Papaconstantinou J, Wong E, Ratrie H, Szpirer C, Szpirer J
Somatic Cell Genet. 1982 May;8(3):363-76. doi: 10.1007/BF01538893.
Hybrids formed by the fusion of mouse hepatoma (BWTG3) and rat fibroblast (JF1) cells exhibit the extinction of mouse albumin and alpha-fetoprotein synthesis. Karyotype analyses suggest that all parental chromosomes are present in the hybrids. The extinction, therefore, of mouse hepatocyte genes is attributed to the inhibitory action of the rat genome. In these studies, we show that these hybrids possess and express the mouse beta-glucuronidase gene (which is encoded on the same chromosome as the mouse albumin and alpha-fetoprotein gene), and we present data of Southern blot analysis which demonstrate that such hybrids have indeed retained both mouse and rat albumin DNA sequences. In addition, using mouse albumin cDNA, we have shown by cDNA-RNA reassociation kinetics that albumin mRNA is virtually absent in these hybrids. We conclude from these studies that the extinction of albumin synthesis involves a mechanism which results in the loss of cytoplasmic albumin mRNA.
由小鼠肝癌细胞(BWTG3)和大鼠成纤维细胞(JF1)融合形成的杂种细胞表现出小鼠白蛋白和甲胎蛋白合成的消失。核型分析表明杂种细胞中存在所有亲代染色体。因此,小鼠肝细胞基因的消失归因于大鼠基因组的抑制作用。在这些研究中,我们表明这些杂种细胞拥有并表达小鼠β-葡萄糖醛酸酶基因(该基因与小鼠白蛋白和甲胎蛋白基因在同一条染色体上编码),并且我们提供了Southern印迹分析数据,这些数据表明此类杂种细胞确实保留了小鼠和大鼠的白蛋白DNA序列。此外,使用小鼠白蛋白cDNA,我们通过cDNA-RNA重缔合动力学表明这些杂种细胞中几乎不存在白蛋白mRNA。我们从这些研究中得出结论,白蛋白合成的消失涉及一种导致细胞质白蛋白mRNA丢失的机制。