Madrer Nimrod, Vaknine-Treidel Shani, Zorbaz Tamara, Tzur Yonat, Bennett Estelle R, Drori Paz, Suissa Nitzan, Greenberg David S, Lerner Eitan, Soreq Eyal, Paldor Iddo, Soreq Hermona
Edmond and Lily Safra Center for Brain Sciences, Hebrew University of Jerusalem, Jerusalem, Israel.
Department of Biological Chemistry, Alexander Silberman Institute of Life Sciences, Faculty of Mathematics and Science, Hebrew University of Jerusalem, Jerusalem, Israel.
Nat Aging. 2025 May;5(5):868-882. doi: 10.1038/s43587-025-00851-z. Epub 2025 Apr 11.
Early, efficient Parkinson's disease (PD) tests may facilitate pre-symptomatic diagnosis and disease-modifying therapies. Here we report elevated levels of PD-specific transfer RNA fragments carrying a conserved sequence motif (RGTTCRA-tRFs) in the substantia nigra, cerebrospinal fluid and blood of patients with PD. A whole blood qPCR test detecting elevated RGTTCRA-tRFs and reduced mitochondrial-originated tRFs (MT-tRFs) segregated pre-symptomatic patients with PD from controls (area under the receiver operating characteristic curve (ROC-AUC) of 0.75 versus 0.71 based on traditional clinical scoring). Strengthening PD relevance, patients carrying PD-related mutations presented higher blood RGTTCRA-tRFs/MT-tRFs ratios than mutation-carrying non-symptomatic controls, and RGTTCRA-tRF levels decreased in patients' blood after deep brain stimulation. Furthermore, RGTTCRA-tRFs complementarity to ribosomal RNA and the translation-supporting LeuCAG3-tRF might aggravate PD via translational inhibition, as reflected by disrupted ribosomal association of RGTTCRA-tRFs in depolarized neuroblastoma cells. Our findings show tRF involvement in PD and suggest a potential simple and safe blood test that may aid clinicians in pre-symptomatic PD diagnosis after validation in larger independent cohorts.
早期、高效的帕金森病(PD)检测可能有助于症状前诊断和疾病修饰疗法。在此,我们报告在PD患者的黑质、脑脊液和血液中,携带保守序列基序(RGTTCRA-tRFs)的PD特异性转移RNA片段水平升高。一项全血定量聚合酶链反应(qPCR)检测可检测到RGTTCRA-tRFs升高和线粒体来源的tRFs(MT-tRFs)减少,该检测将症状前PD患者与对照组区分开来(基于传统临床评分,受试者工作特征曲线下面积(ROC-AUC)为0.75,而对照组为0.71)。与PD相关性更强的是,携带PD相关突变的患者血液中RGTTCRA-tRFs/MT-tRFs比值高于携带突变的无症状对照组,并且在深部脑刺激后患者血液中RGTTCRA-tRF水平降低。此外,RGTTCRA-tRFs与核糖体RNA的互补性以及支持翻译的LeuCAG3-tRF可能通过翻译抑制加重PD,这在去极化神经母细胞瘤细胞中RGTTCRA-tRFs与核糖体的结合被破坏中得到体现。我们的研究结果表明tRF参与了PD,并提示一种潜在的简单安全的血液检测方法,在更大规模的独立队列中验证后可能有助于临床医生进行症状前PD诊断。