Child Psychiatry Branch, National Institute of Mental Health, Bethesda, MD 20892, USA.
Mol Psychiatry. 2011 Sep;16(9):917-26. doi: 10.1038/mp.2010.72. Epub 2010 Jul 13.
Disrupted-in-schizophrenia-1 (DISC1), contains two common non-synonymous single-nucleotide polymorphisms (SNPs)--Leu607Phe and Ser704Cys--that modulate (i) facets of DISC1 molecular functioning important for cortical development, (ii) fronto-temporal cortical anatomy in adults and (iii) risk for diverse psychiatric phenotypes that often emerge during childhood and adolescence, and are associated with altered fronto-temporal cortical development. It remains unknown, however, if Leu607Phe and Ser704Cys influence cortical maturation before adulthood, and whether each SNP shows unique or overlapping effects. Therefore, we related genotype at Leu607Phe and Ser704Cys to cortical thickness (CT) in 255 typically developing individuals aged 9-22 years on whom 598 magnetic resonance imaging brain scans had been acquired longitudinally. Rate of cortical thinning varied with DISC1 genotype. Specifically, the rate of cortical thinning was attenuated in Phe-carrier compared with Leu-homozygous groups (in bilateral superior frontal and left angular gyri) and accelerated in Ser-homozygous compared with Cys-carrier groups (in left anterior cingulate and temporal cortices). Both SNPs additively predicted fixed differences in right lateral temporal CT, which were maximal between Phe-carrier/Ser-homozygous (thinnest) vs Leu-homozygous/Cys-carrier (thickest) groups. Leu607Phe and Ser704Cys genotype interacted to predict the rate of cortical thinning in right orbitofrontal, middle temporal and superior parietal cortices, wherein a significantly reduced rate of CT loss was observed in Phe-carrier/Cys-carrier participants only. Our findings argue for further examination of Leu607Phe and Ser704Cys interactions at a molecular level, and suggest that these SNPs might operate (in concert with other genetic and environmental factors) to shape risk for diverse phenotypes by impacting on the early maturation of fronto-temporal cortices.
精神分裂症相关蛋白 1(DISC1)包含两个常见的非同义单核苷酸多态性(SNP)——亮氨酸 607 苯丙氨酸(Leu607Phe)和丝氨酸 704 半胱氨酸(Ser704Cys)——这些 SNP 分别调节(i)DISC1 分子功能的多个方面,这些功能对皮质发育很重要;(ii)成人额颞皮质的解剖结构;(iii)多种精神疾病表型的风险,这些表型通常在儿童和青少年时期出现,并与额颞皮质发育改变有关。然而,目前尚不清楚 Leu607Phe 和 Ser704Cys 是否会影响成年前的皮质成熟,以及每个 SNP 是否表现出独特或重叠的影响。因此,我们将 Leu607Phe 和 Ser704Cys 的基因型与 255 名 9-22 岁的典型发育个体的皮质厚度(CT)相关联,这些个体在纵向采集了 598 次磁共振成像脑部扫描。皮质变薄的速度随 DISC1 基因型的不同而变化。具体来说,与 Leu 纯合子相比,Phe 携带者组(双侧额上回和左侧角回)的皮质变薄速度减慢,而 Ser 纯合子组(左侧前扣带回和颞叶皮质)的皮质变薄速度加快。两个 SNP 都可预测右侧外侧颞叶 CT 的固定差异,Phe 携带者/Ser 纯合子组(最薄)与 Leu 纯合子/Cys 携带者组(最厚)之间的差异最大。Leu607Phe 和 Ser704Cys 基因型相互作用,预测右侧眶额、中颞和上顶叶皮质的皮质变薄速度,仅在 Phe 携带者/Cys 携带者组中观察到皮质厚度损失率显著降低。我们的研究结果表明,需要进一步在分子水平上研究 Leu607Phe 和 Ser704Cys 的相互作用,并表明这些 SNP 可能通过影响额颞皮质的早期成熟,与其他遗传和环境因素一起,作用于多种表型的风险。