Nahon J L, Gal A, Erdos T, Sala-Trepat J M
Proc Natl Acad Sci U S A. 1984 Aug;81(16):5031-5. doi: 10.1073/pnas.81.16.5031.
We have examined the DNase I sensitivity of the albumin and alpha-fetoprotein (AFP) genes in different rat tissues (adult liver and kidney) and cloned cell lines (hepatoma 7777-C8, JF1 fibroblasts), which show drastic differences in the level of expression of these two genes. This was done by studying the disappearance of defined restriction endonuclease fragments of these genes as a function of limited DNase I digestion. The sensitivity of these genes was compared to that of a gene not expressed in the hepatic cells and to that of a ubiquitously expressed gene. In nuclei from adult rat liver the albumin and AFP genes were preferentially degraded by the nucleolytic action of DNase I, whereas they were not in rat kidney nuclei. In the hepatoma cells the AFP gene was much more sensitive to DNase I digestion than the albumin gene; both genes were very resistant to DNase I action in fibroblastic nuclei. When analyzed in relation to the level of gene expression our results indicate that alterations in the chromatin structure of the albumin and AFP genes might be involved in the early establishment of the tissue-specific potential of overt gene expression; such alterations reflected in an altered DNase I sensitivity do not appear to be responsible for the changes in gene activity occurring during the terminal differentiation of the hepatocyte; and modifications in the chromatin structure of these genes might occur during oncogenic events; these structural modifications could be related to the changes in gene expression observed in hepatocarcinogenic processes.
我们检测了白蛋白和甲胎蛋白(AFP)基因在不同大鼠组织(成年肝脏和肾脏)以及克隆细胞系(肝癌7777-C8、JF1成纤维细胞)中的DNase I敏感性,这些组织和细胞系中这两个基因的表达水平存在显著差异。通过研究这些基因特定限制性内切酶片段随有限DNase I消化的消失情况来进行检测。将这些基因的敏感性与肝细胞中不表达的一个基因以及一个普遍表达的基因的敏感性进行了比较。在成年大鼠肝脏的细胞核中,白蛋白和AFP基因优先被DNase I的核酸酶作用降解,而在大鼠肾脏细胞核中则不然。在肝癌细胞中,AFP基因对DNase I消化的敏感性比白蛋白基因高得多;在成纤维细胞核中,这两个基因对DNase I的作用都非常耐受。当结合基因表达水平进行分析时,我们的结果表明,白蛋白和AFP基因染色质结构的改变可能参与了显性基因表达组织特异性潜能的早期确立;这种反映在DNase I敏感性改变上的改变似乎与肝细胞终末分化过程中发生的基因活性变化无关;这些基因的染色质结构修饰可能在致癌事件中发生;这些结构修饰可能与肝癌发生过程中观察到的基因表达变化有关。