Scheijen B, Jonkers J, Acton D, Berns A
Division of Molecular Genetics, The Netherlands Cancer Institute, Amsterdam.
J Virol. 1997 Jan;71(1):9-16. doi: 10.1128/JVI.71.1.9-16.1997.
Insertional mutagenesis with Moloney murine leukemia virus (MoMLV) in c-myc and Pim-1 transgenic mice permits the identification of oncogenes that collaborate with the transgenes in lymphomagenesis. The recently identified common insertion site pal-1, in MoMLV-induced lymphomas, is located in a region in which several independent integration clusters are found: eis-1, gfi-1, and evi-5. Proviral insertions of MoMLV in the different integration clusters upregulate the transcriptional activity of the Gfi-1 gene, which is located within the pal-1 locus. The eis-1/pal-1/gfi-1/evi-5 locus serves as a target for MoMLV proviral insertions in pre-B-cell lymphomas of Emu-myc transgenic mice (20%) and in T-cell lymphomas of H-2K-myc (75%) and Emu-pim-1 (93%) transgenic mice. Many tumors overexpress both Gfi-1 as well as Myc and Pim gene family members, indicating that Gfi-1 collaborates with Myc and Pim in lymphomagenesis. Proviral integrations in the previously identified insertion site bmi-1 are, however, mutually exclusive with integrations in the eis-1/pal-1/gfi-1/evi-5 locus. This finding suggests that Bmi-1 and Gfi-1 belong to the same complementation group in lymphoid transformation.
利用莫洛尼鼠白血病病毒(MoMLV)对c-myc和Pim-1转基因小鼠进行插入诱变,可鉴定出在淋巴瘤发生过程中与转基因协同作用的癌基因。在MoMLV诱导的淋巴瘤中最近鉴定出的常见插入位点pal-1,位于一个发现了几个独立整合簇的区域:eis-1、gfi-1和evi-5。MoMLV在前病毒插入不同的整合簇中会上调位于pal-1基因座内的Gfi-1基因的转录活性。在Emu-myc转基因小鼠的前B细胞淋巴瘤(20%)以及H-2K-myc(75%)和Emu-pim-1(93%)转基因小鼠的T细胞淋巴瘤中,eis-1/pal-1/gfi-1/evi-5基因座是MoMLV前病毒插入的靶点。许多肿瘤同时过度表达Gfi-1以及Myc和Pim基因家族成员,这表明Gfi-1在淋巴瘤发生过程中与Myc和Pim协同作用。然而,在先前鉴定的插入位点bmi-1处的前病毒整合与在eis-1/pal-1/gfi-1/evi-5基因座的整合相互排斥。这一发现表明,在淋巴细胞转化过程中,Bmi-1和Gfi-1属于同一互补群。