Mullins J I, Brody D S, Binari R C, Cotter S M
Nature. 1984;308(5962):856-8. doi: 10.1038/308856a0.
Feline leukaemia virus (FeLV) is epidemiologically associated with induction of the majority of lymphoid tumours of the domestic cat. However, about one-third of these tumours are devoid of exogenous virus or show evidence of virus integration only after tumour outgrowth. To help define the genetic mechanisms of feline lymphomagenesis we have explored here the possibility that cellular oncogenes (c-onc genes) are rearranged in tumour cell DNA. Of 16 FeLV-positive T-cell tumours among 31 naturally occurring lymphomas, 2 showed evidence of recombinant FeLV proviruses containing myc oncogene sequences. One of the two produced a transmissible myc-containing FeLV. In both cases c-myc and its surrounding DNA appeared unaltered. We believe that the association of myc with FeLV may result in its activation and play a part in the development of a significant fraction of cat T-cell lymphomas. Our findings contrast with studies of experimental induction of chicken lymphoma, in which myc activation occurs by retrovirus promoter insertion near c-myc (refs 3-5), rather than by incorporation into virus.
猫白血病病毒(FeLV)在流行病学上与家猫大多数淋巴瘤的诱发有关。然而,这些肿瘤中约三分之一没有外源病毒,或者仅在肿瘤生长后才显示出病毒整合的迹象。为了帮助确定猫淋巴瘤发生的遗传机制,我们在此探讨了细胞癌基因(c-onc基因)在肿瘤细胞DNA中发生重排的可能性。在31例自然发生的淋巴瘤中的16例FeLV阳性T细胞肿瘤中,有2例显示出含有myc癌基因序列的重组FeLV前病毒的证据。这两例中的一例产生了一种可传播的含myc的FeLV。在这两种情况下,c-myc及其周围的DNA似乎未发生改变。我们认为,myc与FeLV的关联可能导致其激活,并在相当一部分猫T细胞淋巴瘤的发展中起作用。我们的发现与鸡淋巴瘤实验诱导的研究形成对比,在鸡淋巴瘤实验诱导中,myc激活是通过逆转录病毒启动子插入c-myc附近(参考文献3 - 5),而不是通过整合到病毒中。