ATP6V1D和GPHN基因多态性与中国人群抑郁症的关系及功能研究

IF 3.9 4区 医学 Q1 PSYCHIATRY
Peng Liang, Jing-Jie Chen, Xue Yang, Rui Long, Yue Li, Zi-Ling Wang, Ping-Liang Yang, Yun-Dan Liang
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引用次数: 0

摘要

背景:抑郁症是一种全球性的重大社会负担疾病。单核苷酸多态性(snp)与抑郁症的发展有关。本研究旨在探讨GPHN和ATP6V1D基因启动子区域多态性与中国人群抑郁易感性的关系。目的:为识别snp预测中国人群抑郁症提供新的见解。方法:我们进行了一项病例对照研究,涉及555名抑郁症患者和509名健康对照。启动子区域的GPHN rs8020095和ATP6V1D rs3759755、rs10144417、rs2031564和rs8016024采用新一代测序进行基因分型。使用双荧光素酶报告基因来评估每种SNP基因型启动子区域的转录活性,并使用JASPAR数据库预测转录因子与每个位点的结合。结果:与健康对照组相比,ATP6V1D启动子rs10144417 AG基因型(P = 0.015)、rs3759755 AC/CC基因型(P = 0.036)和GPHN基因rs8020095 GA和AA基因型(GA: P = 0.028, GG: P = 0.025)与抑郁症患病率降低显著相关。5个snp存在连锁不平衡,患者的AGATA单倍型频率显著低于健康受试者(P = 0.023)。重组质粒rs3759755-A的荧光素酶活性显著高于重组质粒rs3759755-C (P = 0.026),重组质粒rs8020095-A的荧光素酶活性显著高于重组质粒rs8020095-G (P = 0.001)。转录因子orthodenticle homeobox 2、orthodenticle homeobox 1、forkhead box L1、NK homeobox 3-1和核因子interleukin 3调节与rs3759755A > C和rs8020095A > g具有结合亲和力。结论:本研究证实ATP6V1D启动子区域的SNP (rs3759755和rs10144417)和GPHN的SNP (rs8020095)确实与抑郁症易感性相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association and functional study of ATP6V1D and GPHN gene polymorphisms with depression in Chinese population.

Background: Depression is a disease with a significant global social burden. Single nucleotide polymorphisms (SNPs) are correlated with the development of depression. This study investigates the relationship between polymorphisms in the GPHN and ATP6V1D gene promoter regions and susceptibility to depression in the Chinese population.

Aim: To provide new insights into identifying SNPs for predicting depression in the Chinese population.

Methods: We conducted a case-control study involving 555 individuals with depression and 509 healthy controls. GPHN rs8020095 and ATP6V1D rs3759755, rs10144417, rs2031564, and rs8016024 in the promoter region were genotyped using next-generation sequencing. Dual luciferase reporter genes were employed to assess the transcriptional activity of promoter regions for each SNP genotype, with transcription factors binding to each site predicted using the JASPAR database.

Results: Compared to healthy controls, the ATP6V1D promoter rs10144417 AG genotype (P = 0.015), rs3759755 AC/CC genotype (P = 0.036), and GPHN gene rs8020095 GA and AA genotypes (GA: P = 0.028, GG: P = 0.025) were significantly associated with a lower prevalence of depression. Linked disequilibria were present in five SNPs, with the AGATA haplotype frequency in patients significantly lower than in healthy subjects (P = 0.023). Luciferase activity of the rs3759755-A recombinant plasmid was significantly higher than that of the rs3759755-C recombinant plasmid (P = 0.026), and the rs8020095-A recombinant plasmid activity was significantly higher than that of the rs8020095-G recombinant plasmid (P = 0.001). Transcription factors orthodenticle homeobox 2, orthodenticle homeobox 1, forkhead box L1, NK homeobox 3-1, and nuclear factor, interleukin 3 regulated demonstrated binding affinity with rs3759755A > C and rs8020095A > G.

Conclusion: This study demonstrates that SNPs (rs3759755 and rs10144417) in the promoter region of the ATP6V1D and SNP (rs8020095) of GPHN are indeed associated with susceptibility to depression.

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来源期刊
自引率
6.50%
发文量
110
期刊介绍: The World Journal of Psychiatry (WJP) is a high-quality, peer reviewed, open-access journal. The primary task of WJP is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of psychiatry. In order to promote productive academic communication, the peer review process for the WJP is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJP are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in psychiatry.
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