Ma Shi Liang, Sørensen Annette Balle, Kunder Sandra, Sørensen Karina Dalsgaard, Quintanilla-Martinez Leticia, Morris David W, Schmidt Jörg, Pedersen Finn Skou
Department of Molecular Biology, University of Aarhus, C.F. Møllers Alle, Bldg. 130, DK-8000 Aarhus C, Denmark.
Virology. 2006 Sep 1;352(2):306-18. doi: 10.1016/j.virol.2006.05.006. Epub 2006 Jun 15.
ICSBP (interferon consensus sequence binding protein)/IRF8 (interferon regulatory factor 8) is an interferon gamma-inducible transcription factor expressed predominantly in hematopoietic cells, and down-regulation of this factor has been observed in chronic myelogenous leukemia and acute myeloid leukemia in man. By screening about 1200 murine leukemia virus (MLV)-induced lymphomas, we found proviral insertions at the Icsbp locus in 14 tumors, 13 of which were mature B-cell lymphomas or plasmacytomas. Only one was a T-cell lymphoma, although such tumors constituted about half of the samples screened. This indicates that the Icsbp locus can play a specific role in the development of mature B-lineage malignancies. Two proviral insertions in the last Icsbp exon were found to act by a poly(A)-insertion mechanism. The remaining insertions were found within or outside Icsbp. Since our results showed expression of Icsbp RNA and protein in all end-stage tumor samples, a simple tumor suppressor function of ICSBP is not likely. Interestingly, proviral insertions at Icsbp have not been reported from previous extensive screenings of mature B-cell lymphomas induced by endogenous MLVs. We propose that ICSBP might be involved in an early modulation of an immune response to exogenous MLVs that might also play a role in proliferation of the mature B-cell lymphomas.
ICSBP(干扰素共有序列结合蛋白)/IRF8(干扰素调节因子8)是一种主要在造血细胞中表达的γ干扰素诱导转录因子,在人类慢性粒细胞白血病和急性髓细胞白血病中已观察到该因子的下调。通过筛选约1200例鼠白血病病毒(MLV)诱导的淋巴瘤,我们在14个肿瘤的Icsbp基因座发现了前病毒插入,其中13个是成熟B细胞淋巴瘤或浆细胞瘤。尽管T细胞淋巴瘤约占筛选样本的一半,但只有1个是T细胞淋巴瘤。这表明Icsbp基因座在成熟B系恶性肿瘤的发生发展中可能发挥特定作用。发现在Icsbp最后一个外显子中的两个前病毒插入通过聚腺苷酸插入机制起作用。其余插入位于Icsbp内部或外部。由于我们的结果显示在所有终末期肿瘤样本中都有Icsbp RNA和蛋白质表达,因此ICSBP不太可能具有简单的肿瘤抑制功能。有趣的是,在内源性MLV诱导的成熟B细胞淋巴瘤的先前广泛筛选中,尚未报道Icsbp处的前病毒插入。我们提出,ICSBP可能参与对外源MLV免疫反应的早期调节,这也可能在成熟B细胞淋巴瘤的增殖中起作用。