RNA剪接
生物
拼接因子
髓样
突变
遗传学
表型
骨髓增生异常综合症
疾病
选择性拼接
体细胞
癌症研究
核糖核酸
基因
造血
RNA结合蛋白
点突变
种系突变
髓系白血病
作者
Mario Cazzola,Seishi Ogawa
出处
期刊:Blood
[Elsevier BV]
日期:2026-10-26
标识
DOI:10.1182/blood.2026035568
摘要
The discovery of recurrent somatic mutations affecting the RNA splicing machinery in 2011 revealed an unexpected class of driver mutations in hematologic malignancies. Remarkably, splicing factor (SF) mutations have emerged as some of the most frequent genetic lesions in myelodysplastic syndromes (MDS) and other dysplastic myeloid neoplasms, establishing aberrant RNA splicing as a major pathogenetic pathway in myeloid neoplasia. Subsequent studies have delineated their mutation-specific effects on RNA splicing and established their strong genotype-phenotype associations; consequently, SF mutations are now incorporated into contemporary disease classification and prognostic models. However, the mechanisms underlying their positive clonal selection and striking genotype-phenotype associations remain poorly understood, with co-mutations, clonal architecture, aging, and the hematopoietic microenvironment acting as important modifiers of disease expression. Elucidating how SF mutations interact with these modifiers to shape clonal fitness and disease phenotype remains a key challenge, while translating these biological insights into effective therapies represents the ultimate clinical goal.
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