Cuypers H T, Selten G, Quint W, Zijlstra M, Maandag E R, Boelens W, van Wezenbeek P, Melief C, Berns A
Cell. 1984 May;37(1):141-50. doi: 10.1016/0092-8674(84)90309-x.
A number of mink cell focus-forming (MCF) proviruses was molecularly cloned from mouse lymphoma DNA. From each clone, flanking probes were prepared to detect common integration regions in other MuLV-induced lymphomas. One clone frequently revealed variations in the molecular structure of the corresponding region (Pim-1) in other lymphomas. The results show the following. Changes in the Pim region are seen in 24 out of 93 lymphomas tested. Over 50% of the early T-cell lymphomas show integration in the Pim-1 region. The alterations are seen in different mouse strains and with various MuLVs. The observed variations are caused by the integration of predominantly MCF genomes. All integrations occur in a region spanning less than 20 kb and are associated with the transcriptional activation of a distinct region within the Pim-1 domain. The activated region does not show any homology with 13 known and three putative oncogenes.
从鼠淋巴瘤DNA中分子克隆出了一些貂细胞集落形成(MCF)前病毒。从每个克隆中制备侧翼探针,以检测其他莫氏白血病病毒(MuLV)诱导的淋巴瘤中的共同整合区域。一个克隆在其他淋巴瘤中经常显示出相应区域(Pim-1)分子结构的变异。结果如下。在93个测试的淋巴瘤中,有24个出现了Pim区域的变化。超过50%的早期T细胞淋巴瘤显示在Pim-1区域整合。这些改变在不同的小鼠品系和各种MuLV中均可见。观察到的变异主要是由MCF基因组的整合引起的。所有整合都发生在一个跨度小于20 kb的区域,并且与Pim-1结构域内一个独特区域的转录激活相关。激活区域与13个已知的和3个推定的癌基因没有任何同源性。