Department of Genetic, Faculty of Biological Science, Tarbiat Modares University, Tehran, Iran.
Department of Biology, Faculty of Science, Shahid Bahonar University of Kerman, Kerman, Iran.
Mol Biotechnol. 2023 Feb;65(2):243-251. doi: 10.1007/s12033-022-00494-0. Epub 2022 Apr 25.
Genetic studies of familial forms of Parkinson's disease (PD) have shown that the ZNF543 gene is a candidate gene that operates relevant to this disease. However, until now, there is no evidence for ZNF543 gene function in PD, and mechanisms resulting from its mutation have not been elucidated. Given the same genetic location of the ZNF543 gene with TRIM28 and their effects on PD pathogenesis, we surmised that ZNF543 might act as a transcription factor for TRIM28 gene expression. By knocking out the ZNF543 gene via the CRISPR/Cas9 editing platform, we assessed the functional effect of loss of expression of this gene on TRIM28 gene expression. Four sgRNAs with different PAM sequences were designed against two parts of the regulatory region of ZNF543 gene, and highly efficient disruption of ZNF543 expression in human neuroblastoma cell line was evaluated by polymerase chain reaction and T7 endonuclease assay. Moreover, evaluation of TRIM28 gene expression in ZNF543-knocked-out cells indicated a significant increase in TRIM28 gene expression, suggesting that ZNF543 probably regulates the expression of TRIM28. This approach offers a window into pinpointing the mechanism by which ZNF543 gene mutations mediate PD pathogenicity.
家族性帕金森病(PD)的遗传研究表明,ZNF543 基因是与该疾病相关的候选基因。然而,到目前为止,还没有证据表明 ZNF543 基因在 PD 中的功能,其突变导致的机制也尚未阐明。鉴于 ZNF543 基因与 TRIM28 具有相同的遗传位置,并且它们对 PD 发病机制有影响,我们推测 ZNF543 可能作为 TRIM28 基因表达的转录因子发挥作用。我们通过 CRISPR/Cas9 编辑平台敲除 ZNF543 基因,评估了该基因表达缺失对 TRIM28 基因表达的功能影响。针对 ZNF543 基因调控区的两个部分设计了 4 个具有不同 PAM 序列的 sgRNA,并通过聚合酶链反应和 T7 内切酶分析评估了其在人神经母细胞瘤细胞系中对 ZNF543 表达的高效破坏。此外,对 ZNF543 敲除细胞中 TRIM28 基因表达的评估表明,TRIM28 基因表达显著增加,提示 ZNF543 可能调节 TRIM28 的表达。这种方法为确定 ZNF543 基因突变介导 PD 发病机制的机制提供了一个切入点。