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通过全外显子组测序鉴定房室结折返性心动过速中的潜在候选基因和信号通路。

Identification of potential candidate genes and pathways in atrioventricular nodal reentry tachycardia by whole-exome sequencing.

作者信息

Luo Rong, Zheng Chenqing, Yang Hao, Chen Xuepin, Jiang Panpan, Wu Xiushan, Yang Zhenglin, Shen Xia, Li Xiaoping

机构信息

Institute of Geriatric Cardiovascular Disease, Chengdu Medical College, Chengdu, People's Republic of China.

State Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, China.

出版信息

Clin Transl Med. 2020 Jan;10(1):238-257. doi: 10.1002/ctm2.25.

Abstract

BACKGROUND

Atrioventricular nodal reentry tachycardia (AVNRT) is the most common manifestation of paroxysmal supraventricular tachycardia (PSVT). Increasing data have indicated familial clustering and participation of genetic factors in AVNRT, and no pathogenic genes related to AVNRT have been reported.

METHODS

Whole-exome sequencing (WES) was performed in 82 patients with AVNRT and 100 controls. Reference genes, genome-wide association analysis, gene-based collapsing, and pathway enrichment analysis were performed. A protein-protein interaction (PPI) network was then established; WES database in the UK Biobank and one only genetic study of AVNRT in Denmark were used for external data validation.

RESULTS

Among 95 reference genes, 126 rare variants in 48 genes were identified in the cases (minor allele frequency < 0.001). Gene-based collapsing analysis and pathway enrichment analysis revealed six functional pathways related to AVNRT as with neuronal system/neurotransmitter release cycles and ion channel/cardiac conduction among the top 30 enriched pathways, and then 36 candidate pathogenic genes were selected. By combining with PPI analysis, 10 candidate genes were identified, including RYR2, NOS1, SCN1A, CFTR, EPHB4, ROBO1, PRKAG2, MMP2, ASPH, and ABCC8. From the UK Biobank database, 18 genes from candidate genes including SCN1A, PRKAG2, NOS1, and CFTR had rare variants in arrhythmias, and the rare variants in PIK3CB, GAD2, and HIP1R were in patients with PSVT. Moreover, one rare variant of RYR2 (c.4652A > G, p.Asn1551Ser) in our study was also detected in the Danish study. Considering the gene functional roles and external data validation, the most likely candidate genes were SCN1A, PRKAG2, RYR2, CFTR, NOS1, PIK3CB, GAD2, and HIP1R.

CONCLUSION

The preliminary results first revealed potential candidate genes such as SCN1A, PRKAG2, RYR2, CFTR, NOS1, PIK3CB, GAD2, and HIP1R, and the pathways mediated by these genes, including neuronal system/neurotransmitter release cycles or ion channels/cardiac conduction, might be involved in AVNRT.

摘要

背景

房室结折返性心动过速(AVNRT)是阵发性室上性心动过速(PSVT)最常见的表现形式。越来越多的数据表明AVNRT存在家族聚集现象且遗传因素参与其中,但尚未有与AVNRT相关的致病基因被报道。

方法

对82例AVNRT患者和100例对照进行全外显子测序(WES)。进行了参考基因、全基因组关联分析、基于基因的合并分析和通路富集分析。随后建立了蛋白质-蛋白质相互作用(PPI)网络;使用英国生物银行的WES数据库和丹麦一项仅有的AVNRT基因研究进行外部数据验证。

结果

在95个参考基因中,病例组中48个基因鉴定出126个罕见变异(次要等位基因频率<0.001)。基于基因的合并分析和通路富集分析显示,在前30个富集通路中,有6个与AVNRT相关的功能通路,如神经系统/神经递质释放周期和离子通道/心脏传导,然后选择了36个候选致病基因。结合PPI分析,鉴定出10个候选基因,包括RYR2、NOS1、SCN1A、CFTR、EPHB4、ROBO1、PRKAG2、MMP2、ASPH和ABCC8。从英国生物银行数据库中,包括SCN1A、PRKAG2、NOS1和CFTR在内的候选基因中的18个基因在心律失常中有罕见变异,PIK3CB、GAD2和HIP1R中的罕见变异存在于PSVT患者中。此外,丹麦研究中也检测到了我们研究中RYR2的一个罕见变异(c.4652A>G,p.Asn1551Ser)。考虑到基因功能作用和外部数据验证,最可能的候选基因是SCN1A、PRKAG2、RYR2、CFTR、NOS1、PIK3CB、GAD2和HIP1R。

结论

初步结果首次揭示了潜在的候选基因,如SCN1A、PRKAG2、RYR2、CFTR、NOS1、PIK3CB、GAD2和HIP1R,以及由这些基因介导的通路,包括神经系统/神经递质释放周期或离子通道/心脏传导,可能参与AVNRT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66c0/7240861/bdf8355634a9/CTM2-10-238-g001.jpg

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