Zhou R P, Kan N, Papas T, Duesberg P
Proc Natl Acad Sci U S A. 1985 Oct;82(19):6389-93. doi: 10.1073/pnas.82.19.6389.
Avian carcinoma virus MH2 contains two potential transforming genes, delta gag-mht and delta gag-myc. Thus, MH2 may be a model for two-gene carcinogenesis in which transformation depends on two synergistic genes. Most other directly oncogenic viruses contain single, autonomous transforming (onc) genes and are models for single-gene carcinogenesis. To determine which role each potential onc gene of MH2 plays in oncogenesis, we have prepared deletion and frameshift mutants of each of the two MH2 genes by in vitro mutagenesis of cloned proviral DNA and have tested transforming function and virus production in cultured primary quail cells. We have found that mht deletion mutants and wild-type virus transform primary cells and that myc deletion and frameshift mutants do not. The morphologies of cells transformed by the mht deletion mutants and by wild-type MH2 are similar yet vary considerably. Nevertheless, typical mutant transformed cells can often be distinguished from cells transformed by wild-type MH2. We conclude that the delta gag-myc gene transforms primary cells by itself, without the second potential onc gene. This myc-related gene is the smallest that has direct transforming function. delta gag-mht is without detectable transforming function but may affect transformation by delta gag-myc. Thus, MH2 behaves like a virus with a single onc gene, although it expresses two potential onc genes, and it appears not to be a model for two-gene carcinogenesis. Further work is necessary to determine whether the delta gag-mht gene possibly enhances oncogenic function of delta gag-myc or has independent oncogenic function in animals.
禽癌病毒MH2含有两个潜在的转化基因,δgag - mht和δgag - myc。因此,MH2可能是双基因致癌作用的一个模型,其中转化依赖于两个协同基因。大多数其他直接致癌病毒含有单个自主转化(致癌)基因,是单基因致癌作用的模型。为了确定MH2的每个潜在致癌基因在致癌过程中所起的作用,我们通过对克隆的前病毒DNA进行体外诱变,制备了这两个MH2基因各自的缺失和移码突变体,并在培养的原代鹌鹑细胞中测试了转化功能和病毒产生情况。我们发现mht缺失突变体和野生型病毒能转化原代细胞,而myc缺失和移码突变体则不能。由mht缺失突变体和野生型MH2转化的细胞形态相似但差异很大。然而,典型的突变体转化细胞通常可以与野生型MH2转化的细胞区分开来。我们得出结论,δgag - myc基因自身就能转化原代细胞,无需第二个潜在致癌基因。这个与myc相关的基因是具有直接转化功能的最小基因。δgag - mht没有可检测到的转化功能,但可能影响δgag - myc的转化作用。因此,MH2的行为类似于具有单个致癌基因的病毒,尽管它表达两个潜在致癌基因,而且它似乎不是双基因致癌作用的模型。有必要进一步开展工作来确定δgag - mht基因是否可能增强δgag - myc的致癌功能,或者在动物中是否具有独立的致癌功能。