Keszler Gergely, Vékony Bálint, Elek Zsuzsanna, Nemoda Zsófia, Angyal Nóra, Bánlaki Zsófia, Kovács-Nagy Réka, Rónai Zsolt, Réthelyi János M
Department of Molecular Biology, Institute of Biochemistry and Molecular Biology, Semmelweis University, 1094 Budapest, Hungary.
Doctoral School, Semmelweis University, 1085 Budapest, Hungary.
Int J Mol Sci. 2024 Apr 19;25(8):4477. doi: 10.3390/ijms25084477.
Plasma levels of glial cell line-derived neurotrophic factor (GDNF), a pivotal regulator of differentiation and survival of dopaminergic neurons, are reportedly decreased in schizophrenia. To explore the involvement of GDNF in the pathogenesis of the disease, a case-control association analysis was performed between five non-coding single nucleotide polymorphisms (SNP) across the GDNF gene and schizophrenia. Of them, the 'G' allele of the rs11111 SNP located in the 3' untranslated region (3'-UTR) of the gene was found to associate with schizophrenia. In silico analysis revealed that the rs11111 'G' allele might create binding sites for three microRNA (miRNA) species. To explore the significance of this polymorphism, transient co-transfection assays were performed in human embryonic kidney 293T (HEK293T) cells with a luciferase reporter construct harboring either the 'A' or 'G' allele of the 3'-UTR of GDNF in combination with the hsa-miR-1185-1-3p pre-miRNA. It was demonstrated that in the presence of the rs11111 'G' (but not the 'A') allele, hsa-miR-1185-2-3p repressed luciferase activity in a dose-dependent manner. Deletion of the miRNA binding site or its substitution with the complementary sequence abrogated the modulatory effect. Our results imply that the rs11111 'G' allele occurring more frequently in patients with schizophrenia might downregulate GDNF expression in a miRNA-dependent fashion.
据报道,作为多巴胺能神经元分化和存活的关键调节因子,胶质细胞源性神经营养因子(GDNF)的血浆水平在精神分裂症患者中有所下降。为了探究GDNF在该疾病发病机制中的作用,我们对GDNF基因的五个非编码单核苷酸多态性(SNP)与精神分裂症进行了病例对照关联分析。其中,位于该基因3'非翻译区(3'-UTR)的rs11111 SNP的“G”等位基因被发现与精神分裂症相关。生物信息学分析表明,rs11111“G”等位基因可能会产生三个微小RNA(miRNA)物种的结合位点。为了探究这种多态性的意义,我们在人胚肾293T(HEK293T)细胞中进行了瞬时共转染实验,将携带GDNF 3'-UTR的“A”或“G”等位基因的荧光素酶报告基因构建体与hsa-miR-1185-1-3p前体miRNA共同转染。结果表明,在存在rs11111“G”(而非“A”)等位基因的情况下,hsa-miR-1185-2-3p以剂量依赖的方式抑制荧光素酶活性。删除miRNA结合位点或用互补序列替代它可消除这种调节作用。我们的结果表明,在精神分裂症患者中更频繁出现的rs11111“G”等位基因可能以miRNA依赖的方式下调GDNF表达。