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神经细胞黏附分子1基因上的启动子变体rs2301228赋予汉族人患精神分裂症的风险。

Promoter variant rs2301228 on the neural cell adhesion molecule 1 gene confers risk of schizophrenia in Han Chinese.

作者信息

Zhang Wen, Xiao Mei-Sheng, Ji Shuang, Tang Jinsong, Xu Ling, Li Xiao, Li Ming, Wang Hui-Zhen, Jiang Hong-Yan, Zhang Deng-Feng, Wang Jicai, Zhang Shuliang, Xu Xiu-Feng, Yu Li, Zheng Ping, Chen Xiaogang, Yao Yong-Gang

机构信息

Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences & Yunnan Province, Kunming Institute of Zoology, Kunming, Yunnan, China.

State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, China.

出版信息

Schizophr Res. 2014 Dec;160(1-3):88-96. doi: 10.1016/j.schres.2014.09.036. Epub 2014 Oct 16.

Abstract

BACKGROUND

Schizophrenia is recognized as a disorder of the brain and neuronal connectivity. The neural cell adhesion molecule 1 (NCAM1) gene plays a crucial role in regulating neuronal connectivity.

METHODS

We conducted a two-stage association analysis on 17 NCAM1 SNPs in two independent Han Chinese schizophrenia case-control cohorts (discovery sample from Hunan Province: 986 patients and 1040 normal controls; replication sample from Yunnan Province: 564 cases and 547 healthy controls). Allele, genotype and haplotype frequencies were compared between case and control samples. Transcription factor binding site prediction and luciferase reporter assays were employed to assess the potential function of promoter SNPs. We detected developmental changes at the transcriptional level of NCAM1 during neuron differentiation in Macaca mulatta neural progenitor cells (NPC). Serum levels of NCAM1 were measured in 72 cases and 88 controls.

RESULTS

A promoter variant, rs2301228, was found to be associated with schizophrenia at the allelic level and was validated in a replication cohort. Luciferase reporter assays demonstrated that risk allele rs2301228-A significantly down-regulated NCAM1 gene transcription compared to the G-allele. Concordantly, schizophrenia patients had a significantly lower level of serum NCAM1 compared to healthy donors. During the NPC neuronal differentiation, NCAM1 mRNA was significantly increased, suggesting a critical role of this gene in neural development.

CONCLUSIONS

Our results provide direct evidence for NCAM1 as a susceptibility gene for schizophrenia, which offers support to a neurodevelopmental model and neuronal connectivity hypothesis in the onset of schizophrenia.

摘要

背景

精神分裂症被认为是一种大脑和神经元连接的疾病。神经细胞黏附分子1(NCAM1)基因在调节神经元连接中起关键作用。

方法

我们在两个独立的汉族精神分裂症病例对照队列中对17个NCAM1单核苷酸多态性(SNP)进行了两阶段关联分析(来自湖南省的发现样本:986例患者和1040例正常对照;来自云南省的重复样本:564例病例和547例健康对照)。比较病例组和对照组样本之间的等位基因、基因型和单倍型频率。采用转录因子结合位点预测和荧光素酶报告基因检测来评估启动子SNP的潜在功能。我们检测了猕猴神经祖细胞(NPC)神经元分化过程中NCAM1转录水平的发育变化。测量了72例病例和88例对照的血清NCAM1水平。

结果

发现一个启动子变异体rs2301228在等位基因水平上与精神分裂症相关,并在重复队列中得到验证。荧光素酶报告基因检测表明,与G等位基因相比,风险等位基因rs2301228-A显著下调了NCAM1基因转录。同样,与健康供体相比,精神分裂症患者的血清NCAM1水平显著降低。在NPC神经元分化过程中,NCAM1 mRNA显著增加,表明该基因在神经发育中起关键作用。

结论

我们的结果为NCAM1作为精神分裂症的易感基因提供了直接证据,这为精神分裂症发病的神经发育模型和神经元连接假说提供了支持。

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