Nahon J L, Venetianer A, Sala-Trepat J M
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2135-9. doi: 10.1073/pnas.84.8.2135.
We have examined the chromatin structure of the 5'-flanking region of the albumin and alpha-fetoprotein (Afp) genes in different developing rat tissues and cloned cell lines that display various functional states of these genes. Nuclease-hypersensitive sites were probed with DNase I, using an indirect end-labeling technique. In albumin-producing rat cells two major DNase I-hypersensitive sites were found near the promoter region and one additional site was located approximately 3 kilobases (kb) upstream. Similarly, in Afp-producing rat tissues and cell lines we mapped one DNase I-hypersensitive region close to the promoter region and two cleavage sites further upstream at approximately 2.2 and approximately 3.8 kb from the cap site. The DNase I-hypersensitive sites of both genes were absent in nonhepatic rat cells and therefore appear to be tissue specific. Loss of specific sets of DNase I-hypersensitive sites accompanies the cessation of transcription for the Afp gene in adult rat liver and in a "dedifferentiated" hepatoma cell line. Likewise, specific sets of DNase I-hypersensitive sites disappear during the inactivation of the albumin gene in hepatoma cells. The distal upstream sites of the Afp and albumin genes display the same DNase I sensitivity in expressing and potentially expressible states. These findings suggest that reversible changes in short chromatin regions may be involved in the actual transcription of the albumin and Afp genes, while more permanent tissue-specific changes at other sites correlate with the capacity of these genes to be expressed during hepatic differentiation and neoplasia.
我们研究了不同发育阶段大鼠组织及克隆细胞系中白蛋白和甲胎蛋白(Afp)基因5'侧翼区的染色质结构,这些细胞系展现出这些基因的各种功能状态。使用间接末端标记技术,用DNase I探测核酸酶超敏位点。在产生白蛋白的大鼠细胞中,在启动子区域附近发现了两个主要的DNase I超敏位点,另外一个位点位于上游约3千碱基(kb)处。同样,在产生Afp的大鼠组织和细胞系中,我们绘制了一个靠近启动子区域的DNase I超敏区域以及两个位于上游更远位置的切割位点,分别距离帽位点约2.2 kb和约3.8 kb。这两个基因的DNase I超敏位点在非肝大鼠细胞中不存在,因此似乎具有组织特异性。在成年大鼠肝脏和一个“去分化”的肝癌细胞系中,随着Afp基因转录的停止,特定的DNase I超敏位点组会消失。同样,在肝癌细胞中白蛋白基因失活期间,特定的DNase I超敏位点组也会消失。Afp和白蛋白基因的远端上游位点在表达状态和潜在可表达状态下表现出相同的DNase I敏感性。这些发现表明,短染色质区域的可逆变化可能参与了白蛋白和Afp基因的实际转录,而其他位点更持久的组织特异性变化与这些基因在肝脏分化和肿瘤形成过程中表达的能力相关。