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DUT(p.Y116C)突变诱导的兔血小板减少症。

DUT (p.Y116C)-Mutation-Induced Thrombocytopenia in Rabbits.

作者信息

Fang Mengmeng, Yang Shujun, Liu Ruonan, Wu Xinyu, Jiang Liqiang, Yang Jie, Liu Xin, Wang Gerong, Mu Chao, Wang Xiuwen, Song Yuning

机构信息

State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases, Key Laboratory for Zoonosis Research of the Ministry of Education, and College of Veterinary Medicine, Jilin University, Changchun 130062, China.

College of Life Sciences, Jilin Normal University, No. 1301, Hai Feng Street, Tiexi District, Siping 136000, China.

出版信息

Int J Mol Sci. 2025 Apr 28;26(9):4169. doi: 10.3390/ijms26094169.

Abstract

Thrombocytopenia is a hematologic disorder characterized by an abnormally low platelet count in peripheral blood. Recent studies have identified mutations in DUT as the primary cause of bone marrow failure and diabetes mellitus syndrome (BMFDMS), a condition commonly associated with thrombocytopenia. In this study, a novel rabbit model of thrombocytopenia carrying the DUT c.3020A>G (p.Y116C) mutation was established using SpRY-ABEmax-mediated base editing. This model accurately recapitulates the clinical manifestations of human thrombocytopenia. Phenotypic analysis has revealed that mutant rabbits exhibited significant reductions in megakaryocyte numbers, platelet counts, and survival rates when compared to wild-type controls. Mechanistic investigations showed that the DUT mutation leads to mitochondrial structural abnormalities and functional impairments. Notably, platelets from DUT (p.Y116C)-mutant rabbits exhibited markedly reduced DUT protein expression and enhanced mitophagy, potentially mediated through the Park2 pathway. This study presents the first genetic model of thrombocytopenia that closely mimics the human DUT (p.Y116C) mutation, offering new insights into the relationship between DUT mutations and platelet function, and highlighting potential therapeutic targets for human thrombocytopenia.

摘要

血小板减少症是一种血液系统疾病,其特征为外周血中血小板计数异常降低。最近的研究已确定DUT基因的突变是骨髓衰竭和糖尿病综合征(BMFDMS)的主要病因,而BMFDMS通常与血小板减少症相关。在本研究中,利用SpRY-ABEmax介导的碱基编辑技术建立了一种携带DUT基因c.3020A>G(p.Y116C)突变的新型兔血小板减少症模型。该模型准确地再现了人类血小板减少症的临床表现。表型分析显示,与野生型对照相比,突变兔的巨核细胞数量、血小板计数和存活率均显著降低。机制研究表明,DUT突变导致线粒体结构异常和功能受损。值得注意的是,来自DUT(p.Y116C)突变兔的血小板表现出DUT蛋白表达明显降低,且线粒体自噬增强,这可能是通过Park2途径介导的。本研究提出了首个紧密模拟人类DUT(p.Y116C)突变的血小板减少症遗传模型,为DUT突变与血小板功能之间的关系提供了新的见解,并突出了人类血小板减少症潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e73f/12072063/f895a905d6e7/ijms-26-04169-g001.jpg

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