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全面综合分析鉴定 TYW5 为精神分裂症风险基因。

Comprehensive and integrative analyses identify TYW5 as a schizophrenia risk gene.

机构信息

Mental Health Center and Psychiatric Laboratory, the State Key Laboratory of Biotherapy, West China Hospital of Sichuan University, Chengdu, Sichuan, China.

Department of Neurobiology, Affiliated Mental Health Center & Hangzhou Seventh People's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, 310013, People's Republic of China.

出版信息

BMC Med. 2022 May 9;20(1):169. doi: 10.1186/s12916-022-02363-8.

Abstract

BACKGROUND

Identifying the causal genes at the risk loci and elucidating their roles in schizophrenia (SCZ) pathogenesis remain significant challenges. To explore risk variants associated with gene expression in the human brain and to identify genes whose expression change may contribute to the susceptibility of SCZ, here we report a comprehensive integrative study on SCZ.

METHODS

We systematically integrated the genetic associations from a large-scale SCZ GWAS (N = 56,418) and brain expression quantitative trait loci (eQTL) data (N = 175) using a Bayesian statistical framework (Sherlock) and Summary data-based Mendelian Randomization (SMR). We also measured brain structure of 86 first-episode antipsychotic-naive schizophrenia patients and 152 healthy controls with the structural MRI.

RESULTS

Both Sherlock (P = 3. 38 × 10) and SMR (P = 1. 90 × 10) analyses showed that TYW5 mRNA expression was significantly associated with risk of SCZ. Brain-based studies also identified a significant association between TYW5 protein abundance and SCZ. The single-nucleotide polymorphism rs203772 showed significant association with SCZ and the risk allele is associated with higher transcriptional level of TYW5 in the prefrontal cortex. We further found that TYW5 was significantly upregulated in the brain tissues of SCZ cases compared with controls. In addition, TYW5 expression was also significantly higher in neurons induced from pluripotent stem cells of schizophrenia cases compared with controls. Finally, combining analysis of genotyping and MRI data showed that rs203772 was significantly associated with gray matter volume of the right middle frontal gyrus and left precuneus.

CONCLUSIONS

We confirmed that TYW5 is a risk gene for SCZ. Our results provide useful information toward a better understanding of the genetic mechanism of TYW5 in risk of SCZ.

摘要

背景

确定风险基因座的因果基因并阐明它们在精神分裂症(SCZ)发病机制中的作用仍然是重大挑战。为了探索与人类大脑基因表达相关的风险变异,并确定其表达变化可能导致 SCZ 易感性的基因,我们在此报告了一项对 SCZ 的综合综合研究。

方法

我们使用贝叶斯统计框架(Sherlock)和基于汇总数据的孟德尔随机化(SMR)系统地整合了大规模 SCZ GWAS(N=56418)和大脑表达数量性状基因座(eQTL)数据(N=175)的遗传关联。我们还使用结构 MRI 测量了 86 名首发抗精神病药物治疗的精神分裂症患者和 152 名健康对照者的大脑结构。

结果

Sherlock(P=3.38×10)和 SMR(P=1.90×10)分析均显示 TYW5 mRNA 表达与 SCZ 风险显著相关。基于大脑的研究还确定了 TYW5 蛋白丰度与 SCZ 之间存在显著关联。单核苷酸多态性 rs203772 与 SCZ 显著相关,风险等位基因与前额叶皮质中 TYW5 的转录水平升高相关。我们进一步发现,与对照组相比,SCZ 病例的脑组织中 TYW5 显著上调。此外,与对照组相比,来自精神分裂症病例多能干细胞诱导的神经元中 TYW5 的表达也显著升高。最后,结合基因分型和 MRI 数据分析表明,rs203772 与右侧额中回和左侧楔前叶的灰质体积显著相关。

结论

我们证实 TYW5 是 SCZ 的风险基因。我们的研究结果为更好地理解 TYW5 在 SCZ 风险中的遗传机制提供了有用的信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a3/9082878/8f54bab16e19/12916_2022_2363_Fig1_HTML.jpg

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