Slagle B L, Wheeler D A, Hager G L, Medina D, Butel J S
Virology. 1985 May;143(1):1-15. doi: 10.1016/0042-6822(85)90091-1.
The preneoplastic D-2 hyperplastic outgrowth line, which was derived from a hormone-induced hyperplastic alveolar nodule (HAN) of a BALB/c mouse, was used for a detailed analysis of mouse mammary tumor virus (MMTV) expression. The D-2 HAN line has previously been shown to express viral RNA representative of the entire genome, although viral particles have been noted only rarely. The MMTV-specific mRNA, protein, and DNA content of the D-2 tissues was defined in an effort to better understand the molecular basis of the aberrant virus expression. Northern blotting techniques demonstrated the presence of properly processed 8.9 kb (genomic) and 3.6 kb (envelope) mRNA. Protein electroblotting procedures established the presence of properly processed viral core protein p28. In contrast, the envelope precursor polyprotein was not processed into detectable levels of gp52. Analysis of MMTV proviral content by Southern blot methodology revealed the presence of a newly acquired provirus which serves as a marker for the clonal nature of the D-2 line. The origin of the new provirus is unknown. Methylation studies established that the new proviral insert is hypomethylated and, therefore, is likely serving as the template for the MMTV expression observed in the D-2 HAN line. These characteristics of the D-2 line make it an excellent system in which to study the role, if any, of MMTV in the progression of D-2 preneoplastic tissues to the tumor phenotype.
前肿瘤性D - 2增生性外生细胞系源自BALB/c小鼠的激素诱导增生性肺泡结节(HAN),用于对小鼠乳腺肿瘤病毒(MMTV)表达进行详细分析。此前已表明D - 2 HAN细胞系表达代表整个基因组的病毒RNA,尽管仅很少观察到病毒颗粒。确定了D - 2组织中MMTV特异性mRNA、蛋白质和DNA的含量,以更好地理解异常病毒表达的分子基础。Northern印迹技术证明存在经过正确加工的8.9 kb(基因组)和3.6 kb(包膜)mRNA。蛋白质电印迹程序确定存在经过正确加工的病毒核心蛋白p28。相比之下,包膜前体多蛋白未加工成可检测水平的gp52。通过Southern印迹法分析MMTV前病毒含量,发现存在一种新获得的前病毒,它是D - 2细胞系克隆性质的标志物。新前病毒的起源尚不清楚。甲基化研究表明新的前病毒插入片段是低甲基化的,因此可能是D - 2 HAN细胞系中观察到的MMTV表达的模板。D - 2细胞系的这些特征使其成为一个极好的系统,可用于研究MMTV在D - 2前肿瘤组织发展为肿瘤表型过程中(如果有)所起的作用。