Ishikawa Maho, Yagasaki Fumiharu, Okamura Daisuke, Maeda Tomoya, Sugahara Yuichi, Jinnai Itsuro, Bessho Masami
Division of Hematology, Department of Internal Medicine, Faculty of Medicine, Saitama Medical University, Saitama, Japan.
Int J Hematol. 2007 Oct;86(3):238-45. doi: 10.1532/IJH97.07054.
We identified a novel gene fusion of ANKRD28 (ankyrin repeat domain 28) on 3p25 to NUP98 on 11p15 in a patient with adult myelodysplastic syndrome/acute myelogenous leukemia. A partially cryptic 3-way translocation, t(3;5;11)(p25;q35;p15), that had initially been supposed to be t(3;5)(p25;q35) was revealed by precise breakpoint mapping via fluorescence in situ hybridization analysis with bacterial artificial chromosome clones. This translocation produces the expression of 2 in-frame fusion transcripts, the novel ANKRD28-NUP98 and NUP98-NSD1, and 1 out-of-frame NSD1-ANKRD28 transcript. Transient overexpression of ANKRD28-NUP98 in NIH/3T3 cells, but not the C-terminal deletion mutant of ANKRD28 (DeltaC-ANKRD28), caused significantly increased focus formation compared with mock-transfectant controls. ANKRD28-NUP98 was localized in the nucleolus and cytoplasm, whereas ANKRD28 and DeltaC-ANKRD28 were found exclusively in the cytoplasm. Alteration of the subcellular localization of ANKRD28 might have contributed to the leukemogenesis in this case. This report is the first of ANKRD28 as an NUP98 fusion partner, and this case implies that this fusion may be responsible for hematologic malignancies.
我们在一名成年骨髓增生异常综合征/急性髓系白血病患者中鉴定出一个新的基因融合,即3p25上的ANKRD28(锚蛋白重复结构域28)与11p15上的NUP98融合。通过使用细菌人工染色体克隆进行荧光原位杂交分析的精确断点定位,揭示了一个最初被认为是t(3;5)(p25;q35)的部分隐匿性3向易位,即t(3;5;11)(p25;q35;p15)。这种易位产生了2种读框内融合转录本的表达,即新的ANKRD28-NUP98和NUP98-NSD1,以及1种读框外的NSD1-ANKRD28转录本。与空载体转染对照相比,ANKRD28-NUP98在NIH/3T3细胞中的瞬时过表达,但不是ANKRD28的C端缺失突变体(DeltaC-ANKRD28),导致集落形成显著增加。ANKRD28-NUP98定位于核仁和细胞质,而ANKRD28和DeltaC-ANKRD28仅存在于细胞质中。在这种情况下,ANKRD28亚细胞定位的改变可能促成了白血病的发生。本报告首次报道ANKRD28作为NUP98融合伴侣,且该病例提示这种融合可能与血液系统恶性肿瘤有关。