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与遗传性大血小板减少症相关的新型突变T853fs

Novel mutation T853fs associated with inherited macrothrombocytopenia.

作者信息

Xie Haixiao, Tang Shiyi, Shao Jianmin, Yang Ming, Tong Huida, Zhang Linhua, Zhong Mingzhu, Yu Xiaomin, Bi Laixi, Wang Yuming, Ou Rongying, Ling Chen, Zhu Liqing

机构信息

Department of Clinical Laboratory, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang 325000, China.

Department of Blood Transfusion, Zhuzhou Center Hospital, Zhuzhou, Hunan 412000, China.

出版信息

Mol Ther Nucleic Acids. 2025 May 7;36(2):102554. doi: 10.1016/j.omtn.2025.102554. eCollection 2025 Jun 10.

Abstract

-related inherited thrombocytopenia (-related IT) is a hereditary disorder involving ribosomopathy and platelet dysfunction. Affected patients exhibit significant bleeding tendencies. To date, five affected pedigrees have been reported, all harboring mutations within the "ATPase associated with diverse cellular activities" (AAA) domain. In this study, we identified a novel T853fs variant located in the "helicase" domain. SLFN14 expression was markedly reduced in platelets from the patients and in Meg-01 cells transfected with T853fs plasmid. Functional assays revealed a defection of T853fs variant in both arachidonic acid (AA)-induced aggregation and fibrinogen-induced adhesion. Unlike previously reported mutations in the AAA domain, which significantly upregulate ribosomal protein genes and mitochondrial translation pathways, the T853fs mutation identified in this study did not affect mitochondrial translation. Immunofluorescence assay showed that T853fs variant exhibited diffuse cytoplasmic localization. Further RNA sequencing (RNA-seq) analysis revealed the significant regulation of T853fs mutation on pathways related to ion channels and dense granule, which are crucial to platelet function. In conclusion, this study identifies a new mutation and highlights the phenotypic diversity of SLFN14-RT.

摘要

相关遗传性血小板减少症(-相关IT)是一种涉及核糖体病和血小板功能障碍的遗传性疾病。受影响的患者表现出明显的出血倾向。迄今为止,已报道了五个受影响的家系,所有家系在“与多种细胞活动相关的ATP酶”(AAA)结构域内都存在突变。在本研究中,我们鉴定了一个位于“解旋酶”结构域的新型T853fs变体。患者血小板和转染T853fs质粒的Meg-01细胞中SLFN14表达明显降低。功能测定显示T853fs变体在花生四烯酸(AA)诱导的聚集和纤维蛋白原诱导的粘附中均存在缺陷。与先前报道的AAA结构域突变不同,先前报道的突变显著上调核糖体蛋白基因和线粒体翻译途径,而本研究中鉴定的T853fs突变不影响线粒体翻译。免疫荧光测定显示T853fs变体表现出弥漫性细胞质定位。进一步的RNA测序(RNA-seq)分析揭示了T853fs突变对与离子通道和致密颗粒相关途径的显著调节,这些途径对血小板功能至关重要。总之,本研究鉴定了一个新的突变,并突出了SLFN14-RT的表型多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fdb/12159219/569abaeb3de6/fx1.jpg

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