The INO80E at 16p11.2 locus increases risk of schizophrenia in humans and induces schizophrenia-like phenotypes in mice.

IF 9.7 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL EBioMedicine Pub Date : 2025-03-14 DOI:10.1016/j.ebiom.2025.105645
Bo Hu, Mei-Yu Yin, Chu-Yi Zhang, Zhe Shi, Lu Wang, Xiaoming Lei, Ming Li, Shi-Wu Li, Qin-Hui Tuo
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Abstract

Background: Chromosome 16p11.2 is one of the most significant loci in the genome-wide association studies (GWAS) of schizophrenia. Despite several integrative analyses and functional genomics studies having been carried out to identify possible risk genes, their impacts in the pathogenesis of schizophrenia remain to be fully characterized.

Methods: We performed expression quantitative trait loci (eQTL) and summary-data-based Mendelian randomization (SMR) analyses to identify schizophrenia risk genes in the 16p11.2 GWAS locus. We constructed a murine model with dysregulated expression of risk gene in the medial prefrontal cortex (mPFC) using stereotaxic injection of adeno-associated virus (AAV), followed by behavioural assessments, dendritic spine analyses and RNA sequencing.

Findings: We identified significant associations between elevated INO80E mRNA expression in the frontal cortex and risk of schizophrenia. The mice overexpressing Ino80e in mPFC (Ino80e-OE) exhibited schizophrenia-like behaviours, including increased anxiety behaviour, anhedonia, and impaired prepulse inhibition (PPI) when compared with control group. The neuronal sparse labelling assay showed that the density of stubby spines in the pyramidal neurons of mPFC was significantly increased in Ino80e-OE mice compared with control mice. Transcriptomic analysis in the mPFC revealed significant alterations in the mRNA levels of schizophrenia-related genes and processes related to synapses upon overexpressing Ino80e.

Interpretation: Our results suggest that upregulation of the Ino80e gene in mPFC may induce schizophrenia-like behaviours in mice, further supporting the hypothesis that INO80E is an authentic risk gene.

Funding: This project received support from the National Key Research and Development Program of China, National Natural Science Foundation of China, Key Research and Development Projects of Hunan Provincial Science and Technology Department, Science and Technology Innovation team of Hunan Province, etc.

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16p11.2 基因座上的 INO80E 会增加人类患精神分裂症的风险,并诱导小鼠出现类似精神分裂症的表型。
背景:染色体16p11.2是精神分裂症全基因组关联研究(GWAS)中最重要的基因位点之一。尽管已经开展了多项综合分析和功能基因组学研究来确定可能的风险基因,但这些基因在精神分裂症发病机制中的影响仍有待全面鉴定:我们对16p11.2 GWAS位点进行了表达量性状位点(eQTL)和基于汇总数据的孟德尔随机化(SMR)分析,以确定精神分裂症风险基因。我们利用立体定向注射腺相关病毒(AAV)的方法构建了内侧前额叶皮层(mPFC)风险基因表达失调的小鼠模型,随后进行了行为评估、树突棘分析和 RNA 测序:我们发现额叶皮层中 INO80E mRNA 表达量的升高与精神分裂症风险之间存在明显的关联。与对照组相比,在mPFC中过表达Ino80e的小鼠(Ino80e-OE)表现出类似精神分裂症的行为,包括焦虑行为增加、失张力和冲动前抑制(PPI)受损。神经元稀疏标记实验表明,与对照组相比,Ino80e-OE 小鼠 mPFC 锥体神经元中的短棘密度显著增加。mPFC的转录组分析显示,过度表达Ino80e后,精神分裂症相关基因和突触相关过程的mRNA水平发生了显著变化:我们的研究结果表明,Ino80e基因在mPFC中的上调可能诱导小鼠出现类似精神分裂症的行为,进一步支持了INO80E是一个真实的风险基因的假说:本项目得到了国家重点研发计划、国家自然科学基金、湖南省科技厅重点研发项目、湖南省科技创新团队等的支持。
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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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