Pirota Valentina, Rey Federica, Esposito Letizia, Fantini Valentina, Pandini Cecilia, Maghraby Erika, Di Gerlando Rosalinda, Doria Filippo, Mella Mariella, Pansarasa Orietta, Gandellini Paolo, Freccero Mauro, Carelli Stephana, Cereda Cristina
Department of Chemistry, University of Pavia, Pavia, Italy; G4-INTERACT, USERN, Pavia, Italy.
G4-INTERACT, USERN, Pavia, Italy; Pediatric Clinical Research Center "Fondazione Romeo ed Enrica Invernizzi", Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy; Center of Functional Genomics and Rare diseases, Buzzi Children's Hospital, Milan, Italy.
Int J Biol Macromol. 2024 Oct;277(Pt 4):134417. doi: 10.1016/j.ijbiomac.2024.134417. Epub 2024 Aug 3.
Alpha-synuclein, encoded by the SNCA gene, is a pivotal protein implicated in the pathogenesis of synucleinopathies, including Parkinson's disease. Current approaches for modulating alpha-synuclein levels involve antisense nucleotides, siRNAs, and small molecules targeting SNCA's 5'-UTR mRNA. Here, we propose a groundbreaking strategy targeting G-quadruplex structures to effectively modulate SNCA gene expression and lowering alpha-synuclein amount. Novel G-quadruplex sequences, identified on the SNCA gene's transcription starting site and 5'-UTR of SNCA mRNAs, were experimentally confirmed for their stability through biophysical assays and in vitro experiments on human genomic DNA. Biological validation in differentiated SH-SY5Y cells revealed that well-known G-quadruplex ligands remarkably stabilized these structures, inducing the modulation of SNCA mRNAs expression, and the effective decrease in alpha-synuclein amount. Besides, a novel peptide nucleic acid conjugate, designed to selectively disrupt of G-quadruplex within the SNCA gene promoter, caused a promising lowering of both SNCA mRNA and alpha-synuclein protein. Altogether our findings highlight G-quadruplexes' key role as intriguing biological targets in achieving a notable and successful reduction in alpha-synuclein expression, pointing to a novel approach against synucleinopathies.
由SNCA基因编码的α-突触核蛋白是一种关键蛋白,与包括帕金森病在内的突触核蛋白病的发病机制有关。目前调节α-突触核蛋白水平的方法包括反义核苷酸、小干扰RNA和靶向SNCA基因5'-UTR mRNA的小分子。在此,我们提出了一种开创性的策略,即靶向G-四链体结构以有效调节SNCA基因表达并降低α-突触核蛋白的含量。在SNCA基因的转录起始位点和SNCA mRNA的5'-UTR上鉴定出的新型G-四链体序列,通过生物物理测定和对人类基因组DNA的体外实验,实验证实了它们的稳定性。在分化的SH-SY5Y细胞中的生物学验证表明,著名的G-四链体配体显著稳定了这些结构,诱导了SNCA mRNA表达的调节,并有效降低了α-突触核蛋白的含量。此外,一种设计用于选择性破坏SNCA基因启动子内G-四链体的新型肽核酸偶联物,有望降低SNCA mRNA和α-突触核蛋白的含量。总之,我们的研究结果突出了G-四链体作为有趣的生物学靶点在显著且成功降低α-突触核蛋白表达方面的关键作用,为治疗突触核蛋白病指出了一种新方法。