INSERM, Unité Mixte de Recherche (UMR) 1170, Villejuif, France.
Université Paris XI, UMR 1170, Gustave Roussy, Villejuif, France.
Nat Genet. 2015 Oct;47(10):1131-40. doi: 10.1038/ng.3380. Epub 2015 Aug 17.
No major predisposition gene for familial myeloproliferative neoplasms (MPN) has been identified. Here we demonstrate that the autosomal dominant transmission of a 700-kb duplication in four genetically related families predisposes to myeloid malignancies, including MPN, frequently progressing to leukemia. Using induced pluripotent stem cells and primary cells, we demonstrate that overexpression of ATG2B and GSKIP enhances hematopoietic progenitor differentiation, including of megakaryocytes, by increasing progenitor sensitivity to thrombopoietin (TPO). ATG2B and GSKIP cooperate with acquired JAK2, MPL and CALR mutations during MPN development. Thus, the germline duplication may change the fitness of cells harboring signaling pathway mutations and increases the probability of disease development.
尚未发现家族性骨髓增生性肿瘤(MPN)的主要易感基因。在这里,我们证明了四个遗传相关家族中常染色体显性传递的 700kb 重复序列会导致髓系恶性肿瘤,包括 MPN,常进展为白血病。我们通过诱导多能干细胞和原代细胞证明,ATG2B 和 GSKIP 的过表达通过增加祖细胞对血小板生成素(TPO)的敏感性,增强造血祖细胞的分化,包括巨核细胞的分化。在 MPN 发展过程中,ATG2B 和 GSKIP 与获得性 JAK2、MPL 和 CALR 突变协同作用。因此,种系重复可能会改变携带信号通路突变的细胞的适应性,并增加疾病发展的可能性。