Weinreb Joshua T, Bowman Teresa V
Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY, USA.
Albert Einstein College of Medicine, Gottesman Institute for Stem Cell Biology and Regenerative Medicine, Bronx, NY, USA.
FEBS Lett. 2022 Nov;596(21):2736-2745. doi: 10.1002/1873-3468.14487. Epub 2022 Sep 9.
DEAD-box Helicase 41 (DDX41) is a member of the DExD/H-box helicase family that has a variety of cellular functions. Of note, germline and somatic mutations in the DDX41 gene are prevalently found in myeloid malignancies. Here, we present a comprehensive and analytic review covering relevant clinical, translational and basic science findings on DDX41. We first describe the initial characterisation of DDX41 mutations in patients affected by myelodysplastic syndromes, their associated clinical characteristics, and current treatment modalities. We then cover the known cellular functions of DDX41, spanning from its discovery in Drosophila as a neuroregulator through its more recently described roles in inflammatory signalling, R-loop metabolism and snoRNA processing. We end with a summary of the identified basic functions of DDX41 that when perturbed may contribute to the underlying pathology of haematologic neoplasms.
DEAD盒解旋酶41(DDX41)是DExD/H盒解旋酶家族的成员,具有多种细胞功能。值得注意的是,DDX41基因的种系和体细胞突变在髓系恶性肿瘤中普遍存在。在此,我们对DDX41的相关临床、转化和基础科学研究结果进行全面的分析性综述。我们首先描述了骨髓增生异常综合征患者中DDX41突变的初步特征、其相关的临床特征以及当前的治疗方式。然后,我们涵盖了DDX41已知的细胞功能,从其在果蝇中作为神经调节因子的发现,到其最近在炎症信号传导、R环代谢和小核仁RNA加工中所描述的作用。最后,我们总结了已确定的DDX41的基本功能,这些功能受到干扰时可能导致血液系统肿瘤的潜在病理变化。