Nazarov V, Wolff L
Laboratory of Genetics, National Cancer Institute, Bethesda, Maryland 20892-4255, USA.
J Virol. 1995 Jun;69(6):3885-8. doi: 10.1128/JVI.69.6.3885-3888.1995.
In BALB/c nu/nu and sublethally irradiated DBA/2 mice, promonocytic leukemia was induced by intravenous inoculation of Friend murine leukemia virus (F-MuLV) strain C57 in conjunction with intraperitoneal injection of pristane. These tumors appear to be identical morphologically to previously reported ones induced by other MuLVs, such as Moloney, amphotropic 4070A, and F-MuLV FB29, which most commonly have provirus integrations in the 5' end of the c-myb locus. Interestingly, 2 of the 16 F-MuLV-induced tumors had viruses integrated in the distal 3' end of c-myb. To determine the precise locations of these integrations, it was necessary to clone sequences encoding the 3' c-myb exons and to prepare a physical map of this region. Exons 10 to 15 were positioned on the map, and it was found that the proviruses in the aforementioned tumors were located within narrow region in the beginning of the large (greater than 11 kb) intron 14. The predicted protein product encoded by the affected alleles is truncated by 38 amino acids. This represents a novel virus integration site which is most likely associated with oncogenic activation of the c-myb gene during leukemogenesis.
在BALB/c裸鼠和亚致死剂量照射的DBA/2小鼠中,通过静脉注射Friend鼠白血病病毒(F-MuLV)C57株并腹腔注射 pristane 诱导前单核细胞白血病。这些肿瘤在形态上似乎与先前报道的由其他MuLV诱导的肿瘤相同,例如莫洛尼病毒、嗜双性4070A病毒和F-MuLV FB29,它们最常见的情况是在c-myb基因座的5'端有前病毒整合。有趣的是,16个F-MuLV诱导的肿瘤中有2个病毒整合在c-myb的3'远端。为了确定这些整合的精确位置,有必要克隆编码c-myb 3'外显子的序列并绘制该区域的物理图谱。外显子10至15定位在图谱上,并且发现上述肿瘤中的前病毒位于大的(大于11 kb)内含子14起始处的狭窄区域内。受影响等位基因编码的预测蛋白质产物被截短了38个氨基酸。这代表了一个新的病毒整合位点,很可能与白血病发生过程中c-myb基因的致癌激活有关。