Centre for Neuroimaging, Cognition and Genomics (NICOG), School of Biological and Chemical Sciences and School of Psychology, University of Galway, University Road, Galway, H91 CF50, Ireland.
Discipline of Bioinformatics, School of Mathematical and Statistical Sciences, University of Galway, University Road, Galway, H91 CF50, Ireland.
Hum Mol Genet. 2023 Nov 3;32(22):3194-3203. doi: 10.1093/hmg/ddad142.
The myocyte enhancer factor 2 C (MEF2C) gene encodes a transcription factor important for neurogenesis and synapse development and contains common variants associated with intelligence (IQ) and educational attainment (EA). Here, we took gene expression data from the mouse cortex of a Mef2c mouse model with a heterozygous DNA binding-deficient mutation of Mef2c (Mef2c-het) and combined these data with MEF2C ChIP-seq data from cortical neurons and single-cell data from the mouse brain. This enabled us to create a set of genes that were differentially regulated in Mef2c-het mice, represented direct target genes of MEF2C and had elevated in expression in cortical neurons. We found this gene-set to be enriched for genes containing common genetic variation associated with IQ and EA. Genes within this gene-set that were down-regulated, i.e. have reduced expression in Mef2c-het mice versus controls, were specifically significantly enriched for both EA and IQ associated genes. These down-regulated genes were enriched for functionality in the adenylyl cyclase signalling system, which is known to positively regulate synaptic transmission and has been linked to learning and memory. Within the adenylyl cyclase signalling system, three genes regulated by MEF2C, CRHR1, RGS6, and GABRG3, are associated at genome-wide significant levels with IQ and/or EA. Our results indicate that genetic variation in MEF2C and its direct target genes within cortical neurons contribute to variance in cognition within the general population, and the molecular mechanisms involved include the adenylyl cyclase signalling system's role in synaptic function.
肌细胞增强因子 2 C(MEF2C)基因编码一种对神经发生和突触发育很重要的转录因子,其包含与智力(IQ)和教育程度(EA)相关的常见变体。在这里,我们利用 Mef2c 杂合 DNA 结合缺陷突变的 Mef2c 小鼠模型(Mef2c-het)的小鼠皮质的基因表达数据,将这些数据与皮质神经元的 MEF2C ChIP-seq 数据和小鼠大脑的单细胞数据相结合。这使我们能够创建一组在 Mef2c-het 小鼠中差异表达的基因,这些基因是 MEF2C 的直接靶基因,并且在皮质神经元中的表达水平升高。我们发现这个基因集富集了与 IQ 和 EA 相关的常见遗传变异的基因。这个基因集中下调的基因,即与对照相比在 Mef2c-het 小鼠中表达减少的基因,特别显著富集与 EA 和 IQ 相关的基因。这些下调的基因在腺苷酸环化酶信号系统中具有功能富集,该系统已知可正向调节突触传递,并与学习和记忆有关。在腺苷酸环化酶信号系统中,三个受 MEF2C 调节的基因,即 CRHR1、RGS6 和 GABRG3,与 IQ 和/或 EA 具有全基因组显著相关。我们的研究结果表明,皮质神经元中 MEF2C 及其直接靶基因的遗传变异会导致一般人群认知能力的差异,涉及的分子机制包括腺苷酸环化酶信号系统在突触功能中的作用。