Nakayama H, Ishimaru F, Katayama Y, Nakase K, Sezaki N, Takenaka K, Shinagawa K, Ikeda K, Niiya K, Harada M
Department of Medicine, University of Okayama, Okayama, Japan.
Exp Hematol. 2000 Nov;28(11):1232-8. doi: 10.1016/s0301-472x(00)00530-0.
The Ikaros gene has been implicated in lymphoid development and proliferation from the results of gene targeting studies in mice. Recently we reported that the Ikaros gene may be involved in the disease progression of chronic myelogenous leukemia (CML). In this report, we investigated Ikaros isoforms in human non-lymphoid leukemia cell lines and normal granulocyte/macrophage (CFU-GM) and erythroid (BFU-E)-derived colonies. We evaluated Ikaros gene expression by RT-PCR, Southern blotting, sequencing analysis, Northern blotting, and immunoblotting.Ikaros isoforms Ik-1 and Ik-2, 3 were predominantly expressed in human non-lymphoid leukemia cell lines. Ik-4 and Ik-8 were also detectable as a minor population. In contrast to the previous report in mice, multiple Ikaros isoforms were expressed in human CFU-GM and BFU-E-derived colonies, and the dominant-negative isoform Ik-6 was not detectable. We also showed that human Ikaros isoforms contained an additional coding sequence in the N-terminal region, which was highly homologous to the sequence reported in mice. These observations suggest that the Ikaros gene may play some role in the development of human non-lymphoid lineage hematopoiesis. Moreover, the finding that the dominant-negative isoform Ik-6, which was overexpressed in patients with blast crisis of CML, was rarely detectable in non-lymphoid lineages supports its pathogenetic role in human hematologic malignancies.
从小鼠基因靶向研究结果来看,Ikaros基因与淋巴细胞发育和增殖有关。最近我们报道Ikaros基因可能参与慢性粒细胞白血病(CML)的疾病进展。在本报告中,我们研究了人非淋巴细胞白血病细胞系以及正常粒细胞/巨噬细胞(CFU-GM)和红系(BFU-E)来源集落中的Ikaros异构体。我们通过逆转录聚合酶链反应(RT-PCR)、Southern印迹法、测序分析、Northern印迹法和免疫印迹法评估Ikaros基因表达。Ikaros异构体Ik-1、Ik-2和Ik-3在人非淋巴细胞白血病细胞系中主要表达。Ik-4和Ik-8也可作为少数群体被检测到。与之前关于小鼠的报道不同,多种Ikaros异构体在人CFU-GM和BFU-E来源的集落中表达,且未检测到显性负性异构体Ik-6。我们还表明,人Ikaros异构体在N端区域含有一个额外的编码序列,该序列与小鼠中报道的序列高度同源。这些观察结果表明,Ikaros基因可能在人非淋巴细胞系造血发育中发挥某种作用。此外,在CML急变期患者中过表达的显性负性异构体Ik-6在非淋巴细胞系中很少被检测到这一发现,支持了其在人类血液系统恶性肿瘤中的致病作用。