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基因剂量对认知能力的影响:一项基于功能的跨大脑和非大脑过程的关联研究。

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

作者信息

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

机构信息

Centre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, QC, Canada.

Centre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, QC, Canada; Department of Biochemistry and Molecular Medicine, Université de Montréal, Montréal, QC, Canada.

出版信息

Cell Genom. 2024 Dec 11;4(12):100721. doi: 10.1016/j.xgen.2024.100721.

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.

摘要

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,由于其稀缺性,此类CNV的研究仍然具有挑战性,这限制了我们对与认知能力相关的基因剂量敏感生物学过程的理解。我们对258292名个体进行了全基因组关联研究(GWAS),首次确定了2q12.3处的一个重复与较高的认知表现相关。我们开展了一项功能负担分析,测试认知与破坏6502个在组织、细胞类型和本体论上生物学定义的基因集的CNV之间的关联。其中,864个基因集与认知相关,缺失和重复的效应大小呈负相关。后者表明,所有生物学过程中的功能对缺失(如皮质下区域、突触后)或重复(如大脑皮质、突触前)均敏感。非脑组织与认知之间的关联部分由受限基因驱动,这可能为神经发育障碍中的医学共病提供线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b007/11701252/2fcc2d721a94/fx1.jpg

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