatory cascade that controls left/right asymmetry in chemosensory neurons of C. elegans. Genes Dev 2003; 17: 2123–2137.

  39. 39

    Hagmann P, Cammoun L, Gigandet X, Meuli R, Honey CJ, Wedeen VJ et al. Mapping the structural core of human cerebral cortex. PLoS Biol 2008; 6: e159.

  40. 40

    Kwee LC, Liu D, Lin X, Ghosh D, Epstein MP . A powerful and flexible multilocus association test for quantitative traits. Am J Hum Genet 2008; 82: 386–397.

  41. 41

    Liu D, Lin X, Ghosh D . Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models. Biometrics 2007; 63: 1079–1088.

  42. 42

    Faye LL, Sun L, Dimitromanolakis A, Bull SB . A flexible genome-wide bootstrap method that accounts for ranking and threshold-selection bias in GWAS interpretation and replication study design. Stat Med 2011; 30: 1898–1912.

  43. 43

    Tversky A, Kahneman D . Belief in the law of small numbers. Psychol Bull 1971; 75: 105–110.

  44. 44

    Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM et al. Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet 2012; 44: 552–561.

  45. 45

    Hill IE, Selkirk CP, Hawkes RB, Beesley PW . Characterization of novel glycoprotein components of synaptic membranes and postsynaptic densities, gp65 and gp55, with a monoclonal antibody. Brain Res 1988; 461: 27–43.

  46. 46

    Dapretto M, Bookheimer SY . Form and content: dissociating syntax and semantics in sentence comprehension. Neuron 1999; 24: 427–432.

  47. 47

    Bearden CE, van Erp TG, Dutton RA, Tran H, Zimmermann L, Sun D et al. Mapping cortical thickness in children with 22q11.2 deletions. Cereb Cortex 2007; 17: 1889–1898.

  48. 48

    Gerdes M, Solot C, Wang PP, Moss E, LaRossa D, Randall P et al. Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion. Am J Med Genet 1999; 85: 127–133.

  49. 49

    Smalla KH, Matthies H, Langnase K, Shabir S, Bockers TM, Wyneken U et al. The synaptic glycoprotein neuroplastin is involved in long-term potentiation at hippocampal CA1 synapses. Proc Natl Acad Sci USA 2000; 97: 4327–4332.

  50. 50

    Empson RM, Buckby LE, Kraus M, Bates KJ, Crompton MR, Gundelfinger ED et al. The cell adhesion molecule neuroplastin-65 inhibits hippocampal long-term potentiation via a mitogen-activated protein kinase p38-dependent reduction in surface expression of GluR1-containing glutamate receptors. J Neurochem 2006; 99: 850–860.

  51. 51

    Owczarek S, Soroka V, Kiryushko D, Larsen MH, Yuan Q, Sandi C et al. Neuroplastin-65 and a mimetic peptide derived from its homophilic binding site modulate neuritogenesis and neuronal plasticity. J Neurochem 2011; 117: 984–994.

  52. 52

    Vernes SC, Oliver PL, Spiteri E, Lockstone HE, Puliyadi R, Taylor JM et al. Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain. PLoS Genet 2011; 7: e1002145.

  53. 53

    Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP . A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 2001; 413: 519–523.

  54. 54

    Groszer M, Keays DA, Deacon RM, de Bono JP, Prasad-Mulcare S, Gaub S et al. Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits. Curr Biol 2008; 18: 354–362.

  55. 55

    Shu W, Cho JY, Jiang Y, Zhang M, Weisz D, Elder GA et al. Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene. Proc Natl Acad Sci USA 2005; 102: 9643–9648.

  56. 56

    Haesler S, Wada K, Nshdejan A, Morrisey EE, Lints T, Jarvis ED et al. FoxP2 expression in avian vocal learners and non-learners. J Neurosci 2004; 24: 3164–3175.

  57. 57

    Saito A, Fujikura-Ouchi Y, Kuramasu A, Shimoda K, Akiyama K, Matsuoka H et al. Association study of putative promoter polymorphisms in the neuroplastin gene and schizophrenia. Neurosci Lett 2007; 411: 168–173.

  58. 58

    Huttenlocher PR . Dendritic and synaptic pathology in mental retardation. Pediatr Neurol 1991; 7: 79–85.

  59. 59

    Purpura DP . Dendritic spine ‘dysgenesis’ and mental retardation. Science 1974; 186: 1126–1128.

  60. 60

    Gilman SR, Chang J, Xu B, Bawa TS, Gogos JA, Karayiorgou M et al. Diverse types of genetic variation converge on functional gene networks involved in schizophrenia. Nat Neurosci 2012; 15: 1723–1728.

  61. 61

    van Bokhoven H . Genetic and epigenetic networks in intellectual disabilities. Annu Rev Genet 2011; 45: 81–104.

  62. 62

    Gilman SR, Iossifov I, Levy D, Ronemus M, Wigler M, Vitkup D . Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses. Neuron 2011; 70: 898–907.

  63. 63

    Clement JP, Aceti M, Creson TK, Ozkan ED, Shi Y, Reish NJ et al. Pathogenic SYNGAP mutations impair cognitive development by disrupting maturation of dendritic spine synapses. Cell 2012; 151: 709–723.

Download references

Acknowledgements

We thank Dr Gary Hardiman for the microarray hybridizations and Professor Jack Price for giving us the SPC04 cells. This work was supported by the European Union-funded FP6 Integrated Project IMAGEN (Reinforcement-related behavior in normal brain function and psychopathology) (LSHM-CT- 2007-037286), the German Ministry of Education and Research (BMBF Grant # 01EV0711 and eMED ‘Alcoholism’), the FP7 project IMAGEMEND (Development of effective imaging tools for diagnosis, monitoring and management of mental disorders) and the Innovative Medicine Initiative Project EU-AIMS (115300-2), as well as the Medical Research Council Programme Grant ‘Developmental pathways into adolescent substance abuse’ (G93558), the Swedish Research Council (FORMAS) and the United Kingdom National Institute for Health Research (NIHR) Biomedical Research Centre Mental Health.

Author information

Correspondence to S Desrivières.

Ethics declarations

Competing interests

Dr Barker receives honoraria for teaching from General Electric and acts as a consultant for IXICO. Dr Banaschewski served in an advisory or consultancy role for Hexal Pharma, Lilly, Medice, Novartis, PCM scientific, Shire and Viforpharma. He received conference attendance support and conference support or received speaker’s fee by Lilly, Janssen McNeil, Medice, Novartis and Shire. He is/has been involved in clinical trials conducted by Lilly, Shire and Viforpharma. The present work is unrelated to the above grants and relationships. The remainig authors declare no conflict of interest.

Additional information

Supplementary Information accompanies the paper on the Molecular Psychiatry website

Supplementary information

PowerPoint slides

Rights and permissions

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

Reprints and Permissions

About this article

Cite this article

Desrivières, S., Lourdusamy, A., Tao, C. et al. Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents. Mol Psychiatry 20, 263–274 (2015). https://doi.org/10.1038/mp.2013.197

Download citation

Keywords

  • adolescent
  • cortical thickness
  • intelligence
  • lateralization
  • neural stem cell
  • neuroimaging

Further reading