Michalides R, Wagenaar E, Hilkens J, Hilgers J, Groner B, Hynes N E
J Virol. 1982 Sep;43(3):819-29. doi: 10.1128/JVI.43.3.819-829.1982.
Male mice of strain GR develop T-cell leukemia at a low frequency late in life. These leukemia cells contain large amounts of mouse mammary tumor virus (MMTV) RNA and MMTV proteins in a precursor form (Nusse et al., J. Virol. 32:251-258, 1979). We used restriction enzyme analysis and molecular hybridization to identify MMTV proviruses in the DNA of these leukemia cells. GR leukemia cells contained additional integrated MMTV proviruses at various sites in the genome. This amplification of MMTV proviruses in GR leukemia cells is not restricted to one particular endogenous MMTV provirus of strain GR. The number and location of the extra MMTV proviruses present in transplants of GR leukemia cells did not change upon serial transplantation of the leukemia cells. Acquisition of MMTV proviruses was also found in a similar leukemia, L1210 of the DBA/2 mouse strain, but not in three other leukemias, SL2 of DBA/2, BW5147 of AKR, and a spontaneous thymoma of BALB/c. The two main classes of MMTV RNA, 35S and 24S, were present in the cytoplasmic RNA of GR leukemia cells, indicating that the aberrant processing of MMTV precursor proteins is not due to anomolously sized RNAs. We could not detect extra RNAs in GR leukemia cells which would represent read-through transcripts of cellular genes adjacent to the extra MMTV proviruses, initiated by a promoter signal in the right MMTV long terminal repeat sequence. These data suggest that acquisition of MMTV proviruses may coincide with the onset of leukemogenesis in GR male mice.
GR品系的雄性小鼠在生命后期会以较低频率发生T细胞白血病。这些白血病细胞含有大量处于前体形式的小鼠乳腺肿瘤病毒(MMTV)RNA和MMTV蛋白(努斯等人,《病毒学杂志》32:251 - 258,1979年)。我们使用限制性内切酶分析和分子杂交技术来鉴定这些白血病细胞DNA中的MMTV前病毒。GR白血病细胞在基因组的不同位点含有额外整合的MMTV前病毒。GR白血病细胞中MMTV前病毒的这种扩增并不局限于GR品系的一种特定内源性MMTV前病毒。GR白血病细胞移植中存在的额外MMTV前病毒的数量和位置在白血病细胞的连续移植后并未改变。在DBA/2小鼠品系的类似白血病L1210中也发现了MMTV前病毒的获得,但在其他三种白血病中未发现,即DBA/2的SL2、AKR的BW5147以及BALB/c的自发性胸腺瘤。MMTV RNA的两种主要类别,35S和24S,存在于GR白血病细胞的细胞质RNA中,这表明MMTV前体蛋白的异常加工并非由于异常大小的RNA所致。我们在GR白血病细胞中未检测到额外的RNA,这些RNA可能代表由右侧MMTV长末端重复序列中的启动子信号引发的、与额外MMTV前病毒相邻的细胞基因的通读转录本。这些数据表明,MMTV前病毒的获得可能与GR雄性小鼠白血病发生的起始同时发生。