Nephrology Hospital, The First Affiliated Hospital of Zhengzhou University, Institute of Nephrology, Zhengzhou University, No.1, Jianshe Road, Erqi District, Zhengzhou, 4500052, Henan, People's Republic of China.
School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, People's Republic of China.
Sci Rep. 2021 Mar 4;11(1):5186. doi: 10.1038/s41598-021-84236-3.
Systemic lupus erythematosus (SLE) is a typical autoimmune disease with a strong genetic disposition. Genetic studies have revealed that single-nucleotide polymorphisms (SNPs) in zinc finger protein (ZNF)-coding genes are associated with susceptibility to autoimmune diseases, including SLE. The objective of the current study was to evaluate the correlation between ZNF76 gene polymorphisms and SLE risk in Chinese populations. A total of 2801 individuals (1493 cases and 1308 controls) of Chinese Han origin were included in this two-stage genetic association study. The expression of ZNF76 was evaluated, and integrated bioinformatic analysis was also conducted. The results showed that 28 SNPs were associated with SLE susceptibility in the GWAS cohort, and the association of rs10947540 was successfully replicated in the independent replication cohort (P = 1.60 × 10, OR 1.19, 95% CI 1.03-1.37). After meta-analysis, the association between rs10947540 and SLE was pronounced (P = 9.62 × 10, OR 1.29, 95% CI 1.15-1.44). Stratified analysis suggested that ZNF76 rs10947540 C carriers were more likely to develop relatively high levels of serum creatinine (Scr) than noncarriers (CC + CT vs. TT, p = 9.94 × 10). The bioinformatic analysis revealed that ZNF76 rs10947540 was annotated as an eQTL and that rs10947540 was correlated with decreased expression of ZNF76. Remarkably, significantly reduced expression of ZNF76 was confirmed by expression data from both our laboratory and an array-based expression database. Taken together, these results suggest that ZNF76 rs10947540 is a possible susceptibility factor associated with SLE susceptibility. The mechanism underlying the relationship between ZNF76 and SLE pathogenesis still requires further investigation.
系统性红斑狼疮(SLE)是一种典型的具有强烈遗传倾向的自身免疫性疾病。遗传研究表明,锌指蛋白(ZNF)编码基因中的单核苷酸多态性(SNPs)与自身免疫性疾病(包括 SLE)的易感性相关。本研究旨在评估中国人群中 ZNF76 基因多态性与 SLE 易感性的相关性。这项两阶段遗传关联研究共纳入了 2801 名中国汉族个体(1493 例病例和 1308 例对照)。评估了 ZNF76 的表达,并进行了综合的生物信息学分析。结果显示,在 GWAS 队列中,28 个 SNP 与 SLE 易感性相关,rs10947540 的关联在独立的复制队列中得到了成功复制(P=1.60×10,OR 1.19,95%CI 1.03-1.37)。经荟萃分析,rs10947540 与 SLE 的关联更为显著(P=9.62×10,OR 1.29,95%CI 1.15-1.44)。分层分析表明,ZNF76 rs10947540 C 携带者发生相对较高水平血清肌酐(Scr)的可能性高于非携带者(CC+CT 与 TT,p=9.94×10)。生物信息学分析表明,ZNF76 rs10947540 被注释为一个 eQTL,rs10947540 与 ZNF76 表达降低相关。值得注意的是,我们实验室和基于阵列的表达数据库的表达数据均证实 ZNF76 的表达明显降低。综上所述,这些结果表明 ZNF76 rs10947540 是一个可能与 SLE 易感性相关的易感因素。ZNF76 与 SLE 发病机制之间的关系的机制仍需要进一步研究。