Belli B, Wolff L, Nazarov V, Fan H
Department of Molecular Biology and Biochemistry, University of California, Irvine 92717, USA.
J Virol. 1995 Aug;69(8):5138-41. doi: 10.1128/JVI.69.8.5138-5141.1995.
Moloney murine leukemia virus induces myeloid leukemia when inoculated intravenously into pristane-primed adult BALB/c mice. One hundred percent of these tumors show insertional activation of the c-myb proto-oncogene, and reverse transcriptase PCR assays have shown that the c-myb activation could be detected soon after infection. We tested BALB/c and NIH Swiss mice that had been inoculated as newborns with Moloney murine leukemia virus, under which conditions they develop T lymphomas exclusively. Reverse transcriptase-PCR assays indicated that c-myb activations were detectable soon after neonatal infection. However, none of the resulting T lymphomas contained c-myb activations. The implications of these results to the timing of proto-oncogene activations in leukemogenesis and the specificity of proto-oncogene activations for different diseases are discussed.
将莫洛尼鼠白血病病毒静脉注射到用 pristane 预处理的成年 BALB/c 小鼠体内时,可诱发髓系白血病。这些肿瘤中有 100% 显示 c-myb 原癌基因的插入激活,逆转录酶 PCR 分析表明,感染后不久即可检测到 c-myb 的激活。我们测试了新生时接种莫洛尼鼠白血病病毒的 BALB/c 和 NIH 瑞士小鼠,在这种情况下它们仅发生 T 淋巴瘤。逆转录酶 -PCR 分析表明,新生感染后不久即可检测到 c-myb 的激活。然而,所产生的 T 淋巴瘤均未出现 c-myb 的激活。本文讨论了这些结果对白血病发生中原癌基因激活时间以及不同疾病中原癌基因激活特异性的影响。