Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes.

IF 11.1 Q1 CELL BIOLOGY
Guillaume Huguet, Thomas Renne, Cécile Poulain, Alma Dubuc, Kuldeep Kumar, Sayeh Kazem, Worrawat Engchuan, Omar Shanta, Elise Douard, Catherine Proulx, Martineau Jean-Louis, Zohra Saci, Josephine Mollon, Laura M Schultz, Emma E M Knowles, Simon R Cox, David Porteous, Gail Davies, Paul Redmond, Sarah E Harris, Gunter Schumann, Guillaume Dumas, Aurélie Labbe, Zdenka Pausova, Tomas Paus, Stephen W Scherer, Jonathan Sebat, Laura Almasy, David C Glahn, Sébastien Jacquemont
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引用次数: 0

Abstract

Copy-number variants (CNVs) that increase the risk for neurodevelopmental disorders also affect cognitive ability. However, such CNVs remain challenging to study due to their scarcity, limiting our understanding of gene-dosage-sensitive biological processes linked to cognitive ability. We performed a genome-wide association study (GWAS) in 258,292 individuals, which identified-for the first time-a duplication at 2q12.3 associated with higher cognitive performance. We developed a functional-burden analysis, which tested the association between cognition and CNVs disrupting 6,502 gene sets biologically defined across tissues, cell types, and ontologies. Among those, 864 gene sets were associated with cognition, and effect sizes of deletion and duplication were negatively correlated. The latter suggested that functions across all biological processes were sensitive to either deletions (e.g., subcortical regions, postsynaptic) or duplications (e.g., cerebral cortex, presynaptic). Associations between non-brain tissues and cognition were driven partly by constrained genes, which may shed light on medical comorbidities in neurodevelopmental disorders.

基因剂量对认知能力的影响:一项基于功能的脑和非脑过程关联研究。
增加神经发育障碍风险的拷贝数变异(CNV)也会影响认知能力。然而,由于这类 CNVs 数量稀少,研究起来仍具有挑战性,这限制了我们对与认知能力相关的基因剂量敏感性生物过程的了解。我们对 258292 人进行了全基因组关联研究(GWAS),首次发现了 2q12.3 的重复与较高的认知能力相关。我们进行了功能负担分析,测试了认知能力与破坏 6502 个基因组的 CNV 之间的关联,这些基因组在生物学上被定义为跨组织、跨细胞类型和跨本体。其中,864 个基因组与认知相关,缺失和重复的效应大小呈负相关。后者表明,所有生物过程的功能对缺失(如皮层下区域、突触后)或重复(如大脑皮层、突触前)都很敏感。非脑组织与认知之间的关联部分是由受限基因驱动的,这可能会揭示神经发育障碍的医学合并症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
7.10
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0.00%
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