Science. 2020 Mar 20;367(6484). doi: 10.1126/science.aay6690.
The cerebral cortex underlies our complex cognitive capabilities, yet little is known about the specific genetic loci that influence human cortical structure. To identify genetic variants that affect cortical structure, we conducted a genome-wide association meta-analysis of brain magnetic resonance imaging data from 51,665 individuals. We analyzed the surface area and average thickness of the whole cortex and 34 regions with known functional specializations. We identified 199 significant loci and found significant enrichment for loci influencing total surface area within regulatory elements that are active during prenatal cortical development, supporting the radial unit hypothesis. Loci that affect regional surface area cluster near genes in Wnt signaling pathways, which influence progenitor expansion and areal identity. Variation in cortical structure is genetically correlated with cognitive function, Parkinson's disease, insomnia, depression, neuroticism, and attention deficit hyperactivity disorder.
大脑皮层是我们复杂认知能力的基础,但对于影响人类皮质结构的特定基因座知之甚少。为了确定影响皮质结构的遗传变异,我们对 51665 个人的大脑磁共振成像数据进行了全基因组关联荟萃分析。我们分析了整个皮层的表面积和平均厚度,以及 34 个具有已知功能特化的区域。我们确定了 199 个显著的基因座,并发现了在皮质发育过程中活跃的调控元件内影响总表面积的基因座的显著富集,支持了放射状单位假说。影响区域表面积的基因座聚集在 Wnt 信号通路的基因附近,这些基因影响祖细胞的扩张和区域身份。皮质结构的变异与认知功能、帕金森病、失眠、抑郁、神经质和注意力缺陷多动障碍具有遗传相关性。